Quock R M, Best J A, Chen D C, Vaughn L K, Portoghese P S, Takemori A E
Department of Basic Sciences, Marquette University School of Dentistry, Milwaukee, WI 53233.
Eur J Pharmacol. 1990 Jan 3;175(1):97-100. doi: 10.1016/0014-2999(90)90158-3.
Exposure to nitrous oxide produced concentration-dependent analgesia in the mouse abdominal constriction test. Intracerebroventricular or intrathecal pretreatment with naltrexone or nor-binaltorphimine significantly reduced nitrous oxide analgesia. However, similar pretreatment with beta-funaltrexamine had no appreciable effect. These findings suggest that nitrous oxide analgesia involves spinal and supraspinal kappa-opioid receptors.
在小鼠腹部收缩试验中,暴露于一氧化二氮产生浓度依赖性镇痛作用。用纳曲酮或去甲二氢吗啡酮进行脑室内或鞘内预处理可显著降低一氧化二氮的镇痛作用。然而,用β-氟纳曲胺进行类似预处理则没有明显效果。这些发现表明,一氧化二氮镇痛涉及脊髓和脊髓上的κ-阿片受体。