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Effects of serotoninergic drugs on tremor induced by physostigmine in rats.

机译:5-羟色胺能药物对毒扁豆碱致大鼠震颤的影响。

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We investigated the effects of various serotoninergic drugs and serotonin (5-HT) depletion on physostigmine-induced visible tremor in rats. Physostigmine (0.25-1.5 mg/kg) caused dose-dependent tremor, initiated at 3-5 min (latency decreases as dose increases) and lasted for 30-35 min. Serotonin agonists, 8-hydroxy-2-(di-n-propylamino) tetralin (2.5 mg/kg) and buspirone (5 mg/kg) augmented the tremor response caused by physostigmine. The 5-HT(1)/5-HT(2) receptor antagonist, metergoline (1 mg/kg), and 5-HT(2) blocker, cyproheptadine (10 mg/kg) significantly decreased the duration (40%) as well as intensity (45-50%) of physostigmine-tremor. The 5-HT(2a)/5-HT(2c) antagonist ritanserin (5 mg/kg) significantly reduced the duration (60%) without affecting the intensity of the tremor. In 5-HT depleted rats (p-chlorophenylalanine; 300 mg/kg, for 3 days), physostigmine failed to produce tremor. Interestingly, in these animals, administration of a non-specific 5-HT agonist, 5-methoxy-N,N-dimethyl tryptamine, caused high intensity tremor. These results suggest that presence of 5-HT at the pre-synaptic terminals is needed for the tremor response by physostigmine and the response is greatly mediated via post-synaptic 5-HT receptors. The overall data indicated a direct involvement of central 5-HT system in the cholinergic tremor induced by physostigmine.
机译:我们调查了各种5-羟色胺能药物和5-羟色胺(5-HT)耗竭对毒扁豆碱诱导的大鼠可见震颤的影响。毒扁豆碱(0.25-1.5 mg / kg)引起剂量依赖性震颤,在3-5分钟时开始(潜伏期随剂量增加而降低),并持续30-35分钟。 5-羟色胺激动剂8-羟基-2-(二-正丙基氨基)四氢化萘(2.5 mg / kg)和丁螺环酮(5 mg / kg)增强了毒扁豆碱引起的震颤反应。 5-HT(1)/ 5-HT(2)受体拮抗剂美特古林(1 mg / kg)和5-HT(2)阻断剂赛庚啶(10 mg / kg)显着降低了持续时间(40%)以及毒扁豆碱震颤的强度(45-50%)。 5-HT(2a)/ 5-HT(2c)拮抗剂利坦色林(5 mg / kg)显着减少了持续时间(60%),而不会影响震颤的强度。在5-HT耗竭的大鼠(对氯苯丙氨酸; 300 mg / kg,持续3天)中,毒扁豆碱不能产生震颤。有趣的是,在这些动物中,施用非特异性5-HT激动剂5-甲氧基-N,N-二甲基色胺导致高强度震颤。这些结果表明,毒扁豆碱的震颤反应需要在突触前末端存在5-HT,并且该反应很大程度上由突触后5-HT受体介导。总体数据表明,中央5-HT系统直接参与了由毒扁豆碱引起的胆碱能性震颤。

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