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Efficacy of sodium butyrate adjunct therapy in shigellosis: a randomized, double-blind, placebo-controlled clinical trial

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TLDR
Adjunct therapy with butyrate during shigellosis led to early reduction of inflammation and enhanced LL-37 expression in the rectal epithelia with prolonged release of LL-36 in the stool and improvement in rectal histopathology.
Abstract
Treatment of shigellosis in rabbits with butyrate reduces clinical severity and counteracts the downregulation of cathelicidin (CAP-18) in the large intestinal epithelia Here, we aimed to evaluate whether butyrate can be used as an adjunct to antibiotics in the treatment of shigellosis in patients A randomized, double-blind, placebo-controlled, parallel-group designed clinical trial was conducted Eighty adult patients with shigellosis were randomized to either the Intervention group (butyrate, n = 40) or the Placebo group (normal saline, n = 40) The Intervention group was given an enema containing sodium butyrate (80 mM), twice daily for 3 days, while the Placebo group received the same dose of normal saline The primary endpoint of the trial was to assess the efficacy of butyrate in improving clinical, endoscopic and histological features of shigellosis The secondary endpoint was to study the effect of butyrate on the induction of antimicrobial peptides in the rectum Clinical outcomes were assessed and concentrations of antimicrobial peptides (LL-37, human beta defensin1 [HBD-1] and human beta defensin 3 [HBD-3]) and pro-inflammatory cytokines (interleukin-1β [IL-1β] and interleukin-8 [IL-8]) were measured in the stool Sigmoidoscopic and histopathological analyses, and immunostaining of LL-37 in the rectal mucosa were performed in a subgroup of patients Compared with placebo, butyrate therapy led to the early reduction of macrophages, pus cells, IL-8 and IL-1β in the stool and improvement in rectal histopathology Butyrate treatment induced LL-37 expression in the rectal epithelia Stool concentration of LL-37 remained significantly higher in the Intervention group on days 4 and 7 Adjunct therapy with butyrate during shigellosis led to early reduction of inflammation and enhanced LL-37 expression in the rectal epithelia with prolonged release of LL-37 in the stool ClinicalTrialsgov, NCT00800930

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Regulation of Bacterial Pathogenesis by Intestinal Short-Chain Fatty Acids

TL;DR: The biological role of short-chain fatty acids (SCFA), which are fermentation end products of the intestinal microbiota, in host-pathogen interactions, are dissected to highlight the importance of the chemical environment where the biology of the host, the microbiota, and the pathogen intersects, which provides a basis for designing effective infection prevention and control.
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Gut Microbiota and Colonization Resistance against Bacterial Enteric Infection

TL;DR: Current knowledge on how the gut microbiota can mediate colonization resistance against bacterial enteric infection and on how bacterial enteropathogens can overcome this resistance are summarized.
References
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Journal ArticleDOI

Antimicrobial peptides of multicellular organisms

TL;DR: As the need for new antibiotics becomes more pressing, could the design of anti-infective drugs based on the design principles these molecules teach us?
Journal ArticleDOI

Review article: the role of butyrate on colonic function

TL;DR: Butyrate is an important energy source for intestinal epithelial cells and plays a role in the maintenance of colonic homeostasis, and is a main end‐product of intestinal microbial fermentation of mainly dietary fibre.
Journal ArticleDOI

Butyrate inhibits inflammatory responses through NFκB inhibition: implications for Crohn's disease

TL;DR: Butyrate decreases proinflammatory cytokine expression via inhibition of NFκB activation and IκBα degradation and these anti-inflammatory properties provide a rationale for assessing butyrate in the treatment of CD.
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Potential beneficial effects of butyrate in intestinal and extraintestinal diseases

TL;DR: A wide spectrum of positive effects exerted by butyrate is suggested, with a high potential for a therapeutic use in human medicine, at the extraintestinal and intestinal level.
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