Yoon Michung, Jeong Sunhyo, Nicol Christopher J, Lee Hyunghee, Han Miyoung, Kim Jung-Jae, Seo Yun-Jeong, Ryu Chilyeol, Oh Goo Taeg
Department of Life Sciences, Mokwon University, Taejon 302-729, Korea.
Exp Mol Med. 2002 Dec 31;34(6):481-8. doi: 10.1038/emm.2002.67.
To determine whether the PPARalpha agonist fenofibrate regulates obesity and lipid metabolism with sexual dimorphism, we examined the effects of fenofibrate on body weight, white adipose tissue (WAT) mass, circulating lipids, and the expression of PPARalpha target genes in both sexes of high fat diet-fed C57BL/6J mice. Both sexes of mice fed a high-fat diet for 14 weeks exhibited increases in body weight, visceral WAT mass, as well as serum triglycerides and cholesterol, although these effects were more pronounced among males. Feeding a high fat diet supplemented with fenofibrate (0.05% w/w) reduced all of these effects significantly in males except serum cholesterol level. Females on a fenofibrate-enriched high fat diet had reduced serum triglyceride levels, albeit to a smaller extent compared to males, but did not exhibit decreases in body weight, WAT mass, and serum cholesterol. Fenofibrate treatment resulted in hepatic induction of PPARalpha target genes encoding enzymes for fatty acid beta-oxidation, the magnitudes of which were much higher in males compared to females, as evidenced by results for acyl-CoA oxidase, a first enzyme of the beta-oxidation system. These results suggest that observed sexually dimorphic effects on body weight, WAT mass and serum lipids by fenofibrate may involve sexually related elements in the differential activation of PPARalpha.
为了确定过氧化物酶体增殖物激活受体α(PPARα)激动剂非诺贝特是否以性别差异方式调节肥胖和脂质代谢,我们研究了非诺贝特对高脂饮食喂养的C57BL/6J小鼠雌雄两性的体重、白色脂肪组织(WAT)质量、循环脂质以及PPARα靶基因表达的影响。高脂饮食喂养14周的雌雄小鼠体重、内脏WAT质量以及血清甘油三酯和胆固醇均增加,尽管这些影响在雄性中更为明显。喂食添加非诺贝特(0.05% w/w)的高脂饮食可显著降低雄性小鼠的所有这些影响,但血清胆固醇水平除外。食用富含非诺贝特的高脂饮食的雌性小鼠血清甘油三酯水平降低,尽管与雄性相比程度较小,但体重、WAT质量和血清胆固醇并未降低。非诺贝特治疗导致肝脏中编码脂肪酸β氧化酶的PPARα靶基因的诱导,与雌性相比,雄性中这些基因的诱导程度要高得多,β氧化系统的第一种酶酰基辅酶A氧化酶的结果证明了这一点。这些结果表明,非诺贝特对体重、WAT质量和血清脂质的性别差异影响可能涉及PPARα差异激活中的性别相关因素。