High fat fed hamster, a unique animal model for treatment of diabetic dyslipidemia with peroxisome proliferator activated receptor alpha selective agonists
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Wang, PR
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Merck & Co Inc, Merck Res Lab R80W250, Dept Atherosclerosis & Endocrinol, Rahway, NJ 07065 USAMerck & Co Inc, Merck Res Lab R80W250, Dept Atherosclerosis & Endocrinol, Rahway, NJ 07065 USA
Wang, PR
[1
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Qiu, G
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机构:Merck & Co Inc, Merck Res Lab R80W250, Dept Atherosclerosis & Endocrinol, Rahway, NJ 07065 USA
Qiu, G
Ippolito, M
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Ippolito, M
Wu, M
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Wu, M
Milot, D
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Milot, D
Ventre, J
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Ventre, J
Doebber, T
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Doebber, T
Wright, SD
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Wright, SD
Chao, YS
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Chao, YS
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[1] Merck & Co Inc, Merck Res Lab R80W250, Dept Atherosclerosis & Endocrinol, Rahway, NJ 07065 USA
[2] Merck & Co Inc, Merck Res Lab, Dept Metab Disorders, Rahway, NJ 07065 USA
Dyslipidemia, a major risk factor for cardiovascular disease, may be directly linked to diabetic hyperglycemia and insulin resistance. An appropriate dyslipidemic animal model that has diabetes would provide an important tool for research on the treatment of diabetic dyslipidemia. Ten days of high fat feeding in golden Syrian hamsters resulted in a significant increase in insulin resistance and baseline serum lipid levels accompanied by a pronounced dyslipidemia. Thirteen days of treatment with fenofibrate, a peroxisome proliferator-activated receptor alpha (PPAR alpha) selective agonist, produced a dose-dependent decrease in serum lipid levels. The pattern observed was characterized by lowered very-low-density lipoprotein (VLDL) and low-density lipoprotein (LDL) and raised hi.-h-density lipoprotein (HDL) cholesterol in a fashion similar to that seen in man. Diabetic conditions were also significantly improved by fenofibrate with a normalization of impaired glucose tolerance and an improvement of insulin sensitivity during an oral glucose tolerance test. These data suggest that fenofibrate may correct not only the dyslipidemia but also the insulin resistance caused by a high fat diet, and the high fat fed hamster may be a good animal model for research on the treatment of diabetic dyslipidemia with PPAR alpha selective agonists. (C) 2001 Published by Elsevier Science B.V.