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小鼠多微生物脓毒症盲肠结扎和穿刺模型的实验方案及血管功能评估

Experimental Protocol for Cecal Ligation and Puncture Model of Polymicrobial Sepsis and Assessment of Vascular Functions in Mice.

作者信息

Mishra Santosh Kumar, Choudhury Soumen

机构信息

Division of Pharmacology & Toxicology, Indian Veterinary Research Institute, Bareilly, Uttar Pradesh, India.

, Bhubaneswar, Odisha, India.

出版信息

Methods Mol Biol. 2018;1717:161-187. doi: 10.1007/978-1-4939-7526-6_14.

Abstract

Sepsis is the systemic inflammatory response syndrome that occurs during infection and is exacerbated by the inappropriate immune response encountered by the affected individual. Despite extensive research, sepsis in humans is one of the biggest challenges for clinicians. The high mortality rate in sepsis is primarily due to hypoperfusion-induced multiorgan dysfunctions , resulting from a marked decrease in peripheral resistance. Vascular dysfunctions are further aggravated by sepsis-induced impairment in myocardial contractility. Circulatory failure in sepsis is characterized by refractory hypotension and vascular hyporeactivity (vasoplegia) to clinically used vasoconstrictors. To investigate the complex pathophysiology of sepsis and its associated multiple organ dysfunction, several animal models have been developed. However, cecal ligation and puncture (CLP) model of murine sepsis is still considered as 'gold standard' in sepsis research. In this protocol we have described the standard surgical procedure to induce polymicrobial sepsis by cecal ligation and puncture. Further, we have described the protocol to study the molecular mechanisms underlying vascular dysfunctions in sepsis.

摘要

脓毒症是在感染期间发生的全身炎症反应综合征,受影响个体所遭遇的不适当免疫反应会使其加剧。尽管进行了广泛研究,但人类脓毒症仍是临床医生面临的最大挑战之一。脓毒症的高死亡率主要归因于外周阻力显著降低导致的低灌注诱发的多器官功能障碍。脓毒症引起的心肌收缩力损害会进一步加重血管功能障碍。脓毒症中的循环衰竭表现为难治性低血压和对临床使用的血管收缩剂的血管反应性降低(血管麻痹)。为了研究脓毒症及其相关多器官功能障碍的复杂病理生理学,已经开发了几种动物模型。然而,小鼠脓毒症的盲肠结扎和穿刺(CLP)模型在脓毒症研究中仍被视为“金标准”。在本方案中,我们描述了通过盲肠结扎和穿刺诱导多微生物脓毒症的标准手术程序。此外,我们还描述了研究脓毒症中血管功能障碍潜在分子机制的方案。

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