Zakusov V V, Ostrovskaya R U, Kozhechkin S N, Markovich V V, Molodavkin G M, Voronina T A
Arch Int Pharmacodyn Ther. 1977 Oct;229(2):313-26.
Drugs of the benzodiazepine series (clonazepam, lorazepam, diazepam and medazepam) increase the inhibitory processes in the cerebral cortex as it has been shown by means of the recovery cycles of the intracortical response. There is a correlation between the effect on the recovery cycles and their protective action against convulsions induced by GABA deficit. Diazepam enhances the inhibitory effect of GABA applied iontophoretically to rabbit sensorymotor cortex neurons. The drug GABA-ergic effect seems to be specific since it fails to modify the effects of other putative neurotransmitters (glutamate, glycine, acetylcholine). The alteration of rat conflict situation behaviour under diazepam has been eliminated due to the blockade of GABA-receptors by gicuculline and the decrease of the GABA level by thiosemicarbazide. It is inferred that the main effects of benzodiazepines are mediated by GABA and suggested that these agents increase the sensitivity of postsynaptic GABA-ergic receptors.
苯二氮䓬类药物(氯硝西泮、劳拉西泮、地西泮和美达西泮)可增强大脑皮质的抑制过程,这已通过皮质内反应的恢复周期得到证实。对恢复周期的影响与其对由γ-氨基丁酸(GABA)缺乏引起的惊厥的保护作用之间存在相关性。地西泮可增强通过离子导入法施加于兔感觉运动皮质神经元的GABA的抑制作用。该药物的GABA能效应似乎具有特异性,因为它不会改变其他假定神经递质(谷氨酸、甘氨酸、乙酰胆碱)的作用。由于荷包牡丹碱阻断GABA受体以及氨基硫脲降低GABA水平,地西泮对大鼠冲突情境行为的改变已被消除。据推断,苯二氮䓬类药物的主要作用是由GABA介导的,并表明这些药物可增加突触后GABA能受体的敏感性。