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首页> 外文期刊>Seizure: the journal of the British Epilepsy Association >Effect of metal chelating agents on pentylenetetrazole-induced seizure threshold in cholestatic mice.
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Effect of metal chelating agents on pentylenetetrazole-induced seizure threshold in cholestatic mice.

机译:金属螯合剂对胆汁淤积小鼠中戊四唑诱导的癫痫发作阈值的影响。

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Zinc has been proven to be anticonvulsant in several studies which indicate that diphenylthiocarbazone (dithizone) and diethyldithiocarbamate (DEDTC), zinc chelating agents, enhance seizure activities. There is also evidence that nitric oxide (NO) generators increase zinc concentration in the brain. On the other hand, the increased level of NO in the nervous system and the consequently increased seizure threshold in cholestatic mice have been well studied. Thus, it could be hypothesized that one of the reasons for the increased seizure threshold in cholestasis is partly the enhanced endogenous zinc concentration, at least in part, due to the overproduction of NO. In this study, we examined the hypothesis that zinc chelating agents might decrease seizure activity to its pre-cholestatic level in bile duct-ligated (BDL) mice. Mice were intra-peritoneally injected with dithizone and diethyldithiocarbamate (DEDTC) before the induction of seizure by pentylenetetrazole (PTZ) and then the seizure activity was recorded. Dose response (dithizone: 5, 30, 100 and 200mg/kg; DEDTC: 25, 50 and 100mg/kg) and time course (only for dithizone: 15, 30, 60 and 120min) studies were performed first. Then, the effects of cholestasis, with and without dithizone injection, on seizure activity were assessed. Proconvulsant effect of dithizone and DEDTC was proved to be dose dependent although time interval between dithizone and PTZ injections did not play any significant role in the seizure activity. Cholestasis decreased seizure activity and increased lag phase before seizure and both effects were decreased by dithizone injection. It is elicited that zinc may mediate the cholestasis-induced decrement in seizure activity.
机译:锌在一些研究中被证明是抗惊厥药,表明锌螯合剂二苯基硫代卡巴carb(dithizone)和二乙基二硫代氨基甲酸酯(DEDTC)增强了癫痫发作的活性。也有证据表明,一氧化氮(NO)产生剂会增加大脑中的锌浓度。另一方面,对胆汁淤积小鼠中神经系统中一氧化氮水平的升高以及由此引起的癫痫发作阈值的升高进行了深入研究。因此,可以假设胆汁淤积性癫痫发作阈值增加的原因之一部分是内源性锌浓度增加,至少部分是由于NO的过量产生。在这项研究中,我们检查了锌螯合剂可能会使胆管结扎(BDL)小鼠的癫痫发作活性降低至其胆汁淤积前水平的假设。在戊戊四唑(PTZ)诱发癫痫发作之前,腹膜内注射双硫zone和二乙基二硫代氨基甲酸酯(DEDTC),然后记录癫痫发作活性。首先进行剂量反应(双硫i:5、30、100和200mg / kg; DETTC:25、50和100mg / kg)和时程(仅双硫th:15、30、60和120min)研究。然后,评估胆汁淤积,注射和不注射双硫zone对癫痫发作活动的影响。尽管双硫th和PTZ注射之间的时间间隔在癫痫发作活动中没有任何重要作用,但双硫i和DETTC的前惊厥作用被证明是剂量依赖性的。胆汁淤积会降低癫痫发作的活动性,并增加癫痫发作前的滞后阶段,并且双硫zone注射液都会降低这两种作用。据认为,锌可能介导了胆汁淤积症诱发的癫痫发作活动的减少。

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