Barbara L. Bernardo
Transcription
Barbara L. Bernardo
Barbara L. Bernardo 43 Seabury Avenue Ledyard, CT 06339 (860) 464-9687 (h) (860) 686-2190 (w) Barbara.bernardo@pfizer.com (w), barbvinozmis@yahoo.com (h) CAREER SUMMARY • • • • • Research Scientist with 15 years experience in metabolic disease (frailty, diabetes, and obesity), oncology and safety pharmacology research in a pharmaceutical industry setting Provide in-vivo scientific expertise to investigate disease mechanisms, provide derisking strategies and evaluate new and established targets in diabetes, whole body metabolism, muscle metabolism and muscle wasting Utilize standard pre-clinical models and develop novel in vivo models to characterize and dissect out mechanisms of disease pathogenesis Team and project focus and the ability to work on varied projects Thorough experience in analyzing, collating, reporting and presenting data results PROFESSIONAL SKILL SET In-vivo (Mice, Rats, Dogs, Non-Human Primates) • Cardiovascular assessment using radio-telemetry • Whole body metabolism characterization through indirect calorimetry • Glucose Homeostasis tests: Hyperglycemic clamp, OGTT, IPGTT, IVGTT, ITT • Whole Body imaging techniques (micro-CT, MRI, DEXA, IVIS, ultrasound) • Functional in-vivo tests (treadmill running, running wheel, grip strength, rotorod) • In-vivo and in-situ evoked muscle strength • Animal model development (ex. Flow-Mediated Dilation, Hyperglycemic clamp, Models of Brown Adipose activity, hindlimb immobilization, steroid myopathy, whole body vibration, graft vs. host) • Sciatic nerve denervation • Dosing (p.o., i.p., i.m., i.t., i.v. and s.c.) • Blood collection (cardiac puncture, jugular, tail, facial, saphenous, cephalic and orbital bleeds) • Necropsies, Muscle, fat pad, bone and tissue dissection • Administration of anesthesia: (Isoflurane, Pentobarbital, Ketamine, Midazolam) • Surgery (osmotic mini-pump implants, iBAT removal) • Tumor cell implantation (s.c., i.v., i.c.), tumor fragment implantation (s.c.) • Animal handling, restraint In-vitro • ELISA and multiplex assays • SDS-PAGE & Western Blot • RNA isolation • Cell culture (human and mouse lines); Prepare cell and tissue lysates • Extract and measure tissue levels of glycogen, triglycerides and free fatty acids • Solid phase extractions • Plasma/Serum Clinical Chemistry analysis • Angiogenic assay development Animal Model Experience • Frailty/Muscle Wasting: hindlimb immobilization, aged mice and rats, steroid myopathy, denervation • Diabetes/Metabolism: ob/ob, db/db, DIO, STZ-induced, Zucker, ZDF, ex-iBAT, GEMM including CRE-Luciferase mice, obese NHP • Oncology: immunocompromised mice and rats, xenograft models, angiogenesis and metastasis models • Immunology: GvH Barbara L. Bernardo 860-464-9687 `page 2 of 5 PROFESSIONAL EXPERIENCE Pfizer Inc., Groton, CT Present Senior Scientist – Department of Safety Pharmacology – Physiology Group • Provide safety risk assessments and de-risking strategies for multiple project teams across therapeutic areas • Study director role for in-vivo safety and efficacy studies; responsible for protocol design , execution and report generation • Established and validated a mouse cardiovascular safety assessment model using radio-telemetry • Development of a large animal model (non-human primate) of insulin secretion (hyperglycemic clamp) to assess novel compounds for T2DM • Design and execute small animal studies to investigate the role of brown fat and temperature on metabolic outcomes and in response to novel treatments for obesity & metabolic disease • Assist in the development of a primate model to assess vascular reactivity (flowmediated dilation) using ultrasound techniques • Work in a multi-disciplinary fashion to provide research support for the Cambridge based research unit • Responsible for collecting, analyzing and presenting data to drive decision making Pfizer Inc., Groton, CT 2006-2012 Scientist – Department of Cardiovascular, Metabolic & Endocrine Disease • Design and execute primary in-vivo assays and models to characterize lead compounds for their effect on glucose homeostasis and/or whole body energy metabolism as well as establish and implement appropriate secondary and tertiary in-vivo models to fully characterize lead molecules • Develop in-vivo research models and methods to promote mechanism-based drug discovery for disease-mediated alterations in muscle metabolism, muscle growth and wasting, brown fat activity and whole body metabolism • Characterize metabolic and functional (strength, exercise capacity, balance/coordination, etc) gains/losses of modulating skeletal muscle mass, composition and oxidative capacity • Perform ex-vivo and in-vitro experiments for the evaluation of Biomarker and/or Protein changes in response to compound and/or functional/mechanical intervention in-vivo • Manage and author animal use protocols and act as primary liaison between CVMED and Comparative Medicine for vivarium related operations and activities Pfizer Inc. (Nucon Group), Groton, CT 2005-2006 Associate Scientist – CVMED Department, Obesity Biology • Execute therapeutic in-vivo efficacy studies for obesity drug development • Operating MRI, PIXImus and DEXA x-ray machines to determine body composition • Operating and optimizing spontaneous food intake system to monitor food intake and activity • Maintain accurate study findings, analyze and present data • Review and search relevant scientific literature CGI Pharmaceuticals, Branford, CT 2005 Senior Associate Scientist - Department of Immunology and Inflammation • Design and execute therapeutic in-vivo studies, ex-vivo and in-vitro assays • Characterization of animal models for Lupus (GvH model) and Rheumatoid Arthritis (CIA model) • Trained staff on in-vivo techniques • Assisted Oncology department with animal model development (metastasis models) • Maintained accurate study findings, analyze, organize, and present data Barbara L. Bernardo 860-464-9687 `page 3 of 5 Bayer Corporation, West Haven, CT 2001-2005 Senior Associate Scientist - Department of Cancer Research • Critical role in advancing preclinical drug discovery projects by scheduling, organizing and conducting in vivo studies (Tumor Growth Inhibition, PK/PD and Tox). • Design in-vivo studies to support various projects • Expertise in all aspects of cancer in vivo models and techniques • Proficient in cell culture techniques (human and mouse lines) • Tumor model development • Trained new staff on in-vivo techniques • Maintained accurate study findings, analyze, organize, and present data • Development of a Matrigel-plug assay as an in-vivo angiogenesis assay • Assisted in the development of a tube-formation assay as an in-vitro angiogenesis assay • Assisted in implementing a cell line repository to improve data quality and consistency across Oncology department. • Member of the Safety Committee Bayer Corporation, West Haven, CT 1999-2001 Assistant Laboratory Animal Technician - Department of Research Technologies • Handled all aspects of animal husbandry • Animal handling, assessment of animal health • Cage washing, cage changing • Knowledge of proper housing and enrichment programs • Compliance of federal, state, and facility guidelines • Ensuring proper sanitation of all parts of animal facility • Followed and developed SOP’s for all aspects of animal husbandry • Reviewing and learning animal use protocols • Following proper waste management procedures, including bio-hazardous waste • Daily communication with in-vivo associates • Performing monthly safety evaluations of the animal facilities • Training new husbandry associates EDUCATION B.S., Health Science, Quinnipiac University, Hamden, CT ACCREDITATIONS Certified by the American Association of Laboratory Animal Science as an Assistant Laboratory Animal Technician AWARDS Received an award for Animal Technician of the Year 2000 by the Southern New England Branch of the American Association of Laboratory Animal Science. Barbara L. Bernardo 860-464-9687 `page 4 of 5 EQUIPMENT DSI telemetry platforms including Ponemah and OpenArt IVIS ® Imaging System for use with real time imaging La-Theta micro-CT 4 in 1 Echo MRI PIXImus DEXA CLAMS (Columbus Instruments) Spontaneous Food Intake System (Columbus Instruments) Neuromuscular Function Equipment Sector Imager 6000 (Meso-scale discovery) Spectramax Plus, Spectramax Gemini Fugifilm Imager & Developer Bio-Plex (Bio-Rad) Hitachi Roche 912 Clinical Chemistry Analyzer Hitachi Roche Cobas c311 Clinical Chemistry Analyzer Publications 1) Barbara Bernardo, Min Lu, Gautam Bandyopadhyay, Pingping Li, Yingjiang Zhou, Jie Huang, Nancy Levin, Roberto A. Calle, Derek M. Erion, Timothy P. Rolph, Martin Brenner, Saswata Talukdar “FGF21 does not require interscapular brown adipose tissue and improves liver metabolic profile in animal models of obesity and insulin resistance” Submitted 02 Feb 2015, Sci Rep 2) Yan Weng, Jeffrey R Chabot, Barbara Bernardo, Qingyun Yan, Yimin Zhu, Martin B Brenner, Chandra Vage, Alison Logan, Roberto Calle, Saswata Talukdar “Pharmacokinetics (PK), pharmacodynamics (PD) and integrated PK/PD modeling of a novel long acting FGF21 clinical candidate PF-05231023 in dietinduced obese and leptin-deficient obese mice” PONE-D-14-47149R1 (accepted 30 Jan 2015) 3) Yuichi Akasaki, Noriyuki Ouchi, Yasuhiro Izumiya, Barbara L. Bernardo, Nathan K.LeBrasseur, and Kenneth Walsh “Glycolytic fast-twitch muscle fiber restoration counters adverse age-related changes in body composition and metabolism” Aging Cell, 2013, Doi: 10.1111/acel.12153 4) Barbara L. Bernardo, Timothy S. Wachtmann, Patricia G. Cosgrove, Andrew M. Kuhn, Alan C. Opsahl, Kyle M. Judkins, Thomas B. Freeman, John R. Hadcock, Nathan K. LeBrasseur “PPAR δ Activation and Myostatin Inhibition Exert Distinct yet Complimentary Effects on the Metabolic Profile of ob/ob Mice” PLoS ONE 5(6): e11307. doi:10.1371/journal.pone.0011307 5) Nathan K. LeBrasseur, Theresa M. Schelhorn, Barbara L. Bernardo, Patricia G. Cosgrove, Paula M. Loria, Thomas A. Brown “Myostatin inhibition enhances the effects of exercise on performance and metabolic outcomes in aged mice” J Gerontol A Biol Sci Med Sci doi:10.1093/gerona/glp068 Barbara L. Bernardo 860-464-9687 `page 5 of 5 Abstracts and Posters 1. Barbara L. Bernardo, David A. Griffith, Margaret S. Landis, Debbie Wanapun, David Tess, Tom McDonald, Amit Kalgutkar, Brent Kuzmiski, Nick Edmunds. “Development of a hyperglycemic clamp in non-human primates to assess GLP-1 mediated insulin secretion” American Diabetes Association, San Francisco 2014 2. Janice Chin, Barbara Bernardo, Martin Brenner, Joanne Buxton, John Cheng, Kentaro Futatsugi, Denise Gautreau, John Hadcock, Terri Hinchey, Ann Janssen, Dawn Kelly-Sullivan, Dave Piotrowski, Nicole Roush, Suvi Simila, Joe Warmus, Angela Wolford. “A Small Molecule TGR5 (GPBAR1) Agonist Shows Metabolic and Anti-inflammatory Effects in Cells Expressing Human TGR5” American Diabetes Association, Chicago. 2013 3. Darwin V. Lee, Barbara Bernardo, Saswata Talukdar & Martin B. Brenner “Fibroblast Growth Factor-21 (FGF-21) synergizes with insulin in human adipose stem cell-derived (hASC) adipocytes” EASD, 2012 4. Kyle Kuszpit, Laigao Chen, Aijun Zhu, Gwen Currier, Kenneth Zasadny, Lucinda Thiede, Barbara Bernardo, Martin Brenner “Using [18F]FDG PET as a biomarker for brown adipose tissue (BAT) metabolism in diabetes/obesity research” 2011 World Molecular Imaging Congress, Sept. 2011 5. Salatto CT, Salter EB, Bernardo B, Smith E, Loria PM, Brown TA “DIO Mice Treated with an anti-Myostatin mAB Exhibit Increased Insulin Sensitivity and Decreased Tissue Triglycerides” APPL PHYSIOL NUTR METAB 2009; 34(6)(DEC):1153 (Abstr 144) 6. D. Auclair, D. Miller, C. Carter, Y. Chang, B. Polony, X. Zhang, V. Yatsula, W. Pickett, A. Burd, H. Shi, S. Rocks, R. Gedrich, L. Abriola, D. Apanovitch, H. Vasavada, I. Enyedy, S. Heald, J. Dumas, B. Riedl, S.M. Wilhelm, P.A. Trail “BAY 43-9006 (Sorafinib) is a potent inhibitor of FLT3 tyrosine kinase signaling in AML Cells” AACR (2005) 7. Y. Chang, C. Cortes, B. Polony, C. Brink, J. Elting “Preclinical chemotherapy with the VEGFR-2 and PDGFR inhibitor, BAY 57-9352, in combination with Capecitabine and Paclitaxel” AACR (2005) 8. P. Vincent, X. Zhang, C. Chen, L. Lantz, C. Rembiesa, B. Polony, C. Carter “Chemotherapy with the raf kinase inhibitor BAY 43-9006 in combination with irinotecan, vinorelbine, or gemcitabine is well tolerated and efficacious in preclinical xenograft models” ASCO (2002)