• 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

大鼠棕色和白色脂肪组织中肥胖基因表达的调节。

Modulation of obese gene expression in rat brown and white adipose tissues.

作者信息

Moinat M, Deng C, Muzzin P, Assimacopoulos-Jeannet F, Seydoux J, Dulloo A G, Giacobino J P

机构信息

Département de Biochimie Médicale, Centre Médical Universitaire, Genève, Switzerland.

出版信息

FEBS Lett. 1995 Oct 9;373(2):131-4. doi: 10.1016/0014-5793(95)01030-i.

DOI:10.1016/0014-5793(95)01030-i
PMID:7589451
Abstract

The ob gene mRNA expression in rat brown adipose tissue (BAT) and epididymal white adipose tissue (WAT) was measured on Northern blots hybridized with a rat ob gene probe. The level of ob gene mRNA in BAT was about 40% of that in WAT. Fasting (36 h) or semi-starvation (10 days) decreased the ob gene mRNA level in both tissues by 62-68%, and cold exposure at 6 degrees C (24 h) decreased it in BAT (-84%) but not in WAT. Acute administration of the beta 3-adrenergic agonist Ro 16-8714 decreased the ob gene mRNA level in BAT (-51%) and WAT (-28%) of lean Zucker rats and only in BAT (-74%) of obese falfa rats. This study demonstrates that, in the rat, the ob gene is not only expressed in WAT but also in BAT, and suggests that in these two tissues, the modulation of the ob gene expression might be more closely associated with known alterations in cell lipid content than with changes in sympathetic activity.

摘要

用大鼠ob基因探针进行Northern杂交,测定大鼠棕色脂肪组织(BAT)和附睾白色脂肪组织(WAT)中ob基因mRNA的表达。BAT中ob基因mRNA水平约为WAT中的40%。禁食(36小时)或半饥饿(10天)使两种组织中的ob基因mRNA水平降低62 - 68%,6℃冷暴露(24小时)使BAT中的ob基因mRNA水平降低(-84%),但WAT中未降低。急性给予β3 - 肾上腺素能激动剂Ro 16 - 8714可使瘦型Zucker大鼠的BAT(-51%)和WAT(-28%)以及肥胖型fa/fa大鼠的BAT(-74%)中的ob基因mRNA水平降低。本研究表明,在大鼠中,ob基因不仅在WAT中表达,也在BAT中表达,提示在这两种组织中,ob基因表达的调节可能与细胞脂质含量的已知改变关系更密切,而非与交感神经活性的变化相关。

相似文献

1
Modulation of obese gene expression in rat brown and white adipose tissues.大鼠棕色和白色脂肪组织中肥胖基因表达的调节。
FEBS Lett. 1995 Oct 9;373(2):131-4. doi: 10.1016/0014-5793(95)01030-i.
2
Molecular cloning of rat obese cDNA and augmented gene expression in genetically obese Zucker fatty (fa/fa) rats.大鼠肥胖cDNA的分子克隆及遗传性肥胖Zucker脂肪型(fa/fa)大鼠中基因表达的增强
J Clin Invest. 1995 Sep;96(3):1647-52. doi: 10.1172/JCI118204.
3
Acute injection of beta-adrenoceptor agonist BRL 35135 corrects both impaired uncoupling protein and lipoprotein lipase gene expression but not hypercapacity of lipogenesis in brown adipose tissue of suckling fa/fa rats.急性注射β-肾上腺素能受体激动剂BRL 35135可纠正乳鼠fa/fa大鼠棕色脂肪组织中解偶联蛋白和脂蛋白脂肪酶基因表达的受损情况,但不能纠正脂肪生成的超能力。
Int J Obes Relat Metab Disord. 1994 May;18(5):273-9.
4
Overexpression of the obese gene in the genetically obese JCR:LA-corpulent rat.肥胖基因在遗传性肥胖的JCR:LA-corpulent大鼠中的过表达。
Biochem Biophys Res Commun. 1995 Nov 2;216(1):148-53. doi: 10.1006/bbrc.1995.2603.
5
Differential regulation of beta3-adrenoceptors in gut and adipose tissue of genetically obese (ob/ob) C57BL/6J-mice.基因肥胖(ob/ob)C57BL/6J小鼠肠道和脂肪组织中β3-肾上腺素能受体的差异调节
Br J Pharmacol. 1998 Jun;124(4):763-71. doi: 10.1038/sj.bjp.0701867.
6
Induction of uncoupling protein expression in brown and white adipose tissue by leptin.瘦素诱导棕色和白色脂肪组织中解偶联蛋白的表达。
Endocrinology. 1999 Jan;140(1):292-300. doi: 10.1210/endo.140.1.6399.
7
Regulated expression of the obese gene product (leptin) in white adipose tissue and 3T3-L1 adipocytes.肥胖基因产物(瘦素)在白色脂肪组织和3T3-L1脂肪细胞中的调控表达。
Proc Natl Acad Sci U S A. 1995 Sep 26;92(20):9034-7. doi: 10.1073/pnas.92.20.9034.
8
Direct effects of leptin on brown and white adipose tissue.瘦素对棕色和白色脂肪组织的直接作用。
J Clin Invest. 1997 Dec 1;100(11):2858-64. doi: 10.1172/JCI119834.
9
Increased adipose expression of the uncoupling protein-3 gene by thiazolidinediones in Wistar fatty rats and in cultured adipocytes.噻唑烷二酮类药物使Wistar肥胖大鼠及培养的脂肪细胞中解偶联蛋白-3基因的脂肪表达增加。
Diabetes. 1998 Nov;47(11):1809-14. doi: 10.2337/diabetes.47.11.1809.
10
The effects of the beta3-adrenoceptor agonist BRL 35135 on UCP isoform mRNA expression.β3-肾上腺素能受体激动剂BRL 35135对解偶联蛋白(UCP)亚型mRNA表达的影响。
Biochem Biophys Res Commun. 1998 Nov 18;252(2):450-4. doi: 10.1006/bbrc.1998.9667.

引用本文的文献

1
Altered leptin signaling and attenuated cardiac vagal activity in rats with type 2 diabetes.2型糖尿病大鼠中瘦素信号改变及心脏迷走神经活动减弱
Front Physiol. 2025 Feb 26;16:1547901. doi: 10.3389/fphys.2025.1547901. eCollection 2025.
2
Dysfunction of the Brown Adipose Organ in HFD-Obese Rats and Effect of Tart Cherry Supplementation.高脂饮食诱导肥胖大鼠棕色脂肪组织功能障碍及酸樱桃补充剂的影响
Antioxidants (Basel). 2024 Mar 23;13(4):388. doi: 10.3390/antiox13040388.
3
Tissue-Specific Effects of Leptin on Glucose and Lipid Metabolism.
瘦素对葡萄糖和脂代谢的组织特异性作用。
Endocr Rev. 2021 Jan 28;42(1):1-28. doi: 10.1210/endrev/bnaa027.
4
Adipocyte Gs but not Gi signaling regulates whole-body glucose homeostasis.脂肪细胞 Gs 信号而非 Gi 信号调节全身葡萄糖稳态。
Mol Metab. 2019 Sep;27:11-21. doi: 10.1016/j.molmet.2019.06.019. Epub 2019 Jun 22.
5
Metabolic Association between Leptin and the Corticotropin Releasing Hormone.瘦素与促肾上腺皮质激素释放激素之间的代谢关联
Endocr Metab Immune Disord Drug Targets. 2019;19(4):458-466. doi: 10.2174/1871530319666190206165626.
6
The Role of Leptin in Maintaining Plasma Glucose During Starvation.瘦素在饥饿期间维持血糖水平中的作用。
Postdoc J. 2018 Mar;6(3):3-19. doi: 10.14304/surya.jpr.v6n3.2.
7
POMC neurons expressing leptin receptors coordinate metabolic responses to fasting via suppression of leptin levels.表达瘦素受体的 POMC 神经元通过抑制瘦素水平来协调对禁食的代谢反应。
Elife. 2018 Mar 12;7:e33710. doi: 10.7554/eLife.33710.
8
Leptin and brain-adipose crosstalks.瘦素与脑-脂肪相互作用。
Nat Rev Neurosci. 2018 Feb 16;19(3):153-165. doi: 10.1038/nrn.2018.7.
9
The glucoregulatory actions of leptin.瘦素的糖调节作用。
Mol Metab. 2017 May 4;6(9):1052-1065. doi: 10.1016/j.molmet.2017.04.011. eCollection 2017 Sep.
10
Counterregulation of insulin by leptin as key component of autonomic regulation of body weight.瘦素对胰岛素的反馈调节作用作为自主调节体重的关键组成部分。
World J Diabetes. 2014 Oct 15;5(5):606-29. doi: 10.4239/wjd.v5.i5.606.