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胞壁酰二肽可保护补体缺失的小鼠免受手术诱导感染。

Muramyl dipeptide protects decomplemented mice from surgically-induced infection.

作者信息

Cobb J P, Brown C M, Brown G L, Polk H C

出版信息

Int J Immunopharmacol. 1986;8(7):799-803. doi: 10.1016/0192-0561(86)90017-2.

Abstract

Muramyl dipeptide (MDP) is a natural product of bacterial cell-wall breakdown, which can now be produced synthetically; it is the smallest component of the mycobacterial cell wall capable of reproducing the adjuvant activities of Freund's complete adjuvant. We tested the well-documented, protective effect of MDP to increase survival in a murine model simulating surgically-induced bacteremia. The protocol involved the bacterial innoculation of control and decomplemented mice in the presence and the absence of pretreatment with MDP. Bacteremia in both the control and decomplemented groups pretreated with MDP was decreased statistically at 24 h (P less than 0.01) as compared to controls. Likewise, survival was increased significantly at 24 h (P less than 0.05), 48 h (P less than 0.001), and 72 h (P less than 0.001) using the same group comparisons. We conclude, therefore, that MDP maintains its protective effect in the absence of complement, supporting the view that the mechanism of action of MDP is complement independent.

摘要

胞壁酰二肽(MDP)是细菌细胞壁分解的天然产物,现在也可人工合成;它是分枝杆菌细胞壁中能够重现弗氏完全佐剂佐剂活性的最小成分。我们在模拟手术诱导菌血症的小鼠模型中测试了MDP提高生存率的、有充分文献记载的保护作用。实验方案包括在有和没有MDP预处理的情况下,对对照小鼠和补体缺陷小鼠进行细菌接种。与未预处理的对照组相比,用MDP预处理的对照组和补体缺陷组在24小时时菌血症均有统计学意义的降低(P小于0.01)。同样,使用相同的组间比较,在24小时(P小于0.05)、48小时(P小于0.001)和72小时(P小于0.001)时生存率显著提高。因此,我们得出结论,MDP在没有补体的情况下仍保持其保护作用,这支持了MDP的作用机制不依赖补体的观点。

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