Division of Life Science, College of Natural Sciences and Applied Life Science (Brain Korea 21), Gyeongsang National University, Chinju, South Korea.
Synapse. 2010 Mar;64(3):181-90. doi: 10.1002/syn.20712.
GABA(B) receptors (R) are widely expressed and distributed in the nervous system, and have been implicated in variety of neurodegenerative and pathophysiological disorders. However, the exact molecular mechanism regarding responsibility of GABA(B1)R in downstream signaling pathway is not well understood. The present study was undertaken to explore the downstream signaling and role of GABA(B1)R upon acute ethanol and pentylenetetrazol (PTZ) exposure for (20 min) in cortical and hippocampal neuronal cell cultures by using GABA(B1)R RNA interference (i) (30 nM, 48 h) at gestational days 17.5. The results showed that GABA(B1)R and protein kinase A-alpha (PKA) showed decreased expression upon ethanol and PTZ exposure in cortical and hippocampal neurons during transfected and nontransfected conditions, whereas these effects could lead to significant changes in phosphorylation of cAMP-response element binding protein (p-CREB) expression where GABA(B1)R was knocked down. Furthermore, intracellular Ca(+2) concentrations were also reduced in some groups after transfection with GABA(B1)R RNAi. These results showed a critical role of GABA(B1)R upon ethanol and PTZ exposure by modulating downstream signaling pathway. Finally, these findings suggested that inhibition of GABA(B1)R results in the modulation of PKA, p-CREB pathway may play a role in long-term changes in the nervous system, and may be an underlying cause of ethanol's effects.
GABA(B) 受体 (R) 在神经系统中广泛表达和分布,并与多种神经退行性和病理生理紊乱有关。然而,GABA(B1)R 在下游信号通路中的确切分子机制尚不清楚。本研究旨在通过使用 GABA(B1)R RNA 干扰 (i)(30 nM,48 h)在妊娠第 17.5 天,探讨急性乙醇和戊四氮(PTZ)暴露(20 分钟)后 GABA(B1)R 在皮质和海马神经元细胞培养物中的下游信号转导和作用。结果表明,在转染和未转染条件下,皮质和海马神经元中 GABA(B1)R 和蛋白激酶 A-α (PKA) 的表达在乙醇和 PTZ 暴露后均降低,而这些效应可能导致 cAMP 反应元件结合蛋白 (p-CREB) 表达的磷酸化发生显著变化,其中 GABA(B1)R 被敲低。此外,在转染 GABA(B1)R RNAi 后,一些组的细胞内 Ca(+2)浓度也降低。这些结果表明,GABA(B1)R 在乙醇和 PTZ 暴露时通过调节下游信号通路发挥关键作用。最后,这些发现表明,抑制 GABA(B1)R 会导致 PKA 的调节,p-CREB 途径可能在神经系统的长期变化中起作用,并且可能是乙醇作用的潜在原因。