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分析重复给予吗啡对大鼠运动行为的影响。

Profiling the Effects of Repetitive Morphine Administration on Motor Behavior in Rats.

机构信息

School of Pharmacy and Pharmacology, University of Tasmania, Hobart, TAS 7001, Australia.

Medical School, University of Cyprus, Nicosia 1678, Cyprus.

出版信息

Molecules. 2021 Jul 19;26(14):4355. doi: 10.3390/molecules26144355.

Abstract

Efficient repetitive clinical use of morphine is limited by its numerous side effects, whereas analgesic tolerance necessitates subsequent increases in morphine dose to achieve adequate levels of analgesia. While many studies focused on analgesic tolerance, the effect of morphine dosing on non-analgesic effects has been overlooked. This study aimed to characterize morphine-induced behavior and the development and progression of morphine-induced behavioral tolerance. Adult male Sprague-Dawley rats were repetitively treated with subcutaneous morphine for 14 days in two dose groups (A: 5 mg/kg/day (b.i.d.) → 10 mg/kg/day; B: 10 mg/kg/day (b.i.d.) → 20 mg/kg/day). Motor behavior was assessed daily (distance traveled, speed, moving time, rearing, rotation) in an open-field arena, before and 30 min post-injections. Antinociception was measured using tail-flick and hot-plate assays. All measured parameters were highly suppressed in both dosing groups on the first treatment day, followed by a gradual manifestation of behavioral tolerance as the treatment progressed. Animals in the high-dose group showed increased locomotor activity after 10 days of morphine treatment. This excitatory phase converted to an inhibition of behavior when a higher morphine dose was introduced. We suggest that the excitatory locomotor effects of repetitive high-dose morphine exposure represent a signature of its behavioral and antinociceptive tolerance.

摘要

吗啡的频繁重复临床应用受到其众多副作用的限制,而镇痛耐受则需要随后增加吗啡剂量以达到足够的镇痛水平。尽管许多研究都集中在镇痛耐受上,但吗啡剂量对非镇痛作用的影响却被忽视了。本研究旨在描述吗啡诱导的行为以及吗啡诱导的行为耐受的发展和进展。成年雄性 Sprague-Dawley 大鼠在两个剂量组(A:5mg/kg/天(b.i.d.)→10mg/kg/天;B:10mg/kg/天(b.i.d.)→20mg/kg/天)中接受重复皮下吗啡治疗 14 天。在注射前和 30 分钟,在一个开阔场中每天评估运动行为(行进距离、速度、运动时间、站立、旋转)。使用尾巴闪烁和热板测定法测量镇痛作用。在第一天的治疗中,两个剂量组的所有测量参数均高度抑制,随着治疗的进行,逐渐出现行为耐受。接受高剂量吗啡治疗 10 天后,动物的运动活性增加。当引入更高剂量的吗啡时,这种兴奋相转换为行为抑制。我们认为,重复高剂量吗啡暴露的兴奋运动效应代表了其行为和镇痛耐受的特征。

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