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苯丙胺诱导的镇痛作用不涉及脑内阿片类物质。

Amphetamine-induced analgesia does not involve brain opioids.

作者信息

Drago F, Caccamo G, Continella G, Scapagnini U

出版信息

Eur J Pharmacol. 1984 Jun 1;101(3-4):267-9. doi: 10.1016/0014-2999(84)90168-7.

Abstract

The intrinsic analgesic properties of amphetamine were studied in rats. Subcutaneous injection of amphetamine exerted an additive effect on morphine-induced analgesia in the hot-plate test. Amphetamine itself showed intrinsic analgesic activity in a dose-dependent manner. Administration of naloxone failed to affect the analgesia induced by amphetamine. However, injection of haloperidol totally suppressed the amphetamine-induced change in pain response latency. Both naloxone and haloperidol failed to affect the pain threshold when injected alone, but inhibited morphine-induced analgesia. It is concluded that amphetamine possesses intrinsic analgesic properties which involve catecholamine but not opioid transmission in the brain.

摘要

研究了苯丙胺在大鼠体内的内在镇痛特性。在热板试验中,皮下注射苯丙胺对吗啡诱导的镇痛产生相加作用。苯丙胺本身呈剂量依赖性地表现出内在镇痛活性。给予纳洛酮未能影响苯丙胺诱导的镇痛作用。然而,注射氟哌啶醇完全抑制了苯丙胺诱导的疼痛反应潜伏期变化。纳洛酮和氟哌啶醇单独注射时均未影响痛阈,但抑制了吗啡诱导的镇痛作用。得出的结论是,苯丙胺具有内在镇痛特性,其涉及大脑中的儿茶酚胺传递而非阿片类传递。

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