Treinamento de Força e Hipertrofia HOMEOSTASE
Transcription
Treinamento de Força e Hipertrofia HOMEOSTASE
9/24/14& Modelo&de&Ganhos&de&Força& Musculação¶&Academia:& treinamento&de&força&e&hipertrofia&& & Prof.&Dr.&Carlos&Ugrinowitsh& Sale,&1992& Unidade Motora Placa Motora Neurônio Motor Fibra Muscular 1& 9/24/14& Limiar&de&A*vação Alta&Força Alta Alta&Potência Hipertrofia&Muscular& 1RM 5RM Moderada 10&RM 15&RM Baixa 20&RM Unidade&Motora& Tipo&I &Tipo&II Tesch&et&al.,&JSCR&&1998 Goldspink,&1992 Músculo - Idoso Músculo - Jovem Proximal Proximal Medial Medial Distal Distal 2& 9/24/14& Músculo&K&Treino& Síntese&Proteíca& Tang&et&al.,&2008& Vias&do&Trofismo&Celular& Glass&et&al.,&2005& KNIGHT&&&&KOTHARY&2011& 3& 9/24/14& Células Satélites Domínio Nuclear e Hipertrofia • Cada núcleo é responsável por um determinado volume de sarcoplasma. Essa proporção é mantida constante mesmo com a hipertrofia • Então, para haver hipertrofia é necessário primeiro adicionar núcleo à célula muscular • O núcleo irá aumentar a síntese das proteínas contráteis Deschenes & Kraemer, 2002 Domínio Mionuclear Hipertrofia Alterações com o Treinamento de Força • Para que haja hipertrofia as células satélites precisam adicionar núcleo ás células musculares para que haja um aumento da síntese protéica Hawke, 2005 Kadi et al., 2004 4& 9/24/14& Alterações com o Treinamento de Força • Somente&quando&a&hipertrofia&foi&maior&que&&& ~&20%&é&que&as&células&satélites&par]ciparam& do&processo&de&hipertrofia& Kadi et al., 2004 Fatores&que&“&parecem”&gerar& hipertrofia&muscular& • • • • Dano&muscular& Hipóxia& Alongamento& Escmulo&mecânico& Volume&Total& • Séries&x&repe*ções&x&carga&(kg)& 3&x&10&x&100&kg&=&3.000&kg& ACSM,&2009& 5& 9/24/14& Excêntrico x Concêntrico Ações excêntricas produzem mais força, com ativação muscular semelhante Linnamo et al., 2000 Relação Força - Comprimento • Ações musculares excêntricas usam tanto a força produzida ativa quanto passivamente • A força passiva é produzida pelo tecido conectivo que envolve o tecido muscular, proteínas do citoesqueleto e tendões Tensão Ativa e Passiva Miosina Força (N) Força (% máximo) Actina Por que somos capazes de produzir mais tensão em ações musculares excêntricas do que concêntricas? Comprimento (cm) Enoka, 2003 6& 9/24/14& Ação Muscular Excêntrica Dano Muscular • Marcadores Diretos • Então…. – A tensão passiva pode sobrecarregar as proteínas do citoesqueleto produzindo dano estrutural – Essa sobrecarga parece ocorrer na fase descendente da curva força-comprimento – O dano estrutural produz uma série de sintomas conhecidos como Dor Muscular Tardia Dano Muscular – Marcadores Indiretos • Exercício&excêntrico& aumenta&CK&sérica& • Exercício&concêntrico&não& aumenta&CK&sérica& – Alterações na linha Z – Ruptura da desmina • Marcadores Indiretos – Perda de força – Edema – Diminuição da amplitude do movimento – Vazamento de proteínas intramusculares – Dor muscular tardia – Pico de torque em maior ângulo do movimento Dano Muscular – Marcadores Indiretos • CK plasmática é mais alta após exercício excêntrico de intensidade máxima que submáxima (50% max) Linnamo et al., 2000 Nosaka & Newton, 2002 7& 9/24/14& Marcados Indiretos de Dano e Velocidade da Ação Excêntrica Ações Excêntricas 80.00 • Exercício excêntrico veloz não produz diferenças 70.00 * * 60.00 Torque (N.m) • A acentuação da sobrecarga excêntrica produziu maiores ganhos no supino que uma sobrecarga regular * Ecc60 50.00 Ecc180 40.00 – Na diminuição da força – Aumento da CK 30.00 20.00 pre pos 48 96 Time 40000.00 * * CK (U/L) 30000.00 Doan et al., 2002 20000.00 Ecc60 Ecc180 10000.00 0.00 Barroso et al., 2008 pre pos 24 48 72 96 -10000.00 Tim e Intensidade do Treinamento e Marcadores Indiretos Table 3: Mean and range (in the parentheses) of plasma CK activity of subjects for the baseline (Pre) and peak values following exercise for the control, 50%1RM, 75%-1RM, 90%-1RM, and 110 %-1RM groups. * indicates a significant (P<0.05) difference from the pre-value. Pre Peak CONTROL 187 (117 - 210) 238 (153 - 356) 50%-1RM 213 (43 - 200) 535 (109 - 919)* 75%-1RM 157 (91 - 201) 668 (192 – 1353)* 90%-1RM 178 (118 - 241) 311 (240 - 518)* 110%-1RM 151 (49 - 205) 623 (317 - 3110)* • Intensidades distintas de supino produziram aumentos similares na CK quando o volume total foi equalizado (2000 kg) Uchida&et&al.,&2009& Dano Muscular • Durante a parte descendente da curva força x coprimento, os sarcômeros não são alongados uniformemente • Alguns desses sarcômeros são alongados além do ponto de sobreposição de actina e miosina Friden & Liber, 2001 8& 9/24/14& Efeito do Exercício Repetido • A diminuição da força muscular e os sintomas associados ao dano muscular após exercício excêntrico são menos pronunciados após a segunda sessão de exercício Efeito do Exercício Repetido (EER) • Há evidências de que exercícios excêntricos máximo e sub-máximo, concêntrico e isométrico produzem o efeito do exercício repetido Lavander & Nosaka, 2008 Kim, Ugrinowitsch, Craig, 2009 Lavander & Nosaka, 2008 Diminuição da Produção de Força após Exercício Excêntrico Table 2 – Percentual MVIC (mean± sd) after performing 3 bouts * p<0.05 comparing to pre-values of each bout # p<0.05 compared to the same time point in bout 1 Bout 1 2 3 pre 100 (0.0) 100 (0.0) 100 (0.0) Time pos 48h 65.3 63.6 (8.2) * (14.0) * 78.4 94.6 (7.0) * (9.1) # 72.9 89.1 (16.4) * (11.3) *# 96h 67.3 (19.2) * 102.2 (11.7) # 102.8 (11.2) # Barroso et al., 2008 EER– Linha Z • Não houve ondulação significante da linha Z após a primeira sessão de exercício • Não houve diferença entre os gêneros Stupka et al., 2001 9& 9/24/14& EER- Variação de Exercício • A variação de exercício pode aumentar o estresse em diferentes porções do músculo evitando a ocorrência do EER EER – Variação de Exercícios • A variação do exercício entre sessões de treinamento não aumentou a magnitude dos sintomas de dano muscular após a segunda sessão • Essa adaptação parece ser importante já que o dano muscular está associado à hipertrofia muscular Ugrinowitsch & Kim Dano Muscular Dano Muscular – Marcadores Diretos Linha Z intacta Linha Z rompida Linha Z destruída Crameri et al., 2007 10& 9/24/14& Dano Muscular- Desmina Dano Muscular – Estrutura do Sarcômero • Há regiões de alargamento da linha Z e regiões de linhas Z duplas • Regiões de linha Z duplas indicam a formação de novos sarcômeros Barash et al., 2002 Dano Muscular x Remodelagem Muscular Yu et al., 2004 Dano Muscular x Remodelagem Muscular • A microscopia dos sarcômeros e os dados de actinina e desmina (não mostrados) indicam que não há dano muscular, mas sim aumento da remodelagem com a adição de novos sarcômeros após o exercício excêntrico • Flechas indicam áreas em que novos sarcômeros foram adicionados à miofibrila Yu et al., 2004 Yu et al., 2004 11& No soreness 0 1 2 3 4 5 6 7 Training week 8 9 10 11 Fig. 4: Values of perceived muscle soreness as measured on a visual analog scale (fixed-length line) assessed before each workout session (N 7 each group; ±s.e.m.). Values remained relatively low throughout the 12-week training period for the PT group, but higher levels of soreness were recorded in weeks 4–7 for the NA group, with a statistical difference (*) in week 4 (P 0.022). 9#%8##.' /,1)3*' 8&*' .1%' *%&%-*%-+&$$5' *-/.-2-+&.%' =$ A:RZV>: !%,#./%4'-.+,#&*#0'21,'&$$'3&,%-+-3&.%*'-.'%4#'*%)05'T'%4#'`X'/,1)3 *418#0'&'(#&.'@Ri'-.+,#&*#7'&.0'%4#'HG'/,1)3'&'@Vi'-.+,#&*#I &' 3&-,8-*#' +1(3&,-*1.' 12' %4#' %81' /,1)3*' *418#0' .1' *%&%-*%-+&$ 0-22#,#.+#'=X&9$# @>: LNOMDU&'`PJ'&.&$5*-*'12'%4#'9-13*-#*'%&"#.'-.'8##"B'*418#0 %4&%'&$$'@B'=*#6#.'3,#D'&.0'*#6#.'31*%D9-13*-#*'21,'#&+4'/,1)3>'+?HG *&(3$#*'/#.#,&%#0'+1,,#+%'3,10)+%'8-%4'(#&*),&9$#'+,1**-./'31-.%*: H1,(&$-C#0'LNODMU&'(JHG'$#6#$*'-.+,#&*#0'-.'&$$'*)9d#+%*:'L.'%4# `X'/,1)37'%4#'3,#f31*%'*4-2%'8&*'&'RRi'-.+,#&*#'=$ A:AA]'0#%#,(-.#0 Is 95'(#&.*'12'&'%81D%&-$#0'#D%#*%>'&.0'BRi'-.+,#&*#'-.'%4#'HG'/,1)3 muscle damage required for muscle remodeling? 677 =$ A:AA@>:' g4-$#' %4#*#' -.+,#&*#*' 8#,#' *%&%-*%-+&$$5' *-/.-2-+&.% Table 1. Participant demographics pre-training 8-%4-.'91%4'/,1)3*'+1(3&,#0'8-%4'%4#-,'9&*#$-.#'6&$)#*7'8#'0#%#+%#0 Age (years) Height (cm) Mass (kg) Quadriceps strength (N) .1' 0-22#,#.+#' 9#%8##.' p (PT) 20.3±4 172±13 68.2±7.3%41*#' *4-2%*' +1(3&,-./' 105±65 /,1)3*' =$ A:MB] ) 19.7±3 170±10 70.4±9.5 108±81 0#%#,(-.#0'%4,1)/4'&'1.#D%&-$#07'%53# M'#D%#*%>: ht, mass and quadriceps strength of the PT and NA groups (N 14, ±s.e.m.) before the 12-week resistance training period. c6#,&$$7'%4#'%1%&$'81,"'#221,%'#<3#.0#0'16#,'%4#'MMD8##"'%,&-.-./ *#**-1.'8&*'-0#.%-+&$'21,'91%4'/,1)3*:'E5'+1.%,&*%7'()*+$#'0&(&/# ]!7' R!DXXPGGGXNXGPXXP'PXXPXNNNXPXD]!I 8#,#' )*#0' %1' +1(3&,#' (#&.' /,1)3' &.0' 3#,D*)9d#+%' 3,#D' 1,' 31*%D ' =3#3%-05$3,1$5$' -*1(#,&*#' G>7' @@@D93e' R!DNPG'D .1,(&$-C#0'LNODMU&'(JHG',&%-1'$#6#$*'-.'%4#'%81'9-13*5'*&(3$#*: 8&*'*%&%-*%-+&$$5'0-22#,#.%'9#%8##.'%4#'/,1)3*'T'8-%4'%4#'HG'/,1)3 PXNNPGXPD]!7' R!DXPNGNXX'NXPPG'PGNX'D *418-./'0#(1.*%,&9$#'*5(3%1(*'12'()*+$#'0&(&/#'&.0'*1,#.#**7 RESULTS J`^M]&' =,-91*1(&$' 3,1%#-.' ^M]&>7' MKZD93e 84#,#&*'%4#'`X'/,1)3'#<3#,-#.+#0'.1'*5(3%1(*'12'#-%4#,'0&(&/# E1%4'%4#'3,#D%,&-.#0'=`X>'/,1)3'&.0'%4#'.&-6#'=HG>'/,1)3'+1(3,-*#0 NNGXNGGPGPPGGPD]!7' R!DXNPPNXP'GGGPG'D %4,##'81(#.'&.0'21),'(#.:'X4#'(#&.'&/#7'9105'(&**7'4#-/4%'&.0 PD]!:'G33,1<-(&%#$5'@R ./'+?HG'8&*')*#0'-.'#&+4 1,'*1,#.#**:'L.0#3#.0#.%'12'$#6#$*'12'-.-%-&$'0&(&/#7'%4#'+4&./#*'-. F)&0,-+#3*'61$)(#'8#,#'*%&%-*%-+&$$5'%4#'*&(#'21,'91%4'/,1)3*'9#21,# +%-1.:'X4#'*&(#'(-<'3#,'+?HG'*&(3$#'=+1.%&-.-./ ()*+$#'61$)(#7'/,18%4'2&+%1,'$#6#$*'&.0'F)&0,-+#3*'*%,#./%4'8#,# %,&-.-./'=X&9$# M>: <+#3%'`PJ'3,-(#,*>'8&*')*#0'21,'91%4'%4#'LNODMU& L.+,#&*-./' 81,"' %1%&$*' 8#,#' 19*#,6#0' %4,1)/41)%' %4#' *%)05' 21, ' %4#' `PJ' ,).*' 12' %4#' %81' .1,(&$-C#,' %,&.*+,-3%*: %4#'*&(#'21,'91%4'/,1)3*: #*'=$1/'+?HG'!" +,1**-./D31-.%'+5+$#'.)(9#,>'8#,# 5'%4#'^-/4%P5+$#,'*12%8&,#'21,'#&+4'&(3$-+1.7'8-%4-. 7' )*-./' &' .-.#D31-.%' %-%,&%-1.' =VT]V ./>' 12' +1(3-$#0 12' &$$' @B' +?HG' *&(3$#*:' X81' ()$%-D,).' `PJ #,#'3#,21,(#07'#&+4'+1.%&-.-./'#-%4#,'1.#'1,'%81'LNOD 1.#',).'12'#&+4'12'91%4'.1,(&$-C#,*:'X4#',&8'LNOD &$)#'3#,'`PJ'#<3#,-(#.%'8&*'0-6-0#0'95'%4#'&6#,&/# )#*'12'%4#'%81'.1,(&$-C#,*'3#,'#<3#,-(#.%7'%1'&,,-6# .1,(&$-C#0'LPODMU&'6&$)#*'12'%4#'@B'+?HG*:'O-.&$$57 0'LNODMU&'(JHG'6&$)#*'12'%4#'%81'#<3#,-(#.%*'8#,# #&+4'+?HG'*&(3$#'&.0'%4#'21),'+&%#/1,-#*'12'*#6#. 8#,#'+1(3&,#0:'H1%#'%4&%'8#'%11"'%4#'3,#f31*%',&%-1 LNODMU&'(JHG'$#6#$'3#,'*)9d#+%'&.0'%4#.'&6#,&/#0 &+4',#/-(#.'+&%#/1,5: Statistical analysis 5*#*'8#,#'3#,21,(#0')*-./'%4#'g-$+1<1.'(&%+4#0'3&-,* &(3$#'#D%#*%*'&%'&'3,#*#%'$#6#$'12'*-/.-2-+&.+#'12' A:AR: &9$#*'%4&%'8#,#'+1(3&,#0')*-./'%4#'g-$+1<1.'%#*%'8#,# 1$)(#*' 3,#D%,&-.-./' &.0' 31*%D%,&-.-./7' &.0' -*1(#%,-+ *'3,#D%,&-.-./'&.0'31*%D%,&-.-./:'`&-,#0'%81D*&(3$#'#D 0'%1'+1(3&,#'8##"$5'0-22#,#.+#*'9#%8##.'%4#'HG'&.0 $)0-./e' (#&.' Ph' 6&$)#*7' ()*+$#' 61$)(#7' 3#,+#-6#0 -6#0'#<#,%-1.7'()*+$#'*%,#./%4'&.0'%1%&$'81,"7'&.0'%4#5 91%4'%4#'`X'&.0'HG'/,1)3I'%4#'(#&.'8##"$5'81,"'%1%&$*'(1,#'%4&. 01)9$#0'21,'91%4'/,1)3*'95'%4#'#.0'12'%4#'*%)05:'c6#,&$$7'%4#'[81," DISCUSSION #F)-6&$#.%\'n%4#'%,&-.-./'#221,%'&*'0#*+,-9#0'3,#6-1)*$5'=?-99$#'#% &$:7'@AAVI'N#,9#,'#%'&$:7'@AAV>o7'16#,'%4#'#.%-,#'BD'1,'MMD8##"'%,&-.-./ L.'%4-*'*%)057'1.#'/,1)3'12'3&,%-+-3&.%*'#<3#,-#.+#0'&.'-.-%-&$'91)% *#**-1.' 8&*' %4#' *&(#' =]:@"MA] "p>' 21,' 91%4' /,1)3*:' X4#*#' 81," 12'0&(&/-./'#<#,+-*#'&.0'%4#'1%4#,'4&0'.1'0#%,-(#.%&$'*5(3%1(* %1%&$*'-.+$)0#0'%4#'%4,##D8##"',&(3D)3'*#**-1.'=8##"*'MT]>'21,'%4# `X'/,1)3:'X4-*'8&*'&++1(3$-*4#0'%4,1)/4'*$-/4%$5'4-/4#,7'9)%'.1% 12' 0&(&/#:' ?#*3-%#' %4#' 0-22#,#.%' -.-%-&$' +1.0-%-1.*7' 91%4' /,1)3* *-/.-2-+&.%$5'4-/4#,'=$qA:AR>7'6&$)#*'21,'8##"$5'81,"'&6#,&/#*'21, #<3#,-#.+#0'%4#'*&(#'.#%'-.+,#&*#'-.'()*+$#'*-C#'&.0'*%,#./%4:'X4#*# %4#'HG'/,1)3'2,1('8##" K'%4,1)/4'%1'8##" MM'=O-/: @>: ,#*)$%*' *)//#*%' -%' -*' %4#'*-/.-2-+&.%$5' %1%&$' 81,"' 01.#' 0),-./' X4#' %81' /,1)3*'%4&%' #<3#,-#.+#0' 0-22#,#.%' $#6#$*' 12%,&-.-./' %4&% Dano Muscular e Hipertrofia 800 2 3 4 5 6 7 8 9 10 11 Training week * Pre-trained * ag 15 e th 0 re U sh l –1 o ld 400 200 0 ls throughout eccentric exercise training protocols, ean weekly work totals (N 7, each group, ±s.e.m.; note bars are hidden by the symbols). Mean weekly work totals the pre-trained (PT, circles) and naive group (NA, all weekly work totals (weeks 4–11) were not different the two groups (P>0.05). The histogram on the right otal work performed over the eight-week training session y statistically between the groups (P>0.05). * 600 0 * D am 1000 Total training (kJ) 2000 PT NA Plasma CK (U l–1) Naive 3000 minimal influence on the outcome of this study. Also, because the subjects were randomized, a possible effect should be similar in both groups. Performance Tests The subjects were tested twice on each performance test on four separate days, both before and after the training period. The coefficient of variation of the strength tests were approximately 2%. The highest score from each test was used for later analysis. 9/24/14& Maximum concentric strength Maximum concentric strength was measured as the concentric 1RM in the elbow flexion. The range of motion of the elbow joint started from a slightly flexed (160-) position to an end position of 75- in the elbow joint. The subjects completed three to four sets of three to five repetitions as a warm-up. Thereafter, single lifts were performed, with the load increased gradually until the maximum was reached. Each lift was separated by a pause of 3–5 min to ensure full recovery between the attempts. This same rest protocol was used for all performance tests in the study. The specific concentric strength was defined as the maximum concentric strength divided by the mean anatomical cross-sectional area of the elbow flexors. Maximum eccentric strength Treino Excêntrico x Concêntrico – The eccentric 1RM was measured as the maximum load the subject could lower from 75 to 160- in the elbow joint Indivíduos Treinados cally only. The subjects in ECC were instructed to use 3–4 s ()*+$#'0&(&/#7'&*'&**#**#0'%4,1)/4'0#%#,(-.-./'%4#'$#6#$*'12'3$&*(& Ph:' X4#' `X' /,1)3' 4&0' &' (#&.' Ph' $#6#$' %4&%'Table ,#(&-.#0' 9#$18 2. Quadriceps muscle volume and isometric strength MAZ _ $TM n MRA _ $TM = .1,(&$>o7'-.0-+&%-./'.1'0#(1.*%,&9$#'()*+$# 0&(&/#'%4,1)/41)%'%4#'%,&-.-./'3#,-10:'E5'+1.%,&*%7'%4#'HG'/,1)3Pre-trained group (PT) Naive group (NA) ,#+1,0#0'(#&.'Ph'6&$)#*'8#$$'&916#'.1,(&$7'3#&"-./'1.'8##" R Pre-training Post-training %! Pre-training Post-training %! #$#6&%#0' -. &%' RBArMVA _ $TM:' `$&*(&' Ph' ,#(&-.#0' *-/.-2-+&.%$5' 8##"*'KTZ'=$sA:AR>'84#.'%4#'%81'/,1)3*'8#,#'+1(3&,#0'=O-/: ]>: 3 Quadriceps volume (cm ) =8##" K>' 8&*' *%&%-*%-+&$$5' 1651±145 1751±141 6.5* 1906±175 2041±176 7.5* L.-%-&$' 3#,+#-6#0' *1,#.#**' *-/.-2-+&.%$5 #$#6&%#0'-.'%4#'HG'/,1)3'=O-/: K>: Quadriceps strength (N) 104.5±64.5 130.5±28.5 24.8* 108.4±81 136.4±118.6 25.8* E1%4'()*+$#'*%,#./%4'&.0'*-C#'-.+,#&*#0'#F)&$$5'-.'*)9d#+%*'-. E F F E CTS OF Mean values (N 14, ±s.e.m.) of the PT and NA groups before and after the 12-week resistance training. *Significant difference (P<0.05) was seen within the 91%4'/,1)3*:'L.+,#&*#*'-.'61$)(#'12'%4#'F)&0,-+#3*'()*+$#'8#,# *-/.-2-+&.%'21,'91%4'%4#'`X'&.0'HG'/,1)37',#*3#+%-6#$5'=$sA:AAM7 groups for pre- and post-cross volume values as well as pre- and post-strength results. No statistical difference (P>0.05), however, was present between the $sA:AM>:'X4#'`X'/,1)3'4&0'&'V:Ri'-.+,#&*#'-.'()*+$#'61$)(#7 NA and PT groups for either muscle volume or strength. &.0'%4#'HG'/,1)3'&'Z:Ri'-.+,#&*#'=X&9$# @>7'&.0'%4#'0-22#,#.+# PT weekly mean NA weekly mean 4000 %4#'#<%,&+#$$)$&,'(&%,-<7'9&*&$'$&(-.&'&.0'*&,+1$#((&'&*'8#$$'&* 0&(&/#'8-%4-.'%4#'()*+$#'2-9#,'%1'%4#'+1.%,&+%-$#'&.0'+5%1*"#$#%&$ 3,1%#-.*'=H#84&('#%'&$:7'MQB]>:'!&,+1$#((&'0-*,)3%-1.'-*'+1.2-,(#0 95'&.'-.+,#&*#'-.'9$110D91,.#'$#6#$*'12'-.%,&()*+)$&,'3,1%#-.*'*)+4 &*'+,#&%-.#'"-.&*#'=Ph>7'84-+4'-.'%),.'4&*'9##.'$-."#0'%1'3,10)+%-1. 12' &.' -.2$&((&%1,5' ,#*31.*#' =P&..1.' #%' &$:7' MQBQI' J1).0' #%' &$:7 MQBZ>:'X4#'0&(&/#'%1'%4#'+1.%,&+%-$#'3,1%#-.*')*)&$$5'$#&0*'%1'&'$1** FIGURE 1—The test and training apparatus for the elbow flexion 12'*%,#./%4'=(&<-(&$'-*1(#%,-+'21,+#>'=P$&,"*1.'#%'&$:7'MQQ@>: used in the present study. L.'%4#'+),,#.%'*%)057'&'0&(&/-./'-.-%-&$'#<#,+-*#'91)%'8&*'+1.2-,(#0 95' #$#6&%#0' Ph' $#6#$*' -.' %4#' HG' /,1)3I' -.' 8##"*' KTZ7' 3$&*(& +1.+#.%,&%-1.*'8#,#'8#$$'&916#'%4#'0&(&/#'%4,#*41$0'&.0'16#,'2-6# %-(#*'%4&%'12'%4#'`X'/,1)3:'X4#*#'#$#6&%#0'Ph'$#6#$*'8#,#'.1%'-.%#.0#0 Training Protocol %1'F)&.%-25'%4#'&(1).%'12'0&(&/#'9)%'-.*%#&0'%1'*#,6#'&*'&'(&,"#, %1' +1.2-,(' %4&%' )$%,&*%,)+%),&$' 0&(&/#' %1' %4#' ()*+$#' 4&0' 1++),,#0 The subjects exercised both arms during the training =G,(*%,1./7'MQBKI'P$&,"*1.7'MQQZ>:'G.1%4#,'(&,"#,'12'0&(&/#'8&* &$*1'19*#,6#0'T'%4-*'9#-./'%4#'*-/.-2-+&.%'-.+,#&*#'-.'3#,+#-6#0'*1,#.#** sessions, but only the nondominant arm was tested and -.'%4#'HG'/,1)37'84-+4'8&*'&9*#.%'-.'%4#'`X'/,1)3: analyzed. The training program is given in Table 2 and G.'#++#.%,-+'#<#,+-*#',#/-(#'8&*')*#0'-.'%4-*'*%)05'*3#+-2-+&$$5 consisted of 2–3 training sessions per week for 12 wk. The 9#+&)*#'%4#'4-/4#*%'21,+#'3,10)+%-1.'-.'*"#$#%&$'()*+$#'1++),*'0),-./ $#./%4#.-./' ()*+$#' +1.%,&+%-1.*' &.0' %4)*' 3,16-0#*' %4#' /,#&%#*% exercise sessions alternated between either maximum *%-()$)*'21,'()*+$#'/,18%4'=^&!%&51'#%'&$:7'@AAA>:'E#+&)*#'12'%4#*# (repetition maximum, RM) or medium loads. The max4-/4'21,+#*7'()*+$#'0&(&/#'-*'+1((1.$5'&**1+-&%#0'8-%4'#++#.%,-+ +1.%,&+%-1.*:'G$%41)/4'0&(&/#'+&.'9#'&'+1((1.'(&.-2#*%&%-1.'12 imum load was defined as the greatest load that could be #++#.%,-+'#<#,+-*#7'-2'%4#'(&/.-%)0#'12'21,+#'-*'-.+,#&*#0'/,&0)&$$5 lifted a given number of repetitions and sets (4- to 8RM). &.0'3,1/,#**-6#$57'()*+$#*'&0&3%'%1'&.5'3&%%#,.'12')*#7'-.+$)0-./ The21,+#*7' medium load -.d),5' was ,#*31.*# set to a value of 85–90% of 4-/4' #++#.%,-+' 8-%4' .1'training 0#%#+%&9$#' ()*+$#' =^&!%&51' #%' MQQQI' H#84&(7'load. MQBB>:' During X4#' /,&0)&$'any ,&(3D)3 the&$:7'maximum given 2 wk of training, 3,1%1+1$')*#0'-.'%4-*'*%)05'8&*'*)++#**2)$'-.'&+4-#6-./'4-/4'%,&-.-./ each subject completed three sessions with the maximum 21,+#*'84-$#'&61-0-./'0#%#+%&9$#'0&(&/#'-.'%4#'`X'/,1)3: load%4&%' and sessions the load. As a warm-up g#' 19*#,6#0' %4#'two -.+,#&*#' -.' ()*+$#'with 61$)(#' 21,'medium %4#' %81 /,1)3*' 8&*'before #F)-6&$#.%' ,#/&,0$#**' 12' O,1(' &. training, all&' 0&(&/-./' subjects91)%:' completed two to three sets of #./-.##,-./' 3#,*3#+%-6#7' 0&(&/#' &*' &' .#+#**&,5' 3,#+),*1,' 21, 6–12 repetitions of the designated action type while ,#*%,)+%),-./'81)$0'*##('%1'9#'&'311,'[0#*-/.'2#&%),#\7',#F)-,-./ gradually the CON group, the subjects )..#+#**&,5' 6)$.#,&9-$-%5' increasing =-:#:' *&,+1$#((&'load. 0&(&/#7'In *1,#.#**' &.0 8#&".#**>'-.',#*31.*#'%1'&',#F)-,#(#.%'21,'&00-%-1.&$'*%,#./%4:'L% lifted the load from a starting angle of 160- to an end *##(*'%4&%'&'.##0'21,'&00#0'*%,#./%4'%1'9#'+1)3$#0'%1'&',#F)-,#(#.% position of approximately 70- in the elbow joint. Similarly, 12'0&(&/#D-.0)+#0'0-(-.-*4#0'*%,#./%4'81)$0'+#,%&-.$5'9#'&61-0#0 95'.&%),&$'*#$#+%-1.'-2'31**-9$#:'L.0##07'0),-./'+4,1.-+',#*-*%&.+# the ECC group lowered the load from approximately 70 to %,&-.-./7' 84#%4#,' &.' &%4$#%#' #<3#,-#.+#*' ()*+$#' *1,#.#**' &.0 160-. An assistant returned the load to the starting position, 0&(&/#' &%' %4#' 1.*#%' 12' %,&-.-./' 81)$0' *##(' %1' 4&6#' .1' -(3&+% thus letting the subjects train concentrically or eccentri84&%*1#6#,'84#.'%,&-.-./'+1.%-.)#*').-.%#,,)3%#0'16#,'(1.%4*'1, 0 1 2 3 4 5 6 7 8 9 10 11 Training week Fig. 3. Plasma creatine kinase (CK) levels were measured in each participant weekly. CK levels increased significantly in the NA group for the weeks 5T8 (* statistical difference between groups; P<0.05). By contrast, the PT group was never above the control CK level (150 U l–1), representing the muscle damage threshold. for each lowering of the load, and the subjects in CON were TABLE 2. The training program for the concentric exercise and eccentric instructed to use maximum effort in every lift. To ensure exercise groups. progression in training, the relative training load was Training Session Each Week gradually increased every fourth week as the target number CONCE NTRIC AND E CCE NTRIC TRAINING 2175 Week 1 2 3 Reps per week of repetitions in each set was decreased from eight to six 1 3 ! 8RM 3 ! 8 medium 3 ! 8RM 72 repetitions in week 4by andt hthen week bject s in CG r epor a lt er in g4 !t h8RM eir level of ph ysica l 56 a n d pr a ct ice, wer e followed r ee to m afour xim arepetitions l isokin et after ic su 2 3 !t ed 8 medium addition, the individual absolute ivit y. m u scle a ct8.ionIn s for ea ch isokin et ic t est m ode. Thtraining e m u scleloada ctwas 3 4 ! 8RM 3 ! 8 medium 4 ! 8RM 88 4an alysis. 3 !In8tmedium 4! 8RM S tatistical r a cla ss cor r ela t ion coefficien t s wer e 56 a ct ion s werprogressively e sepa r a t ed by a r est inas t erthe va lsubjects of 25 s. Du r in g t stronger. he increased became If ! e-wa 6RM y ANOVA 3 ! 6t omedium 6RM bilit y 66 ca lcu la t ed by 5u sin g a 4on a ssess t h4e!r elia 25-s r est per t h e Kin -Com dynwere a m om et er leverduring a r m mthe oved alliod, repetitions and sets completed maximum 6 3 ! 6 medium 4 ! 6RM t or qu e, CSA, a n d iE MG a ct ivit y m ea su r em en t s. Th e st a t is- 42 a t 30°/s t otraining slowly bout, r et u r nthet hload e legwas t o tincreased h e in it ia l(0.25–1 t est posit kg)ion at theofnext 7 4 ! 6RM 4 ! 6 medium 4 ! 6RM 72 en ces in pr et est -t o-post t est ch a n ges 48 wit h ou t r equ ir in g a n y m u scu la r a ct ivit y fr om t h e lim b. t ica l sign ifica8n ce of differ 4 ! 6 medium 4 ! 6RM maximum session. If the subject failed to complete on g gr ou ps9 wa s det m in ed by 4a!t 4h medium r ee- (gr ou5p!34RM t im e 3 56 In t r a cla ss r elia bilit y coefficien t s, det er m in ed by u sin g a a mthe 5 !er4RM session for as described, nextm ode) or10t wo- (n4o!t 4est m ode for a dr iceps CSA) fa ct or 36 on e-wa y ANOVA a sin gle t rthe ia l, load wer e was 0.84unaltered for a ver aat ge thet est medium 5 ! qu 4RM 5 !m 4RM 4 !t s4 medium 5! ea su r em en on t h e t im e 4RM a n d t est 56 t or qu e du rmaximum in g m a ximsessions a l Con muntil u scleit awas ct ionsuccessfully s a n d 0.83 du r in g ANOVA completed. The wit h 11r epea t ed mediumh oc t5est ! 4RM ode fa ct or s 12 followed4 !by4 post s for sim ple effect s a n d 36 m a xim a l Enumber cc m u scle ct ionin s. each maximum session rose from mthree ofasets a n dtraining sim ple t r session a st s aiss given a pprasopr t e (23). DifferWh ile t h e su bject wa s per for m in g t h e m a xim a l-effor t iso- in t er a ct ion The withincon each theia number of sets times the number of during the first week to five during the last weeks. There eacht set. of teach training session a da pt aint ion o t rThe a indesignated in g werintensity e in dica ed by sign ifi- is termed kin et ic m u scle a ct ion s, E MG da t a wer e obt a in ed fr om t h e en ces in t h erepetitions tou6-min Three subjects RMt im (maximum medium thaninmaximum). ca n tingr ou p 3 e or grload) ou por3 t im e(10–15% 3 t est lower m ode t er a ct ion s. con t r a ct in gwas r ighat 3va st s la t er pause a lis a nbetween d va st u s each m ediaset. lis m u scles. Treino Excêntrico x Concêntrico – Indivíduos Treinados All show the training sessions circles, dashed line). The horizontal arrows 41.2 T (rep). 11.4 B.0.3The T 0.3 48.5 T 12.1 7.8 T 9.7 2.3 T 2.9 that employed the described number of Pre repetitions Post 37.5before T 9 and2.0 T 3.9 54.9 T 12.4 4.5 T 5.9 1.1 T 2.4 maximum concentric strength and eccentric strength after T 12.1 1.7 are T4 6.4 T 14.4 j3.3 T 8.4 j1.2 T 3.2 the training in CON (filled bars) and ECCDiff (openj3.7 bars). The data given as mean T SD. *Significantly different from pre values, P G Values are means T SD in percent. CON, concentric exercise; ECC, eccentric 0.001; †significantly greater increase than for CON, P G 0.001. exercise. * Significantly different from pre values (P = 0.03); † significantly different from CON (P = 0.005). Vikne et al., 2006 FIGURE 6—Serial anatomical cross-sectional areas (ACSA) of the elbow flexors in the concentric exercise (CON; panel A) and eccentric exercise (ECC; panel B) groups before (filled circles, solid lines) and after (open circles, dashed lines) the training period. Serial ACSA are given at intervals of one-eighth the length of humerus from the distal (left) to the proximal (right) end. * Significantly different from pre values, P G 0.005. The data are mean T SD. Downloaded from http://jap.physiology.org/ at CAPES - Usage on October 4, 2012 Th e r a n ge of m ot ion du r in g wh ich t h ese da t a wer e collect ed Sim ple a n d m u lt iple cor r ela t ion a n d r egr ession a n a lysis wer e of the American Sports u sed t o det er m in e t h e r ela t ive con t r ibu t ion s http://www.acsm-msse.org of ch a n ges in wa s t h e sa1772 m e a s tOfficial h a t forJournal a ver a et ge t or qu e. Th e College E MG aof ct ivit y Medicine Flann al., 2011 Vikne et al., 2006 da t a fr om t h e t wo m u scles wer e su m m ed a n d u sed t o a ssess qu a dr iceps CSA a n d n eu r a l a ct iva t ion t o ch a n ges in st r en gt h . t h e degr ee of elect r ica l excit a t ion (n eu r a l a ct iva t ion ) of t h e An a lph a level of P # 0.05 wa s u sed for a ll t est s of sign ifiu n der lyin g m u scu la t u r e. E MG a ct ivit y wa s r ecor ded wit h a ca n ce. by wit thehAmerican of pliSports Medicine. Unauthorized reproduction of this article is prohibited. t wo-ch a n n el Copyright Cou lbou r n@r2006 ecor der a h igh -gaCollege in bioa m fier, ba n d-pa ss filt er wit h cu t offs of 8 a n d 1,000 H z, a n d a ga in RES U LTS of 10,000. Two silver-silver ch lor ide su r fa ce elect r odes wer e Th e pa t t er n of r esu lt s for pea k a n d a ver a ge t or qu e, pla ced 30 m m a pa r t over ea ch m u scle a ppr oxim a t ely over t h e m ea su r ed du r in g m a xim a l Con a n d E cc m u scle a ct ion s, m ot or poin t . Th e t wo gr ou n d elect r odes wer e pla ced 30 m m wa s t h e sa m e. Th er efor e, on ly t h e da t a for a ver a ge a pa r t over t h e r igh t a n t er ior su per ior ilia c spin e of t h e pelvis. Befor e t h e elect r odes wer e pla ced, t h e skin wa s t h or ou gh ly t or qu e a r e r epor t ed. Ch a n ges in a ver a ge t or qu e of t h e clea n ed wit h isopr opyl a lcoh ol a n d sligh t ly scr a t ch ed wit h a r igh t qu a dr iceps m u scle for t h e t h r ee gr ou ps m ea su r ed st er ile n eedle t o r edu ce in t er elect r ode im peda n ce below 5,000 du r in g m a xim a l Con a n d E cc isokin et ic m u scle a ct ion s V. Acet a t e pa per wa s u sed t o t r a ce t h e elect r ode pla cem en t t o a r e pr esen t ed in Ta ble 2. Wh en t est ed in t h e E cc m ode, en su r e t h e sa m e elect r ode pla cem en t wa s m a de in su bse- t h e m ea n a n d per cen t ch a n ges for E TG, CTG, a n d CG qu en t t est s. Th e E MG da t a wer e r ect ified a n d in t egr a t ed over wer e 34.0 (36.2%), 12.5 (12.8%), a n d 21.8 (21.7%) within nor between the two groups. In addition, when the t h e sa m e t im etwo per iodwere a s pooled t h e atogether, ver a ge for ceno m ea su r em en t s. Th e N · m , r espect ively. Ma xim u m a ver a ge t or qu e in E TG groups we found statistically iE MG da t a forsignificant t h r eechanges t r ia lsin the forfiber-type ea ch proportions. t est m ode wer e a ver a ged. a n d CTG in cr ea sed sign ifica n t ly m or e t h a n in CG. Th e In t r a cla ss r elia bilit y coefficien t s for t h e m a xim a l iE MG a ct iv- in cr ea se in a ver a ge t or qu e in E TG wa s sign ifica n t ly it y du r in g Con a n dcross-sectional E cc m u scle Muscle areaa ct ion s wer e 0.90 a n d 0.88, gr ea t er t h a n t h e in cr ea se in CTG. r espect ively. As seen in Figure 6, the anatomical cross-sectional areas Wh en t est ed in t h e Con m ode, t h e m ea n a n d per cen t distal regions (one- and Lh)r ed wit h MRI Th e CSA of were t h egreater qu aindrtheiceps m u scle watwo-eighths s m ea su than in the proximal regions of the elbow-flexor group by u sin g a Gen er a l E lect r ic Sigm a Adva n t a ge u n it wit h ch a n ges in a ver a ge t or qu e for E TG, CTG, a n d CG wer e (three- and four-eighths Lh). The mean anatomical elbowsoft wa r e ver sion T2 pr ot(mean on den sittoy four-eighths im a ges fr om 5-m m - 5.4 (6.8%), 14.4 (18.4%), a n d 3.8 (4.7%) N · m , r especflexor 4.6.8. cross-sectional area of one2 Lh)nof 4.9 cm not change t h ick a xia l sca s 26.8 a t T20, 30,of the 40,CON 50,group 60,did 70, a n d 80% of t h e t ively. Th e ch a n ge in a ver a ge t or qu e wa s sign ifica n t ly during the training period (+0.7 T 1.1 cm2, +3%; P = 0.1). fem u r len gt h For wer obtgroup, a inthe edmean by area u sin g aT 3.4 m ucmlt2 islice spin -ech o gr ea t er in CTG t h a n in CG. Th er e wa s n o sign ifica n t theeECC of 25.4 rose 2 by 2.8 T 1.4 cm (11%; P G 0.001) during the training pu lse sequ en ce (r epet it ion t im e 5 2,000 m s; ech o t im e 5 10 differ en ce in t h e ch a n ge in a ver a ge t or qu e bet ween period. The effect thus differed between the two groups m s), 24-cm field-of-view, a n d 256 3 192 pixel E TG a n d CG. Th e in cr ea se in a ver a ge t or qu e in CTG (P = 0.004; Fig. 6). Increases in absolute area were greaterm a t r ix. Tot a l flexor grouppu had its largest sca n t im e wa swhere 6.8 the m in . Com t er-a ssistportions ed pla(onen im et r y a n a ly- wa s sign ifica n t ly gr ea t er t h a n t h a t for E TG. ), but the relative hypertrophy was sis wa s u sedand t otwo-eighths det er mLhin e CSA m ea su r em en t s fr om t h e E cc isokin et ic t r a in in g in cr ea sed st r en gt h m or e t h a n comparable between the four individual regions (one- to im a ges wit h afour-eighths pixel cou t in g(10–12%). r ou t inThe e. corresponding In t r a cla ss r elia bilit y Con isokin et ic t r a in in g wh en m ea su r em en t s wer e m a de Lh) inn ECC increasesa tof t2–4% in CONen were likewise r a n ged fr om coefficien t s fornonsignificant m u scle CSA h e differ t levels by u sin g t h e sa m e m u scle a ct ion a s t h a t u sed du r in g 0.97 t o 0.99. t r a in in g. Th e ch a n ge in a ver a ge t or qu e m ea su r ed du r Hreduced eavy-resistan train in g. E a ch exper im en t a l su bject 1RM, the loads were to mean values of 78ce T 4, 60 T 3, FIGURE 5—Relative load–velocity therespectively. concentric After the normalization of 43 Trelationship 3, and 26tTrin 2%, a(ECC; inwased exercise (CON; panel A) and eccentric exercise panel hB)er r igh t leg on t h e Kin -Com dyn a m om et er u sin g the test therecircles, little difference in the velocity of groups before (filled circles, solid lines) andloads, after (open dashed eitare hnormalized er Con E cc(Fig. isokin et ic m u scle a ct ion s, depen din g on t h e Ta ble 2. Average torqu e at pretest an d posttest shortening that before the training 5). lines) the study. The loads V90, V70, V50, andfrom V30 to or period both pre- and postconcentric strength. The test loads were reduced at r athe inpost in g1RM,gr ou p t o wh ich sh e wa s a ssign ed. Tr a in in g wa s 3 for CON an d E CC test m od es posttesting to 78 T 4, 60 T 3, 43 T 3, and 26 Tt2% proportions respectively. The data are mean T Fiber-type SD. da ys/wk for 10 wk for a t ot a l of 30 t r a in in g session s. Du r in g The proportion of the type I fibers differed between the Gr ou p P r et est P ost t est Mea n Ch a n ge Mea n % Ch a n ge t r a in in g, su bject s per for m ed t h r ee set s of 10 r epet it ion s wit h two groups before the training period (P = 0.005; Table 3). during the training period, Before although there was a trend the study, subjects hadween relatively rfew IIX (2%) n othe r est bet epet it ion s. A 3-m in r est wa s given bet ween E CC Test M od e toward a reduced proportion and in the ECC group (P five = 0.08). IIA/X fibers (8%); subjects had no IIX fibers, and set s. groups Su bject werfibers. e stThea bilized for t r a in in g wit h t h e sa m e subjects the hadtwo less than 2% Also, there was no differencesixbetween in typesIIA/X CTG 97.7 6 23.5 110.2 6 30.2 12.5* 12.8 proportions ofpr type I fibers did the proportions of the type I fibers after the training period. ocedu r enotachange s forin either t estgroup in g. Beca u se speed, n ot for ce, is con E TG 93.9 6 18.7 127.9 6 22.0 34.0*† 36.2 There were likewise few alterations in the subgroups of the t r olled by t h e Kin -Com dyn a m om et er du r in g isokin et ic m u scle CG 104.6 6 24.3 102.8 6 26.2 21.8 21.7 type II fibers. Only the 2.8% reduction of IIX fibers in ct ion for ce of m u scle a ct ion s va r ied wit h in dividu a l effor t . CON was statistically significant, whereasathere was s, a trend CON Test M od e for reduction in the proportion of the IIAX Dufibers. r in gThere t h e fir st week of t r a in in g, a for ce m a r ker on t h e were no other significant differences or changes neither Kin -Com scr een wa s set a t t h e pr et est pea k for ce m ea su r ed CTG 78.4 6 18.5 92.8 6 23.4 14.4*‡ 18.4 E TG 79.5 6 11.7 84.9 6 13.8 5.4 6.8 du r in g Con or E cc m u scle a ct ion s. Th e su bject wa s a sked t o TABLE 3. Fiber-type proportions (%) in the CON and ECC groups before and after the CG 81.7 6 16.2 85.5 6 18.8 3.8 4.7 training period. r ea ch or exceed t h e for ce m a r ker wit h ea ch r epet it ion . Th e Type I Type IIC Type IIA Type IIAX Type IIX for ce m a r ker pla cem en t wa s a dju st ed ea ch week ba sed on Va lu es a r e m ea n s 6 SD in N · m . Ba sed on gr ou p 3 t im e pa r t ia l CON (N = 8) Pre 34.5 T 10.7 0.3 T 0.4 50.5 T 14.9 11.3isokin T 11.4 3.3 et T 3.2ic st r en gt h t est s. in t er a ct ion fr om a n a lysis of va r ia n ce (ANOVA): * sign ifica n t ly differPost 35 T 9.3 1.1 T 1.7 58.9 T 12.7 4.5 T 5.9 0.5 T 0.6* Diff 0.5 T 12.2 0.8 T 1.9 8.4 T 17.6 j6.8 T 9.4Su j2.8 T3 bject s in CG wer e in st r u ct ed t o m a in t a in t h eir pr eviou s en t (P , 0.05) com pa r ed wit h CG; † sign ifica n t ly gr ea t er (P , 0.05) ECC (N = 6) Preload 50.1 T 3.5† 0.2 T 0.3 45.7 T 7.5 3.1level T 4.1 0.9of T 1.9 a ct ivit y a n d n ot begin a lower-ext r em it y st r en gt h FIGURE 3— A. Progression of the training during the training com pa r ed wit h CTG a n d CG; ‡ sign ifica n t ly gr ea t er (P , 0.05) com Post exercise 40.9 T 8.1 3.1 T 5.8 49.6 T 10.8 4.5 T 6.4 1.9 T 3.6 period from sessions 1 to 29 in the concentric group (CON; Diff j9.2 T 10.4 T 5.9 3.9 T 9.7 1.4tTr3.6 1 Tg 1.8 pr ogr a m a in in u n t il t h e st u dy wa s over. Non e of t h e pa r ed wit h E TG a n d CG. filled circles, solid line) and the eccentric exercise group (ECC;2.9 open Treino Excêntrico x Concêntrico – Indivíduos Destreinados Higbie et al., 1996 post- vs pretraining tests; Fig. 3B). The improvements were 1776 Official Journal of the American College of Sports Medicine http://www.acsm-msse.org 4.7 T 2.2 kg (18%) and 3.9 T 1.3 kg (14%) after training for CON and ECC, respectively. The eccentric 1RM improved more for ECC (8.6 T 3.3 kg, 26%) than for CON (3.1 T 1.3 kg, 9%; P G 0.001 for ECC vs CON). Consequently, thethe American College of Sports Medicine. Unauthorized reproduction of this article is prohibited. Copyright @ 2006 by ratio between the eccentric 1RM and the concentric 1RM developed differently (P G 0.001). For CON, the ratio decreased from 1.30 T 0.10 to 1.20 T 0.12 during the training period (P = 0.007), whereas for ECC, the ratio increased from 1.21 T 0.08 to 1.33 T 0.12 (P = 0.008). Maximum angular velocity Both groups increased the maximum angular velocities at all loads during the training period (P G 0.05; Fig. 4), and there was no difference between the two groups. The increase in the absolute angular velocity was similar in all tests (V2–V90) and ranged from 18 (V2) to 53-Isj1 (V90). Because the absolute angular velocity decreased as the load increased, the relative effect of training was greatest at the highest loads. When the test loads of 90, 70, 50, and 30% of the preconcentric 1RM were normalized to the postconcentric RESISTANCE TRAINING IN TRAINED MEN FIGURE 4—Maximum angular velocity at loads 90% (V90), 70% (V70), 50% (V50), and 30% (V30) of the maximum concentric strength at pretest and the common 2-kg load (V2). All velocities are taken at 115- in the elbow joint before (filled circles, solid lines) and after (open circles, dashed lines) the study in the concentric exercise group (CON; panel A) and the eccentric exercise group (ECC; panel B). * Significantly different from pre values, P G 0.05. The data are mean T SD. Medicine & Science in Sports & Exercised 1775 Copyright @ 2006 by the American College of Sports Medicine. Unauthorized reproduction of this article is prohibited. 12& 9/24/14& Treino Excêntrico x Concêntrico – Indivíduos Destreinados 2176 Velocidade da Fase Excêntrica e Hipertrofia E F F E CTS OF CONCE NTRIC AND E CCE NTRIC TRAINING Higbie et al., 1996 in g E cc m u scle a ct ion s a ft er E cc t r a in in g (36.2%) wa s sign ifica n t ly gr ea t er t h a n t h e cor r espon din g ch a n ge in a ver a ge t or qu e m ea su r ed du r in g Con m u scle a ct ion s a ft er Con t r a in in g (18.4%). Ch a n ges in t h e CSA of t h e qu a dr iceps m u scle det erm in ed fr om MRI sca n s a ft er t r a in in g a r e pr esen t ed in F ig. 1. F or t h e seven levels (20 – 80% fem u r len gt h ), t h e m ea n a n d per cen t in cr ea ses in CSA of t h e qu a dr iceps for E TG a n d CTG r a n ged fr om 1.9 t o 3.3 cm 2 (6.0 – 7.8%) a n d fr om 1.7 t o 2.8 cm 2 (3.5 – 8.6%), r espect ively. F or t h e su m of t h e seven levels, t h e CSA of t h e qu a dr iceps in cr ea sed 19.9 cm 2 (6.6%) in E TG com pa r ed wit h 15.0 cm 2 (5.0%) for CTG (Ta ble 3). No in cr ea se in CSA of t h e qu a dr iceps m u scle wa s fou n d in CG. Th e in cr ea ses in CSA of t h e qu a dr iceps for t h e t wo t r a in in g gr ou ps wer e sign ifica n t ly gr ea t er t h a n t h e in cr ea se for CG. Th e in cr ea ses for E TG wer e sign ifica n t ly gr ea t er t h a n for CTG a t t h e 40, 50, 60, a n d 70% levels a n d for t h e su m of t h e seven levels. Th e sign ifica n ce of t h e sm a ll E TG-t oCTG differ en ces m a y h a ve been du e in pa r t t o t h e gr ea t er va r ia bilit y of t h e ch a n ges in CTG (see F ig. 2). Ch a n ges in iE MG of t h e r igh t qu a dr iceps m u scle for t h e t h r ee gr ou ps m ea su r ed du r in g m a xim a l volu n t a r y Gr ou p P r et est P ost t est Mea n Ch a n ge Mea n % Ch a n ge CTG E TG CG 295.4 6 52.0 300.8 6 41.3 323.7 6 52.8 310.3 6 56.2 320.7 6 43.7 320.9 6 53.0 15.0* 19.9*† 22.8 5.0 6.6 20.9 Va lu es a r e m ea n s 6 SD in cm 2 of su m of cr oss-sect ion a l a r ea s fr om 7 levels (20 – 80% fem u r len gt h ). Ba sed on gr ou p 3 t im e pa r t ia l in t er a ct ion fr om ANOVA: * sign ifica n t ly gr ea t er (P , 0.05) com pa r ed wit h CG; † sign ifica n t ly gr ea t er (P , 0.05) com pa r ed wit h CTG a n d CG. Downloaded from http://jap.physiology.org/ at CAPES - Usage on October 4, 2012 F ig. 1. Va lu es a r e m ea n s 6 SE . Ch a n ge in cr oss-sect ion a l a r ea (CSA; cm 2 ) of qu a dr iceps m u scle m ea su r ed fr om m a gn et ic r eson a n ce im a gin g sca n s a t 7 levels a t pr et est a n d post t est in con cen t r ic (Con ; A ), eccen t r ic (E cc; B ), a n d con t r ol (C ) gr ou ps. * Sign ifica n t ly gr ea t er com pa r ed wit h con t r ol gr ou p a t P # 0.05. ** Sign ifica n t ly differ en t com pa r ed wit h Con gr ou p a t P # 0.05. Ta ble 3. Cross-section al area of qu ad riceps m u scle (su m of 7 levels) at pretest an d posttest • O exercício excêntrico veloz produziu maiores ganhos de torque do que o exercício excêntrico lento CTRL ECC CON Farthing & Chilibeck, 2003 F ig. 2. Sca t t er plot s of ch a n ge in a ver a ge t or qu e m ea su r ed du r in g m a xim a l Con a n d E cc kn ee ext en sion s t o ch a n ges in qu a dr iceps CSA (su m of 7 slices) a n d in t egr a t ed volt a ge fr om E MG (iE MG) in E cc t r a in in g gr ou p (E TG) a n d Con t r a in in g gr ou p (CTG). Lin ea r r egr ession lin es a r e sh own . F or E TG t est ed du r in g E cc m u scle a ct ion s (A a n d B ; s), ch a n ge in (D) t or qu e 5 1.63 · DCSA 1 1.47; r 5 0.51; st a n da r d er r or of est im a t e (SE E ) 5 18.1 Nm a n d D · t or qu e 5 1.69 3 10 4 · DiE MG 1 26.68; r 5 0.48; SE E 5 18.6 N · m . F or E TG t est ed du r in g Con m u scle a ct ion s (A a n d B ; r), Dt or qu e 5 0.29 · DCSA 2 0.34; r 5 0.20; SE E 5 9.1 N · m a n d Dt or qu e 5 4.39 3 10 4 · DiE MG 1 4.68; r 5 0.43; SE E 5 8.4 N · m . F or CTG t est ed du r in g Con m u scle a ct ion s (C a n d D; s), Dt or qu e 5 1.11 · DCSA 2 3.95; r 5 0.70; SE E 5 9.3 N · m a n d Dt or qu e 5 1.29 3 10 5 · DiE MG 1 8.6; r 5 0.68; SE E 5 9.5 N · m . F or CTG t est ed du r in g E cc m u scle a ct ion s (C a n d D; r), Dt or qu e 5 1.09 · DCSA 2 3.95; r 5 0.44; SE E 5 17.8 N · m a n d Dt or qu e 5 6.6 3 10 4 · DiE MG 1 9.65; r 5 0.19; SE E 5 19.5 N · m . Velocidade da Fase Excêntrica e Hipertrofia Velocidade da Fase Excêntrica e Hipertrofia • O exercício excêntrico veloz produziu uma maior hipertrofia nas porções proximal, média e distal do bíceps braquial • O treino excêntrico veloz produziu sempre maiores torques do que o treino excêntrico lento Farthing & Chilibeck, 2003 Shepstone et al., 2005 13& 9/24/14& Velocidade da Fase Excêntrica e Hipertrofia Velocidade da Fase Excêntrica e Hipertrofia • O treino excêntrico produziu uma maior quantidade de lesão nas fibras de contração rápida • Durante contrações excêntricas há uma reversão do princípio do tamanho. Fato que produz maior hipertrofia nas fibras de contração rápida • O treino excêntrico rápido produziu uma maior hipertrofia nas fibras de contração rápida • Qual é a explicação para tal fato? Shepstone et al., 2005 Tipos&de&Ação&Hormonal& Shepstone et al., 2005 Fatores&Endócrinos&x&Locais& • O&grupo&do&Dr.&Kraemer&e&Dr.&Hakkinnen&vem& nos&úl]mos&10&anos&tentando&relacionar&os& ganhos&de&força&à&magnitude&da&resposta& endócrina&após&sessões&de&exercício&de&força&e& períodos&de&treinamento& • && Gyton&&&Hall,&2008& West&et&al.,&2010& 14& 9/24/14& Fatores&Endócrinos&x&Locais& • Por&outro&lado,&outros&grupos&vem&tentando& demonstrar&que&não&há&relação&entre&as& respostas&endócrinas&e&os&ganhos&de&força&e& hipertrofia&muscular&decorrentes&do& treinamento&de&força& Lactato&x&Séries& • A&quan]dade&de&lactato& produzida&em&uma& sessão&não&parece&ser& afetada&pelo&número&de& séries& • && Smilios&et&al.,&2003& West&et&al.,&2010& Lactato&x&Repe]ções& • Quanto&maior&o&número& de&repe]ções&na&série& maior&é&a&concentração& de&lactato&no&sangue& Smilios&et&al.,&2003& Testosterona&x&Séries& • O&número&de&séries&não& parece&afetar&a& liberação&de& testosterona&de&forma& aguda& Smilios&et&al.,&2003& 15& 9/24/14& Testosterona&x&Repe]ções& GH&x&Séries& • O&número&de&repe]ções& nas&séries&também& parece&não&afetar&a& liberação&de& testosterona&de& maneira&aguda& • Um&maior&número&de&séries& parece&aumentar&a&liberação& de&GH&após&o&treino.&& Smilios&et&al.,&2003& Smilios&et&al.,&2003& GH&x&Repe]ções& Cor]sol&x&Séries& • 10&repe]ções&parecem& maximizar&a&liberação& de&GH&agudamente& • Quando&as&séries&têm& 10&ou&mais&repe]ções,& um&maior&número&de& séries&incrementa&a& liberação&de&cor]sol& Smilios&et&al.,&2003& Smilios&et&al.,&2003& 16& 9/24/14& Cor]sol&x&Repe]ções& • Quanto&maior&o&número& de&repe]ções&maior&a& liberação&de&cor]sol& • L&+&A&=&2&x&6V10&RM& • Leg&press,&extensão&e&flexão&dos&joelhos,&flexão&dos& cotovelos& • A&=&2&x&6V10&RM& • Flexão&dos&cotovelos& 2x/sem.& Smilios&et&al.,&2003& 11&semanas& Ronnestad&et&al.,&2010& Ronnestad&et&al.,&2010& 17& 9/24/14& Dose&Testosterona&K&Hipertrofia& • Testosterona&com&ação&endócrina&parece& produzir&hipertrofia&de&uma&maneira&doseK dependente& • Ela&produz&hipertrofia&tanto&de&fibras& musculares&]po&I&quanto&]po&II& SinhaKHikim&et&al.&(2003)&& Fatores&Endócrinos&x&Locais& • Treinamento¶&os& flexores&de&cotovelo& • Treinamento¶&os& flexores&de&cotovelo& mais&séries&de&leg&press& Dose&Testosterona&K&Hipertrofia& • A&hipertrofia&muscular&só& foi&produzida&pela& testosterona&com&função& endócrina&quando&a&dose& era&suprafisiológica& • A&hipertrofia&foi&causada& por&a]vação&de&células& satélites&e&consequente& aumento&de&mionúcleos& nas&fibras&(domínio& mionuclear)& SinhaKHikim&et&al.&(2003)&& Fatores&Endócrinos&x&Locais& • A&resposta&de&lactato&e&testosterona&total&foi&mais& elevada&antes&e&após&o&treinamento&na&condição&de& alta&produção&hormonal&& – Produzir&uma&maior& elevação&aguda&dos& hormônios& anabolizantes& West&et&al.,&2010& West&et&al.,&2010& 18& 9/24/14& Fatores&Endócrinos&x&Locais& • A&resposta&de&GH&e&testosterona&livre&foi&mais& elevada&antes&e&após&o&treinamento&na&condição&de& alta&produção&hormonal&& West&et&al.,&2010& Fatores&Endócrinos& &x&Locais& Fatores&Endócrinos&x&Locais& • A&resposta&de&IGFK1&foi&mais&elevada&antes&e&após&o& treinamento&na&condição&de&alta&produção&hormonal&& West&et&al.,&2010& Fatores&Endócrinos&x&Locais& West&et&al.,&2010& West&et&al.,&2009& 19& 9/24/14& Fatores&Endócrinos& &x&Locais& Modelo de Esfigmomanômetro para Promover a Oclusão Vascular 180 mm X 900 mm LAURENTINO, et al. (2008) Int J Sports Med; 29: 664–667. West&et&al.,&2009& Oclusão Vascular Oclusão • A oclusão do fluxo sanguíneo parece ser um fator importante para os ganhos de força muscular • Ela estimularia a hipóxia, fadiga local, produzindo maiores ganhos em força Takarada, 2000 20& 9/24/14& Oclusão • A oclusão permitiu uma maior ativação muscular, mesmo com cargas mais baixas Oclusão • Os ganhos em hipertrofia foram semelhantes com baixa intensidade e oclusão ao treino com alta intensidade sem oclusão Takarada, 2000 Oclusão • Os ganhos de força, em várias velocidades, foram iguais com oclusão Takarada, 2000 Oclusão • Verificar o efeito do treinamento com oclusão vascular na hipertrofia e ganho de força de jovens Takarada, 2000 Laurentino et al., 2011 21& 9/24/14& Kaatsu-Walk Training • Usa a oclusão vascular como estímulo de treinamento • Pressão mantida durante o treino a 120 mmHg • 3 semanas de treino • 6 vezes por semana • 2 vezes por dia • 5X2minX1min • 3 km/h Kaatsu-Walk Training • O grupo que andou com oclusão vascular teve hipertrofia muscular Abe et al., 2006 Oclusão&Vascular&x&Expressão&Miosta]na& • • • • Abe et al., 2006 Oclusão&Vascular&x&& Expressão&Miosta]na& 8&semanas&de&treinamento& Pressão&de&Oclusão&–&80%&da&PA&de&oclusão& Grupos&20%&e&20%Ocl&K&3&x&15&RM/4&x&15&RM& Grupo&80%&K&3&x&8RM/4&x&8RM& Lauren]no&et&al.,&2012& Lauren]no&et&al.,&2012& 22& 9/24/14& 23& 9/24/14& 210 Training & Testing Statistical analysis After normality (i. e. Shapiro Wilk) and variance assurance (i. e., Levene), a mixed model was performed for each dependent variable, having group and time as fixed factors, and subjects as a random factor [37] (SAS® 9.2). Whenever a significant F-value was obtained, a post-hoc test with a Tukey’s adjustment was performed for multiple comparison purposes. Whenever p-values of the F-tests indicated a trend towards significant values, the percentage change from pre- to post-training was calculated for each participant and a one way-ANOVA was used to compare the groups (i. e., VO2max and time to exhaustion). A Tukey posthoc test was used for the multiple comparisons when necessary. The significance level was set at p < 0.05. Results are expressed as mean ± standard error (SE). Results 7–8 10–12 RM 3 30–36 120 s 80 % vVO2max 20 60 s 45 s 85–90 % vVO2max 20 60 s 60 s 95 % vVO2max 20 60 s 60 s 95–100 % vVO2max 15 60 s 90 s De&Souza&et&al.,&2013& connected to the gas analyzer for breath-by-breath measurements of gaseous exchange. VO2max was defined when 2 or more of the following criteria were met: an increase in VO2 of less than 2.1 ml·kg 1·min 1 between 2 consecutive stages, a respiratory exchange ratio greater than 1.1, a blood lactate concentration higher that 8.0 mmol·l 1, and a ± 10 bpm of the predicted maximal heart rate (i. e. 220-age) [21]. The data was smoothed averaging the data over 10-s intervals and VO2max was obtained from the average of the 3 highest values obtained during the test. In addition, the time taken to exhaustion was recorded as an endurance performance variable. Verbal encouragement was provided to ensure that maximal values were reached. Muscle cross-sectional area Quadriceps cross-sectional area was obtained through magnetic resonance imaging (MRI) (Signa LX 9.1, GE Healthcare, Milwaukee, WI, USA). Subjects lay in the device in a supine position with straight legs. A bandage was used to restrain leg movements during image acquisition. All images were captured from both legs. An initial image was captured to determine the perpendicular distance from the greater trochanter to the inferior border of the lateral epicondyle of the femur, which was defined as *! *! 2 *! *! *! *! 2 52 Muscle analyses 46 Immunoblotting 40 20 10 a Downloaded by: Dot. Lib Information. Copyrighted material. 5–6 6–8 RM 5 30–40 120 s Pre- and post-training muscle samples were taken from the Leg press (LP) 1 RM, left (LT) and right (RT) cross-sectional area for the dominant control (C), interval training (IT), strength training (ST), and concurrent midportion Table of 2the vastus lateralis ofthigh the participants’ training (CT) groups pre- and post-training (mean ± SE). legs using the percutaneous biopsy Ctechnique withIT suction. ST CT LP-1RM (kg) were dissected Pre 261.2 ±from 56.1 268.4 ± 47.6 Muscle specimens free blood 255.4 and± 56.4 connec- 270.3 ± 45.5 Post 262.8 ± 60.6 263.8 ± 51.5 320.3 ± 57.0 315.7 ± 63.5 tive tissue and washed in Pre deionized8 347.3 water, in liquid 8 332.4 ± 893.3 LT-CSA (mm ) ± 1 643.1then frozen 8 390.3 ± 817.5 8 340.8 ± 1 000.0 Post 8 556.3 ± 1 579.7 8 658.2 ± 922.3 8 849.5 ± 893.3 8 996.8 ± 919.5 nitrogen andRT-CSA stored 80 The pre- 8 215.4 ± 898.8 (mm ) at Pre °C for protein 8 332.7 ± 1 511.6extraction. 8 483.5 ± 920.9 8 261.4 ± 1 002.0 Post 8 508.3 ± 1 467.4 8 756.1 ± 1 001.6 8 668.0 ± 952.4 8 882.7 ± 868.4 training and *-post-training biopsies were taken, respectively, 4 Post-test values greater than pre-test values (p < 0.001) !- Post-test values forof the ST and CT groups greater than48 the C h and after IT groups (p the < 0.001) last training days before the start training and session. The a post-training sample bwas obtained from a site Fig. 1 Aerobic fitness for the control (C), interval 58 30 training (IT), strength training (ST), and concur3 cm proximal to the pre-training incision. a rent training (CT) groups. Pre- and Post-training (mean ± SE). a – greater than C and ST groups (p < 0.05). b – lower than IT, ST and CT groups (p < 0.05). 0 Post Pre –10 AMPK, phospho-Thr172 AMPK (p-AMPK), Akt, phospho-Ser473Akt IT CT C ST S6K1 and phospho-Thr389-p70 (p-p70S6K1) expres(p-Akt), p70S6K1 c d 15 800 sion levels were evaluated by immunoblotting in total vastus 10 700 Briefly, samples were 5subjected to SDS-PAGE lateralis extracts. 0 in polyacrylamide gels (6–15 %) depending upon protein molec600 –5 ular weight. After electrophoresis, proteins were electrotransb 500 –10 Pre Post ferred to nitrocellulose membranes (BioRad Biosciences; Piscataway, NJ, USA). Equal gel loading and transfer e ciency de Souza EO et al. Molecular Adaptations to Concurrent training. Int J Sports Med 2013; 34: 207–213 were monitored using 0.5 % Ponceau S staining of blot membrane. Blotted membrane was then blocked (5 % BSA, 10 mM Tris-HCl (pH = 7.6), 150 mM NaCl, and 0.1 % Tween 20) for 2 h at room temperature and then incubated overnight at 4 °C with specific antibodies against AMPK, p-AMPK, Akt, pAkt, p70S6K1 and p-p70S6K1 (Cell Signaling Tech., MA, USA) and GAPDH (Advanced Immunochemical, CA, USA). Binding of the primary antibody was detected with the use of peroxidase-conjugated secondary antibodies (rabbit or mouse, depending on the protein, for 2 h at room temperature) and developed using enhanced chemiluminescence (Amersham Biosciences, NJ, USA) detected by autoradiography. Quantification analysis of blots was performed with the use of Image J software (Image J based on NIH image). Samples were normalized to relative changes in GAPDH. In addition, AMPK, Akt, and p70S6K1 phosphorylated/total ratios De&Souza&et&al.,&2013& ed by: Dot. Lib Information. Copyrighted material. 3–4 8–10 RM 4 32–40 120 s Aerobic fitness was significantly improved in the interval2max was improved in 5 ± 0.95 % and 15 ± 1.3 % (pre- to post-test) in groups CT and IT, respectively, Muscle biopsy trained groups after training. VO % Change VO2max (ml.kg –1.min –1) bouts bout time rest interval 1–2 12 RM 3 36 90 s Aerobic fitness Treinamento&Concorrente& % Change time to exhaustion (seconds) weeks intensity sets total volume rest interval interval training intensity AMPK total protein content remained unchanged across time in the ST, CT, IT, and C groups (p = 0.90). Significantly greater Akt protein content was observed at the post-test in the ST group when compared with the C and IT groups (p 0.03). The CT group presented a significant pre- to post-training increment in p70S6K1 protein content (p = 0.04). Additionally, ST and CT groups showed greater p70S6K1 protein content when compared with both the C (p 0.03) and IT (p 0.01) groups at post-test. The IT group showed increased AMPK phosphorylation from the preto the post-training assessment and greater activity when compared with C, CT and ST groups (p = 0.01) at the post-testing. The ST group presented a significantly increased Akt phosphorylation Training & Testing 209 VO2max (ml.kg–1.min–1) Strength Training The ST and CT groups increased leg-press 1RM similarly from pre- to post-test (p 0.001) and presented greater maximum strength values than the C group in the post-test (p 0.001). There were no training e ects in leg press 1RM for the IT and C groups (p 0.93) ( Table 2). Time to exhaustion (seconds) Table 1 Strength and interval training progressions throughout 8 weeks. Muscle hypertrophy Left and right legs quadriceps CSA were significantly increased in both the ST (6.2 ± 1.4 % and 5.5 ± 1.42 %, p 0.0005) and CT groups (7.8 ± 1.66 % and 7.5 ± 1.96 %, p < 0.0001) in the post-test. Quadriceps CSA was greater in the ST and CT groups compared to the C group in the post-test (p 0.05). No di erences were observed in both the C and IT groups (p 0.75. and p 0.18, respectively) ( Table 2). Molecular responses Maximal strength Treinamento&Concorrente& (p = 0.003 and p = 0.003 when compared to the C group). There were no significant di erences in maximal aerobic power increments between CT and IT (p 0.05). All of the training groups presented similar and significant percentage increase in time to exhaustion (TE) when compared to C (CT = 6.1 ± 0.58 %, p = 0.04; IT = 8.3 ± 0.88 %, p = 0.04; ST = 3.2 ± 0.66 %, p = 0.04) ( Fig. 1). 24& 9/24/14& groups covered approximately 5 065 m ( ± 371.5) per training session. The IT protocol used in the present study was based on previous findings that demonstrate: a) a significant superiority of intermittent vs. continuous training regimens in increasing aerobic fitness [16]; and b) the acute interference of the present IT protocol in muscle force production capacity [10]. Despite the expected increase in time to exhaustion in the IT group, the increase in this variable observed in the ST group is in accordance with previous studies demonstrating that maximal strength training may positively a ect the TE [35]. Regarding the muscle strength, some studies have reported reduced gains after CT regimens [19, 34]. For instance, Hickson [19] and Kraemer et al. [24] presented significant di erences in strength gains from pre- to post-training for the ST and CT groups (30 % and 19.5 %, and 35 % and 24 %, respectively). However, it should be emphasized that it might be di cult to compare CT studies [19, 24] due to some confounding factors, such as the type and the intensity of endurance training. Hickson [19] and Kraemer et al. [24] employed a constant workload and traditional endurance exercise (i. e. continuous running) as a greater part of their endurance regimens. In addition, these authors used a longer duration than the current study (i. e., 10–12 weeks of training) and a very high training volume (5 and 4 sessions of each training mode per week, respectively) [19, 24]. Such an unusual high strength training volume may have hampered recovery between training sessions, causing the reduction in strength gains. On the other hand, the low-volume strength training protocol used in our CT regimen produced similar gains over time (p = 0.03). Moreover, Akt activity was significantly greater in the ST group when compared with both the C and IT groups (p 0.03) at the post-test. The ST group presented a trend toward higher p70S6K1 phosphorylation (p = 0.06). The ST group presented significantly greater p70S6K1 phosphorylation when compared with the C and the IT groups (p 0.02) at the post-test. Finally, there were no changes in AMPK, Akt, and p70S6K1 phosphorylated/total ratios from pre- to post-training assessments (p 0.61) ( Fig. 2). Training Regimens and Gene Expression Discussion Forward Reverse GTACGAGCCACCCCCGACAGC TGCTGTCTCCATGTTTGATGTATCT CCAGGCTGGGAACTGCTGGC GGATTTCTGGAGGCCTGCTT GACCAGGAGAAGATGGGCTGAATCCGTT CAGATACCCGATGGATTTTCTCA AGCGCCCCCGAGCCTTGAT TCTCTGCTCCCCACCTCTAAGT TCTCTGCTCCCCACCTCTAAGT TCCAGAGGTGTGAGCCAGTCT GCTCATCACAGTCAAGACCAAAATCCCTT CCCTGTTTCAGCGGAGGAA Hipertrofia&–&Treinamento&Concorrente& for the leg-press 458, knee extension, and knee flexion exercises. All the exercises were performed at constant-speed eccentric and concentric muscle actions, and through a 908 range of motion at the knee joint. The subjects in the IT group performed high-intensity IT on a treadmill. The targeted training intensity was 80–100% of the speed needed to elicit V_ O2max (vV_ O2max). Concurrent training group performed the same ST and IT training protocols described The purpose of this study was to investigate the chronic e ects of CT on skeletal muscle hypertrophy as well as phosphorylation of selected AMPK and Akt/mTOR/p70S6K1 proteins. We hypothesized that in a CT regimen, the activation of the AMPK pathway produced by the IT component would blunt the strength exercise-induced muscle hypertrophy and impair increases in muscle strength. Our findings do not support the proposed hypothesis ( Fig. 2). Conversely, the novel finding of the present study was that, in humans, the muscle hypertrophy stimuli produced by CT seem to override the AMPK hypertrophy-blunting e ect observed in the IT regimen. This data is further supported by the similar muscle strength and hypertrophy gains after CT and ST regimens. The interval training regimen used in the present study was e ective in increasing aerobic fitness in both groups that performed the IT ( Fig. 1). The participants from the IT and CT Treinamento&Concorrente& Pre kDa C 62 Post IT ST CT C Pre IT ST CT kDa C AMPK 62 60 AKT 60 70 p70 70 p-AMPK (a.u.) AMPK total (a.u.) 1.0 0.5 0.0 Pre p70S6k1 total (a.u.) the TM De&Souza&et&al.,&2014& Hipertrofia&–&Intensidade&e&Exercício& Fonseca&et&al.,&2014& p-Akt (a.u.) Pre d,f c,d,f 1.0 0.5 0.0 Pre C IT ST Post CT 1.0 0.5 Pre Pre d,f 1.0 0.5 Pre C IT ST Post CT C Post IT ST CT p-AKTser473 AKT p-p70thr389 p70 p-AMPKthr172 AMPK 2 1 0 Pre Post 1.5 1.0 0.5 0.0 Post 1.5 Pre IT ST CT 3 c,d,f 0.5 0.0 kDa C 60 p-AMPKthr172 60 p-AKTser473 70 70 p-p70thr389 62 GAPDH 62 Post 1.0 0.0 Post 1.5 p-p70S6k1 (a.u.) Akt total (a.u.) 0.5 1.5 1.5 d,f 1.0 0.0 Journal of Strength and Conditioning Research ST CT 2.0 0.0 Post 1.5 Figure 1. Muscle fibers types cross-sectional area responses before (Pre) and after (Post) the training regimens. *p # 0.05 for within-group comparisons (Pre vs. Post). C = control; CSA = cross-sectional area; CT = concurrent training; IT = interval training; ST = strength training. IT c,d,g,h 2.5 1.5 4 C GAPDH 36 36 AU10 Post IT ST CT AMPK Phospho/ Total (a.u.) ActIIb FOXO-3a FLST-3 GASP-1 MSTN SMAD-7 Akt Phospho/ Total (a.u.) Genes p70S6k1 Phospho/ Total (a.u.) TABLE 1. Sequence of primers used in real-time polymerase chain reaction. Downloaded by: Dot. Lib Information. Copyrighted material. Training & Testing 211 Pre Post 1.5 1.0 0.5 0.0 Pre C Post IT ST CT Fig. 2 Total, phosphorylated and phosphorylated/total ratio AMPK, Akt, and p70S6K1 protein expression for the control (C), interval training (IT), strength training (ST), and concurrent training (CT) groups. Pre- and Post-training (mean ± SE). Protein expression was normalized by GAPDH. c – post-training values greater than pre-training values (p < 0.05). d- post-training values greater than the C group, at the same time point (p < 0.05). f – post-training values for the ST group greater than for the IT group, at the same time point (p < 0.05). g – post-training values for the IT group greater than for the ST group, at the same time point (p < 0.05). h – post-training values for the IT group greater than for the CT group, at the same time point (p < 0.05). De&Souza&et&al.,&2013& de Souza EO et al. Molecular Adaptations to Concurrent training. Int J Sports Med 2013; 34: 207–213 Hipertrofia&–&Intensidade&e&Exercício& Fonseca&et&al.,&2014& 25& 9/24/14& 40 Hipertrofia&–&Intensidade&e&Exercício& (e.g., volume total, séries, repetições e intervalo de descanso). O intervalo entre as séries (i.e. 2 minutos) foi mantido durante toda a duração do estudo, o número total de Periodização&e&Hipertrofia& séries, as repetições e a carga levantada foram controlados semanalmente para evitar distorções entre os grupos na variável no volume total (i.e., [séries • repetições •quilos (agachamento) + séries • repetições •quilos (cadeira extensora]) TABELA 3. TABELA 3 - Progressão do volume, da intensidade e dos exercícios utilizados durante as doze semanas de treinamento. Grupos Semanas 1- Semanas 5- 4 Semanas 9- Volum 12 e 9 GNP Seg Qui Seg Qui Seg Qui Agachamento 3x8 3x8 3x8 3x8 3x8 3x8 C.Extensora 2x8 2x8 2x8 2x8 2x8 2x8 320 reps 320 reps 320 reps GPL Seg Qui Seg Qui Seg Qui Agachamento 3x12 2x12 4x8 4x8 3x4 3x4 C.Extensora 2x12 2x12 2x8 2x8 2x4 2x4 GPO Seg Qui Seg Qui Seg Qui Agachamento 2*12 4*6 3x10 4x6 2x8 4x4 C.Extensora 3x12 3x6 2x10 2x6 2x8 2x4 423 reps 408 reps 384 reps 344 reps 160 reps 224 reps Reps/dia 960 40 976 40,6 976 40,6 GNP-grupo não-periodizado; GPL- grupo periodizado-linear; GPO- grupo periodizadoondulado. Reps- repetições. Seg- segunda-feira; Qui- quinta-feira. C.Extensoracadeira extensora. Fonseca&et&al.,&2014& 4.9. Análise estatística De&Souza,&2014& Técnicas de inspeção visual e o teste de Shapiro-Wilk confirmaram a ausência 41 de observações extremas e a normalidade dos dados. Então, foi utilizado um modelo misto assumindo grupo (quatro níveis) e tempo (três níveis) como fatores fixos e os sujeitos como fator aleatório para cada variável dependente. Na ocorrência de razão de valores F significante, foi utilizado um ajustamento de Tukey para efeito de comparações múltiplas. O valor de significância adotado foi de p<0,05 e os dados estão apresentados como média e desvio padrão. Adicionalmente, foram calculados o tamanho do efeito (TE) intragrupo (e.g. médias 6 e 12 semanas- média prétreinamento/ desvio padrão pré-treinamento) (COHEN, 1988; UGRINOWITSCH, FELLINGHAM e RICARD, 2004). 5. RESULTADOS 5.1. Volume total de treinamento Ao final do período experimental foi observado um volume total de treino similar entre os grupos GNP, GPL e GPO: 92.598 ± 15.340kg, 92.973kg ± 10.760kg e 108.367 Periodização&e&Hipertrofia& ± 18.316kg (p>0,05, FIGURA 4A e 4B). Em média, os participantes dos grupos experimentais treinaram com um volume total de 4.450,7 (±160kg) por sessão de Periodização&e&Hipertrofia& 45 treinamento. FIGURA 4- A) dados de volume total ( [séries x repetições x kg (agachamento) + séries FIGURA 7 – Valores de área de secção transversa muscular do quadríceps (ASTM) x repetições x kg (cadeira extensora]) para os grupos não-periodizado (GNP), (média ± DP). * - p<0,05 diferença significantes com relação aos valores (Pré). #- periodizado-linear (GPL) e periodizado-ondulado (GPO). B) intervalos de confiança p<0,05 diferença significante com relação aos valores de seis semanas. GNP- grupo das comparações múltiplas do volume total. não-periodizado, GPL- grupo periodizado-linear, GPO- grupo periodizado-ondulado. De&Souza,&2014& De&Souza,&2014& 26& 9/24/14& Força&x&Potência& Força&x&Potência& Lamas&et&al.,&2010& Lamas&et&al.,&2009& Molecular adaptation to resistance training Table 5. Fiber types cross sectional area (mm2) before and after training for strength, power, and control groups (mean " SEM) Strength training w Type I Type Iia* Type IIb* Power training Control Pre Post Pre Post Pre Post 5186.4 " 444.0 5753.2 " 379.4 4647.9 " 343.8 5968.1 " 516.4 6820.1 " 373.3 6569.6 " 364.5 5358.4 " 454.9 5605.2 " 402.1 5509.2 " 453.1 5063.4 " 456.4 6463.0 " 394.7 6579.6 " 418.8 5567.7 " 521.5 5911.6 " 521.2 4946.0 " 465.3 5330.6 " 572.0 6159.8 " 462.1 5388.8 " 424.7 Força&x&Potência& Velocidade&Exercício&Excêntrico& Post-test values greater than pre-test values (time main effect, Po0.05). w *Post-test values greater than pre-test values (time main effect, Po0.0001). Roschel et al. 287 Fig. 3. mTOR, RICTOR, RAPTOR and 4EBP-1 (AU) gene expression (ratio between the mRNA expression of the gene of interest and the internal standard) for the strength (ST) and power training (PT) and control (C) groups pre and post a 8-week period (mean SEM). aPost-test values greater than pre-test values (Po0.0001). b Post-test for the strength and the PT groups greater than the control group (Po0.0001). cPost-test values for the strength group greater than the post-test values for the power group (Po0.001). dPosttest values for the ST and PT pooled greater than the pre-test values (Po0.05). muscle fiber hypertrophy for all fiber types were produced mainly by the ST group effect. Gene expression analysis revealed that mTOR (effect sizes of 2.8 and 2.3 for the ST and PT, respectively) and RICTOR (effect sizes 2.2 and 1.4) mRNA levels increased for both experimental groups from pre- to post-test (Po0.01). There was no difference in mTOR and RICTOR between the ST and the PT in the post-test (P40.05) but they had higher expression of these genes than the control group in the post-test [Po0.001, Fig. 3(b) and (c)]. Overall, RAPTOR gene expression showed a similar behavior but the ST presented higher post-test values than the PT [Po0.001, Fig. 3(a)]. However, effect sizes were similar between groups (i.e. 3.0 and 3.1). There was a main time effect for 4EBP-1. In order to determine whether this main effect was due to changes in the training groups, the ST and PT groups were pooled and compared with the control group. The pooled data revealed a decreased 4EBP-1 after training [Po0.05, Fig. 3(d), effect size of ! 1.24]. Lamas&et&al.,&2009& Calcineurin gene expression did not change in response to both training regimens. Calcipressin expression was found to increase for both groups from pre- to post-test (Po0.01) [Fig. 4(a)]. Calcipressin mRNA level was also increased after both training regimens compared with the control group in the post-test (Po0.001) [Fig. 4(b)]. Discussion In this study, we compared the effect of different two resistance training regimens on maximum strength gains, muscle fiber hypertrophy and phenotype shift and determined the expression of the genes involved in skeletal muscle plasticity. Our main findings were: (1) strength increased similarly between training protocols; (2) fiber cross-sectional area increased for both training regimens; however, there was a trend toward greater increases in the ST group; (3) mTOR, RAPTOR and RICTOR gene expression Appl. Physiol. Nutr. Metab. Downloaded from www.nrcresearchpress.com by 201.81.148.68 on 04/17/11 For personal use only. Fig. 1. Mechanical output during EE. (a) Peak eccentric torque over 5 sets of 8 eccentric contractions. (b) Total work performed over 5 sets of 8 eccentric contractions. (c) Total impulse over 5 sets of 8 eccentric contractions. (d) Impulse in each of the 5 sets. *, p < 0.05 compared with EF. EE, eccentric exercise; ES, slow EE; EF, fast EE. Fig. 2. Mechano growth factor (MGF) mRNA expression in ES and EF. EE, eccentric exercise; ES, slow EE; EF, fast EE; B, baseline; T1, immediately after EE; and T2, 2 h after EE. *, p < 0.05 compared with B. torque production through the range of motion and time under tension (Crewther et al. 2005). Therefore, contraction velocity has a direct effect on time under tension, accounting for the significant differences observed for total impulse values. Indeed, time under tension in the ES group was 10-fold that of the EF. While the ES group performed the EE at 20°·s–1, resulting in a 4.5-s (90° range of motion) time under tension, the fast velocity of the EF group allowed only 0.43 s under tension because of the high movement speed (210°·s–1). Despite the lesser time under tension in the EF group, it is possible that fast EE may have induced a higher mechanical overload than slow EE (Enoka 1996; Chapman et al. 2008). In fact, it is known that resistance-exercise–induced mechanical overload increases MGF mRNA expression (Rommel et al. 2001; Goldspink 2005; Heinemeier et al. 2007; Liu et al. 2008), which in turn is related to Akt/mTORCI/p70S6K pathway activation (Kimball et al. 2002; Sartorelli and Fulco 2004). Interestingly, although only the ES protocol induced a significant increase in MGF mRNA expression from B to T2, these values were not different between the groups, and greater Akt/mTORCI/p70S6K activation, compared with EF, was not observed. Again, it may be that the greater muscle tension imposed during EF accounted for an increased mechanotransduction, resulting in similar downstream signaling activation (Burkholder 2007). In fact, it has been proposed that the skeletal muscle hypertrophy following EF is related to Z band streaming (Shepstone et al. 2005). Z bands are critical sites for mechanotransduction, because of the presence of phospholipase D (Hornberger et al. 2006a). The increased muscle tension during EF may lead to greater activation of phospholipase D; it has been suggested that this mediates stretch-induced signaling, activating mTORCI/p70S6K Roschel&et&al.,2011&& Published by NRC Research Press 5 27& 9/24/14& 288 Velocidade&Exercício&Excêntrico& Appl. Physiol. Nutr. Metab. Vol. 36, 2011 Appl. Physiol. Nutr. Metab. Downloaded from www.nrcresearchpress.com by 201.81.148.68 on 04/17/11 For personal use only. Fig. 3. Changes in total protein and protein phosphorylation. (a) Akt. (b) Akt phosphorylation. (c) mTOR. (d) mTOR phosphorylation. (e) p70S6k1. (f ) p70S6k1 phosphorylation. EE, eccentric exercise; ES, slow EE; EF, fast EE; B, baseline; T1, immediately after EE; T2, 2 h after EE. *, p < 0.05 compared with B. OBRIGADO&!!!!!& & UGRINOWITSCH@GMAIL.COM& in an Akt-independent way (Hornberger et al. 2006a, 2006b). Additionally, it has been demonstrated that phosphatidic acid (resulting from increased phospholipase D activity) may activate p70S6K in an mTOR-independent fashion (Lehman et al. 2007). Thus, it is possible that muscle tension plays a role in velocity-specific hypertrophy pathway activation, which may have compensated for the time-under-tension difference observed between EF and ES. Regardless of the interesting findings herein, caution should be exercised when interpreting and extrapolating these data. Given the inherent heterogeneity in the molecular responses after resistance training, a within-subject and (or) within-leg design would be optimal. However, it is important to note that even though such a design would be the most efficient in minimizing data variability, it would add great bias to our findings. EE is known to induce muscle damage, which may increase protein synthesis, activating the pathways we assessed in this study. Conversely, a single bout of EE is known to produce the repeated-bout effect, which is characterized by a strong minimization of EE-induced muscle damage (Nosaka and Clarkson 1995; Barroso et al. 2010) and activation of the Akt/mTORCI/p70S6K pathway (V. Tricoli, A. Blazevich, C. Ugrinowitsch, M.S. Aoki, and K, No- saka 2010, unpublished data). The repeated-bout effect induced by a within-leg design could negatively affect our results, masking the effect of exercise velocity. Furthermore, EE is known to cause the greatest cross-education among muscle actions (Hortobágyi et al. 1997; Farthing and Chilibeck 2003a), affecting peak torque and total work between testing sessions. Finally, there is evidence of a contralateral repeated-bout effect (Howatson and Van Someren 2007), hampering the adoption of a within-subject design. In addition, one may argue that the EE was not matched for time under tension (TUT). However, matching TUT would require a far greater number of contractions in the EF group. Exercise volume has been demonstrated to play a role in the magnitude of exercise-induced muscle damage (Nosaka et al. 2001, 2002; Chapman et al. 2006, 2008; Chen and Nosaka 2006), affecting protein phosphorylation. Despite the importance of understanding the molecular responses to EE in TUT-matched conditions, previous studies have shown greater muscle hypertrophy with fast EE when total work, but not TUT, was matched (Farthing and Chilibeck 2003b; Shepstone et al. 2005). Last, it has been demonstrated that type II fibers contribute to a larger degree to the increase in the phosphorylation of p70S6K after EE (Tannerstedt et al. Roschel&et&al.,2011&& Published by NRC Research Press 28&