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G蛋白介导的大鼠海马CA3区细胞代谢型谷氨酸能和毒蕈碱能反应的脱敏作用

G-protein-mediated desensitization of metabotropic glutamatergic and muscarinic responses in CA3 cells in rat hippocampus.

作者信息

Guérineau N C, Bossu J L, Gähwiler B H, Gerber U

机构信息

Brain Research Institute, University of Zurich, Switzerland.

出版信息

J Physiol. 1997 Apr 15;500 ( Pt 2)(Pt 2):487-96. doi: 10.1113/jphysiol.1997.sp022035.

DOI:10.1113/jphysiol.1997.sp022035
PMID:9147332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1159398/
Abstract
  1. Desensitization of a metabotropic response was investigated in CA3 pyramidal neurons in hippocampal slice cultures using the patch-clamp technique. 2. 1S,3R-1-aminocyclopentane-1,3-dicarboxylate (1S,3R-ACPD), an agonist at metabotropic glutamate receptors (mGluRs), and metacholine (MCh), an agonist at muscarinic receptors, induced a cationic current that appears to be activated through a G-protein-independent transduction process, as previously shown. Prolonged or repetitive bath application of agonists led to rapid desensitization of the cationic current with a time constant of approximately 20 s. 3. Complete recovery from desensitization was observed within 6 min. 4. These responses mediated by mGluRs and muscarinic receptors cross-desensitized. 5. Preventing the activation of G-proteins by loading cells with GDP beta S strongly reduced or suppressed desensitization, and resulted in a sustained inward cationic current. When cells were filled with GTP gamma S to irreversibly activate G-proteins, the desensitization process was enhanced such that a first application of agonist caused a markedly reduced response. 6. These results show that a cationic current induced by metabotropic agonists in hippocampal pyramidal cells undergoes apparent desensitization and suggests that this process occurs through a G-protein-mediated inhibition of the underlying membrane conductance.
摘要
  1. 运用膜片钳技术,在海马脑片培养物的CA3锥体神经元中研究了代谢型反应的脱敏作用。2. 代谢型谷氨酸受体(mGluRs)的激动剂1S,3R-1-氨基环戊烷-1,3-二羧酸(1S,3R-ACPD)和毒蕈碱受体的激动剂乙酰甲胆碱(MCh),如先前所示,诱导出一种阳离子电流,该电流似乎是通过与G蛋白无关的转导过程激活的。长时间或重复浴用激动剂会导致阳离子电流迅速脱敏,时间常数约为20秒。3. 在6分钟内观察到脱敏后的完全恢复。4. 由mGluRs和毒蕈碱受体介导的这些反应发生交叉脱敏。5. 通过用GDPβS加载细胞来阻止G蛋白的激活,强烈降低或抑制了脱敏作用,并导致持续的内向阳离子电流。当细胞用GTPγS填充以不可逆地激活G蛋白时,脱敏过程增强,以至于首次应用激动剂会导致反应明显减弱。6. 这些结果表明,海马锥体细胞中代谢型激动剂诱导的阳离子电流会发生明显的脱敏作用,并表明该过程是通过G蛋白介导的对潜在膜电导的抑制而发生的。

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