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苯二氮䓬类镇静剂美达西泮与促智药甲氯芬酯联合使用对大鼠脑毒蕈碱受体活性的影响。

Effect of the combination of the benzodiazepine tranquilizer medazepam and the nootropic agent meclofenoxate on the activity of rat brain muscarinic receptors.

作者信息

Popova J S, Petkov V D

机构信息

Institute of Physiology, Bulgarian Academy of Sciences, Sofia.

出版信息

Gen Pharmacol. 1990;21(6):927-30. doi: 10.1016/0306-3623(90)90456-v.

Abstract
  1. The effect of 7-day treatment with the benzodiazepine tranquilizer medazepam (5 mg/kg), the nootropic agent meclofenoxate (100 mg/kg) and their combination in the same doses on the binding activity of muscarinic receptors in four rat brain structures (cerebral cortex, striatum, hippocampus and hypothalamus) were studied using the antagonist [3H]-1-quinuclidinyl benzylate [( 3H]-QNB) as radio-ligand. 2. Medazepam treatment caused significant decrease of muscarinic receptor binding affinity (Kd) and of the receptor binding capacity (Bmax) in the brain structures studied. The number of muscarinic binding sites was unsignificantly decreased only in the hippocampus. 3. Meclofenoxate treatment caused an increase of muscarinic receptor affinity and a decrease of the binding capacity in the cerebral cortex and hypothalamus and an increase of the binding affinity in the striatum and hippocampus. 4. The combination of medazepam and meclofenoxate caused no significant changes of both muscarinic receptor characteristics in the hippocampus and of the receptor affinity in the striatum and hypothalamus in comparison with control rats. The Bmax values were decreased in the cerebral cortex, striatum and hypothalamus when compared with control animals. The differences observed were slighter than those determined after the comparison of medazepam treated rats with control rats. 5. The results obtained afford an opportunity to suggest that the nootropic agent meclofenoxate acts to moderate the effect of the benzodiazepine tranquilizer medazepam on the activity of rat brain muscarinic receptors.
摘要
  1. 研究了苯二氮䓬类镇静剂美达西泮(5毫克/千克)、促智药甲氯芬酯(100毫克/千克)及其相同剂量组合对大鼠四个脑区(大脑皮层、纹状体、海马体和下丘脑)毒蕈碱受体结合活性的7天治疗效果,使用拮抗剂[3H]-1-喹核醇苄酯[(3H]-QNB)作为放射性配体。2. 美达西泮治疗导致所研究脑区中毒蕈碱受体结合亲和力(Kd)和受体结合容量(Bmax)显著降低。仅海马体中毒蕈碱结合位点数量无显著减少。3. 甲氯芬酯治疗导致大脑皮层和下丘脑中毒蕈碱受体亲和力增加、结合容量降低,纹状体和海马体中结合亲和力增加。4. 与对照大鼠相比,美达西泮和甲氯芬酯的组合导致海马体中毒蕈碱受体特征以及纹状体和下丘脑受体亲和力均无显著变化。与对照动物相比,大脑皮层、纹状体和下丘脑的Bmax值降低。观察到的差异比美达西泮治疗大鼠与对照大鼠比较后确定的差异更小。5. 所得结果表明,促智药甲氯芬酯可调节苯二氮䓬类镇静剂美达西泮对大鼠脑毒蕈碱受体活性的影响。

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