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诺龙调节非阿片类和阿片类镇痛以及耐受性/依赖性:性别差异的作用。

Nandrolone modulates the non-opioid and opioid analgesia and tolerance/dependence: role of sexual dimorphism.

作者信息

Philipova Tz, Ivanova T, Pavlova E, Kasakov L, Vlaskovska M

机构信息

Institute of Physiology, Bulgarian Academy of Sciences, 1113 Sofia, Bulgaria.

出版信息

Arch Physiol Biochem. 2003 Dec;111(5):429-36. doi: 10.3109/13813450312331342283.

Abstract

The aim of this investigation was to study the effect of the doping steroid nandrolone on metamizol and morphine-induced analgesia and tolerance/dependence in rats. Nandrolone per se did not change the basal nociceptive thresholds in both sexes. It diminished the analgesic effect of metamizol in females, revealed by tail flick test, and males, revealed by paw pressure and hot plate tests. In general, the action of nandrolone was to decrease the morphine-induced analgesia in female and male rats. This was strongly manifested by paw pressure and tail flick tests in male, and tail flick tests in female animals. Nandrolone slowed the development of opioid tolerance/dependence. It aggravated the withdrawal syndrome in the females and invigorated aggression in the males. The data provide evidence that anabolic steroid nandrolone might decrease the analgesic action of metamizol or morphine. The doping steroid could modulate opioid tolerance/dependence and the aggressive behavior in a gender dependent manner. The action of nandrolone is most likely due to profound long-term effects on the central nervous system and might be a gateway to addiction of other drugs of abuse.

摘要

本研究的目的是探讨兴奋剂类固醇诺龙对大鼠安乃近和吗啡诱导的镇痛作用以及耐受性/依赖性的影响。诺龙本身并未改变两性的基础痛觉阈值。它减弱了通过甩尾试验在雌性大鼠以及通过爪压痛试验和热板试验在雄性大鼠中所显示的安乃近的镇痛效果。总体而言,诺龙的作用是降低雌性和雄性大鼠中吗啡诱导的镇痛作用。这在雄性大鼠的爪压痛试验和甩尾试验以及雌性动物的甩尾试验中表现得尤为明显。诺龙减缓了阿片类药物耐受性/依赖性的发展。它加剧了雌性大鼠的戒断综合征,并增强了雄性大鼠的攻击性。这些数据表明,合成代谢类固醇诺龙可能会降低安乃近或吗啡的镇痛作用。这种兴奋剂类固醇可能以性别依赖的方式调节阿片类药物耐受性/依赖性和攻击行为。诺龙的作用很可能是由于对中枢神经系统产生了深远的长期影响,并且可能是导致滥用其他药物成瘾的一个途径。

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