Effects of Pseudomonas aeruginosa mannose-sensitive hemagglutinin (PA-MSHA) pretreatment on septic rats.

Int Immunopharmacol

Department of Critical Care Medicine, Huashan Hospital, Fudan University, China. Electronic address:

Published: November 2013

AI Article Synopsis

  • The study examined the effects of different doses and durations of PA-MSHA injection on the survival rates of rats after cecal ligation and puncture (CLP).
  • The 0.5 ml PA-MSHA group administered for 8 days had the highest survival rate at 91.7%, noticeably better than the 33.3% survival in the CLP-only group.
  • PA-MSHA treatment altered inflammatory responses, boosting pro-inflammatory cytokines initially and anti-inflammatory cytokines later, while also increasing TLR4 expression and inducing endotoxin tolerance in macrophages.

Article Abstract

To evaluate the effects of Pseudomonas aeruginosa mannose-sensitive hemagglutinin (PA-MSHA) injection on the survival rate of rats post cecal ligation and puncture (CLP), Sprague-Dawley (SD) rats were subcutaneously injected with 0.125 ml, 0.25 ml or 0.5 ml PA-MSHA for 8 days or 16 days before CLP. The survival rate and physiological appearance of rats in each group were monitored daily post CLP. The expression of Toll-like receptor 4 (TLR4) and cytokines related to inflammation was evaluated. We found that the 0.5 ml-8d (0.5 ml PA-MSHA injected for 8 days) group had the highest 7-day survival rate (91.7%), which was significantly improved compared with the CLP-only group (33.3%). Furthermore, our results showed that PA-MSHA effectively increased serum pro-inflammatory mediators (TNF-α, IL-1β and IL-6) at the early stage (8 days) but increased anti-inflammatory mediators (IL-4 and IL-10) at the late stage (16 days). PA-MSHA significantly up-regulated the mRNA expression of TLR4 at 8 and 16 days. After PA-MSHA pretreatment, CLP had no marked effect on the levels of most inflammatory factors. To explore potential protective mechanisms of PA-MSHA against CLP, we examined the effect of PA-MSHA on murine macrophage-like RAW264.7 cells and found that PA-MSHA induced endotoxin tolerance. In conclusion, this study suggested that precisely controlling the dosage and time of PA-MSHA administration can effectively increase the rat survival rate post CLP, which may be mediated through regulating inflammatory mediators and inducing endotoxin tolerance.

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Source
http://dx.doi.org/10.1016/j.intimp.2013.09.006DOI Listing

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