High‐fat diet–induced alterations to gut microbiota and gut‐derived lipoteichoic acid contributes to the development of enteric neuropathy
Open Access
- 13 March 2020
- journal article
- research article
- Published by Wiley in Neurogastroenterology & Motility
- Vol. 32 (7) , e13838
Abstract
Background: High‐fat diet, microbial alterations and lipopolysaccharide (LPS) are thought to cause enteric diabetic neuropathy and intestinal dysmotility. However, the role of the gut microbiota, lipoteichoic acid (LTA) from Gram‐positive bacteria and short‐chain fatty acids (SCFAs) in the development of diabetic enteric neuropathy and intestinal dysmotility is not well understood. Our aim was to examine the role of the gut microbiota, LTA and SCFAs in the development of diabetic enteric neuropathy and intestinal dysmotility.Methods: We fed germ‐free (GF) and conventionally raised (CR) mice either a high‐fat (HFD) or standard chow diet (SCD) for 8 weeks. We analyzed the microbial community composition in CR mice using 16S rRNA sequencing and damage to myenteric neurons using immunohistochemistry. We also studied the effects of LPS, LTA, and SCFAs on duodenal muscularis externa contractions and myenteric neurons using cultured preparations.Key Results: High‐fat diet ingestion reduced the total number and the number of nitrergic myenteric neurons per ganglion in the duodenum of CR but not in GF‐HFD mice. GF mice had fewer neurons per ganglion compared with CR mice. CR mice fed a HFD had increased abundance of Gram‐positive bacteria. LTA and LPS did not affect the frequency of duodenal muscularis contractions after 24 hours of cultured but reduced the density of nitrergic myenteric neurons and increased oxidative stress and TNFα production in myenteric ganglia. SCFAs did not affect muscularis contractions or injure myenteric neurons.Conclusions & Inferences: Gut microbial alterations induced increase in Gram‐positive bacterial LTA may contribute to enteric neuropathy.Keywords
Funding Information
- National Center for Research Resources (P20 GM103408)
- National Institutes of Health (R01 DK114007, R01 DK106011)
- National Institute of General Medical Sciences (P20 RR016454)
This publication has 61 references indexed in Scilit:
- High-Fat Diet Reduces the Formation of Butyrate, but Increases Succinate, Inflammation, Liver Fat and Cholesterol in Rats, while Dietary Fibre Counteracts These EffectsPLOS ONE, 2013
- Butyrate and Propionate Protect against Diet-Induced Obesity and Regulate Gut Hormones via Free Fatty Acid Receptor 3-Independent MechanismsPLOS ONE, 2012
- Evaluation of Methods for the Extraction and Purification of DNA from the Human MicrobiomePLOS ONE, 2012
- Vaginal microbiome of reproductive-age womenProceedings of the National Academy of Sciences, 2010
- Short-Chain Fatty Acids Regulate the Enteric Neurons and Control Gastrointestinal Motility in RatsGastroenterology, 2010
- The Bacterial Cell EnvelopeCold Spring Harbor Perspectives in Biology, 2010
- Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic AdultsPLOS ONE, 2010
- Lipoteichoic Acid Induces Unique Inflammatory Responses when Compared to Other Toll-Like Receptor 2 LigandsPLOS ONE, 2009
- The enteric nervous system: normal functions and enteric neuropathiesNeurogastroenterology & Motility, 2008
- Mechanisms underlying the resistance to diet-induced obesity in germ-free miceProceedings of the National Academy of Sciences, 2007