4.7 Article

Soybean Meal-Dependent Intestinal Inflammation Induces Different Patterns of Bone-Loss in Adult Zebrafish Scale

期刊

BIOMEDICINES
卷 9, 期 4, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines9040393

关键词

zebrafish; bone; osteoporosis; inflammatory bowel disease; intestinal inflammation; scale; soy

资金

  1. Ministry of Health (Ricerca Corrente), Italy
  2. 5 x 1000 anno 2017 progetto SoyFish (Grupposandonato Foundation)

向作者/读者索取更多资源

Inflammatory bowel disease has been found to be associated with low bone mineral density. Zebrafish is a suitable model for studying the effects of intestinal inflammation on bone metabolism. Research shows that soybean meal can induce intestinal inflammation in zebrafish, leading to changes in bone structure and activity of bone cells.
Inflammatory bowel disease have been linked to several health issues, including high risk of low bone mineral density. Danio rerio (zebrafish) is a good model to verify the effects of intestinal inflammation, since its gastrointestinal and immune systems are closely related to that of mammalians. Zebrafish is also a powerful model to study bone metabolism using the scale as the read-out model. Food strongly impacts zebrafish gut physiology, and it is well known that soybean meal induces intestinal inflammation. Adult zebrafish fed with defatted soybean meal (SBM) exhibited an intestinal inflammation evidenced by morphological alterations, inflammatory infiltrate, and increased mRNA expression of inflammatory cytokines (IL-1 beta, IL-6, IL-8, IL-10, TGF beta, TNF-alpha). The peak of acute intestinal inflammation, spanning between week 2 and 3, correlates with a transitory osteoporosis-like phenotype in the scale border. Later, a chronic inflammatory condition, associated with persistent IL-8 expression, correlates with the progression of resorption lacunae in the scale center. Both types of resorption lacunae were associated with intense osteoclastic tartrate-resistant acid phosphatase (TRAP) activity. After 3 weeks of SBM treatment, osteoclast activity decreased in the scale border but not in the center. At the same time, alkaline phosphatase (ALP) is activated in the border to repair the bone matrix. This model can contribute to elucidate in vivo the molecular mechanisms that links intestinal inflammation and bone metabolism in IBD.

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