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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Nitrous oxide-antinociception is mediated by opioid receptors and nitric oxide in the periaqueductal gray region of the midbrain.
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Nitrous oxide-antinociception is mediated by opioid receptors and nitric oxide in the periaqueductal gray region of the midbrain.

机译:一氧化二氮的抗伤害感受作用是由阿片受体和中脑导水管周围灰色区域的一氧化氮介导的。

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摘要

Previous studies have shown that nitrous oxide (N(2)O)-induced antinociception is sensitive to antagonism by blockade of opioid receptors and also by inhibition of nitric oxide (NO) production. The present study was conducted to determine whether these occur within the same brain site. Mice were stereotaxically implanted with microinjection cannulae in the periaqueductal gray (PAG) area of the midbrain. In saline-pretreated mice, exposure to 70% N(2)O resulted in a concentration-dependent antinociceptive effect in the mouse abdominal constriction test. Pretreatment with an opioid antagonist in the PAG significantly antagonized the antinociceptive effect. Pretreatment with an inhibitor of NO production in the PAG also significantly antagonized the antinociceptive effect. These findings suggest that N(2)O acts in the PAG via an NO-dependent, opioid receptor-mediated mechanism to induce antinociception.
机译:以前的研究表明,一氧化二氮(N(2)O)诱导的抗伤害感受作用对阿片类药物受体的拮抗作用很敏感,因为它可以阻断阿片受体并抑制一氧化氮(NO)的产生。进行本研究以确定它们是否在同一大脑部位内发生。在中脑导水管周围灰色(PAG)区域中,将小鼠显微注射立体定位。在盐水预处理的小鼠中,暴露于70%N(2)O会导致小鼠腹部收缩试验中浓度依赖性的镇痛作用。在PAG中使用阿片类拮抗剂进行预处理可显着拮抗镇痛作用。在PAG中用NO生成抑制剂进行预处理也明显拮抗了伤害感受作用。这些发现表明,N(2)O通过NO依赖性阿片受体介导的机制在PAG中起作用,以诱导抗伤害感受。

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