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苯二氮䓬受体激动剂对兔红核电活动影响的相对效能

Relative efficacies of benzodiazepine receptor agonists in affecting red nucleus electrical activity in rabbits.

作者信息

Massotti M, De Medici D, De Luca C

机构信息

Laboratorio di Farmacologia, Istituto Superiore di Sanità, Roma, Italy.

出版信息

Psychopharmacology (Berl). 1990;102(4):479-84. doi: 10.1007/BF02247128.

Abstract

The effects of benzodiazepine receptor agonists on the electrical activity of red nucleus (RN) and neocortex were studied in rabbits. Under basal conditions, 30-40 microV, 40-50 Hz waves were recorded in RN. An increase of the amplitude (Emax, 75-90 microV) was found after IV injection of flunitrazepam (ED50, 0.14 mg/kg), diazepam (ED50, 0.28 mg/kg), alpidem (ED50, 1.57 mg/kg) and zolpidem (ED50, 0.73 mg/kg). Clonazepam (ED50, 0.12 mg/kg) and Cl 218,872 (ED50, 0.63 mg/kg) were less effective. In contrast, 2-10-fold higher doses were required to induce a slight decrease of the frequency. At the level of the cortex all benzodiazepine agonists induced synchronization and spindles. The effects of diazepam (5 mg/kg IV) in both areas were antagonized by flumazenil (0.04 mg/kg IV) and bicuculline (0.2 mg/kg IV). Pentamethylentetrazole (10-30 mg/kg IV) selectively abated the effect at the level of the cortex, whereas both clonazepam (2 mg/kg IV) and beta-CCM (0.6 mg/kg IV) selectively suppressed only the effects on the RN. These results suggest that activation of benzodiazepine receptor mainly influences the RN waves amplitude. The efficacy in increasing the amplitude appears related to the reported relative efficacy of the compound in potentiating GABA responses. The possibility exists that these effects are dependent upon the partial or full agonist action of the drugs or upon their binding at distinct benzodiazepine receptor types.

摘要

在兔身上研究了苯二氮䓬受体激动剂对红核(RN)和新皮质电活动的影响。在基础条件下,RN中记录到30 - 40微伏、40 - 50赫兹的波。静脉注射氟硝西泮(ED50,0.14毫克/千克)、地西泮(ED50,0.28毫克/千克)、阿普唑仑(ED50,1.57毫克/千克)和唑吡坦(ED50,0.73毫克/千克)后,振幅增加(Emax,75 - 90微伏)。氯硝西泮(ED50,0.12毫克/千克)和Cl 218,872(ED50,0.63毫克/千克)的效果较差。相比之下,需要高2 - 10倍的剂量才能引起频率略有下降。在皮质水平,所有苯二氮䓬激动剂都能诱导同步化和纺锤波。氟马西尼(0.04毫克/千克静脉注射)和荷包牡丹碱(0.2毫克/千克静脉注射)能拮抗地西泮(5毫克/千克静脉注射)在这两个区域的作用。戊四氮(10 - 30毫克/千克静脉注射)选择性地减弱皮质水平的作用,而氯硝西泮(2毫克/千克静脉注射)和β-CCM(0.6毫克/千克静脉注射)仅选择性地抑制对RN的作用。这些结果表明苯二氮䓬受体的激活主要影响RN波的振幅。增加振幅的效力似乎与该化合物在增强GABA反应方面报道的相对效力有关。这些作用有可能取决于药物的部分或完全激动剂作用,或者取决于它们与不同类型苯二氮䓬受体的结合。

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