Impacts of Fructose on Intestinal Barrier Function, Inflammation and Microbiota in a Piglet Model.

Abstract

The metabolic disorder caused by excessive fructose intake was reported extensively and often accompanied by intestinal barrier dysfunction. And the rising dietary fructose was consumed at an early age of human. However, related researches were almost conducted in rodent models, while in the anatomy and physiology of gastrointestinal tract, pig is more similar to human beings than rodents. Hence, weaned piglets were chosen as the model animals in our study to investigate the fructose's impacts on intestinal tight junction, inflammation response and microbiota structure of piglets. Herein, growth performance, inflammatory response, oxidation resistance and ileal and colonic microbiota of piglet were detected after 35-day fructose supplementation. Our results showed decreased tight junction gene expressions in piglets after fructose addition, with no obvious changes in the growth performance, antioxidant resistance and inflammatory response. Moreover, fructose supplementation differently modified the microbiota structures in ileum and colon. In ileum, the proportions of Streptococcus and Faecalibacterium were higher in Fru group (fructose supplementation). In colon, the proportions of Blautia and Clostridium sensu stricto 1 were higher in Fru group. All the results suggested that tight junction dysfunction might be an earlier fructose-induced event than inflammatory response and oxidant stress and that altered microbes in ileum and colon might be the potential candidates to alleviate fructose-induced intestinal permeability alteration.

• Authors: Pingting Guo, Haichao Wang, Linbao Ji, Peixia Song, Xi Ma
• Journal: Nutrients (Nutrients) Vol. 13 Issue 10 (Oct 06 2021) ISSN: 2072-6643 [Electronic] Switzerland
• PMID: 34684516 (Publication Type: Journal Article)

Chemical References

• Fructose

Topics

• Animals
• Colitis (chemically induced)
• Colon (drug effects)
• Dietary Supplements (adverse effects)
• Fructose (adverse effects)
• Gastrointestinal Microbiome (drug effects)
• Ileum (drug effects)
• Intestinal Mucosa (drug effects)
• Models, Animal
• Oxidative Stress (drug effects)
• Permeability (drug effects)
• Swine
• Tight Junctions (drug effects)