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在小鼠最大电休克诱发惊厥实验中,别嘌醇不影响卡马西平和丙戊酸的抗惊厥活性。

Allopurinol does not affect the anticonvulsant activity of carbamazepine and valproate in maximal electroshock-induced convulsions in mice.

作者信息

Parada-Turska Jolanta, Czuczwar Mirosław, Kiś Jacek, Czuczwar Piotr, Cioczek Anna, Łuszczki Jarogniew, Czuczwar Stanisław J

机构信息

Department of Rheumatology, Medical University, Jaczewskiego 8, PL 20-090 Lublin, Poland.

出版信息

Pol J Pharmacol. 2004 Jan-Feb;56(1):67-72.

Abstract

Allopurinol, an inhibitor of xanthine oxidase, is indicated in the management of patients with elevated serum and urinary uric acid levels. It was also reported to be beneficial in patients with epilepsy when added to traditional antiepileptic drug. Here, we investigated the effect of allopurinol upon the electrical seizure threshold and its effect on the protective efficacy of common antiepileptic drugs, carbamazepine (CBZ) and valproate (VPA) against maximal electroshock (MES)-induced convulsions in mice. We found that allopurinol administered at doses of 5, 15 or 45 mg/kg, did not affect electrical seizure threshold. When administered acutely or for a prolonged period of time (5 times every 24 h), it did not affect anticonvulsant activity of CBZ and VPAin MES. Free plasma concentration of both anticonvulsants was not affected by allopurinol given at a dose of 45 mg/kg for 5 days. Thus, our results did not support suggestions that allopurinol can be beneficial as add-on drug in the management of epilepsy at least in patients treated with CBZ or VPA.

摘要

别嘌醇是一种黄嘌呤氧化酶抑制剂,适用于治疗血清和尿酸水平升高的患者。据报道,当与传统抗癫痫药物联合使用时,它对癫痫患者也有益处。在此,我们研究了别嘌醇对电惊厥阈值的影响,以及它对常用抗癫痫药物卡马西平(CBZ)和丙戊酸盐(VPA)对小鼠最大电休克(MES)诱导惊厥的保护效果的影响。我们发现,以5、15或45mg/kg的剂量给药别嘌醇,并不影响电惊厥阈值。急性给药或长期给药(每24小时给药5次)时,它并不影响CBZ和VPA对MES的抗惊厥活性。以45mg/kg的剂量给药别嘌醇5天,两种抗惊厥药物的血浆游离浓度均未受影响。因此,我们的结果并不支持以下观点,即至少在接受CBZ或VPA治疗的患者中,别嘌醇作为附加药物治疗癫痫有益。

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