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模拟人类败血症的临床表现和疾病进展:一种用于动物模型的单细菌注射方法。

Simulating the clinical manifestations and disease progression of human sepsis: A monobacterial injection approach for animal modeling.

机构信息

Department of Clinical Laboratory, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, China.

School of Medical Technology and Information Engineering, Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Virulence. 2024 Dec;15(1):2395835. doi: 10.1080/21505594.2024.2395835. Epub 2024 Sep 1.

DOI:10.1080/21505594.2024.2395835
PMID:39219264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11370922/
Abstract

Sepsis is defined as life-threatening organ dysfunction caused by a dysregulated host response to infection, with great clinical heterogeneity, high morbidity, and high mortality. At the same time, there are many kinds of infection sources, the pathophysiology is very complex, and the pathogenesis has not been fully elucidated. An ideal animal model of sepsis can accurately simulate clinical sepsis and promote the development of sepsis-related pathogenesis, treatment methods, and prognosis. The existing sepsis model still uses the previous Sepsis 2.0 modelling standard, which has some problems, such as many kinds of infection sources, poor repeatability, inability to take into account single-factor studies, and large differences from clinical sepsis patients. To solve these problems, this study established a new animal model of sepsis. The model uses intravenous tail injection of a single bacterial strain, simplifying the complexity of multibacterial infection, and effectively solving the above problems.

摘要

脓毒症是指由宿主对感染的失调反应引起的危及生命的器官功能障碍,具有很大的临床异质性、高发病率和高死亡率。同时,感染源种类繁多,病理生理学非常复杂,发病机制尚未完全阐明。一个理想的脓毒症动物模型可以准确模拟临床脓毒症,并促进与脓毒症相关的发病机制、治疗方法和预后的发展。现有的脓毒症模型仍然使用以前的 Sepsis 2.0 建模标准,存在一些问题,如多种感染源、重复性差、不能考虑单因素研究以及与临床脓毒症患者的差异较大。为了解决这些问题,本研究建立了一种新的脓毒症动物模型。该模型采用静脉尾注射单一细菌菌株,简化了多细菌感染的复杂性,并有效地解决了上述问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/3461ef437ec7/KVIR_A_2395835_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/ddacf94ed2ef/KVIR_A_2395835_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/44ca1ee494cf/KVIR_A_2395835_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/75ee672898a8/KVIR_A_2395835_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/9ffa663c4c29/KVIR_A_2395835_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/3461ef437ec7/KVIR_A_2395835_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/ddacf94ed2ef/KVIR_A_2395835_UF0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/44ca1ee494cf/KVIR_A_2395835_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/75ee672898a8/KVIR_A_2395835_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/9ffa663c4c29/KVIR_A_2395835_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c59e/11370922/3461ef437ec7/KVIR_A_2395835_F0004_OC.jpg

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Initial antimicrobial management of sepsis.脓毒症的初始抗菌治疗。
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Sepsis, a 2020 review for the internist.脓毒症,2020年内科医生综述。
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Intensive Care Med. 2020 Feb;46(2):266-284. doi: 10.1007/s00134-020-05950-6. Epub 2020 Feb 11.
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α -AR antagonism by BRL-44408 maleate attenuates acute lung injury in rats with downregulation of ERK1/2, p38MAPK, and p65 pathway.马来酸 BRL-44408 拮抗 α-AR 可下调 ERK1/2、p38MAPK 和 p65 通路,减轻大鼠急性肺损伤。
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