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氯化镍对戊四氮致痫小鼠的逆转作用。

Reversal of pentylenetetrazole-induced seizure activity in mice by nickel chloride.

机构信息

Department of Pharmaceutical Sciences and Drug Research, Punjabi University, Patiala - 147 002, India.

出版信息

Indian J Pharmacol. 2009 Feb;41(1):15-8. doi: 10.4103/0253-7613.48885.

DOI:10.4103/0253-7613.48885
PMID:20177575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2825007/
Abstract

OBJECTIVE

The present study was designed to investigate the anticonvulsant potential of nickel which is shown to selectively block t-type calcium channels by using nickel choride on pentylenetetrazole (80 mg/kg) induced seizure activity model in mice.

MATERIALS AND METHODS

Seizures were assessed in terms of onset of Straub's tail phenomenon and onset of jerky movements of the whole body, convulsions, and death. Sodium valproate served as a standard control in the present study.

RESULTS

Nickel chloride (5 mg/kg i.p. and 10 mg/kg i.p.) attenuated pentylenetetrazole-induced seizure activity in mice, as reflected by a significant increase in the onset time of Straub's tail phenomenon and onset of jerky movements of the whole body, convulsions, and death. High dose of nickel chloride showed more pronounced anticonvulsant action than sodium valproate.

CONCLUSIONS

The anticonvulsant action of nickel chloride was noticeable in this study. However, further studies are required to elucidate its full anticonvulsant potential.

摘要

目的

本研究旨在通过氯化镍对戊四氮(80mg/kg)诱导的小鼠癫痫发作模型的作用,研究镍的抗惊厥潜力,镍被证明可选择性地阻断 T 型钙通道。

材料和方法

以 Straub 尾巴现象的开始和整个身体的抽搐运动的开始、抽搐和死亡为指标评估癫痫发作。本研究中,丙戊酸钠作为标准对照。

结果

氯化镍(腹腔注射 5mg/kg 和 10mg/kg)可减轻戊四氮诱导的小鼠癫痫发作活动,表现为 Straub 尾巴现象的开始和整个身体的抽搐运动的开始、抽搐和死亡时间明显延长。高剂量的氯化镍显示出比丙戊酸钠更明显的抗惊厥作用。

结论

本研究中观察到氯化镍的抗惊厥作用。然而,需要进一步的研究来阐明其全部的抗惊厥潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/eb4f5cb30886/IJPharm-41-15-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/14a4d0c2a856/IJPharm-41-15-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/f3ce76744108/IJPharm-41-15-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/3a5359cdbdff/IJPharm-41-15-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/eb4f5cb30886/IJPharm-41-15-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/14a4d0c2a856/IJPharm-41-15-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/f3ce76744108/IJPharm-41-15-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/3a5359cdbdff/IJPharm-41-15-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c760/2825007/eb4f5cb30886/IJPharm-41-15-g004.jpg

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CNS drug specificity as determined by the mouse intravenous pentylenetetrazol technique.通过小鼠静脉注射戊四氮技术测定的中枢神经系统药物特异性。
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Cortical and subcortical electrical activity in experimental seizures induced by metrazol.由戊四氮诱发的实验性癫痫发作中的皮质和皮质下电活动。
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Actions of U-92032, a T-type Ca2+ channel antagonist, support a functional linkage between I(T) and slow intrathalamic rhythms.T型钙通道拮抗剂U-92032的作用支持了低阈值钙电流(I(T))与丘脑内缓慢节律之间的功能联系。
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