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纳洛酮和 N-甲基-D-天冬氨酸对抗刺激引起的镇痛:阿片类受体和 N-甲基-D-天冬氨酸受体的作用。

Antagonism of stimulation-produced analgesia by naloxone and N-methyl-D-aspartate: role of opioid and N-methyl-D-aspartate receptors.

机构信息

Department of Physiology, University College of Medical Sciences, Delhi, India.

出版信息

Hum Exp Toxicol. 2012 Jan;31(1):51-6. doi: 10.1177/0960327111417908. Epub 2011 Jul 29.

Abstract

The present study aims to investigate the influence of electrical stimulation of periaqueductal gray (PAG) following peripheral nerve injury and its modulation by naloxone and N-methyl-D-aspartate (NMDA). Chronic neuropathic pain was induced by chronic constriction injury of the sciatic nerve, and subsequently a cannula was implanted in the PAG area for the purpose of electrical stimulation and intra-PAG drug administration. Intra-PAG administration of morphine, ketamine, and their combination were found to elicit antinociceptive response on hot-plate test. Electrical stimulation of PAG was also observed to demonstrate decreased pain response on hot-plate test, and this effect was reversed by the administration of naloxone, NMDA, and their combination, when injected into the PAG area. These findings suggest that apart from the opioid receptors, probably NMDA receptors also have a role to play in stimulation-produced analgesia.

摘要

本研究旨在探讨周围神经损伤后导水管周围灰质(PAG)电刺激的影响及其对纳洛酮和 N-甲基-D-天冬氨酸(NMDA)的调制作用。慢性神经病理性疼痛通过坐骨神经慢性缩窄性损伤诱导,随后在 PAG 区域植入导管,用于电刺激和 PAG 内药物给药。研究发现,PAG 内给予吗啡、氯胺酮及其组合可在热板试验中产生镇痛反应。电刺激 PAG 也观察到在热板试验中疼痛反应减轻,当将纳洛酮、NMDA 及其组合注入 PAG 区域时,这种作用被逆转。这些发现表明,除了阿片受体外,NMDA 受体可能也在刺激引起的镇痛中发挥作用。

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