BACKGROUND: Alkaline sphingomyetinase, an enzyme found exclusively in bile and the intestinal brush border, hydrolyzes sphingomyetin into ceramide, sphingosine and sphingosine-I-phosphate, thereby inducing epithelial apoptosis. Reduced levels of alkaline sphingomyelinase have been found in premalignant and malignant intestinal epithelia and in ulcerative colitis tissue. Probiotic bacteria can be a source of sphingomyelinase. OBJECTIVE: To determine the effect of VSL#3 probiotic therapy on mucosal levels of alkaline sphingomyelinase, both in a Mouse model of colitis and in patients with ulcerative colitis. METHODS: Interleukin, 10 gene-deficient (IL 10KO) and wild type control mice were treated with VSL#3 (10(9) colony-forming units per day) for three weeks, after which alkaline sphingomyelinase activity was measured in ileal and colonic tissue. As welt, 15 patients with ulcerative colitis were treated with VSL#3 (900 billion bacteria two times per day for five weeks). Alkaline sphingomyelinase activity was measured through biopsies and comparison of ulcerative cotitis disease activity index scores obtained before and after treatment. RESULTS: Lowered alkaline sphingomyelinase levels were seen in the colon (P=0.02) and ileum (P=0.04) of IL10KO mice, as compared with controls. Treatment of these truce with VSL#3 resulted in Upregulation Of mucosal alkaline sphingomyelinase activity in both the colon (P=0.04) and the ileum (P=0.01). VSL#3 treatment of human patients who had ulcerative colitis decreased mean ( +/- SEM) ulcerative colitis disease activity index scores from 5.3 +/- 1.8946 to 0.70 +/- 0.34 (P=0.02) and increased mucosat alkaline sphingomyelinase activity. CONCLUSION: Mucosal alkaline sphingomyelinase activity is reduced in the intestine of IL10KO mice with colitis and in humans with ulcerative colitis. VSL#3 probiotic therapy upregulates mucosal alkaline sphingomyelinase activity.

VSL#3 probiotic upregulates mucosal alkaline sphingomyelinase and reduces inflammation.

DI MARZIO, Luisa;
2008-01-01

Abstract

BACKGROUND: Alkaline sphingomyetinase, an enzyme found exclusively in bile and the intestinal brush border, hydrolyzes sphingomyetin into ceramide, sphingosine and sphingosine-I-phosphate, thereby inducing epithelial apoptosis. Reduced levels of alkaline sphingomyelinase have been found in premalignant and malignant intestinal epithelia and in ulcerative colitis tissue. Probiotic bacteria can be a source of sphingomyelinase. OBJECTIVE: To determine the effect of VSL#3 probiotic therapy on mucosal levels of alkaline sphingomyelinase, both in a Mouse model of colitis and in patients with ulcerative colitis. METHODS: Interleukin, 10 gene-deficient (IL 10KO) and wild type control mice were treated with VSL#3 (10(9) colony-forming units per day) for three weeks, after which alkaline sphingomyelinase activity was measured in ileal and colonic tissue. As welt, 15 patients with ulcerative colitis were treated with VSL#3 (900 billion bacteria two times per day for five weeks). Alkaline sphingomyelinase activity was measured through biopsies and comparison of ulcerative cotitis disease activity index scores obtained before and after treatment. RESULTS: Lowered alkaline sphingomyelinase levels were seen in the colon (P=0.02) and ileum (P=0.04) of IL10KO mice, as compared with controls. Treatment of these truce with VSL#3 resulted in Upregulation Of mucosal alkaline sphingomyelinase activity in both the colon (P=0.04) and the ileum (P=0.01). VSL#3 treatment of human patients who had ulcerative colitis decreased mean ( +/- SEM) ulcerative colitis disease activity index scores from 5.3 +/- 1.8946 to 0.70 +/- 0.34 (P=0.02) and increased mucosat alkaline sphingomyelinase activity. CONCLUSION: Mucosal alkaline sphingomyelinase activity is reduced in the intestine of IL10KO mice with colitis and in humans with ulcerative colitis. VSL#3 probiotic therapy upregulates mucosal alkaline sphingomyelinase activity.
File in questo prodotto:
File Dimensione Formato  
Can J Gastroenterol 2008 copia autori.pdf

Solo gestori archivio

Tipologia: Abstract
Dimensione 292.01 kB
Formato Adobe PDF
292.01 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11564/114500
Citazioni
  • ???jsp.display-item.citation.pmc??? 28
  • Scopus 75
  • ???jsp.display-item.citation.isi??? 64
social impact