• 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

在转染了异源三聚体G蛋白β1亚基的培养心房肌细胞中,β-肾上腺素能受体激活毒蕈碱型钾电流。

Activation of muscarinic K+ current by beta-adrenergic receptors in cultured atrial myocytes transfected with beta1 subunit of heterotrimeric G proteins.

作者信息

Bender K, Wellner-Kienitz M C, Meyer T, Pott L

机构信息

Institut für Physiologie, Abteilung Zelluläre Physiologie, Ruhr-Universität Bochum, Germany.

出版信息

FEBS Lett. 1998 Nov 13;439(1-2):115-20. doi: 10.1016/s0014-5793(98)01350-7.

DOI:10.1016/s0014-5793(98)01350-7
PMID:9849890
Abstract

Muscarinic K+ channels (IK(ACh)) in native atrial myocytes are activated by betagamma subunits of pertussis toxin (Ptx)-sensitive heterotrimeric G proteins coupled to different receptors. betagamma subunits of Ptx-insensitive Gs, coupled to beta-adrenergic receptors, do not activate native IK(ACh). In atrial myocytes from adult rats transfected with rat brain beta1 subunit IK(ACh) can be activated by stimulation of beta-adrenergic receptors using isoprenaline. This effect is insensitive to Ptx. These findings demonstrate for the first time promiscuous (Ptx-insensitive) coupling of Gsbetagamma to GIRK channels in their native environment.

摘要

天然心房肌细胞中的毒蕈碱钾通道(IK(ACh))由与不同受体偶联的百日咳毒素(Ptx)敏感异源三聚体G蛋白的βγ亚基激活。与β肾上腺素能受体偶联的Ptx不敏感Gs的βγ亚基不会激活天然IK(ACh)。在用大鼠脑β1亚基转染的成年大鼠心房肌细胞中,使用异丙肾上腺素刺激β肾上腺素能受体可激活IK(ACh)。这种效应对Ptx不敏感。这些发现首次证明了在其天然环境中Gsβγ与GIRK通道存在混杂(Ptx不敏感)偶联。

相似文献

1
Activation of muscarinic K+ current by beta-adrenergic receptors in cultured atrial myocytes transfected with beta1 subunit of heterotrimeric G proteins.在转染了异源三聚体G蛋白β1亚基的培养心房肌细胞中,β-肾上腺素能受体激活毒蕈碱型钾电流。
FEBS Lett. 1998 Nov 13;439(1-2):115-20. doi: 10.1016/s0014-5793(98)01350-7.
2
Isoprenaline can activate the acetylcholine-induced K+ current in canine atrial myocytes via Gs-derived betagamma subunits.异丙肾上腺素可通过Gs衍生的βγ亚基激活犬心房肌细胞中乙酰胆碱诱导的钾电流。
J Physiol. 1999 Jan 15;514 ( Pt 2)(Pt 2):413-23. doi: 10.1111/j.1469-7793.1999.413ae.x.
3
Overexpression of beta 1 and beta 2 adrenergic receptors in rat atrial myocytes. Differential coupling to G protein-gated inward rectifier K(+) channels via G(s) and G(i)/o.大鼠心房肌细胞中β1和β2肾上腺素能受体的过表达。通过G(s)和G(i)/o与G蛋白门控内向整流钾通道的差异偶联。
J Biol Chem. 2001 Oct 5;276(40):37347-54. doi: 10.1074/jbc.M106234200. Epub 2001 Aug 8.
4
Coupling to Gs and G(q/11) of histamine H2 receptors heterologously expressed in adult rat atrial myocytes.组胺H2受体与成年大鼠心房肌细胞中异源表达的Gs和G(q/11)的偶联
Biochim Biophys Acta. 2003 Sep 23;1642(1-2):67-77. doi: 10.1016/s0167-4889(03)00101-0.
5
G protein-independent inhibition of GIRK current by adenosine in rat atrial myocytes overexpressing A1 receptors after adenovirus-mediated gene transfer.腺病毒介导的基因转移后,在过表达A1受体的大鼠心房肌细胞中,腺苷对GIRK电流的G蛋白非依赖性抑制作用。
J Physiol. 2003 Aug 1;550(Pt 3):707-17. doi: 10.1113/jphysiol.2003.041962. Epub 2003 Jun 18.
6
Activation of muscarinic K+ current in guinea-pig atrial myocytes by a serum factor.血清因子对豚鼠心房肌细胞毒蕈碱钾电流的激活作用
J Physiol. 1993 Feb;461:263-81. doi: 10.1113/jphysiol.1993.sp019513.
7
Gating properties of GIRK channels activated by Galpha(o)- and Galpha(i)-coupled muscarinic m2 receptors in Xenopus oocytes: the role of receptor precoupling in RGS modulation.非洲爪蟾卵母细胞中由与Gα(o)和Gα(i)偶联的毒蕈碱m2受体激活的GIRK通道的门控特性:受体预偶联在RGS调节中的作用
J Physiol. 2002 Dec 1;545(2):355-73. doi: 10.1113/jphysiol.2002.032151.
8
Activation of inwardly rectifying potassium channels by muscarinic receptor-linked G protein in isolated human ventricular myocytes.毒蕈碱受体偶联G蛋白对人离体心室肌细胞内向整流钾通道的激活作用
J Membr Biol. 1997 May 1;157(1):71-81. doi: 10.1007/s002329900217.
9
On the mechanism of basal and agonist-induced activation of the G protein-gated muscarinic K+ channel in atrial myocytes of guinea pig heart.豚鼠心脏心房肌细胞中G蛋白门控毒蕈碱型钾通道的基础激活和激动剂诱导激活机制
J Gen Physiol. 1991 Sep;98(3):517-33. doi: 10.1085/jgp.98.3.517.
10
Antisense oligonucleotides against receptor kinase GRK2 disrupt target selectivity of beta-adrenergic receptors in atrial myocytes.针对受体激酶GRK2的反义寡核苷酸破坏心房肌细胞中β-肾上腺素能受体的靶点选择性。
FEBS Lett. 1999 May 28;451(3):279-83. doi: 10.1016/s0014-5793(99)00594-3.

引用本文的文献

1
A Collision Coupling Model Governs the Activation of Neuronal GIRK1/2 Channels by Muscarinic-2 Receptors.一种碰撞偶联模型调控毒蕈碱-2受体对神经元GIRK1/2通道的激活。
Front Pharmacol. 2020 Aug 12;11:1216. doi: 10.3389/fphar.2020.01216. eCollection 2020.
2
Acute desensitization of GIRK current in rat atrial myocytes is related to K+ current flow.大鼠心房肌细胞中GIRK电流的急性脱敏与钾离子电流流动有关。
J Physiol. 2004 Dec 1;561(Pt 2):471-83. doi: 10.1113/jphysiol.2004.072462. Epub 2004 Sep 30.
3
Heterologous facilitation of G protein-activated K(+) channels by beta-adrenergic stimulation via cAMP-dependent protein kinase.
β-肾上腺素能刺激通过环磷酸腺苷(cAMP)依赖性蛋白激酶对G蛋白激活的钾通道的异源易化作用。
J Gen Physiol. 2000 May;115(5):547-58. doi: 10.1085/jgp.115.5.547.