首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Metabotropic glutamate receptor activation enhances the activities of two types of Ca2+-activated k+ channels in rat hippocampal astrocytes.
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Metabotropic glutamate receptor activation enhances the activities of two types of Ca2+-activated k+ channels in rat hippocampal astrocytes.

机译:代谢型谷氨酸受体激活增强了大鼠海马星形胶质细胞中两种类型的Ca2 +激活的k +通道的活性。

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摘要

The influence of activation of glutamate receptor (GluR) on outward K(+) current in cultured neonate rat hippocampal astrocytes was investigated. Patch-clamp analysis of K(+) channel currents in cultured astrocytes identified the existence of 71 +/- 6 and 161 +/- 11 pS single-channel K(+) currents that were sensitive to changes in voltage and [Ca(2+)](i) and blocked by external TEA but not by charybdotoxin, iberiotoxin, apamin, or 4-aminopyridine. Reverse transcriptase (RT)-PCR and Northern blot analysis revealed transcripts of the Ca(2+)-activated K(+) channel (K(Ca)) beta(4)-subunit (beta4) (KCNMB4) in cultured astrocytes. Expression of the metabotropic glutamate receptor (mGluR) subtypes mGluR1 and mGluR5 and the ionotropic glutamate receptor (iGluR) subtypes iGluR1 and iGluR4 were detected by RT-PCR and immunofluorescence analysis in cultured astrocytes. The mGluR agonists L-glutamate and quisqualate increased the open state probability (NP(o)) of the 71 and 161 pS K(+) channel currents that were prevented by the mGluR receptor antagonists 1-aminoindan-1,5-dicarboxylic acid or L-(+)-2-amino-3-phosphonopropionic acid and not by the iGluR antagonists (+)-5-methyl-10,11-dihydro-5H-dibenzo [a,d] cyclohepten-5,10-imine maleate or CNQX. Activation of the two types of K(+) channel currents by mGluR agonists was attenuated by pertussis toxin and by inhibition of phospholipase C (PLC) or cytochrome P450 arachidonate epoxygenase. These results indicate that brain astrocytes contain the KCNMB4 transcript and express two novel types of K(Ca) channels that are gated by activation of a G-protein coupled metabotropic glutamate receptor functionally linked to PLC and cytochrome P450 arachidonate epoxygenase activity.
机译:谷氨酸受体(GluR)的激活对培养的新生大鼠海马星形胶质细胞外向K(+)电流的影响进行了调查。对培养的星形胶质细胞中的K(+)通道电流进行膜片钳分析,确定存在71 +/- 6和161 +/- 11 pS单通道K(+)电流,这些电流对电压和[Ca(2 +)](i)并被外部TEA阻断,但未被charybdotoxin,iberiotoxin,apapamin或4-aminopyridine阻断。逆转录酶(RT)-PCR和Northern印迹分析揭示了在培养的星形胶质细胞中Ca(2+)激活的K(+)通道(K(Ca))beta(4)-亚基(beta4)(KCNMB4)的转录本。通过RT-PCR和免疫荧光分析在培养的星形胶质细胞中检测了代谢型谷氨酸受体(mGluR)亚型mGluR1和mGluR5以及离子型谷氨酸受体(iGluR)亚型iGluR1和iGluR4的表达。 mGluR激动剂L-谷氨酸和喹喹啉增加了被mGluR受体拮抗剂1-aminoindan-1,5-dihydroxy或阻止的71和161 pS K(+)通道电流的开态概率(NP(o))。 L-(+)-2-氨基-3-膦酸丙酸而不是由iGluR拮抗剂(+)-5-甲基-10,11-二氢-5H-二苯并[a,d]环庚烯5,10-亚胺马来酸酯或CNQX。百日咳毒素和磷脂酶C(PLC)或细胞色素P450花生四烯酸环氧酶的抑制作用减弱了mGluR激动剂对两种类型的K(+)通道电流的激活。这些结果表明,脑星形胶质细胞含有KCNMB4转录本,并表达两种新型的K(Ca)通道,这些通道通过激活与蛋白质和细胞色素P450花生四烯酸环氧酶活性相关的G蛋白偶联的代谢型谷氨酸受体激活而被门控。

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