选择性阿片受体激动剂R-84760对大鼠伤害感觉、运动和呼吸的影响。

K Fujibayashi, M Kubota-Watanabe, Y Iizuka
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引用次数: 0

摘要

研究了R-84760 [(3R)-3-(1-吡咯烷二基甲基)-4-[(1S)-5,6-二氯-l-丹卡布单基]四氢-1,4-噻嗪盐酸]对大鼠伤害感觉、运动和呼吸的影响。R-84760在福尔马林试验中表现出较强的抗伤感受作用。皮下注射时,其效价分别是U-50488和吗啡的930倍和1500倍。脑室内和鞘内注射以及纳洛酮皮下注射可拮抗R-84760的抗痛觉作用,提示R-84760的作用部位位于脊柱和脊柱上水平。当R-84760的剂量比抗痛感所需剂量高16倍时,会干扰旋转棒的性能。R-84760在抗痛感的最大剂量下对动脉血Pco2、Po2和pH无影响。
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Effects of R-84760, a selective kappa-opioid receptor agonist, on nociception, locomotion and respiration in rats.

The effects of R-84760 [(3R)-3-(1-pyrrolidinylmethyl)-4-[(1S)-5,6-dichloro-l-indancarb onyl] tetrahydro-1,4-thiazine hydrochloride] on nociception, locomotion and respiration were examined in rats. R-84760 induced a potent antinociceptive effect in the formalin test. The potency was 930 and 1500 times higher than that of U-50488 and morphine, respectively, when injected subcutaneously. Intracerebroventricular and intrathecal injection, as well as subcutaneous administration of naloxone antagonized the antinociceptive effect of R-84760, suggesting the sites of action of R-84760 were at the spinal and supraspinal levels. R-84760 disturbed the rotarod performance at doses 16 times higher than those needed for antinociception. R-84760 did not affect the arterial blood Pco2, Po2 and pH at a supramaximal dose for antinociception.

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