Chavis P, Nooney J M, Bockaert J, Fagni L, Feltz A, Bossu J L
C.C.I.P.E., CNRS/INSERM, Montpellier, France.
J Neurosci. 1995 Jan;15(1 Pt 1):135-43. doi: 10.1523/JNEUROSCI.15-01-00135.1995.
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.
运用膜片钳技术的细胞贴附式记录模式,研究了代谢型谷氨酸受体激活对在1微摩尔Bay K 8644存在时所记录的培养小脑颗粒细胞中钙二氢吡啶(DHP)敏感通道的影响。浴槽施加激动剂(反式-ACPD、1S,3R-和1R,3S-ACPD异构体,以及在CPP和CNQX存在下的谷氨酸或喹啉酸),在40%的记录细胞中诱发钙通道活性增加,潜伏期可变,为8.9±8.6秒。L-CCG1、L-AP3、L-AP4、AMPA或NMDA均未激活钙通道。这种细胞类型中存在的两种二氢吡啶敏感通道被反式-ACPD激活:经典的24 pS L型通道和较小电导的7 pS通道。结果表明,该效应既不是由细胞内Ca2+介导,也不是由百日咳毒素(PTX)敏感的G蛋白介导。有趣的是,用BAPTA-AM处理增加了反应性膜片的数量,并且在整个药物应用过程中活性更持久。过夜PTX处理后,即使激动剂被洗脱,钙通道的激活仍持续存在。这些结果表明,mGluR1/mGluR5可能介导二氢吡啶敏感钙通道的易化作用。