首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Involvements of mu- and kappa-opioid receptors in morphine-induced antinociception in the nucleus accumbens of rats.
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Involvements of mu- and kappa-opioid receptors in morphine-induced antinociception in the nucleus accumbens of rats.

机译:mu和阿片受体参与吗啡诱导的伏伏核的镇痛作用。

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摘要

It is well known that there are three types of opioid receptors, mu- (MOR), delta- (DOR), and kappa-opioid receptor (KOR) in the central nervous system. The present study investigated the involvement of opioid receptors in morphine-induced antinociception in the nucleus accumbens (NAc) of rats. The hindpaw withdrawal latencies to thermal and mechanical stimulation increased markedly after intra-NAc administration of morphine. The antinociceptive effects induced by morphine were dose-dependently inhibited by intra-NAc administration of the non-selective opioid receptor antagonist naloxone. Furthermore, the morphine-induced antinociception was significantly attenuated by subsequent intra-NAc injection of the MOR antagonist beta-funaltrexamine or the KOR antagonist nor-binaltorphimine, but not the DOR antagonist naltrindole. The results indicate that MOR and KOR, but not DOR are involved in the morphine-induced antinociception in the NAc of rats.
机译:众所周知,中枢神经系统中存在三种类型的阿片受体,即mu-(MOR),delta-(DOR)和kappa-阿片受体(KOR)。本研究调查了阿片受体在吗啡诱导的伏伏核(NAc)中的抗伤害感受中的作用。 NAc内施用吗啡后,后爪退缩对热和机械刺激的潜伏期显着增加。吗啡诱导的抗伤害感受作用通过非选择性阿片受体拮抗剂纳洛酮的NAc内剂量依赖性抑制。此外,通过随后的NAc内注射MOR拮抗剂β-富氨曲胺或KOR拮抗剂去甲双萘酚,而不是DOR拮抗剂纳曲酮,吗啡诱导的抗伤害感受明显减弱。结果表明,MOR和KOR参与了大鼠NAc中吗啡诱导的抗伤害感受,但未参与DOR。

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