首页 | 本学科首页   官方微博 | 高级检索  
     


Modulation of Ca-channel current by an adenosine analog mediated by a GTP-binding protein in chick sensory neurons
Authors:Haruo Kasai  Toshihiko Aosaki
Affiliation:(1) Department of Physiology, Faculty of Medicine, University of Tokyo, 113 Bunkyo-ku, Tokyo, Japan;(2) Abteilung Membranbiophysik, Max-Planck-Institut für biophysikalische Chemie, D-3400 Göttingen, Federal Republic of Germany
Abstract:Inhibitory modulation of the high-voltage-activated (HVA) Ca-channel current by 2-chloroadenosine (2CA) was studied in chick sensory neurons using the whole-cell clamp method. 2CA reduced the ohgrCTX-sensitive HVA-current (Aosaki and Kasai 1989) in a dose-dependent manner with aKd of 0.8 mgrM. The inhibition by 2CA was also voltage-dependent, being maximal at hyperpolarized potentials, and completely removed at potentials more positive than 30 mV. This voltage-dependence of 2CA action was also evident as a progressive increase in Ca-channel current magnitude during a depolarization which could be described by a single exponential function and which became faster at larger depolarizations. The concentration of 2CA affected the steady-state reduction in Ca-channel current, but did not alter the time-course of current increase during depolarization. The voltage-dependent effect of 2CA was mimicked by intracellular application of GTP-gammaS, but not by phorbol ester, arachidonic acid or nitroprusside. These results are consistent with model in which 2CA activates a G-protein, which then unmasks an additional activation gate on the Ca-channel.
Keywords:Ca-channels  GTP-binding protein  Adenosine    /content/qpgn743kg3325171/xxlarge969.gif"   alt="  ohgr"   align="  BASELINE"   BORDER="  0"  >-Conotoxin  Patch-clamp
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号