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尼莫地平对大鼠模型中吗啡相关戒断综合征的影响:一项观察性研究。

Effect of Nimodipine on Morphine-related Withdrawal Syndrome in Rat Model: An Observational Study.

作者信息

Mishra Pravash Ranjan, Barik Mayadhar, Ray Subrata Basu

机构信息

Department of Anatomy, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.

Department of Nuclear Medicine, All India Institute of Medical Sciences, New Delhi, India.

出版信息

J Pediatr Neurosci. 2017 Jan-Mar;12(1):7-14. doi: 10.4103/1817-1745.205652.

DOI:10.4103/1817-1745.205652
PMID:28553371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5437795/
Abstract

OBJECTIVE

To observe the effect of L-type calcium channel blocker like nimodipine on morphine's withdrawal when it was administered continuously along with morphine versus a single bolus dose of nimodipine, which was administered at the end of the experiment before the precipitation of withdrawal reaction in morphine-dependent rats.

MATERIALS AND METHODS

Four groups of adult male Wistar rats were rendered morphine dependent by subcutaneous injections of morphine at a dose of 10 mg/kg for 10 days. Nimodipine 10 mg/kg intraperitoneally (ip) administered to one group once daily before morphine administration in the entire experimental period, and another group received nimodipine only once at the end of the experiment as a single bolus dose 2 mg/kg before the administration of naloxone. Naloxone 3 mg/kg was administered ip to all the groups to precipitate withdrawal reactions. The withdrawal reactions were evaluated and scored as per the Gellert and Holtzman global withdrawal rating scale.

RESULTS

Nimodipine when administered as a single bolus dose before naloxone administration in morphine-dependant rats reduced the features of withdrawal reactions more effectively than continuous administration of nimodipine along with morphine throughout the experimental period.

CONCLUSION

We discovered that nimodipine helps in attenuating the severity of morphine withdrawal having potential role encountered during pharmacotherapy with morphine management of opioid dependence, well memory, impairement, cell signaling and phosphorylation of neuron.

摘要

目的

观察L型钙通道阻滞剂尼莫地平在与吗啡连续给药时以及在实验结束时于吗啡依赖大鼠戒断反应诱发前单次大剂量给药时,对吗啡戒断反应的影响。

材料与方法

四组成年雄性Wistar大鼠通过皮下注射10mg/kg吗啡,连续给药10天,使其产生吗啡依赖。一组在整个实验期间每天在注射吗啡前腹腔注射10mg/kg尼莫地平,另一组在实验结束时、注射纳洛酮前单次大剂量腹腔注射2mg/kg尼莫地平。所有组均腹腔注射3mg/kg纳洛酮以诱发戒断反应。根据盖勒特和霍尔兹曼整体戒断评分量表对戒断反应进行评估和评分。

结果

在吗啡依赖大鼠中,于注射纳洛酮前单次大剂量给予尼莫地平,比在整个实验期间与吗啡连续给药更有效地减轻了戒断反应的特征。

结论

我们发现尼莫地平有助于减轻吗啡戒断的严重程度,在阿片类药物依赖的吗啡治疗、良好记忆、损伤、细胞信号传导和神经元磷酸化过程中具有潜在作用。

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