• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

非诺贝特通过性二态性调节肥胖和脂质代谢。

Fenofibrate regulates obesity and lipid metabolism with sexual dimorphism.

作者信息

Yoon Michung, Jeong Sunhyo, Nicol Christopher J, Lee Hyunghee, Han Miyoung, Kim Jung-Jae, Seo Yun-Jeong, Ryu Chilyeol, Oh Goo Taeg

机构信息

Department of Life Sciences, Mokwon University, Taejon 302-729, Korea.

出版信息

Exp Mol Med. 2002 Dec 31;34(6):481-8. doi: 10.1038/emm.2002.67.

DOI:10.1038/emm.2002.67
PMID:12526091
Abstract

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.

摘要

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。

相似文献

1
Fenofibrate regulates obesity and lipid metabolism with sexual dimorphism.非诺贝特通过性二态性调节肥胖和脂质代谢。
Exp Mol Med. 2002 Dec 31;34(6):481-8. doi: 10.1038/emm.2002.67.
2
Effects of fenofibrate on high-fat diet-induced body weight gain and adiposity in female C57BL/6J mice.非诺贝特对高脂饮食诱导的雌性C57BL/6J小鼠体重增加和肥胖的影响。
Metabolism. 2004 Oct;53(10):1284-9. doi: 10.1016/j.metabol.2004.05.003.
3
Changes in liver PPARalpha mRNA expression in response to two levels of high-safflower-oil diets correlate with changes in adiposity and serum leptin in rats and mice.大鼠和小鼠肝脏中过氧化物酶体增殖物激活受体α(PPARα)mRNA表达对两种水平的高红花油饮食的反应变化与肥胖和血清瘦素的变化相关。
J Nutr Biochem. 2007 Feb;18(2):86-96. doi: 10.1016/j.jnutbio.2006.03.003. Epub 2006 May 18.
4
Fenofibrate prevents obesity and hypertriglyceridemia in low-density lipoprotein receptor-null mice.非诺贝特可预防低密度脂蛋白受体缺失小鼠的肥胖和高甘油三酯血症。
Metabolism. 2004 May;53(5):607-13. doi: 10.1016/j.metabol.2003.12.010.
5
Fenofibrate modulates cardiac and hepatic metabolism and increases ischemic tolerance in diet-induced obese mice.非诺贝特调节饮食诱导的肥胖小鼠的心脏和肝脏代谢并提高缺血耐受性。
J Mol Cell Cardiol. 2008 Jan;44(1):201-9. doi: 10.1016/j.yjmcc.2007.08.020. Epub 2007 Sep 7.
6
Green tea (-)-epigallocatechin-3-gallate reduces body weight with regulation of multiple genes expression in adipose tissue of diet-induced obese mice.绿茶(-)-表没食子儿茶素-3-没食子酸酯通过调节饮食诱导肥胖小鼠脂肪组织中的多个基因表达来减轻体重。
Ann Nutr Metab. 2009;54(2):151-7. doi: 10.1159/000214834. Epub 2009 Apr 22.
7
Fenofibrate improves lipid metabolism and obesity in ovariectomized LDL receptor-null mice.
Biochem Biophys Res Commun. 2003 Feb 28;302(1):29-34. doi: 10.1016/s0006-291x(03)00088-3.
8
Regulation of obesity and lipid disorders by herbal extracts from Morus alba, Melissa officinalis, and Artemisia capillaris in high-fat diet-induced obese mice.桑叶、香蜂草和茵陈蒿的草药提取物对高脂饮食诱导的肥胖小鼠肥胖和脂质代谢紊乱的调节作用
J Ethnopharmacol. 2008 Jan 17;115(2):263-70. doi: 10.1016/j.jep.2007.09.029. Epub 2007 Oct 5.
9
Inhibition of the actions of peroxisome proliferator-activated receptor alpha on obesity by estrogen.雌激素对过氧化物酶体增殖物激活受体α在肥胖方面作用的抑制
Obesity (Silver Spring). 2007 Jun;15(6):1430-40. doi: 10.1038/oby.2007.171.
10
Trans-10,cis-12 CLA increases liver and decreases adipose tissue lipids in mice: possible roles of specific lipid metabolism genes.反式-10,顺式-12共轭亚油酸可降低小鼠肝脏脂质并减少脂肪组织脂质:特定脂质代谢基因的可能作用
Lipids. 2003 May;38(5):497-504. doi: 10.1007/s11745-003-1090-0.

引用本文的文献

1
Sex Hormone: A Potential Target at Treating Female Metabolic Dysfunction-Associated Steatotic Liver Disease?性激素:治疗女性代谢功能障碍相关脂肪性肝病的潜在靶点?
J Clin Exp Hepatol. 2025 Mar-Apr;15(2):102459. doi: 10.1016/j.jceh.2024.102459. Epub 2024 Nov 19.
2
A sexually dimorphic hepatic cycle of periportal VLDL generation and subsequent pericentral VLDLR-mediated re-uptake.肝内门周 VLDL 生成和随后的中心 VLDLR 介导的再摄取存在性别二态性周期。
Nat Commun. 2024 Sep 28;15(1):8422. doi: 10.1038/s41467-024-52751-2.
3
Adequate enrollment of women in cardiovascular drug trials and the need for sex-specific assessment and reporting.
女性在心血管药物试验中的充分入组以及进行性别特异性评估和报告的必要性。
Am Heart J Plus. 2022 Jun 23;17:100155. doi: 10.1016/j.ahjo.2022.100155. eCollection 2022 May.
4
Fenofibrate alleviates insulin resistance by reducing tissue inflammation in obese ovariectomized mice.非诺贝特通过减轻肥胖去卵巢小鼠的组织炎症来缓解胰岛素抵抗。
Nutr Diabetes. 2023 Nov 7;13(1):19. doi: 10.1038/s41387-023-00249-z.
5
Impact of Sex and Gender on Clinical Management of Patients with Advanced Chronic Liver Disease and Type 2 Diabetes.性别对晚期慢性肝病合并2型糖尿病患者临床管理的影响
J Pers Med. 2023 Mar 20;13(3):558. doi: 10.3390/jpm13030558.
6
Fenofibrate enhances lipid deposition via modulating PPARγ, SREBP-1c, and gut microbiota in mice fed a high-fat diet.非诺贝特通过调节高脂饮食喂养小鼠的过氧化物酶体增殖物激活受体γ(PPARγ)、固醇调节元件结合蛋白-1c(SREBP-1c)和肠道微生物群来增强脂质沉积。
Front Nutr. 2022 Sep 12;9:971581. doi: 10.3389/fnut.2022.971581. eCollection 2022.
7
ILRUN Promotes Atherosclerosis Through Lipid-Dependent and Lipid-Independent Factors.ILRUN 通过脂质依赖和非依赖因素促进动脉粥样硬化。
Arterioscler Thromb Vasc Biol. 2022 Sep;42(9):1139-1151. doi: 10.1161/ATVBAHA.121.317156. Epub 2022 Jul 14.
8
Ferulic Acid Prevents Nonalcoholic Fatty Liver Disease by Promoting Fatty Acid Oxidation and Energy Expenditure in C57BL/6 Mice Fed a High-Fat Diet.阿魏酸通过促进高脂肪饮食喂养的 C57BL/6 小鼠的脂肪酸氧化和能量消耗来预防非酒精性脂肪肝病。
Nutrients. 2022 Jun 18;14(12):2530. doi: 10.3390/nu14122530.
9
Mitochondrial Function, Fatty Acid Metabolism, and Body Composition in the Hyperbilirubinemic Gunn Rat.高胆红素血症Gunn大鼠的线粒体功能、脂肪酸代谢和身体组成
Front Pharmacol. 2021 Mar 8;12:586715. doi: 10.3389/fphar.2021.586715. eCollection 2021.
10
SIRT6 Promotes Hepatic Beta-Oxidation via Activation of PPARα.SIRT6 通过激活 PPARα 促进肝脏β氧化。
Cell Rep. 2019 Dec 17;29(12):4127-4143.e8. doi: 10.1016/j.celrep.2019.11.067.