• 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

瘦素和皮质酮对肥胖(ob)/肥胖(ob)小鼠的食物摄入量及棕色脂肪组织中解偶联蛋白1(UCP1)mRNA的表达具有相反的作用。

Leptin and corticosterone have opposite effects on food intake and the expression of UCP1 mRNA in brown adipose tissue of lep(ob)/lep(ob) mice.

作者信息

Arvaniti K, Ricquier D, Champigny O, Richard D

机构信息

Département de physiologie, Faculté de médecine, Université Laval, Québec, Canada.

出版信息

Endocrinology. 1998 Sep;139(9):4000-3. doi: 10.1210/endo.139.9.6287.

DOI:10.1210/endo.139.9.6287
PMID:9724056
Abstract

The present study was conducted to assess the interaction effect of leptin and corticosterone on food intake and the expression of uncoupling protein 1 (UCP1) mRNA in interscapular brown adipose tissue (IBAT). To this end, a 3 x 3 factorial experiment was designed in which adrenalectomized (ADX) lep(ob)/lep(ob) mice were subjected to three doses of corticosterone and three doses of leptin. The results confirm the anorectic and orexigenic effects of leptin and corticosterone, respectively. The results also emphasize the abilities of leptin and corticosterone to respectively increase and reduce the expression of UCP1 mRNA in IBAT. The effects of leptin and corticosterone on food intake and the expression of UCP1 mRNA translated into effects on body weight and body composition; leptin reduced body weight and corticosterone increased the weight of IBAT. The present results do not provide evidence for leptin-corticosterone interactions in the control of food intake and thermogenesis. Corticosterone increased food intake and reduced the expression of IBAT UCP1 regardless of the leptin status, and leptin reduced food intake and induced the expression of IBAT UCP1 independently of the corticosterone levels.

摘要

本研究旨在评估瘦素和皮质酮对食物摄入量以及肩胛间棕色脂肪组织(IBAT)中解偶联蛋白1(UCP1)mRNA表达的相互作用。为此,设计了一个3×3析因实验,对肾上腺切除的(ADX)lep(ob)/lep(ob)小鼠给予三种剂量的皮质酮和三种剂量的瘦素。结果分别证实了瘦素的厌食作用和皮质酮的促食欲作用。结果还强调了瘦素和皮质酮分别增加和降低IBAT中UCP1 mRNA表达的能力。瘦素和皮质酮对食物摄入量及UCP1 mRNA表达的影响转化为对体重和身体组成的影响;瘦素降低体重,皮质酮增加IBAT的重量。目前的结果并未为瘦素 - 皮质酮在食物摄入控制和产热中的相互作用提供证据。无论瘦素状态如何,皮质酮均增加食物摄入量并降低IBAT中UCP1的表达,而瘦素则独立于皮质酮水平降低食物摄入量并诱导IBAT中UCP1的表达。

相似文献

1
Leptin and corticosterone have opposite effects on food intake and the expression of UCP1 mRNA in brown adipose tissue of lep(ob)/lep(ob) mice.瘦素和皮质酮对肥胖(ob)/肥胖(ob)小鼠的食物摄入量及棕色脂肪组织中解偶联蛋白1(UCP1)mRNA的表达具有相反的作用。
Endocrinology. 1998 Sep;139(9):4000-3. doi: 10.1210/endo.139.9.6287.
2
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.
3
Norepinephrine is required for leptin effects on gene expression in brown and white adipose tissue.去甲肾上腺素是瘦素对棕色和白色脂肪组织基因表达产生作用所必需的。
Endocrinology. 1999 Oct;140(10):4772-8. doi: 10.1210/endo.140.10.7043.
4
Leptin selectively reduces white adipose tissue in mice via a UCP1-dependent mechanism in brown adipose tissue.瘦素通过棕色脂肪组织中一种依赖解偶联蛋白1(UCP1)的机制选择性减少小鼠的白色脂肪组织。
Am J Physiol Endocrinol Metab. 2001 Feb;280(2):E372-7. doi: 10.1152/ajpendo.2001.280.2.E372.
5
Resistance to the anorexic and thermogenic effects of centrally administrated leptin in obese aged rats.肥胖老年大鼠对中枢给予瘦素的厌食和产热作用产生抵抗。
Regul Pept. 2000 Aug 25;92(1-3):65-71. doi: 10.1016/s0167-0115(00)00151-8.
6
Differential regulation of leptin expression and function in A/J vs. C57BL/6J mice during diet-induced obesity.饮食诱导肥胖期间A/J小鼠与C57BL/6J小鼠中瘦素表达和功能的差异调节
Am J Physiol Endocrinol Metab. 2000 Aug;279(2):E356-65. doi: 10.1152/ajpendo.2000.279.2.E356.
7
Severe leptin resistance in brown fat-deficient uncoupling protein promoter-driven diphtheria toxin A mice despite suppression of hypothalamic neuropeptide Y and circulating corticosterone concentrations.尽管下丘脑神经肽Y和循环皮质酮浓度受到抑制,但棕色脂肪缺乏的解偶联蛋白启动子驱动的白喉毒素A小鼠仍存在严重的瘦素抵抗。
Diabetes. 1998 Feb;47(2):230-8. doi: 10.2337/diab.47.2.230.
8
Sex-dependent dietary obesity, induction of UCPs, and leptin expression in rat adipose tissues.大鼠脂肪组织中性别依赖性饮食性肥胖、解偶联蛋白(UCPs)的诱导及瘦素表达
Obes Res. 2001 Sep;9(9):579-88. doi: 10.1038/oby.2001.75.
9
Corticotropin-releasing hormone-mediated pathway of leptin to regulate feeding, adiposity, and uncoupling protein expression in mice.促肾上腺皮质激素释放激素介导的瘦素途径对小鼠进食、肥胖及解偶联蛋白表达的调节
Endocrinology. 2003 Aug;144(8):3547-54. doi: 10.1210/en.2003-0301.
10
Activation of the sympathetic nervous system by galanin-like peptide--a possible link between leptin and metabolism.甘丙肽样肽对交感神经系统的激活作用——瘦素与新陈代谢之间的一种可能联系。
Endocrinology. 2003 Nov;144(11):4709-17. doi: 10.1210/en.2003-0748. Epub 2003 Jul 24.

引用本文的文献

1
The Role of the Stress Response in Metabolic Dysfunction-Associated Fatty Liver Disease: A Psychoneuroendocrineimmunology-Based Perspective.应激反应在代谢相关脂肪性肝病中的作用:基于心理神经内分泌免疫学的观点。
Nutrients. 2023 Feb 3;15(3):795. doi: 10.3390/nu15030795.
2
Sexual Dimorphism in Adipose-Hypothalamic Crosstalk and the Contribution of Aryl Hydrocarbon Receptor to Regulate Energy Homeostasis.脂肪-下丘脑串扰中的性别二态性及芳香烃受体在调节能量平衡中的作用。
Int J Mol Sci. 2022 Jul 12;23(14):7679. doi: 10.3390/ijms23147679.
3
Brown Adipose Tissue-A Translational Perspective.
棕色脂肪组织——转化视角。
Endocr Rev. 2023 Mar 4;44(2):143-192. doi: 10.1210/endrev/bnac015.
4
Activation of Basolateral Amygdala to Nucleus Accumbens Projection Neurons Attenuates Chronic Corticosterone-Induced Behavioral Deficits in Male Mice.基底外侧杏仁核对伏隔核投射神经元的激活可减轻慢性皮质酮诱导的雄性小鼠行为缺陷。
Front Behav Neurosci. 2021 Feb 24;15:643272. doi: 10.3389/fnbeh.2021.643272. eCollection 2021.
5
UBE2E1 Is Preferentially Expressed in the Cytoplasm of Slow-Twitch Fibers and Protects Skeletal Muscles from Exacerbated Atrophy upon Dexamethasone Treatment.UBE2E1在慢肌纤维的细胞质中优先表达,并在 Dexamethasone 治疗时保护骨骼肌免受加剧的萎缩。
Cells. 2018 Nov 16;7(11):214. doi: 10.3390/cells7110214.
6
Dexamethasone reduces energy expenditure and increases susceptibility to diet-induced obesity in mice.地塞米松可降低小鼠的能量消耗,并增加其对饮食诱导肥胖的易感性。
Obesity (Silver Spring). 2013 Sep;21(9):E415-20. doi: 10.1002/oby.20338.
7
Mother to infant or infant to mother? Reciprocal regulation of responsiveness to stress in rodents and the implications for humans.是从母亲到婴儿还是从婴儿到母亲?啮齿动物对应激反应的相互调节及其对人类的影响。
J Psychiatry Neurosci. 2004 Sep;29(5):364-82.
8
Adipose tissue as an endocrine organ? A review of some recent data.脂肪组织是一个内分泌器官?近期一些数据的综述。
Eat Weight Disord. 2000 Sep;5(3):116-23. doi: 10.1007/BF03354441.
9
Hypothalamic-pituitary-adrenal dysfunction in Apoe(-/-) mice: possible role in behavioral and metabolic alterations.载脂蛋白E基因敲除(Apoe(-/-))小鼠的下丘脑-垂体-肾上腺功能障碍:在行为和代谢改变中的可能作用。
J Neurosci. 2000 Mar 1;20(5):2064-71. doi: 10.1523/JNEUROSCI.20-05-02064.2000.