Mitoma H, Konishi S
Mitsubishi Kasei Institute of Life Sciences, Machida-shi, Tokyo, Japan.
Neuroscience. 1999;88(3):871-83. doi: 10.1016/s0306-4522(98)00260-7.
Long-term facilitation of neurotransmission by monoaminergic systems is implicated in the cellular mechanism of memory and learning-related processes at invertebrate synapses. Using whole-cell recording and rat cerebellar slices, we have examined whether mammalian monoamine-containing neurons play analogous roles in synaptic plasticity, and our results suggest that serotonin and noradrenaline are critically involved in short- and long-term modulation of GABAergic transmission in the cerebellar cortex. Exogenously applied serotonin and noradrenaline selectively induced a short-term enhancement of GABAergic transmission between cerebellar interneurons and Purkinje cells, their effect subsiding in 30 min. Successive amine applications converted this effect to long-term facilitation lasting more than 2 h. During the monoamine-induced short- and long-term facilitation, spontaneously occurring miniature inhibitory synaptic responses increased in frequency, without significant changes in their mean amplitude and amplitude distribution, as well as the GABA receptor sensitivity of Purkinje cells. The actions of the two amines on the inhibitory transmission were mimicked by forskolin and blocked by kinase inhibitors, H-7, H-89 and Rp-adenosine 3',5'-cyclic monophosphothioate. Thus, serotonin and noradrenaline are likely to activate cyclic-AMP- and protein kinase-dependent pathways in GABAergic interneurons, thereby reinforcing the inhibitory transmission on to Purkinje cells. Repetitive electrical stimulation within the molecular layer mimicked the facilitatory effect induced by exogenous monoamines: namely, neural stimulation selectively elicited long-lasting enhancement of GABAergic transmission in a manner sensitive to the monoamine receptor antagonists, methiothepin and propranolol, and an uptake inhibitor, imipramine. Synaptically released monoamines thus appear to induce cyclic-AMP- and protein kinase-dependent long-term facilitation of cerebellar GABAergic transmission, thereby providing a likely mechanism of synaptic plasticity associated with motor coordination within the mammalian cerebellar system.
单胺能系统对神经传递的长期促进作用与无脊椎动物突触处记忆和学习相关过程的细胞机制有关。我们使用全细胞记录和大鼠小脑切片,研究了哺乳动物含单胺的神经元在突触可塑性中是否发挥类似作用,结果表明,血清素和去甲肾上腺素在小脑皮质GABA能传递的短期和长期调节中起关键作用。外源性施加血清素和去甲肾上腺素可选择性诱导小脑中间神经元与浦肯野细胞之间GABA能传递的短期增强,其作用在30分钟内消退。连续施加胺可将这种效应转化为持续超过2小时的长期促进作用。在单胺诱导的短期和长期促进过程中,自发出现的微小抑制性突触反应频率增加,其平均幅度、幅度分布以及浦肯野细胞的GABA受体敏感性均无显著变化。福斯可林模拟了这两种胺对抑制性传递的作用,而激酶抑制剂H-7、H-89和Rp-腺苷3',5'-环磷酸硫代酯可阻断其作用。因此,血清素和去甲肾上腺素可能激活GABA能中间神经元中依赖环磷酸腺苷和蛋白激酶的途径,从而加强对浦肯野细胞的抑制性传递。分子层内的重复电刺激模拟了外源性单胺诱导的促进作用:即神经刺激以对单胺受体拮抗剂美噻吨和普萘洛尔以及摄取抑制剂丙咪嗪敏感的方式选择性地引起GABA能传递的长期增强。因此,突触释放的单胺似乎诱导了依赖环磷酸腺苷和蛋白激酶的小脑GABA能传递的长期促进作用,从而为哺乳动物小脑系统内与运动协调相关的突触可塑性提供了一种可能的机制。