Allen I C, Schousboe A, Griffiths R
Department of Biochemistry and Microbiology, University of St. Andrews, Fife, Scotland, U.K.
Neurochem Res. 1986 Nov;11(11):1487-96. doi: 10.1007/BF00965768.
The effect of L-homocysteine and selected derivatives on the high-affinity uptake of the inhibitory neuroeffectors, GABA and taurine, was investigated in synaptosomes, and in cultured neurons and astrocytes. High-affinity uptake of taurine into synaptosomes was inhibited most effectively by L-homocysteine, DL-homocysteine and homocystine whereas neuronal uptake was unaffected by any of the compounds tested. The high affinity uptake of taurine into astrocytes was markedly inhibited by L-homocysteine, L-homocysteic acid and L-homocystine. High-affinity GABA uptake into astrocytes was notably inhibited by L-homocystine, none of the other compounds tested causing appreciable inhibition below a concentration of 5 mM. Neuronal and synaptosomal high-affinity uptake of GABA was not significantly affected by any of the test compounds at concentrations below 5 mM. The implication of these results to the study of the mechanism of homocysteine-induced seizures and their relevance to the genetic disorder homocystinuria is discussed.
研究了L-同型半胱氨酸及其选定衍生物对抑制性神经效应物γ-氨基丁酸(GABA)和牛磺酸在突触体、培养神经元和星形胶质细胞中的高亲和力摄取的影响。L-同型半胱氨酸、DL-同型半胱氨酸和同型胱氨酸对牛磺酸进入突触体的高亲和力摄取抑制作用最为有效,而神经元摄取不受所测试的任何化合物影响。L-同型半胱氨酸、L-同型半胱氨酸酸和同型胱氨酸显著抑制牛磺酸进入星形胶质细胞的高亲和力摄取。同型胱氨酸显著抑制GABA进入星形胶质细胞的高亲和力摄取,在浓度低于5 mM时,其他测试化合物均未引起明显抑制。在浓度低于5 mM时,测试化合物均未对神经元和突触体中GABA的高亲和力摄取产生显著影响。讨论了这些结果对同型半胱氨酸诱导癫痫发作机制研究的意义及其与遗传性疾病同型胱氨酸尿症的相关性。