セッション情報 Poster Presentation(GI)

タイトル

IF-P1-7 The Effect of Dai-kenchu-to in Maintenance of Microbiomal Diversity on Intestinal Inflammation

演者 Kozo Yoshikawa(The University of TokushimaJapan)
共同演者 M Shimada(The University of TokushimaJapan), N Kurita(The University of TokushimaJapan), T Iwata(The University of TokushimaJapan), H Sato(The University of TokushimaJapan), M Nishioka(The University of TokushimaJapan), S Morimoto(The University of TokushimaJapan), T Miyatani(The University of TokushimaJapan), H Kashihara(The University of TokushimaJapan), C Takasu(The University of TokushimaJapan)
抄録 [Purpose]Diversity of microbiome is lost in inflammatory bowel disease (Gastroenterology 2009). We have alreadyreported that the Dai-kenchu-to (DKT) prevented the bacterial translocation through suppression of cy-tokine and apoptosis (Dig Dis Sci 2008). The hypothesis is microbiome related anti-inflammatory effects ofDKT. The aim of this study was to evaluate the effect of DKT on maintenance of microbiomal diversity inintestinal inflammation.[MethodコThe wister rat was received the fast stress for 5 days (F-group). The microbiome of stool was examinedat pre一 and post一 fast stress. ln DKT grouprat was administered the DKT (300mg/kg/day) during the faststress (D-group)and the effect of DKT was examined. Microbiome was examined by terminal restrictionfragment length polymorphism analysis and diversity was analyzed by operational taxonomical unit(OTU) .[Result]]n F-groupErysipelotrichaceae increased to 860/o in post fast stressOTU of pre-fast stress was 111 andpost-fast stress was 46 (changing rate : 58 O/o ) . The diversity of microbiome was severely decreased. On theother handin D-groupdiversity of microbiome was kept after fast stress(Lac加ospiraceae : Ruminococ-caceae: Coriobacteriales 540/o220/o5%)OTU of pre-fast stress was 52 and post-fast stress was 55(changing rate : 50/o ). DKT maintained the diversity of microbiome in fast stress model.[Conclusion]DKT maintained the diversity of microbiome in fast stress modelOur data suggested the new mechanisrnof anti-inflammatory effect of DKT.
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