非洲荆芥叶提取物对脑缺血/再灌注损伤后脑卒中相关关键生化指标的调节作用

Omotayo B Ilesanmi, Afolabi C Akinmoladun, Olanrewaju Sam Olayeriju, Ibrahim Olabayode Saliu, M Tolulope Olaleye, Afolabi A Akindahunsi
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引用次数: 14

摘要

背景:氧化应激在脑卒中发病中起重要作用。因此,富含抗氧化植物化学物质的植物被认为是预防和治疗中风和其他神经系统疾病的有效药物。非洲反法西斯英语。(Moraceae)传统上用于脑相关问题的管理,但缺乏其抗中风潜力的数据。材料与方法:采用双侧颈总动脉闭塞30 min / 2 h再灌注法(BCCAO/R)诱导雄性Wistar大鼠脑缺血再灌注损伤。对照组为假手术组,未进行BCCAO/R治疗;对照组为未进行MEA治疗的BCCAO/R治疗组。用50 mg/kg或100 mg/kg非洲胡麻甲醇叶提取物(MEA)预处理14 d,对BCCAO/ r介导的氧化应激关键标志物(丙二醛、还原性谷胱甘肽、黄嘌呤氧化酶、超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶)、神经化学紊乱和兴奋毒性(髓过氧化物酶、谷氨酰胺合成酶、Na+/K+ atp酶、乙酰胆碱酯酶和酪氨酸羟化酶)的改善作用。并与20 mg/kg槲皮素为标准品处理效果进行了评价和比较。结果:结果显示,与未处理BCCAO/R的对照组相比,MEA预处理可显著减轻或逆转BCCAO/R诱导的氧化应激、神经化学功能障碍和兴奋毒性评价生化标志物的水平或活性变化(p < 0.05)。100 mg/kg MEA的效果与标准品槲皮素相似。结论:这些结果揭示了非洲古树在脑卒中和其他缺血性疾病中的神经保护作用。
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MODULATION OF KEY BIOCHEMICAL MARKERS RELEVANT TO STROKE BY ANTIARIS AFRICANA LEAF EXTRACT FOLLOWING CEREBRAL ISCHEMIA/REPERFUSION INJURY.

Background: Oxidative stress plays a significant role in stroke pathogenesis. Hence, plants rich in antioxidant phytochemicals have been suggested as effective remedies for prevention and treatment of stroke and other neurological diseases. Antiaris africana Engl. (Moraceae) is traditionally used for the management of brain-related problems but there is paucity of data on its anti-stroke potential.

Materials and methods: Ischemia/reperfusion injury was induced by a 30 min bilateral common carotid artery occlusion/ 2 h reperfusion (BCCAO/R) in the brain of male Wistar rats. A sham-operated group which was not subjected to BCCAO/R and a group subjected to BCCAO/R without treatment with MEA served as controls. The ameliorative effect of 14 days of pretreatment with 50 mg/kg or 100 mg/kg A. africana methanol leaf extract (MEA) on BCCAO/R-mediated alterations to key markers of oxidative stress (malondialdehyde, reduced glutathione, xanthine oxidase, superoxide dismutase, catalase and glutathione peroxidase) and neurochemical disturbances and excitotoxicity (myeloperoxidase, glutamine synthetase, Na+/K+ ATPase, acetylcholinesterase and tyrosine hydroxylase), was evaluated and compared with the effect produced by treatment with 20 mg/kg quercetin as a reference standard.

Results: Results show that pretreatment with MEA significantly mitigated or reversed BCCAO/R-induced changes in the level or activity of the evaluated biochemical markers of oxidative stress, neurochemical dysfunction and excitotoxicity compared with the BCCAO/R untreated control group (p < 0.05). The effect produced by 100 mg/kg MEA was similar to that of the reference standard, quercetin.

Conclusion: These results revealed the neuroprotective potential of A. africana in stroke and other ischemia-related pathologies.

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