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尼群洛尔和佐芬普利在大鼠脑缺血再灌注模型中的抗氧化和抗细胞凋亡作用。

The anti-oxidant and anti-apoptotic effects of nebivolol and zofenopril in a model of cerebral ischemia/reperfusion in rats.

机构信息

Department of Neurology, Faculty of Medicine, Dicle University, Diyarbakır, Turkey.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2012 Jan 10;36(1):22-8. doi: 10.1016/j.pnpbp.2011.08.011. Epub 2011 Aug 23.

Abstract

The aim of this experiment was to investigate whether nebivolol and zofenopril have protective effects against oxidative damage and apoptosis induced by cerebral ischemia/reperfusion (I/R). There were seven groups of rats, with each containing eight rats. The groups were: the control group, I/R group, I/R plus zofenopril, I/R plus nebivolol, I/R plus nebivolol and zofenopril, zofenopril only and nebivolol only. Cerebral I/R was induced by clamping the bilateral common carotid artery and through hypotension. The rats were sacrificed 1h after ischemia, and histopathological and biochemical analyses were carried out on their brains. The total antioxidant capacity was evaluated by using an automated and colorimetric measurement method developed by Erel. I/R produced a significant increase in the levels of total oxidant status and malondialdehyde levels, the number of caspase-3 immunopositive cells and activities of prolidase and paraoxonase in brain when compared with the control group (p<0.05). A significant decrease in brain total antioxidant capacity and nitric oxide levels were found in I/R group when compared with the control group (p<0.05). Both nebivolol and zofenopril treatment prevented decreasing of the total antioxidant capacity and nitric oxide levels, produced by I/R in the brain (p<0.05). Both nebivolol and zofenopril treatment prevented the total oxidant status, malondialdehyde levels, activities of paraoxonase and prolidase from increasing in brains of rats exposed to I/R (p<0.05). In conclusion, both nebivolol and zofenopril protected rats from ischemia-induced brain injury. The protection may be due to the indirect prevention of oxidative stress and apoptosis.

摘要

本实验旨在研究奈必洛尔和佐芬普利是否具有对抗脑缺血再灌注(I/R)引起的氧化损伤和细胞凋亡的保护作用。将大鼠分为 7 组,每组 8 只。对照组、I/R 组、I/R+佐芬普利组、I/R+奈必洛尔组、I/R+奈必洛尔和佐芬普利组、佐芬普利组和奈必洛尔组。通过夹闭双侧颈总动脉和低血压诱导脑 I/R。缺血 1h 后处死大鼠,对其大脑进行组织病理学和生化分析。采用 Erel 开发的自动比色法评估总抗氧化能力。与对照组相比,I/R 可显著增加总氧化状态和丙二醛水平、caspase-3 免疫阳性细胞数以及脑内脯氨酸肽酶和对氧磷酶活性(p<0.05)。与对照组相比,I/R 组脑总抗氧化能力和一氧化氮水平显著降低(p<0.05)。奈必洛尔和佐芬普利治疗均可预防 I/R 引起的脑总抗氧化能力和一氧化氮水平降低(p<0.05)。奈必洛尔和佐芬普利治疗均可预防 I/R 大鼠脑总氧化状态、丙二醛水平、对氧磷酶和脯氨酸肽酶活性升高(p<0.05)。结论:奈必洛尔和佐芬普利均可保护大鼠免受缺血性脑损伤。这种保护作用可能是通过间接预防氧化应激和细胞凋亡实现的。

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