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Nutritional modulation of gut microbiota - the impact on metabolic disease pathophysiology. | LitMetric

Nutritional modulation of gut microbiota - the impact on metabolic disease pathophysiology.

J Nutr Biochem

Department of Medicine, Section of Gastroenterology, University of Chicago, Chicago, IL, USA. Electronic address:

Published: February 2016

AI Article Synopsis

  • The obesity epidemic affects over one-third of the U.S. population, highlighting the need for better understanding of systemic causes and new treatments.
  • The intestinal microbiota plays a crucial role in metabolism, influenced by diet, which affects energy intake, nutrient absorption, liver function, and immune response.
  • Potential therapies to modify gut microbiota include prebiotics, probiotics, postbiotics, and fecal microbiota transplantation, offering hope for improved treatments for metabolic disorders.

Article Abstract

The obesity epidemic afflicts over one third of the United States population. With few therapies available to combat obesity, a greater understanding of the systemic causes of this and other metabolic disorders is needed to develop new, effective treatments. The mammalian intestinal microbiota contributes to metabolic processes in the host. This review summarizes the research demonstrating the interplay of diet, intestinal microbiota and host metabolism. We detail the effects of diet-induced modifications in microbial activity and resultant impact on (1) sensory perception of macronutrients and total energy intake; (2) nutrient absorption, transport and storage; (3) liver and biliary function; (4) immune-mediated signaling related to adipose inflammation; and (5) circadian rhythm. We also discuss therapeutic strategies aimed to modify host-microbe interactions, including prebiotics, probiotics and postbiotics, as well as fecal microbiota transplantation. Elucidating the role of gut microbes in shaping metabolic homeostasis or dysregulation provides greater insight into disease development and a promising avenue for improved treatment of metabolic dysfunction.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757500PMC
http://dx.doi.org/10.1016/j.jnutbio.2015.08.013DOI Listing

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