• 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

基因糖尿病(db/db)小鼠脂肪细胞质膜中Gs和Gi的α亚基。

Alpha-subunits of Gs and Gi in adipocyte plasma membranes of genetically diabetic (db/db) mice.

作者信息

Bégin-Heick N

机构信息

Department of Biochemistry, University of Ottawa, Ontario, Canada.

出版信息

Am J Physiol. 1992 Jul;263(1 Pt 1):C121-9. doi: 10.1152/ajpcell.1992.263.1.C121.

DOI:10.1152/ajpcell.1992.263.1.C121
PMID:1322037
Abstract

The adipocyte membrane G protein pattern, beta-adrenergic receptor activity, and adenylyl cyclase were determined in adipocyte membranes of the db/db mouse, a mutant that is a model of diabetes preceded by hyperinsulinemia, hyperglycemia, and extreme obesity. These studies were undertaken to determine whether the alterations already noted in the ob/ob mouse and those in the db/db mouse are similar and related to the hormonal defects, particularly the hyperinsulinemia and hyperglycemia prevalent in these animals (cf. Ref. 11). The ADP ribosylation data show that Gs alpha was more highly labeled in the tissues of the db/db mutant than in the homozygous control, but there was no significant difference in the amount of ADP-ribose incorporated in the Gi alpha-subunits. Quantification of the proteins by immunodetection revealed that the long (46-kDa) form of Gs alpha was significantly less abundant in the db mutant than in its control, whereas there was no difference in the short (42-kDa) form. Gi alpha-peptides corresponding to Gi alpha 2 and Gi alpha 1 were both less abundant in the db mutant than in the homozygous control. These data contrasted with those obtained for ob mutants and their lean homozygous controls reported previously (4) and confirmed here. It is concluded on the basis of these studies that factors other than the hormonal status are responsible for the G protein patterns in the ob and db mutants. Differences in G protein patterns noted in between the control groups (B/Ks or B/6 homozygotes) correlated strongly with the quantitative differences in adenylyl cyclase response in the two strains.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在db/db小鼠的脂肪细胞膜中测定了脂肪细胞膜G蛋白模式、β-肾上腺素能受体活性和腺苷酸环化酶。db/db小鼠是一种突变体,是伴有高胰岛素血症、高血糖症和极度肥胖的糖尿病模型。进行这些研究是为了确定已经在ob/ob小鼠中发现的改变与db/db小鼠中的改变是否相似,以及是否与激素缺陷有关,特别是这些动物中普遍存在的高胰岛素血症和高血糖症(参见参考文献11)。ADP核糖基化数据显示,与纯合对照组相比,db/db突变体组织中的Gsα被标记的程度更高,但Giα亚基中掺入的ADP核糖量没有显著差异。通过免疫检测对蛋白质进行定量分析发现,db突变体中长(46 kDa)形式的Gsα明显比其对照组少,而短(42 kDa)形式则没有差异。与Giα2和Giα1对应的Giα肽在db突变体中均比纯合对照组少。这些数据与先前报道的ob突变体及其瘦纯合对照组的数据形成对比(4),并在此得到证实。基于这些研究得出结论,激素状态以外的因素是ob和db突变体中G蛋白模式的原因。对照组(B/Ks或B/6纯合子)之间G蛋白模式的差异与两种品系中腺苷酸环化酶反应的定量差异密切相关。(摘要截短于250字)

相似文献

1
Alpha-subunits of Gs and Gi in adipocyte plasma membranes of genetically diabetic (db/db) mice.基因糖尿病(db/db)小鼠脂肪细胞质膜中Gs和Gi的α亚基。
Am J Physiol. 1992 Jul;263(1 Pt 1):C121-9. doi: 10.1152/ajpcell.1992.263.1.C121.
2
Quantification of the alpha and beta subunits of the transducing elements (Gs and Gi) of adenylate cyclase in adipocyte membranes from lean and obese (ob/ob) mice.对来自瘦小鼠和肥胖(ob/ob)小鼠的脂肪细胞膜中腺苷酸环化酶转导元件(Gs和Gi)的α和β亚基进行定量分析。
Biochem J. 1990 May 15;268(1):83-9. doi: 10.1042/bj2680083.
3
Liver beta-adrenergic receptors, G proteins, and adenylyl cyclase activity in obesity-diabetes syndromes.肥胖-糖尿病综合征中的肝脏β-肾上腺素能受体、G蛋白和腺苷酸环化酶活性
Am J Physiol. 1994 Jun;266(6 Pt 1):C1664-72. doi: 10.1152/ajpcell.1994.266.6.C1664.
4
Genetically acquired diabetes: adipocyte guanine nucleotide regulatory protein expression and adenylate cyclase regulation.
Biochim Biophys Acta. 1991 Feb 22;1096(2):121-6. doi: 10.1016/0925-4439(91)90049-f.
5
Effect of the genetic background and specific mutation on adenylate cyclase activity in obesity syndromes.
Mol Cell Endocrinol. 1988 Oct;59(3):171-8. doi: 10.1016/0303-7207(88)90101-3.
6
Alterations in G-protein expression, Gi function and stimulatory receptor-mediated regulation of adipocyte adenylyl cyclase in a model of insulin-resistant diabetes with obesity.
Cell Signal. 1992 Jul;4(4):365-77. doi: 10.1016/0898-6568(92)90031-3.
7
RU-486 (Mifepristone) ameliorates diabetes but does not correct deficient beta-adrenergic signalling in adipocytes from mature C57BL/6J-ob/ob mice.RU-486(米非司酮)可改善糖尿病,但不能纠正成熟C57BL/6J-ob/ob小鼠脂肪细胞中β-肾上腺素能信号传导缺陷。
Int J Obes Relat Metab Disord. 1997 Oct;21(10):865-73. doi: 10.1038/sj.ijo.0800479.
8
Impaired expression and functional activity of the beta 3- and beta 1-adrenergic receptors in adipose tissue of congenitally obese (C57BL/6J ob/ob) mice.先天性肥胖(C57BL/6J ob/ob)小鼠脂肪组织中β3 -和β1 -肾上腺素能受体的表达及功能活性受损。
Mol Endocrinol. 1994 Apr;8(4):518-27. doi: 10.1210/mend.8.4.7914350.
9
Alterations of adenylyl cyclase-linked G proteins in rat liver during aging.衰老过程中大鼠肝脏中腺苷酸环化酶相关G蛋白的变化。
Am J Physiol. 1996 Jan;270(1 Pt 1):E126-32. doi: 10.1152/ajpendo.1996.270.1.E126.
10
Tissue-specific alterations in G protein expression in genetic versus diet-induced models of non-insulin-dependent diabetes mellitus in the mouse.在小鼠非胰岛素依赖型糖尿病的遗传模型与饮食诱导模型中,G蛋白表达的组织特异性改变。
Metabolism. 1995 Jun;44(6):771-8. doi: 10.1016/0026-0495(95)90191-4.

引用本文的文献

1
The functional state of hormone-sensitive adenylyl cyclase signaling system in diabetes mellitus.糖尿病中激素敏感性腺苷酸环化酶信号系统的功能状态
J Signal Transduct. 2013;2013:594213. doi: 10.1155/2013/594213. Epub 2013 Sep 28.
2
Early alterations in the brown adipose tissue adenylate cyclase system of pre-obese Zucker rat fa/fa pups: decreased G-proteins and beta 3-adrenoceptor activities.肥胖前期 Zucker 大鼠 fa/fa 幼崽棕色脂肪组织腺苷酸环化酶系统的早期改变:G 蛋白和β3-肾上腺素能受体活性降低。
Biochem J. 1995 Dec 15;312 ( Pt 3)(Pt 3):781-8. doi: 10.1042/bj3120781.
3
Growth hormone decreases the response to anti-lipolytic agonists and decreases the levels of Gi2 in rat adipocytes.
生长激素会降低大鼠脂肪细胞对抗脂解激动剂的反应,并降低Gi2的水平。
Biochem J. 1994 Jan 1;297 ( Pt 1)(Pt 1):41-5. doi: 10.1042/bj2970041.
4
Dietary obesity linked to genetic loci on chromosomes 9 and 15 in a polygenic mouse model.在一个多基因小鼠模型中,饮食性肥胖与9号和15号染色体上的基因位点有关。
J Clin Invest. 1994 Oct;94(4):1410-6. doi: 10.1172/JCI117477.