首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >Xuebijing Protects Rats from Sepsis Challenged with Acinetobacter baumannii by Promoting Annexin A1 Expression and Inhibiting Proinflammatory Cytokines Secretion
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Xuebijing Protects Rats from Sepsis Challenged with Acinetobacter baumannii by Promoting Annexin A1 Expression and Inhibiting Proinflammatory Cytokines Secretion

机译:血必净通过促进膜联蛋白A1的表达并抑制促炎性细胞因子的分泌保护大鼠免受败血症鲍曼不动杆菌的攻击

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摘要

Xuebijing (XBJ) injection is a herbal medicine that has been widely used in the treatment of sepsis in China; however, its role in the development and progression of Acinetobacter baumannii sepsis and the underlying mechanisms remain uninvestigated. In the present study, fifty-four male Wistar rats were randomly assigned to normal-control group, sepsis-control group, and sepsis + XBJ group, each containing three subgroups of different treatment time periods (6, 12, and 24 hrs following injection, resp.). The sepsis model was established by intraperitoneal injection of A. baumannii ATCC 19606. For XBJ treatment, 4 mL/kg XBJ was administrated simultaneously by intravenous injection through caudal vein every 12 hrs. All animals demonstrated ill state, obvious intestinal dysfunction, histopathological lung damages, and overactive inflammatory responses after A. baumannii infection, and these events could be partially reversed by XBJ treatment from the beginning of infection. XBJ induced an increase in the expression of anti-inflammatory mediator annexin A1; however, two proinflammatory cytokines, interleukin-8 (IL-8) and tumor necrosis factor-α (TNF-α), were decreased at the each monitored time point. These findings suggested that XBJ via its cytokine-mediated anti-inflammatory effects might have a potential role in preventing the progression of A. baumannii infection to sepsis by early administration.
机译:血必净注射液是一种在中国已广泛用于治疗败血症的草药。然而,其在鲍曼不动杆菌败血症的发生和发展中的作用及其潜在机制尚待研究。在本研究中,将54只雄性Wistar大鼠随机分为正常对照组,败血症对照组和败血症+ XBJ组,每组包含三个不同治疗时间段(注射后6、12和24小时)的亚组。 ,分别)。通过腹膜内注射鲍曼不动杆菌ATCC 19606建立脓毒症模型。对于XBJ治疗,每12小时通过尾静脉静脉内注射同时施用4mL / kg XBJ。所有动物在鲍曼不动杆菌感染后均表现出病态,明显的肠道功能障碍,肺部病理组织损伤和炎症反应过度,从感染开始就可以通过XBJ治疗部分逆转这些事件。 XBJ诱导抗炎介质膜联蛋白A1的表达增加;然而,在每个监测的时间点,两种促炎细胞因子白细胞介素8(IL-8)和肿瘤坏死因子-α(TNF-α)减少了。这些发现表明,XBJ通过其细胞因子介导的抗炎作用,可能通过早期给药来预防鲍曼不动杆菌感染发展为败血症。

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