Kumar Sandeep, Ren Qinglu, Beckley Jonathon H, O'Buckley Todd K, Gigante Eduardo D, Santerre Jessica L, Werner David F, Morrow A Leslie
Bowles Center for Alcohol Studies, University of North Carolina School of Medicine Chapel Hill, NC, USA.
Front Neurosci. 2012 Apr 9;6:44. doi: 10.3389/fnins.2012.00044. eCollection 2012.
Protein kinases are implicated in neuronal cell functions such as modulation of ion channel function, trafficking, and synaptic excitability. Both protein kinase C (PKC) and A (PKA) are involved in regulation of γ-aminobutyric acid type A (GABA(A)) receptors through phosphorylation. However, the role of PKA in regulating GABA(A) receptors (GABA(A)-R) following acute ethanol exposure is not known. The present study investigated the role of PKA in the effects of ethanol on GABA(A)-R α1 subunit expression in rat cerebral cortical P2 synaptosomal fractions. Additionally, GABA-related behaviors were examined. Rats were administered ethanol (2.0-3.5 g/kg) or saline and PKC, PKA, and GABA(A)-R α1 subunit levels were measured by western blot analysis. Ethanol (3.5 g/kg) transiently increased GABA(A)-R α1 subunit expression and PKA RIIβ subunit expression at similar time points whereas PKA RIIα was increased at later time points. In contrast, PKC isoform expression remained unchanged. Notably, lower ethanol doses (2.0 g/kg) had no effect on GABA(A)-R α1 subunit levels, although PKA type II regulatory subunits RIIα and RIIβ were increased at 10 and 60 min when PKC isozymes are also known to be elevated. To determine if PKA activation was responsible for the ethanol-induced elevation of GABA(A)-R α1 subunits, the PKA antagonist H89 was administered to rats prior to ethanol exposure. H89 administration prevented ethanol-induced increases in GABA(A)-R α1 subunit expression. Moreover, increasing PKA activity intracerebroventricularly with Sp-cAMP prior to a hypnotic dose of ethanol increased ethanol-induced loss of righting reflex (LORR) duration. This effect appears to be mediated in part by GABA(A)-R as increasing PKA activity also increased the duration of muscimol-induced LORR. Overall, these data suggest that PKA mediates ethanol-induced GABA(A)-R expression and contributes to behavioral effects of ethanol involving GABA(A)-R.
蛋白激酶与神经元细胞功能有关,如离子通道功能的调节、转运以及突触兴奋性。蛋白激酶C(PKC)和蛋白激酶A(PKA)都通过磷酸化参与γ-氨基丁酸A型(GABAA)受体的调节。然而,急性乙醇暴露后PKA在调节GABAA受体(GABAA-R)中的作用尚不清楚。本研究调查了PKA在乙醇对大鼠大脑皮质P2突触体组分中GABAA-R α1亚基表达影响中的作用。此外,还检测了与GABA相关的行为。给大鼠注射乙醇(2.0 - 3.5 g/kg)或生理盐水,通过蛋白质免疫印迹分析测量PKC、PKA和GABAA-R α1亚基水平。乙醇(3.5 g/kg)在相似时间点短暂增加了GABAA-R α1亚基表达和PKA RIIβ亚基表达,而PKA RIIα在稍后时间点增加。相比之下,PKC同工型表达保持不变。值得注意的是,较低剂量的乙醇(2.0 g/kg)对GABAA-R α1亚基水平没有影响,尽管当PKC同工酶也升高时,PKA II型调节亚基RIIα和RIIβ在10分钟和60分钟时增加。为了确定PKA激活是否是乙醇诱导的GABAA-R α1亚基升高的原因,在乙醇暴露前给大鼠注射PKA拮抗剂H89。注射H89可阻止乙醇诱导的GABAA-R α1亚基表达增加。此外,在给予催眠剂量的乙醇之前,通过脑室注射Sp-cAMP增加PKA活性,增加了乙醇诱导的翻正反射消失(LORR)持续时间。这种效应似乎部分由GABAA-R介导,因为增加PKA活性也增加了蝇蕈醇诱导的LORR持续时间。总体而言,这些数据表明PKA介导乙醇诱导的GABAA-R表达,并有助于乙醇涉及GABAA-R的行为效应。