Saransaari Pirjo, Oja Simo S
Tampere Brain Research Center, Medical School, University of Tampere, and Tampere University Hospital, Finland.
Neurochem Res. 2005 Dec;30(12):1549-56. doi: 10.1007/s11064-005-8833-9.
GABA is known to be the inhibitory neurotransmitter in the majority of brain stem nuclei. The release of GABA has been extensively studied both in vivo and in vitro in higher brain areas, whereas the mechanisms of release in the brain stem have not been systemically characterized. The properties of preloaded [3H]GABA were now investigated in mouse brain stem slices, using a superfusion system. The basal release was enhanced by K+ stimulation (50 mM K+) and under various cell-damaging conditions (ischemia, hypoglycemia, the presence of free radicals and metabolic poisons). No K+-stimulated release was discernible in the absence of Ca2+, indicating that the release was at least partly Ca2+-dependent. Moreover, the release was increased when Na+ or Cl- was omitted from the superfusion medium. GABA and beta-alanine stimulated the release, confirming the involvement of the reversed function of GABA transporters. Incubation of the slices with the anion channel inhibitors diisothiocyanostilbene and 4-acetamido-4'-isothiocyanostilbene-2,2'-disulphonate and with the Cl- uptake inhibitor 9-anthracenecarboxylic acid also reduced GABA release, demonstrating that a part of it comprises leakage through anion channels. All these mechanisms were involved in the ischemia-induced GABA release, which was over 4-fold greater than the release in normoxia. Contrary to the other brain areas, GABA release in the brain stem was not affected by ionotropic glutamate receptors but may be modulated by metabotropic receptors. This ischemia-induced GABA release might constitute an important mechanism against excitotoxicity, protecting the brain stem under cell-damaging conditions.
γ-氨基丁酸(GABA)是大多数脑干核中的抑制性神经递质。GABA的释放已在高等脑区的体内和体外进行了广泛研究,而脑干中释放的机制尚未得到系统的表征。现在,使用灌注系统在小鼠脑干切片中研究了预加载的[3H]GABA的特性。基础释放通过K+刺激(50 mM K+)以及在各种细胞损伤条件下(缺血、低血糖、自由基存在和代谢毒物)得到增强。在没有Ca2+的情况下,没有可辨别的K+刺激释放,这表明释放至少部分依赖于Ca2+。此外,当从灌注培养基中省略Na+或Cl-时,释放增加。GABA和β-丙氨酸刺激释放,证实了GABA转运体反向功能的参与。用阴离子通道抑制剂二异硫氰酸芪和4-乙酰氨基-4'-异硫氰酸芪-2,2'-二磺酸盐以及Cl-摄取抑制剂9-蒽羧酸孵育切片也减少了GABA释放,表明其中一部分包括通过阴离子通道的泄漏。所有这些机制都参与了缺血诱导的GABA释放,其比常氧下的释放高出4倍以上。与其他脑区相反,脑干中的GABA释放不受离子型谷氨酸受体的影响,但可能受代谢型受体调节。这种缺血诱导的GABA释放可能构成对抗兴奋性毒性的重要机制,在细胞损伤条件下保护脑干。