Kimura H, Okamoto K, Sakai Y
Brain Res. 1985 Mar 25;330(2):235-44. doi: 10.1016/0006-8993(85)90682-1.
For the purpose of revealing the physiological functions or roles of prostaglandins (PGs), PGD2 in particular, in the central nervous system, the effects of PGD2, E2 and F2 alpha on the postsynaptic actions of GABA, taurine, L-glutamate and L-aspartate on Purkinje cell dendrites in guinea pig, cerebellar slices were electrophysiologically investigated using intradendritic recording. Iontophoretic application of PGD2 alone either depolarized or hyperpolarized some Purkinje cell dendrites, while PGE2 and F2 alpha induced only depolarizations. All PGs tested showed fairly strong potentiation of the inhibitory action of GABA or taurine and of the excitatory action of L-glutamate or L-aspartate on Purkinje cell dendrites. As a possible mechanism of action, the change of the cyclic nucleotide level induced by PGs was tentatively suggested as being involved in the potentiating action of PGs on excitatory amino acids.
为了揭示前列腺素(PGs),特别是前列腺素D2(PGD2)在中枢神经系统中的生理功能或作用,利用树突内记录技术,对豚鼠小脑切片浦肯野细胞树突上,PGD2、前列腺素E2(PGE2)和前列腺素F2α(F2α)对γ-氨基丁酸(GABA)、牛磺酸、L-谷氨酸和L-天冬氨酸突触后作用的影响进行了电生理研究。单独离子导入PGD2可使一些浦肯野细胞树突去极化或超极化,而PGE2和F2α仅诱导去极化。所有测试的前列腺素均显示出对GABA或牛磺酸的抑制作用以及对L-谷氨酸或L-天冬氨酸对浦肯野细胞树突的兴奋作用有相当强的增强作用。作为一种可能的作用机制,初步认为PGs诱导的环核苷酸水平变化与PGs对兴奋性氨基酸的增强作用有关。