Tsuchiya T, Fukushima H
Eur J Pharmacol. 1978 Apr 15;48(4):421-4. doi: 10.1016/0014-2999(78)90169-3.
The actions of benzodiazepines and pentobarbitone on GABA-mediated recurrent inhibition of hippocampal pyramidal neurons were investigated in the immobilized unanaesthetized cat. Extracellular action potentials of single neurons were recorded in regions CA1 or CA2 with 4 M NaCl-containing glass micropipettes. Bicuculline (0.1 mg/kg i.v.) reduced the period of inhibition induced by stimulation of the fimbria and the septum, but fludiazepam and diazepam (0.3--1.0 mg/kg i.v.) and pentobarbitone (15--30 mg/kg i.v.) prolonged the inhibition. The prolongation produced by these compounds was antagonized by the administration of bicuculline (0.3 mg/kg i.v.). The results suggest that these two classes of compounds potentiate GABA-mediated recurrent inhibition in hippocampal neurons in a similar way.
在固定未麻醉的猫身上研究了苯二氮䓬类药物和戊巴比妥对海马锥体神经元GABA介导的反复抑制的作用。用含4M氯化钠的玻璃微电极在CA1或CA2区记录单个神经元的细胞外动作电位。荷包牡丹碱(0.1mg/kg静脉注射)缩短了刺激穹窿和隔膜诱导的抑制期,但氟地西泮和地西泮(0.3-1.0mg/kg静脉注射)以及戊巴比妥(15-30mg/kg静脉注射)延长了抑制期。静脉注射荷包牡丹碱(0.3mg/kg)可拮抗这些化合物产生的延长作用。结果表明,这两类化合物以相似的方式增强海马神经元中GABA介导的反复抑制。