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首页> 外文期刊>Methods and findings in experimental and clinical pharmacology >Behavioral pharmacological properties after recovery from the loss of righting reflex induced by benzodiazepine receptor agonists in mice.
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Behavioral pharmacological properties after recovery from the loss of righting reflex induced by benzodiazepine receptor agonists in mice.

机译:从苯二氮卓受体激动剂引起的小鼠对位反射丧失中恢复后的行为药理特性。

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摘要

In this study we examined the behavioral pharmacological side effects after recovery from the loss of righting reflex induced by three benzodiazepine receptor agonists - zolpidem, brotizolam and flunitrazepam - in ddY mice. All agents caused marked motor incoordination in the rotarod test and muscle flaccidity in the traction test until 15 min after recovery of righting reflex. Thereafter, the short-acting hypnotics zolpidem and brotizolam showed a faster recovery than the long-acting benzodiazepine flunitrazepam. However, head twitch responses were observed in the mice treated with flunitrazepam, but zolpidem and brotizolam had no such effect. The flunitrazepam-induced head twitch response was antagonized by ketanserin, a 5- HT(2A) receptor antagonist. These results indicate that flunitrazepam, a long-acting benzodiazepine that is nonselective for type I and II benzodiazepine receptors, induces head twitch responses with muscle flaccidity after recovery from the loss of righting reflex caused by thesedrugs. In addition, these findings suggest the involvement of a 5-HT(2A)-GABA(A) receptor/benzodiazepine interaction in this phenomenon.
机译:在这项研究中,我们研究了在ddY小鼠中,由三种苯并二氮杂receptor受体激动剂-唑吡坦,溴硝唑仑和氟硝西epa引起的扶正反射丧失后,恢复行为后的行为药理副作用。在扶正反射恢复后的15分钟内,所有试剂均在旋转脚架测试中引起明显的运动不协调,在牵引测试中引起肌肉松弛。此后,短效催眠药唑吡坦和溴苯唑仑比长效苯二氮卓氟硝西raz显示出更快的恢复。然而,在用氟尼西epa治疗的小鼠中观察到头部抽搐反应,但是唑吡坦和溴替唑仑没有这种作用。氟硝西epa诱导的头抽搐反应是由5-羟色胺(2A)受体拮抗剂ketanserin拮抗的。这些结果表明,氟硝西epa是一种长效的苯二氮卓类药物,对I型和II型苯二氮卓类受体不具有选择性,在从这些药物引起的矫正反射丧失中恢复后,会诱发头部痉挛,并伴有肌肉松弛。此外,这些发现表明在这种现象中涉及5-HT(2A)-GABA(A)受体/苯并二氮杂pine相互作用。

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