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纳曲吲哚对大鼠吗啡诱导的耐受性和身体依赖性的不同作用。

Differential effects of naltrindole on morphine-induced tolerance and physical dependence in rats.

作者信息

Hepburn M J, Little P J, Gingras J, Kuhn C M

机构信息

Department of Pharmacology, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

J Pharmacol Exp Ther. 1997 Jun;281(3):1350-6.

PMID:9190871
Abstract

This study investigated the effect of delta opioid receptor blockade by naltrindole on the development of physical dependence and tolerance to the antinociceptive and respiratory depressive effects of morphine in rats. Chronic morphine was delivered either by s.c. injection of increasing amounts of morphine over 5 days or by s.c. implantation of morphine pellets. Animals were cotreated with saline or naltrindole. Antinociception and respiratory depression were assessed after administration of a challenge dose of morphine, and withdrawal signs were determined after naloxone challenge. Naltrindole significantly attenuated the development of antinociceptive tolerance after all three chronic treatment regimens. In addition, rats pretreated with naltrindole displayed significantly fewer withdrawal symptoms and less weight loss after a naloxone challenge. In contrast, naltrindole did not prevent the development of tolerance to morphine-induced respiratory depression. These results imply that tolerance to antinociception and physical dependence involves adaptations at interacting mu and delta receptor populations, whereas tolerance to respiratory depression reflects actions of independent mu and delta receptor populations. These findings suggest that delta antagonists may have potential clinical application for decreasing the rapid development of tolerance to opiate-induced analgesia, while allowing for the development of protective tolerance to respiratory depression.

摘要

本研究调查了纳曲吲哚对δ阿片受体的阻断作用,对大鼠吗啡抗伤害感受和呼吸抑制作用的身体依赖性及耐受性发展的影响。慢性吗啡给药方式为:在5天内皮下注射递增剂量的吗啡,或皮下植入吗啡缓释微丸。动物同时接受生理盐水或纳曲吲哚治疗。给予一剂激发剂量的吗啡后评估抗伤害感受和呼吸抑制情况,给予纳洛酮激发后确定戒断症状。在所有三种慢性治疗方案后,纳曲吲哚均显著减弱了抗伤害感受耐受性的发展。此外,用纳曲吲哚预处理的大鼠在接受纳洛酮激发后,出现的戒断症状显著减少,体重减轻也较少。相比之下,纳曲吲哚并未阻止对吗啡诱导的呼吸抑制耐受性的发展。这些结果表明,对抗伤害感受和身体依赖性的耐受性涉及相互作用的μ和δ受体群体的适应性变化,而对呼吸抑制的耐受性反映了独立的μ和δ受体群体的作用。这些发现表明,δ拮抗剂可能具有潜在的临床应用价值,可减少对阿片类药物诱导镇痛耐受性的快速发展,同时允许对呼吸抑制产生保护性耐受性。

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