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酸感受离子通道激活/抑制对大鼠痫性发作的影响 被引量:3

Acid-sensor ion channels activation/inhibition on rats with lithium pilocarpine-induced epilepsy
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摘要 目的观察酸感受离子通道(ASICs)激活/抑制对氯化锂一匹罗卡品大鼠的癫痫皮层脑电图癫痫放电的影响。方法制作匹罗卡品大鼠癫痫模型,分别腹腔注射磷酸盐缓冲液(PBS)、阿米洛利、左乙拉西坦或酸性液体,记录脑电图癫痫样发电次数、波幅、放电间期变化。结果在注射后60~90min,与正常对照组比较,ASICs抑制组癫痫样放电次数(0.69±0.08)、波幅(0.70±0.16)均明显下降(P〈0.05),放电间期(1.46±0.18)延长(P〈0.05);ASICs激活组在注射后30min内,癫痫样放电次数增高(1.05±0.07)(P〈0.05)。结论阿米洛利能抑制锂一匹罗卡品诱导的癫痫发作,酸性液体可促进癫痫发作,其作用机制可能与抑制或激活ASICs通道有关。 Objective To study the effects of acid-sensor ion channels activation or inhibition on the epileptic discharge in EEG of epilepsy rat model induced by Lithium-pilocarpine. Methods Seizures were intraperitoneally induced in rats with lithium-pilocarpine. The rats were divided into four groups: the placebo group, the ASICs inhibitor group, the positive control group and the ASICs activator group by ad- ministrating intraperitoneally PBS, amiloride, Levetiracetam or acidic liquids, respectively. The number of discharge, and amplitude and interval of discharge were selected as the indicators for comparison. Results Sixty-ninety min after the injection, the number of discharge (0. 69 ± 0.08 ) and the amplitude (0. 70± 0. 16) were reduced in the ASICs inhibitor group, while the interval of discharge was increased (1.46 ± 0. 18 ) ( P 〈 0. 05 ) as compared with the placebo group. In the ASICs activator group, the number of discharge ( 1.05 ±0. 07) was increased 30 min after injection. Conclusion Amiloride can inhibit epilepsy induced by lithium-pilocarpine, while acid liquids exert the opposite effects, which may be concerned with the inhibition or activation of ASICs channel.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2012年第8期1566-1568,共3页 Chinese Journal of Experimental Surgery
基金 国家自然科学基金资助项目(30900459) 武汉大学青年教师资助项目(3082012) 国家教育部新教师基金资助项目(090392) 湖北省教育厅科学技术研究计划指导性项目(B类)(B20090102)
关键词 匹罗卡品 阿米洛利 酸感受离子通道 癫痫 Pilocarpine Amiloride Acid-sensing ion channel Epilepsy
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