Weizman A, Fares F, Pick C G, Yanai J, Gavish M
Geha Psychiatric Hospital, Tel Aviv, Israel.
Eur J Pharmacol. 1989 Oct 10;169(2-3):235-40. doi: 10.1016/0014-2999(89)90020-4.
Chronic phenobarbital administration for 20 days to mice resulted in significant increases in the density of peripheral benzodiazepine binding sites in the heart, kidney and cerebellum, but did not affect the density of these sites in the olfactory bulb. No alteration in the affinity (KD) of peripheral benzodiazepine binding sites for their ligand [3H]PK 11195 was observed in any of the organs examined. Phenobarbital treatment did not affect the maximal binding capacity or the affinity of the central benzodiazepine receptors for [3H]flunitrazepam in the cerebral cortex, hippocampus and olfactory bulb. A significant reduction in [3H]muscimol binding in the hippocampus was obtained following chronic phenobarbital treatment. Such an alteration was not detected in the cerebral cortex. The KD values remained unaltered in both tissues. The modulatory effect of phenobarbital on peripheral benzodiazepine binding sites could be related to alterations in the functions of these organs or to the neurochemical effects of the drug.
对小鼠连续20天给予苯巴比妥,导致心脏、肾脏和小脑中外周苯二氮䓬结合位点的密度显著增加,但不影响嗅球中这些位点的密度。在所检查的任何器官中,均未观察到外周苯二氮䓬结合位点对其配体[3H]PK 11195的亲和力(KD)有改变。苯巴比妥治疗不影响大脑皮层、海马体和嗅球中中央苯二氮䓬受体对[3H]氟硝西泮的最大结合容量或亲和力。长期苯巴比妥治疗后,海马体中[3H]蝇蕈醇结合显著减少。在大脑皮层未检测到这种改变。两个组织中的KD值均未改变。苯巴比妥对外周苯二氮䓬结合位点的调节作用可能与这些器官功能的改变或药物的神经化学作用有关。