Galust'ian G E, Ignatov Iu D
Biull Eksp Biol Med. 1983 Jan;95(1):56-8.
Quantitative histochemistry was used to study the effects of phenazepam, medazepam, diazepam, and nitrazepam on GABA-transaminase activity in different rat brain structures. Phenazepam and diazepam, which produced anxiolytic effect in low doses, selectively inhibited GABA-transaminase of the hippocamp. The degree of GABA-transaminase inhibition corresponded with pharmacological activity of the test benzodiazepines. It is assumed that inhibition of brain GABA-transaminase by benzodiazepines is linked with their interaction with GABA-benzodiazepine receptor complex.
采用定量组织化学方法研究了非那西泮、美达西泮、地西泮和硝西泮对不同大鼠脑结构中γ-氨基丁酸转氨酶(GABA-转氨酶)活性的影响。低剂量时产生抗焦虑作用的非那西泮和地西泮选择性抑制海马体的GABA-转氨酶。GABA-转氨酶的抑制程度与受试苯二氮䓬类药物的药理活性相对应。据推测,苯二氮䓬类药物对脑GABA-转氨酶的抑制作用与其与GABA-苯二氮䓬受体复合物的相互作用有关。