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Facilitatory coupling between a glutamate metabotropic receptor and dihydropyridine-sensitive calcium channels in cultured cerebellar granule cells

机译:谷氨酸代谢型受体与小脑颗粒细胞中二氢吡啶敏感性钙通道之间的促进偶联

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摘要

The effect of metabotropic glutamate receptor activation on Ca dihydropyridine (DHP)-sensitive channels recorded in the presence of 1 microM Bay K 8644 was examined on cultured cerebellar granule cells using the patch-clamp technique in the cell-attached configuration. Bath-applied agonist (trans-ACPD, 1S,3R-, and 1R,3S-ACPD isomers, and glutamate or quisqualate in the presence of CPP and CNQX) evoked an increase in Ca channel activity with a variable latency of 8.9 +/- 8.6 sec in 40% of the recorded cells. Neither L-CCG1, L-AP3, L-AP4, nor AMPA or NMDA activated Ca channels. Two dihydropyridine-sensitive channels present in this cell type were activated by trans-ACPD: the classical 24 pS L-type channel and a smaller-conductance 7 pS channel. The effect was shown to be mediated by neither intracellular Ca2+ nor a pertussis toxin (PTX)-sensitive G protein. Interestingly treatment with BAPTA-AM increased the number of responding patches and the activity was more sustained throughout the drug application. After overnight PTX treatment, activation of the Ca channels persisted even after washout of the agonist. These results indicate that mGluR1/mGluR5 probably mediate the facilitation of dihydropyridine-sensitive Ca channels.
机译:使用膜片钳技术在细胞附着的配置下,在培养的小脑颗粒细胞上检查了在1 microM Bay K 8644存在下记录的代谢型谷氨酸受体活化对Ca二氢吡啶(DHP)敏感通道的影响。浴应用的激动剂(反式ACPD,1S,3R和1R,3S-ACPD异构体,以及在CPP和CNQX存在下的谷氨酸或准喹啉)引起Ca通道活性增加,潜伏期为8.9 +/-在40%的已记录单元中为8.6秒。 L-CCG1,L-AP3,L-AP4或AMPA或NMDA均未激活Ca通道。反式ACPD可激活此细胞类型中存在的两个对二氢吡啶敏感的通道:经典的24 pS L型通道和较小电导的7 pS通道。结果表明,这种作用既不是由细胞内Ca2 +介导,也不是由百日咳毒素(PTX)敏感的G蛋白介导的。有趣的是,用BAPTA-AM进行治疗可增加反应性斑块的数量,并且在整个药物应用过程中其活性会更持久。在过夜PTX处理后,即使冲洗了激动剂,Ca通道的激活仍然持续。这些结果表明,mGluR1 / mGluR5可能介导对二氢吡啶敏感的钙通道的促进。

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