首页> 外文期刊>Pharmacology: International Journal of Experimental and Clinical Pharmacology >Tetramethylpyrazine analogue CXC195 protects against cerebral ischemia/reperfusion injury in the rat by an antioxidant action via inhibition of NADPH oxidase and iNOS expression
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Tetramethylpyrazine analogue CXC195 protects against cerebral ischemia/reperfusion injury in the rat by an antioxidant action via inhibition of NADPH oxidase and iNOS expression

机译:四甲基吡嗪类似物CXC195通过抑制NADPH氧化酶和iNOS的表达而具有抗氧化作用,可预防大鼠脑缺血/再灌注损伤

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Aims: This study was conducted to investigate the protective effects of CXC195, a tetramethylpyrazine analogue, in acute focal cerebral ischemia/reperfusion (I/R) injury in rats and to elucidate the potential mechanism. Methods: Middle cerebral artery occlusion for 2 h followed by reperfusion for 24 h was conducted in male Wistar rats and different doses of tetramethylpyrazine and CXC195 were intraperitoneally injected at 30 min after reperfusion. Results: Our results demonstrated that CXC195 at the dosage of 3 and 10 mg/kg significantly reduced the neurological deficit score and the infarct volume compared to the vehicle-treated group. In addition, CXC195 exhibited a protective effect against hippocampus neuronal cell death and significantly restored the brain ATP content. The activities of superoxide dismutase (SOD), glutathione peroxidase (GPx) and total antioxidative capability (T-AOC), as well as production of malondialdehyde (MDA) and reactive oxygen species (ROS) were assayed in ipsilateral hemisphere homogenates to evaluate the redox status after I/R injury. Treatment with CXC195 significantly attenuated the decrease of SOD, GPx and T-AOC activities and inhibited the elevation of MDA content and ROS generation. Furthermore, CXC195 prevented the upregulation of the NADPH oxidase (NOX) 2 and NOX4, and reduced inducible nitric oxide synthase (iNOS) induction and production of nitric oxide induced by I/R. Conclusion: These results suggest that CXC195 has a neuroprotective effect in transient focal ischemia, which is most likely due to its antioxidant activity by inhibiting NOX and iNOS expression.
机译:目的:本研究旨在研究四甲基吡嗪类似物CXC195在大鼠急性局灶性脑缺血/再灌注(I / R)损伤中的保护作用,并阐明其潜在机制。方法:对雄性Wistar大鼠进行大脑中动脉闭塞2 h,然后再灌注24 h,再灌注后30 ​​min腹腔注射不同剂量的川methyl嗪和CXC195。结果:我们的结果表明,与媒介物治疗组相比,CXC195的剂量为3和10 mg / kg时,可显着降低神经功能缺损评分和梗塞体积。此外,CXC195对海马神经元细胞死亡具有保护作用,并能显着恢复大脑ATP含量。在同侧半球匀浆中测定超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GPx)和总抗氧化能力(T-AOC)的活性,以及​​丙二醛(MDA)和活性氧(ROS)的产生,以评估氧化还原I / R受伤后的状态。 CXC195处理显着减弱了SOD,GPx和T-AOC活性的降低,并抑制了MDA含量的升高和ROS的产生。此外,CXC195防止了NADPH氧化酶(NOX)2和NOX4的上调,并减少了I / R诱导型一氧化氮合酶(iNOS)的诱导和一氧化氮的产生。结论:这些结果表明,CXC195在短暂性局灶性局部缺血中具有神经保护作用,这很可能是由于其通过抑制NOX和iNOS表达而具有的抗氧化活性。

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