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首页> 外文期刊>Journal of Pharmacy and Pharmacology >Montelukast, a cysteinyl leukotriene receptor-1 antagonist, attenuates chronic brain injury after focal cerebral ischaemia in mice and rats.
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Montelukast, a cysteinyl leukotriene receptor-1 antagonist, attenuates chronic brain injury after focal cerebral ischaemia in mice and rats.

机译:半胱氨酰白三烯受体1拮抗剂孟鲁司特可减轻小鼠和大鼠局灶性脑缺血后的慢性脑损伤。

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OBJECTIVES: Previously we demonstrated the neuroprotective effect of montelukast, a cysteinyl leukotriene receptor-1 (CysLT(1) ) antagonist, on acute brain injury after focal cerebral ischaemia in mice. In this study, we have determined its effect on chronic brain injury after focal cerebral ischaemia in mice and rats. METHODS: After transient focal cerebral ischaemia was induced by middle cerebral artery occlusion, montelukast was intraperitoneally injected in mice or orally administered to rats for five days. Behavioural dysfunction, brain infarct volume, brain atrophy and neuron loss were determined to evaluate brain lesions. KEY FINDINGS: Montelukast (0.1 mg/kg) attenuated behavioural dysfunction, brain infarct volume, brain atrophy and neuron loss in mice, which was similar to pranlukast, another CysLT(1) receptor antagonist. Oral montelukast (0.5 mg/kg) was effective in rats and was more effective than edaravone, a free radical scavenger. CONCLUSION: Montelukast protected mice and rats against chronic brain injury after focal cerebral ischaemia, supporting the therapeutic potential of CysLT(1) receptor antagonists.
机译:目的:以前我们证明半胱氨酸白三烯受体1(CysLT(1))拮抗剂孟鲁司特对小鼠局灶性脑缺血后急性脑损伤的神经保护作用。在这项研究中,我们已经确定了它对小鼠和大鼠局灶性脑缺血后慢性脑损伤的作用。方法:大脑中动脉闭塞诱发短暂性局灶性脑缺血后,将孟鲁司特腹膜内注射给小鼠或口服给大鼠五天。行为障碍,脑梗死体积,脑萎缩和神经元丢失被确定来评估脑损伤。主要发现:孟鲁司特(0.1 mg / kg)减轻了小鼠的行为障碍,脑梗死体积,脑萎缩和神经元丢失,与另一种CysLT(1)受体拮抗剂普卢司特相似。口服孟鲁司特(0.5 mg / kg)在大鼠中有效,并且比自由基清除剂依达拉奉更有效。结论:孟鲁司特保护小鼠和大鼠免受局部脑缺血后的慢性脑损伤,支持CysLT(1)受体拮抗剂的治疗潜力。

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