AI Article Synopsis

  • - The study investigates the effects of Arabinoxylan (AX) from finger millet on metabolic issues and gut bacteria caused by a high-fat diet (HFD) in mice.
  • - Male Swiss albino mice were fed either a normal diet or a high-fat diet for 10 weeks, with FM-AX supplementation given in two doses to assess various health markers.
  • - Results showed that FM-AX supplementation mitigated weight gain, improved glucose tolerance, reduced liver fat accumulation, and positively affected gut health, suggesting its potential as a nutraceutical for obesity management.

Article Abstract

Arabinoxylan (AX), a non-starch polysaccharide extracted from cereals such as wheat, rice and millets, is known to impart various health promoting effects. Our earlier study suggested that finger millet (FM) could ameliorate high fat diet (HFD)-induced metabolic derangements. The present study is aimed to evaluate the effect of FM-AX supplementation, a key bioactive from finger millet, on HFD-induced metabolic and gut bacterial derangements. Male Swiss albino mice were fed with normal chow diet (NPD) or HFD (60%kcal from fat) for 10 weeks. FM-AX was orally supplemented at doses of 0.5 and 1.0g/kg bodyweight on every alternate day for 10 weeks. Glucose tolerance, serum hormones, hepatic lipid accumulation and inflammation, white adipose tissue marker gene expression, adipocyte size and inflammation; metagenomic alterations in cecal bacteria; cecal short chain fatty acids and colonic tight junction gene expressions were studied. FM-AX supplementation prevented HFD-induced weight gain, alerted glucose tolerance and serum lipid profile, hepatic lipid accumulation and inflammation. Hepatic and white adipose tissue gene expressions were beneficially modulated. Further, AX supplementation prevented metagenomic alterations in cecum; improved ileal and colonic health and overall prevented metabolic endotoxemia. Present work suggests that AX from finger millet can be developed as a nutraceutical for the management of HFD- induced obesity.

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Source
http://dx.doi.org/10.1016/j.ijbiomac.2017.08.100DOI Listing

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