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苯环利定对大鼠脊髓反射的抑制作用。

Inhibitory effect of phencyclidine on rat spinal reflexes.

作者信息

Nagano N, Ono H, Fukuda H

机构信息

Department of Toxicology and Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.

出版信息

Gen Pharmacol. 1988;19(6):795-8.

PMID:3068095
Abstract
  1. The effects of phencyclidine (PCP) on spinal reflexes and the excitability of motoneuron somata were studied in rats. 2. PCP decreased both the monosynaptic reflex (MSR) and the polysynaptic reflex (PSR) in spinal rats as well as in intact rats. 3. The effects of PCP were not antagonized by monoaminergic and cholinergic antagonists. 4. A low dose of PCP antagonized the PSR augmentation but not the MSR augmentation caused by N-methyl-D-aspartate (NMDA). 5. In the excitability test, PCP decreased not only the monosynaptic response but also the excitability of motoneuron somata. 6. These results suggest that the inhibitory effects of PCP on spinal reflexes are not due to mediation of the monoaminergic and cholinergic systems, but partly due to its blockade of NMDA-type receptors and also to a hyperpolarizing action or a membrane-stabilizing action on the motoneuron soma.
摘要
  1. 研究了苯环己哌啶(PCP)对大鼠脊髓反射和运动神经元胞体兴奋性的影响。2. PCP降低了脊髓大鼠和完整大鼠的单突触反射(MSR)和多突触反射(PSR)。3. 单胺能和胆碱能拮抗剂不能拮抗PCP的作用。4. 低剂量的PCP拮抗由N-甲基-D-天冬氨酸(NMDA)引起的PSR增强,但不拮抗MSR增强。5. 在兴奋性测试中,PCP不仅降低了单突触反应,还降低了运动神经元胞体的兴奋性。6. 这些结果表明,PCP对脊髓反射的抑制作用不是由于单胺能和胆碱能系统的介导,而是部分由于其对NMDA型受体的阻断,也由于对运动神经元胞体的超极化作用或膜稳定作用。

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