Zhai J, Stewart R R, Friedberg M W, Li C
Laboratory of Molecular and Cellular Neurobiology, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD 20892, USA.
Brain Res. 1998 Sep 14;805(1-2):116-22. doi: 10.1016/s0006-8993(98)00689-1.
The effect of ethanol on the current activated by 2.5 to 40 microM gamma-aminobutyric acid (GABA) was studied in freshly isolated rat dorsal root ganglion (DRG) neurons under voltage clamp in the whole-cell and perforated-patch recording configurations. Our results confirmed that GABAA-activated current in these neurons was insensitive to ethanol at concentrations from 2.5 to 100 mM [G. White, D.M. Lovinger, F.F. Weight, Ethanol inhibits NMDA-activated current but does not alter GABA-activated current in an isolated adult mammalian neuron, Brain Res. 507 (1990) 332-336.]. In addition, the ethanol sensitivity of GABA receptors was studied under conditions that promote phosphorylation of the PKC site on the gamma2L subunit. The presence of the gamma2L and other subunit mRNAs was detected by reverse transcription (RT) of total RNA purified from adult DRG followed by polymerase chain reaction (PCR) using subunit specific primer sets. We found that the GABA response remained insensitive to 2.5-100 mM ethanol despite: (i) the extracellular preapplication of 5, 20 or 500 nM phorbol 12-myristate 13-acetate (PMA); (ii) raising free intracellular Ca2+ ([Ca2+]i) from 7 to 100 or 600 nM by altering the intracellular Ca2+/EGTA ratio; (iii) intracellular application of PKC (0.247 U ml-1 ); and (iv) combining the intracellular application of 1 microM okadaic acid and 30 microM peptide 3 with the extracellular application of 20 nM PMA. These results suggest that phosphorylation of the gamma2L subunit is not the only requirement for ethanol sensitivity of GABAA receptors.
在全细胞和穿孔膜片钳记录模式下的电压钳条件下,研究了乙醇对新鲜分离的大鼠背根神经节(DRG)神经元中由2.5至40微摩尔γ-氨基丁酸(GABA)激活的电流的影响。我们的结果证实,这些神经元中GABAA激活的电流在2.5至100毫摩尔的浓度范围内对乙醇不敏感[G.怀特、D.M.洛文杰、F.F.韦特,《乙醇抑制NMDA激活的电流,但不改变分离的成年哺乳动物神经元中GABA激活的电流》,《脑研究》507(1990)332 - 336]。此外,在促进γ2L亚基上PKC位点磷酸化的条件下研究了GABA受体的乙醇敏感性。通过对从成年DRG纯化的总RNA进行逆转录(RT),然后使用亚基特异性引物组进行聚合酶链反应(PCR),检测γ2L和其他亚基mRNA的存在。我们发现,尽管存在以下情况,GABA反应对2.5 - 100毫摩尔乙醇仍不敏感:(i)细胞外预先施加5、20或500纳摩尔佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA);(ii)通过改变细胞内Ca2 + / EGTA比率将游离细胞内Ca2 +([Ca2 +]i)从7提高到100或600纳摩尔;(iii)细胞内施加PKC(0.247 U ml-1);以及(iv)将细胞内施加1微摩尔冈田酸和30微摩尔肽3与细胞外施加20纳摩尔PMA相结合。这些结果表明,γ2L亚基的磷酸化不是GABAA受体对乙醇敏感的唯一必要条件。