Georgiev V P, Petkova B P, Petkov V D, Kambourova T S
Acta Physiol Pharmacol Bulg. 1986;12(2):14-20.
The effects of angiotensin II (AT II), GABA, muscimol (administered i.c.v.) and of amino-oxiacetic acid (AOAA) and baclofen (administered i.p.), as well as of the combinations of AT II with these substances and bicuculline, were studied with respect to the threshold of the convulsive seizures induced by timed intravenous infusion of pentylenetetrazol (PTZ) in mice. It was found in the experiments that the threshold-increasing effect of GABA, muscimol and AOAA was potentiated by AT II (applied in a dose which did not change essentially the convulsive threshold). The potentiated effect of GABA, muscimol and AOAA on the convulsive threshold, when applied in combination with AT II, was antagonized by bicuculline. The threshold-increasing effect of baclofen was not affected substantially by AT II; in this case bicuculline had no effect. On the basis of the results obtained it may be assumed that AT II performs the functions of an antocoid predominantly for the GABA-A receptors in the central nervous system.
研究了血管紧张素II(AT II)、γ-氨基丁酸(GABA)、蝇蕈醇(脑室内注射)、氨基氧乙酸(AOAA)和巴氯芬(腹腔注射),以及AT II与这些物质和荷包牡丹碱的组合,对小鼠定时静脉注射戊四氮(PTZ)诱导惊厥发作阈值的影响。实验发现,GABA、蝇蕈醇和AOAA的阈值升高作用被AT II(以基本不改变惊厥阈值的剂量应用)增强。当GABA、蝇蕈醇和AOAA与AT II联合应用时,其对惊厥阈值的增强作用被荷包牡丹碱拮抗。巴氯芬的阈值升高作用基本不受AT II影响;在这种情况下,荷包牡丹碱没有作用。根据所得结果可以推测,AT II主要对中枢神经系统中的GABA-A受体发挥抗惊厥作用。