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青少年和成年大鼠的非阿片类药物耐受。

Non-opioid tolerance in juvenile and adult rats.

机构信息

Department of Neurophysiology, Beritashvili Institute of Physiology, Gotua Street 14, 0160 Tbilisi, Georgia, USA.

出版信息

Eur J Pharmacol. 2010 Mar 10;629(1-3):68-72. doi: 10.1016/j.ejphar.2009.12.016. Epub 2009 Dec 24.

Abstract

It has recently been shown that antinociceptive tolerance develops by repeated systemic administration of non-steroidal anti-inflammatory drugs (NSAIDs) metamizol and lysine-acetylsalicylate. This is similar to the tolerance observed with opioid-induced analgesia [Vanegas and Tortorici, 2002, Cell and Mol. Neurobiol. 22, 655-661]. In the present study, we investigated the development of tolerance to the analgesic effects of the additional NSAIDs analgine, ketorolac and xefocam in juvenile and adult rats. After injection of each drug, tail-flick latencies were significantly elevated on the first day followed by a progressive decrease in tail-flick latency (i.e., tolerance) over the 5-day period, as well as cross-tolerance to morphine-induced analgesia. Tolerance to the analgesic effect of all three NSAIDs developed more rapidly in juvenile compared to adult rats. Pretreatment with naloxone completely prevented the analgesic effects of these drugs in tail-flick and hot plate tests for both juvenile and adult rats. Moreover, each NSAID exhibited cross-tolerance when tolerance to morphine had been induced by systemic morphine delivered repeatedly over 5-day period in both age groups. Our data confirm other recent findings that tolerance to the analgesic action of NSAIDs may depend on an opiate-mediated mechanism.

摘要

最近的研究表明,非甾体类抗炎药(NSAIDs)氨基比林和赖氨酸乙酰水杨酸经重复全身给药后会产生抗伤害感受性耐受。这与阿片类药物引起的镇痛作用观察到的耐受情况相似[Vanegas 和 Tortorici,2002,细胞和分子神经生物学 22,655-661]。在本研究中,我们研究了青少年和成年大鼠对额外的 NSAIDs 安乃近、酮咯酸和昔布类药物镇痛作用的耐受发展情况。在注射每种药物后,第一天空腹舔尾潜伏期明显升高,随后在 5 天内空腹舔尾潜伏期逐渐降低(即耐受),以及对吗啡引起的镇痛作用的交叉耐受。与成年大鼠相比,三种 NSAIDs 的镇痛作用在青少年大鼠中更快地产生耐受。纳洛酮预处理完全阻止了这些药物在青少年和成年大鼠的舔尾和热板试验中的镇痛作用。此外,在两个年龄组中,通过重复 5 天全身给予吗啡诱导吗啡耐受后,每种 NSAID 都表现出交叉耐受。我们的数据证实了其他最近的发现,即 NSAIDs 的镇痛作用的耐受可能依赖于阿片介导的机制。

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