Jeong Sunhyo, Han Miyoung, Lee Hyunghee, Kim Mina, Kim Jaekwang, Nicol Christopher J, Kim Bang Hyun, Choi Jae Hoon, Nam Ki-Hoan, Oh Goo Taeg, Yoon Michung
Department of Life Sciences, Mokwon University, Taejon, Korea.
Metabolism. 2004 Oct;53(10):1284-9. doi: 10.1016/j.metabol.2004.05.003.
Our previous study suggested that fenofibrate affects obesity and lipid metabolism in a sexually dimorphic manner in part through the differential activation of hepatic peroxisome proliferator-activated receptor alpha (PPARalpha) in male and female C57BL/6J mice. To determine whether fenofibrate reduces body weight gain and adiposity in female sham-operated (Sham) and ovariectomized (OVX) C57BL/6J mice, the effects of fenofibrate on not only body weight, white adipose tissue (WAT) mass, and food intake, but also the expression of both leptin and PPARalpha target genes were measured. Compared to their respective low-fat diet-fed controls, both Sham and OVX mice exhibited increases in body weight and WAT mass when fed a high-fat diet. Fenofibrate treatment decreased body weight gain and WAT mass in OVX, but not in Sham mice. Furthermore, fenofibrate increased the mRNA levels of PPARalpha target genes encoding peroxisomal enzymes involved in fatty acid beta-oxidation, and reduced apolipoprotein C-III (apo C-III) mRNA, all of which were expressed at higher levels in OVX compared to Sham mice. However, leptin mRNA levels were found to positively correlate with WAT mass, and food intake was not changed in either OVX or Sham mice following fenofibrate treatment. These results suggest that fenofibrate differentially regulates body weight and adiposity due in part to differences in PPARalpha activation, but not to differences in leptin production, between female OVX and Sham mice.
我们之前的研究表明,非诺贝特以性别二态性方式影响肥胖和脂质代谢,部分原因是雄性和雌性C57BL/6J小鼠肝脏中过氧化物酶体增殖物激活受体α(PPARα)的激活存在差异。为了确定非诺贝特是否能降低雌性假手术(Sham)和去卵巢(OVX)的C57BL/6J小鼠的体重增加和肥胖,我们检测了非诺贝特对体重、白色脂肪组织(WAT)质量、食物摄入量以及瘦素和PPARα靶基因表达的影响。与各自低脂饮食喂养的对照组相比,Sham和OVX小鼠在高脂饮食喂养时体重和WAT质量均增加。非诺贝特治疗可降低OVX小鼠的体重增加和WAT质量,但对Sham小鼠无效。此外,非诺贝特增加了参与脂肪酸β氧化的过氧化物酶体酶编码的PPARα靶基因的mRNA水平,并降低了载脂蛋白C-III(apo C-III)mRNA水平,与Sham小鼠相比,这些基因在OVX小鼠中的表达水平更高。然而,发现瘦素mRNA水平与WAT质量呈正相关,非诺贝特治疗后,OVX和Sham小鼠的食物摄入量均未改变。这些结果表明,非诺贝特对体重和肥胖的调节存在差异,部分原因是雌性OVX和Sham小鼠之间PPARα激活的差异,而非瘦素产生的差异。