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阿片受体在大鼠伏隔核中催产素诱导的抗伤害感受中的作用。

Involvement of opioid receptors in oxytocin-induced antinociception in the nucleus accumbens of rats.

作者信息

Gu Xing-Long, Yu Long-Chuan

机构信息

Neurobiology Laboratory and National Laboratory of Biomembrane and Membrane Biotechnology, College of Life Sciences, Peking University, Beijing, China.

出版信息

J Pain. 2007 Jan;8(1):85-90. doi: 10.1016/j.jpain.2006.07.001. Epub 2006 Nov 9.

DOI:10.1016/j.jpain.2006.07.001
PMID:17097925
Abstract

UNLABELLED

Antinociceptive effects of oxytocin have been demonstrated in mice, rats, dogs, and humans. It has been shown that oxytocin receptors and fibers with oxytocin were distributed in the nucleus accumbens (NAc) of rats. The present study was performed to investigate the regulating role of oxytocin in nociception in the NAc of rats. Intra-NAc administration of oxytocin-induced dose-dependent increases in the hindpaw withdrawal latency (HWL) to noxious thermal and mechanical stimulation in rats, indicating that oxytocin has antinociceptive effects in the NAc of rats. Furthermore, the oxytocin-induced antinociceptive effects were attenuated by intra-NAc administration of the opioid-receptor antagonist naloxone, suggesting that the endogenous opioid system is involved in the oxytocin-induced antinociception in the NAc. Moreover, the oxytocin-induced antinociception was attenuated by intra-NAc injection of the kappa-receptor antagonist nor-binaltorphimine (nor-BNI) and the mu-receptor antagonist beta-funaltrexamine, but not by the delta-receptor antagonist naltrindole, demonstrating the involvements of mu- and kappa-receptors, but not delta-receptor, in the oxytocin-induced antinociception in the NAc of rats.

PERSPECTIVE

This article supplements the evidence that oxytocin regulates nociception in the central nervous system. It presents additional material for clinical application of oxytocin as an analgesia drug.

摘要

未标注

催产素的抗伤害感受作用已在小鼠、大鼠、狗和人类中得到证实。研究表明,催产素受体和含催产素的纤维分布于大鼠的伏隔核(NAc)。本研究旨在探讨催产素在大鼠伏隔核伤害感受中的调节作用。向大鼠伏隔核内注射催产素可使大鼠后爪对有害热刺激和机械刺激的缩爪潜伏期(HWL)呈剂量依赖性增加,这表明催产素在大鼠伏隔核中具有抗伤害感受作用。此外,向伏隔核内注射阿片受体拮抗剂纳洛酮可减弱催产素诱导的抗伤害感受作用,提示内源性阿片系统参与了催产素在伏隔核中诱导的抗伤害感受。而且,向伏隔核内注射κ受体拮抗剂 nor- 环丙甲羟二氢吗啡酮(nor-BNI)和μ受体拮抗剂β - 芬太尼可减弱催产素诱导的抗伤害感受作用,但δ受体拮抗剂纳曲吲哚则无此作用,这表明μ受体和κ受体而非δ受体参与了催产素在大鼠伏隔核中诱导的抗伤害感受。

观点

本文补充了催产素调节中枢神经系统伤害感受的证据。它为催产素作为镇痛药物的临床应用提供了更多资料。

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