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丹红注射液通过增加老龄大鼠的[具体物质]来保护出血性脑损伤。(注:原文中“by Increasing in”表述有误,推测可能是“by increasing [某种物质]”,这里按纠正后的意思翻译,具体需结合完整准确的原文确定)

Danhong Injection Protects Hemorrhagic Brain by Increasing in Aged Rats.

作者信息

Wang Shang, Yu Lie, Sun Guifang, Liu Yu, Hu Wentao, Liu Yanru, Peng Tao, Wang Xiaojun, Cheng Jingliang, Sr Aravintakumar, Qin Bo, Lu Hong

机构信息

Department of Neurology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

Department of Magnetic Resonance, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.

出版信息

Front Pharmacol. 2020 Mar 25;11:346. doi: 10.3389/fphar.2020.00346. eCollection 2020.

Abstract

Intracerebral hemorrhage (ICH) is a severe cerebrovascular disease with a high incidence, mortality and disability rate. Danhong injection (DHI) is beneficial for ischemic stroke, but is prohibited for ICH due to risk of bleeding. The present study aims to explore the potential therapeutic time window and molecular mechanism of DHI in a collagenase-induced ICH model in aged rats. DHI administration after ICH could significantly improve body weight and neurological deficits, and reduce the hematoma volume and brain water content when compared to the vehicle control. Furthermore, the protective effect of DHI administration on days 1-3 after ICH was superior to those on days 3-5 or 7-9 after ICH. DHI remarkably increased the () expression in astrocytes and reduced the expression of inflammatory factors tumor necrosis factor-α (TNF-α) and interleukin-β (IL-1β) after ICH. The immediate treatment of inhibiter chelerythrine (Che) after ICH abolished the protective effect of DHI. Furthermore, the Che treatment reduced the expression of in astrocytes, but increased the expression of TNF-α and IL-1β after ICH. DHI treatment could not reverse these changes. Therefore, the earlier DHI is administered, the better the neuroprotective effect. DHI exerts antioxidative and anti-inflammatory function by increasing in astrocytes. These present results may change the established understanding of DHI, and reveal a novel treatment approach for ICH.

摘要

脑出血(ICH)是一种严重的脑血管疾病,具有高发病率、高死亡率和高致残率。丹红注射液(DHI)对缺血性中风有益,但由于存在出血风险,禁止用于脑出血。本研究旨在探讨丹红注射液在胶原酶诱导的老年大鼠脑出血模型中的潜在治疗时间窗和分子机制。与溶剂对照组相比,脑出血后给予丹红注射液可显著改善体重和神经功能缺损,并减少血肿体积和脑含水量。此外,脑出血后1 - 3天给予丹红注射液的保护作用优于脑出血后3 - 5天或7 - 9天。脑出血后,丹红注射液显著增加星形胶质细胞中()的表达,并降低炎症因子肿瘤坏死因子-α(TNF-α)和白细胞介素-β(IL-1β)的表达。脑出血后立即给予抑制剂白屈菜红碱(Che)可消除丹红注射液的保护作用。此外,Che处理降低了脑出血后星形胶质细胞中()的表达,但增加了TNF-α和IL-1β的表达。丹红注射液处理无法逆转这些变化。因此,丹红注射液给药越早,神经保护作用越好。丹红注射液通过增加星形胶质细胞中的()发挥抗氧化和抗炎功能。这些研究结果可能会改变对丹红注射液的既定认识,并揭示一种新的脑出血治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13e4/7135891/7575383301ee/fphar-11-00346-g001.jpg

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