Yamada K
Department of Neuropsychopharmacology and Hospital Pharmacy, Nagoya University School of Medicine, Japan.
Nihon Yakurigaku Zasshi. 1998 Feb;111(2):87-96. doi: 10.1254/fpj.111.87.
Nitric oxide (NO) is a free radical gas that is synthesized from L-arginine by NO synthase (NOS). Activation of NMDA, non-NMDA or metabotropic glutamate receptors causes NO formation through NOS activation. From data obtained in experiments performed by microdialysis together with nitrate assay, we have proposed that NO production in the cerebellum following non-NMDA and metabotropic glutamate receptor activation may be independent of NOS activity, while NMDA receptor-mediated NO production depends on its activity. Glial cells appear to play a role in modulating NO production by regulating L-arginine availability. Activation of NMDA receptors and the increase in intracellular calcium concentration is a trigger for the long-term potentiation (LTP). NO acts as a retrograde messenger in the hippocampal LTP to enhance glutamate release from presynaptic nerve terminal, in which cyclic GMP may be involved. Behavioral studies demonstrate that NO is involved in some forms of learning and memory. Our studies suggest that NMDA/NO/cyclic GMP signaling plays a role in spatial working memory. Further, it is suggested that NO production in the brain is altered by aging. These results support the hypothesis that NO plays a role in mechanism of synaptic plasticity.
一氧化氮(NO)是一种自由基气体,由一氧化氮合酶(NOS)从L-精氨酸合成。NMDA、非NMDA或代谢型谷氨酸受体的激活通过NOS激活导致NO形成。根据微透析与硝酸盐测定实验获得的数据,我们提出非NMDA和代谢型谷氨酸受体激活后小脑内的NO产生可能独立于NOS活性,而NMDA受体介导的NO产生则依赖于其活性。神经胶质细胞似乎通过调节L-精氨酸的可用性在调节NO产生中发挥作用。NMDA受体的激活和细胞内钙浓度的增加是长时程增强(LTP)的触发因素。NO在海马LTP中作为逆行信使,增强突触前神经末梢的谷氨酸释放, 其中可能涉及环鸟苷酸。行为学研究表明,NO参与某些形式的学习和记忆。我们的研究表明,NMDA/NO/环鸟苷酸信号传导在空间工作记忆中起作用。此外,有人提出大脑中的NO产生会因衰老而改变。这些结果支持了NO在突触可塑性机制中起作用的假说。