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大鼠中的纳洛酮痛觉过敏和应激诱导的镇痛作用。

Naloxone hyperalgesia and stress-induced analgesia in rats.

作者信息

Coderre T J, Rollman G B

出版信息

Life Sci. 1983 May 2;32(18):2139-46. doi: 10.1016/0024-3205(83)90103-0.

Abstract

Since past studies concerning the effects of naloxone on nociception have yielded inconclusive findings, the variables of pain test, baseline sensitivity, and stress condition were examined. Within a pure-bred strain of rats, consistent individual differences did not occur. All three measures of pain responsiveness demonstrated hyperalgesic effects of naloxone, but they differed in their capacity to reflect the effects of analgesia produced by continuous or intermittent electrical shock. By some measures, naloxone reversed the stress-induced analgesia due to intermittent shock; it did not influence the analgesia produced by continuous stress. The data support a model of pain inhibition involving both opioid and non-opioid systems and suggest that the hyperalgesic effects of naloxone can sometimes give rise to erroneous conclusions concerning apparent naloxone-reversability of putative analgesic procedures.

摘要

由于过去关于纳洛酮对痛觉影响的研究结果尚无定论,因此对疼痛测试、基线敏感性和应激条件等变量进行了研究。在纯种种系的大鼠中,并未出现一致的个体差异。所有三种疼痛反应指标均显示出纳洛酮的痛觉过敏作用,但它们在反映连续或间歇性电击产生的镇痛效果的能力上有所不同。通过某些指标,纳洛酮可逆转因间歇性电击导致的应激诱导镇痛;但它并不影响连续应激产生的镇痛作用。这些数据支持了一种涉及阿片类和非阿片类系统的疼痛抑制模型,并表明纳洛酮的痛觉过敏作用有时可能会导致关于假定镇痛程序的明显纳洛酮可逆性得出错误结论。

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