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丹红注射液通过改善缺血半影区细胞内能量代谢耦联减轻脑缺血/再灌注损伤。

Danhong injection alleviates cerebral ischemia/reperfusion injury by improving intracellular energy metabolism coupling in the ischemic penumbra.

机构信息

College of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou 310053, China.

College of Life Science, Zhejiang Chinese Medical University, Hangzhou 310053, China.

出版信息

Biomed Pharmacother. 2021 Aug;140:111771. doi: 10.1016/j.biopha.2021.111771. Epub 2021 May 28.

Abstract

Danhong injection (DHI) is a compound Chinese medicine widely used in China for treatment of ischemic cardio-cerebrovascular diseases. However, limited data are available regarding the protective effect of DHI on the ischemic penumbra in ischemic stroke. This study aimed to investigate the effect of intravenous DHI on neuronal injure in the ischemic penumbra after cerebral ischemia/reperfusion (CI/R), focusing especially on the involvement of intracellular energy metabolism coupling. Male Sprague-Dawley rats were subjected to right middle cerebral artery occlusion for 60 min followed by reperfusion with or without intravenous DHI (0.5, 1.0, or 2.0 mL/kg) once daily for 7 days. Post-treatment with DHI ameliorated neurological defects, diminished cerebral infarction, alleviated cerebral edema, improved microcirculatory perfusion after 7days of reperfusion, and inhibited apoptosis and enhanced neuronal survival in the ischemic penumbra. In addition, DHI significantly ameliorated oxidative stress, reduced DNA damage, and inhibited the activation of PARP1/AIF pathway, thereby restoring cytoplasmic glycolytic activity. Furthermore, this drug increased PDH activity by inhibiting the HIF1α/PDK1 signaling pathway, thus eliminating the inhibitory effect of CI/R on mitochondrial metabolism. The results of this study suggest that DHI can alleviate cerebral edema after CI/R and rescue the ischemic penumbra, and these protective effects are due to the regulation of intracellular energy metabolic coupling.

摘要

丹红注射液(DHI)是一种广泛应用于中国治疗缺血性心脑血管疾病的复方中药。然而,关于 DHI 对缺血性中风缺血半影区的保护作用的数据有限。本研究旨在探讨静脉注射 DHI 对脑缺血再灌注(CI/R)后缺血半影区神经元损伤的影响,特别关注细胞内能量代谢偶联的参与。雄性 Sprague-Dawley 大鼠右侧大脑中动脉闭塞 60min 后,再灌注 7 天,每日 1 次,分别给予 0.5、1.0 或 2.0mL/kg 的 DHI。DHI 治疗后可改善神经缺陷,减少脑梗死,减轻脑水肿,改善再灌注后 7 天的微循环灌注,并抑制缺血半影区的细胞凋亡,增强神经元存活。此外,DHI 还可显著改善氧化应激,减少 DNA 损伤,抑制 PARP1/AIF 通路的激活,从而恢复细胞质糖酵解活性。此外,该药物通过抑制 HIF1α/PDK1 信号通路增加 PDH 活性,从而消除 CI/R 对线粒体代谢的抑制作用。本研究结果表明,DHI 可减轻 CI/R 后脑水肿并挽救缺血半影区,这些保护作用是由于细胞内能量代谢偶联的调节。

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