High fat fed hamster, a unique animal model for treatment of diabetic dyslipidemia with peroxisome proliferator activated receptor alpha selective agonists

被引:58
作者
Wang, PR [1 ]
Qiu, G
Ippolito, M
Wu, M
Milot, D
Ventre, J
Doebber, T
Wright, SD
Chao, YS
机构
[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
关键词
fenofibrate; diabetic dyslipidemia; insulin sensitivity; animal model;
D O I
10.1016/S0014-2999(01)01249-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:285 / 293
页数:9
相关论文
共 42 条
[1]   REGULATION OF GALLBLADDER CHOLESTEROL CONCENTRATION IN THE HAMSTER - ROLE OF HEPATIC CHOLESTEROL LEVEL [J].
ANDERSEN, JM ;
COOK, LR .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 875 (03) :582-592
[2]   FENOFIBRATE - A REVIEW OF ITS PHARMACODYNAMIC AND PHARMACOKINETIC PROPERTIES AND THERAPEUTIC USE IN DYSLIPIDEMIA [J].
BALFOUR, JA ;
MCTAVISH, D ;
HEEL, RC .
DRUGS, 1990, 40 (02) :260-290
[3]   REVIEW OF EUROPEAN CLINICAL-EXPERIENCE WITH FENOFIBRATE [J].
BLANE, GF .
CARDIOLOGY, 1989, 76 :1-13
[4]  
Brewer HB, 1999, AM J CARDIOL, V83, p3F
[5]   Fenofibrate and rosiglitazone lower serum triglycerides with opposing effects on body weight [J].
Chaput, E ;
Saladin, R ;
Silvestre, M ;
Edgar, AD .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 271 (02) :445-450
[6]   Cardiovascular outcomes in type 2 diabetes - A double-blind placebo-controlled study of bezafibrate: the St. Mary's, Ealing, Northwick Park Diabetes Cardiovascular Disease Prevention (SENDCAP) Study [J].
Elkeles, RS ;
Diamond, JR ;
Poulter, C ;
Dhanjil, S ;
Nicolaides, AN ;
Mahmood, S ;
Richmond, W ;
Mather, H ;
Sharp, P ;
Feher, MD .
DIABETES CARE, 1998, 21 (04) :641-648
[7]   DEMONSTRATION OF A CRITICAL ROLE FOR FREE FATTY-ACIDS IN MEDIATING COUNTERREGULATORY STIMULATION OF GLUCONEOGENESIS AND SUPPRESSION OF GLUCOSE-UTILIZATION IN HUMANS [J].
FANELLI, C ;
CALDERONE, S ;
EPIFANO, L ;
DEVINCENZO, A ;
MODARELLI, F ;
PAMPANELLI, S ;
PERRIELLO, G ;
DEFEO, P ;
BRUNETTI, P ;
GERICH, JE ;
BOLLI, GB .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 92 (04) :1617-1622
[8]   RATIONALE AND APPLICATION OF FATTY-ACID OXIDATION INHIBITORS IN TREATMENT OF DIABETES-MELLITUS [J].
FOLEY, JE .
DIABETES CARE, 1992, 15 (06) :773-784
[9]   Bezafibrate and simvastatin combination therapy for diabetic dyslipidaemia: efficacy and safety [J].
Gavish, D ;
Leibovitz, E ;
Shapira, I ;
Rubinstein, A .
JOURNAL OF INTERNAL MEDICINE, 2000, 247 (05) :563-569
[10]   Comparison of the efficacy and safety of fenofibrate and lovastatin in patients with primary type IIa or IIb hyperlipidaemia [J].
Gholami, K ;
Tavakoli, N ;
Maleki, M ;
Shafiee, A .
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS, 1998, 23 (03) :213-221