High Dose Vitamin D supplementation alters faecal microbiome and predisposes mice to more severe colitis

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作者
Simon Ghaly
Nadeem O. Kaakoush
Frances Lloyd
Terence McGonigle
Danny Mok
Angela Baird
Borut Klopcic
Lavinia Gordon
Shelley Gorman
Cynthia Forest
Roger Bouillon
Ian C. Lawrance
Prue H. Hart
机构
[1] The University of Western Australia,Telethon Kids Institute
[2] The University of Western Australia,School of Medicine and Pharmacology
[3] St. Vincent’s Hospital,Department of Gastroenterology and Hepatology
[4] UNSW Sydney,School of Medical Sciences
[5] The Walter and Eliza Hall Institute,Australian Genome Research Facility
[6] PathWest,Department of Anatomical Pathology
[7] Fiona Stanley Hospital,Clinical and Experimental Endocrinology
[8] Katholieke Universiteit Leuven,Centre for Inflammatory Bowel Disease
[9] St. John of God Hospital,undefined
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Vitamin D has been suggested as a possible adjunctive treatment to ameliorate disease severity in human inflammatory bowel disease. In this study, the effects of diets containing high (D++, 10,000 IU/kg), moderate (D+, 2,280 IU/kg) or no vitamin D (D−) on the severity of dextran sodium sulphate (DSS) colitis in female C57Bl/6 mice were investigated. The group on high dose vitamin D (D++) developed the most severe colitis as measured by blinded endoscopic (p < 0.001) and histologic (p < 0.05) assessment, weight loss (p < 0.001), drop in serum albumin (p = 0.05) and increased expression of colonic TNF-α (p < 0.05). Microbiota analysis of faecal DNA showed that the microbial composition of D++ control mice was more similar to that of DSS mice. Serum 25(OH)D3 levels reduced by 63% in the D++ group and 23% in the D+ group after 6 days of DSS treatment. Thus, high dose vitamin D supplementation is associated with a shift to a more inflammatory faecal microbiome and increased susceptibility to colitis, with a fall in circulating vitamin D occurring as a secondary event in response to the inflammatory process.
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