Literature DB >> 11590209

Effects of fenofibrate on lipid parameters in obese rhesus monkeys.

D A Winegar1, P J Brown, W O Wilkison, M C Lewis, R J Ott, W Q Tong, H R Brown, J M Lehmann, S A Kliewer, K D Plunket, J M Way, N L Bodkin, B C Hansen.   

Abstract

Fenofibrate is a member of the fibrate class of hypolipidemic agents used clinically to treat hypertriglyceridemia and mixed hyperlipidemia. The fibrates were developed primarily on the basis of their cholesterol and triglyceride lowering in rodents. Fibrates have historically been ineffective at lowering triglycerides in experimentally-induced dyslipidemia in nonhuman primate models. The spontaneously obese rhesus monkey is a well-recognized animal model for the study of human obesity and type 2 diabetes, and many of these monkeys exhibit naturally occurring lipid abnormalities, including elevated triglycerides and low HDL cholesterol (HDL-C), similar to patients with type 2 diabetes. To explore whether the obese rhesus model was predictive of the lipid lowering effects of fibrates, we evaluated fenofibrate in six hypertriglyceridemic, hyperinsulinemic, nondiabetic animals in a 20-week, dose-escalating study. The study consisted of a 4-week baseline period, two treatment periods of 10 mg/kg twice daily (b.i.d) for 4 weeks and 30 mg/kg b.i.d. for 8 weeks, and a 4-week washout period. Fenofibrate (30 mg/kg b.i.d) decreased serum triglycerides 55% and LDL-C 27%, whereas HDL-C increased 35%. Apolipoproteins B-100 and C-III levels were also reduced 70% and 29%, respectively. Food intake, body weight, and plasma glucose were not affected throughout the study. Interestingly, plasma insulin levels decreased 40% during the 30 mg/kg treatment period, suggesting improvement in insulin sensitivity. These results support the use of obese rhesus monkey as an excellent animal model for studying the effects of novel hypolipidemic agents, particularly agents that impact serum triglycerides and HDL-C.

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Year:  2001        PMID: 11590209

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  15 in total

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Review 2.  Lipid therapy for cardiovascular disease with insulin resistance, diabetes, or the metabolic syndrome.

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3.  Development of a sensitive ELISA to quantify apolipoprotein CIII in nonhuman primate serum.

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Review 4.  Nonhuman primates and other animal models in diabetes research.

Authors:  H James Harwood; Paul Listrani; Janice D Wagner
Journal:  J Diabetes Sci Technol       Date:  2012-05-01

5.  Deep-coverage rhesus red blood cell proteome: a first comparison with the human and mouse red blood cell.

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Journal:  Blood Transfus       Date:  2010-06       Impact factor: 3.443

Review 6.  Use and Importance of Nonhuman Primates in Metabolic Disease Research: Current State of the Field.

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7.  Cell-specific toxicity of fibrates in human embryonal rhabdomyosarcoma cells.

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Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2003-02-08       Impact factor: 3.000

8.  Effects of aleglitazar, a balanced dual peroxisome proliferator-activated receptor α/γ agonist on glycemic and lipid parameters in a primate model of the metabolic syndrome.

Authors:  Barbara C Hansen; Xenia T Tigno; Agnes Bénardeau; Markus Meyer; Elena Sebokova; Jacques Mizrahi
Journal:  Cardiovasc Diabetol       Date:  2011-01-20       Impact factor: 9.951

Review 9.  Obesity and Aging in Humans and Nonhuman Primates: A Mini-Review.

Authors:  Kelli L Vaughan; Julie A Mattison
Journal:  Gerontology       Date:  2016-04-28       Impact factor: 5.140

10.  Increased fibroblast growth factor 21 expression in high-fat diet-sensitive non-human primates (Macaca mulatta).

Authors:  E B Nygaard; C L Møller; P Kievit; K L Grove; B Andersen
Journal:  Int J Obes (Lond)       Date:  2013-05-21       Impact factor: 5.095

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