Heemskerk F M, Schrama L H, de Graan P N, Gispen W H
Biochem Biophys Res Commun. 1987 Aug 31;147(1):94-9. doi: 10.1016/s0006-291x(87)80091-8.
Phosphorylation of synaptosomal plasma membranes from rat hippocampus in the presence of the convulsant drug 4-aminopyridine resulted in the inhibition of the phosphorylation of the nervous tissue specific protein kinase C substrate protein B-50 (48 kDa) and the alpha-subunit of calcium/calmodulin-dependent protein kinase II (50 kDa). Preincubation of SPM with 2-amino-5-phosphonovalerate prevents the inhibition of B-50 phosphorylation by 4-aminopyridine, but had no effect on the inhibition of 50 kDa phosphorylation. 2-Amino-5-phosphonovalerate is known to be a specific N-methyl-D-aspartate antagonist and has anti-epileptic activity in vitro and in vivo. Several other anti-epileptic drugs tested did not influence the 4-aminopyridine-induced inhibition of protein phosphorylation.
在惊厥药物4-氨基吡啶存在的情况下,对大鼠海马突触体细胞膜进行磷酸化处理,结果导致神经组织特异性蛋白激酶C底物蛋白B-50(48 kDa)和钙/钙调蛋白依赖性蛋白激酶II的α亚基(50 kDa)的磷酸化受到抑制。突触体细胞膜与2-氨基-5-磷酸戊酸预孵育可防止4-氨基吡啶对B-50磷酸化的抑制,但对50 kDa磷酸化的抑制没有影响。已知2-氨基-5-磷酸戊酸是一种特异性N-甲基-D-天冬氨酸拮抗剂,在体外和体内均具有抗癫痫活性。测试的其他几种抗癫痫药物并未影响4-氨基吡啶诱导的蛋白磷酸化抑制作用。