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首页> 外文期刊>European neuropsychopharmacology: the journal of the European College of Neuropsychopharmacology >Comparative efficacy of liposome-entrapped amiloride and free amiloride in animal models of seizures and serum potassium in mice.
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Comparative efficacy of liposome-entrapped amiloride and free amiloride in animal models of seizures and serum potassium in mice.

机译:脂质体包裹的阿米洛利和游离阿米洛利在癫痫发作和小鼠血清钾动物模型中的比较功效。

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摘要

The present study was aimed to evaluate a liposomal formulation of amiloride on experimental seizure models including the increasing current electroshock seizure threshold test (ICES), pentylenetetrazole (PTZ)-induced seizures and PTZ-induced status epilepticus in mice. Further, the effect of liposomal amiloride on serum K(+) levels was also investigated using flame photometry. We found an improved anticonvulsant action with liposome-entrapped amiloride as compared to free amiloride. Further, free amiloride showed an increase in serum K(+) levels, however the latter was unaffected with liposomal formulation treatment. These results, together with previously published data, suggest that as drug delivery vehicles, liposomes can enhance the effectiveness of drugs in the CNS without producing peripheral toxicity (hyperkalemia).
机译:本研究旨在评估阿米洛利的脂质体制剂在实验性癫痫模型上的作用,包括增加电流电击癫痫阈值试验(ICES),戊四氮(PTZ)诱导的癫痫发作和PTZ诱导的小鼠癫痫持续状态。此外,还使用火焰光度法研究了脂质体阿米洛利对血清K(+)水平的影响。我们发现与游离阿米洛利相比,脂质体包裹的阿米洛利具有更好的抗惊厥作用。此外,游离的阿米洛利显示出血清K(+)水平升高,但是后者不受脂质体制剂治疗的影响。这些结果以及以前发表的数据表明,脂质体作为药物传递载体,可以增强CNS中药物的效力,而不会产生周围毒性(高钾血症)。

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