长期服用可待因引起Wistar大鼠髓鞘轴突变性和运动功能障碍。

IF 5.1 Q1 SUBSTANCE ABUSE
Substance Abuse and Rehabilitation Pub Date : 2022-11-11 eCollection Date: 2022-01-01 DOI:10.2147/SAR.S365982
Victor Bassey Archibong, Ibe Michael Usman, Ann Monima Lemuel
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引用次数: 2

摘要

目的:含有可待因(一种阿片类药物)的非处方止咳药在尼日利亚广泛使用,因此容易被过度使用或滥用。本研究旨在了解口服可待因对雄性Wistar大鼠大脑皮层和小脑神经元完整性的影响及其行为意义。方法:取体重相当的成年雄性Wistar大鼠30只,随机分为A、B、C、D、E 5组(n = 6)。研究药物为ArchilinTM加可待因和二氢可待因30mg。A组为对照组,给予生理盐水0.5mL/kg。B组和C组分别给予双氢可待因1mg/kg和2mg/kg;D组和E组分别给予ArchilinTM可待因糖浆2mL/kg和4mL/kg。根据动物体重给予ArchilinTM可待因糖浆和二氢可待因溶液,每日口服和口咽管辅助,连续21天。实验动物采用梁行走和开阔场地进行神经行为学研究。在治疗期结束时,动物被盐酸氯胺酮腹腔麻醉。大脑很快被解剖出来,用生理盐水冲洗,组织处理用于髓磷脂研究。结果:束流行走和开放野实验结果显示,长期服用可待因对实验动物的运动功能有干扰作用。给予生理盐水的大鼠的前额叶皮层和小脑切片显示髓鞘正常,而与对照组相比,治疗组的动物显示髓鞘退化。结论:长期服用处方可待因可引起髓鞘变性,影响髓系轴突电脉冲传导,导致运动功能不全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prolonged Codeine Administration Causes Degeneration of Myelinated Axons and Motor Dysfunction in Wistar Rats.

Prolonged Codeine Administration Causes Degeneration of Myelinated Axons and Motor Dysfunction in Wistar Rats.

Prolonged Codeine Administration Causes Degeneration of Myelinated Axons and Motor Dysfunction in Wistar Rats.

Prolonged Codeine Administration Causes Degeneration of Myelinated Axons and Motor Dysfunction in Wistar Rats.

Purpose: Over-the-counter (OTC) anti-cough medications which contain codeine (an opioid) are extensively available in Nigeria, and hence prone to overuse or abuse. The study aimed to understand the effects of oral codeine administration on the integrity of neurons of the cerebral cortex and cerebellum and its behavioral implications in male Wistar rats.

Methods: Thirty adult male Wistar rats of comparable weights were obtained and randomly allocated into 5 groups: A, B, C, D, and E (n = 6). Drugs used for the study were ArchilinTM with codeine and dihydrocodeine 30mg. Group A served as control and was administered 0.5mL/kg of normal saline. Groups B and C were treated with 1mg/kg and 2mg/kg of dihydrocodeine, respectively; Group D and E received 2mL/kg and 4mL/kg of ArchilinTM codeine syrup, respectively. The ArchilinTM codeine syrup and dihydrocodeine solutions were administered to the animals based on their body weight, orally and daily with the aid of oropharyngeal tubes for 21 days. The experimental animals were subjected to neurobehavioral studies using beam walk and open field. At the end of the treatment period, the animals were anesthetized with ketamine-hydrochloride intraperitoneally. The brains were quickly dissected out, rinsed with normal saline, and tissue processed for myelin studies.

Results: The beam walking and open field result revealed that prolonged codeine administration interfered with motor function in the experimental animals. Sections of the prefrontal cortex and cerebellum of rats given normal saline showed normal myelin sheaths, whereas animals in the treatment group showed degenerating myelin compared to the control.

Conclusion: Prolonged consumption of prescription codeine causes degeneration of the myelin sheaths and this may affect the conduction of electrical impulses in myelinated axons thus resulting in motor function insufficiency.

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