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血管紧张素转换酶抑制剂和血管紧张素Ⅱ1型受体拮抗剂对戊四氮诱发小鼠惊厥的影响。

Effect of ACE inhibitors and AT1 receptor antagonists on pentylenetetrazole-induced convulsions in mice.

作者信息

Łukawski Krzysztof, Czuczwar Stanisław Jerzy

机构信息

Department of Physiopathology, Institute of Rural Health, Jaczewskiego 2, Lublin, 20-090, Poland,

出版信息

Neurol Sci. 2015 May;36(5):779-81. doi: 10.1007/s10072-014-2040-x. Epub 2015 Jan 9.

Abstract

Experimental data show that some angiotensin-converting enzyme (ACE) inhibitors and angiotensin AT(1) receptor antagonists that are normally used as antihypertensive drugs can exert anticonvulsant-like activity against audiogenic seizures. In the current study, a number of ACE inhibitors (captopril, enalapril, cilazapril, perindopril and zofenopril) and AT(1) antagonists (losartan, telmisartan and candesartan) were examined against pentylenetetrazole (PTZ)-induced seizures in mice. Captopril (50 mg/kg) administered intraperitoneally significantly raised the PTZ threshold (p < 0.05). The remaining drugs were not protective against PTZ-induced convulsions. The current study indicates that captopril decreases PTZ-evoked seizures in mice, which is an animal model of myoclonic convulsions.

摘要

实验数据表明,一些通常用作抗高血压药物的血管紧张素转换酶(ACE)抑制剂和血管紧张素AT(1)受体拮抗剂可对听源性癫痫发作发挥类似抗惊厥的活性。在本研究中,检测了多种ACE抑制剂(卡托普利、依那普利、西拉普利、培哚普利和佐芬普利)和AT(1)拮抗剂(氯沙坦、替米沙坦和坎地沙坦)对小鼠戊四氮(PTZ)诱导的癫痫发作的作用。腹腔注射卡托普利(50 mg/kg)可显著提高PTZ阈值(p < 0.05)。其余药物对PTZ诱导的惊厥无保护作用。本研究表明,卡托普利可减少小鼠中PTZ诱发的癫痫发作,PTZ诱发的癫痫发作是肌阵挛性惊厥的动物模型。

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