Journal Article

High-fat diet impairs duodenal barrier function and elicits glia-dependent changes along the gut-brain axis that are required for anxiogenic and depressive-like behaviors

Capuano, Riccardo, Lattanzi, Roberta, Sarnelli, Giovanni, Maftei, Daniela, Esposito, Giuseppe, Casano, Fabrizio, Vincenzi, Martina, Del Re, Alessandro, Seguella, Luisa, Pesce, Mirella, Pesce, Marcella, Corpetti, Chiara, Gulbransen, Brian D.

2021

Overview

Background Mood and metabolic disorders are interrelated and may share common pathological processes. Autonomic neurons link the brain with the gastrointestinal tract and constitute a likely pathway for peripheral metabolic challenges to affect behaviors controlled by the brain. The activities of neurons along these pathways are regulated by glia, which exhibit phenotypic shifts in response to changes in their microenvironment. How glial changes might contribute to the behavioral effects of consuming a high-fat diet (HFD) is uncertain. Here, we tested the hypothesis that anxiogenic and depressive-like behaviors driven by consuming a HFD involve compromised duodenal barrier integrity and subsequent phenotypic changes to glia and neurons along the gut-brain axis. Methods C57Bl/6 male mice were exposed to a standard diet or HFD for 20 weeks. Bodyweight was monitored weekly and correlated with mucosa histological damage and duodenal expression of tight junction proteins ZO-1 and occludin at 0, 6, and 20 weeks. The expression of GFAP, TLR-4, BDNF, and DCX were investigated in duodenal myenteric plexus, nodose ganglia, and dentate gyrus of the hippocampus at the same time points. Dendritic spine number was measured in cultured neurons isolated from duodenal myenteric plexuses and hippocampi at weeks 0, 6, and 20. Depressive and anxiety behaviors were also assessed by tail suspension, forced swimming, and open field tests. Results HFD mice exhibited duodenal mucosa damage with marked infiltration of immune cells and decreased expression of ZO-1 and occludin that coincided with increasing body weight. Glial expression of GFAP and TLR4 increased in parallel in the duodenal myenteric plexuses, nodose ganglia, and hippocampus in a time-dependent manner. Glial changes were associated with a progressive decrease in BDNF, and DCX expression, fewer neuronal dendritic spines, and anxiogenic/depressive symptoms in HFD-treated mice. Fluorocitrate (FC), a glial metabolic poison, abolished these effects both in the enteric and central nervous systems and prevented behavioral alterations at week 20. Conclusions HFD impairs duodenal barrier integrity and produces behavioral changes consistent with depressive and anxiety phenotypes. HFD-driven changes in both peripheral and central nervous systems are glial-dependent, suggesting a potential glial role in the alteration of the gut-brain signaling that occurs during metabolic disorders and psychiatric co-morbidity.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Animals / Anxiety / Autonomic nervous system / Barium / Behavior / Behavioral disorders / Biomedical and Life Sciences / Biomedicine / Body Weight / Brain - metabolism / Brain - pathology / Brain research / Brain-derived neurotrophic factor / Dendritic spines / Dentate gyrus / Depression - etiology / Depression, Mental / Development and progression / Diet / Diet, High-Fat - adverse effects / Digestive system / Doublecortin protein / Duodenum / Duodenum - metabolism / Duodenum - pathology / Enteric glia / Enteric nervous system / Ganglia / Gastrointestinal tract / Glial fibrillary acidic protein / Glial signaling / Gut-brain axis / Health aspects / High fat diet / Hippocampus / Immunology / Intestinal hyper-permeability / Male / Mental Disorders - etiology / Metabolic disorders / Mice / Mice, Inbred C57BL / Microenvironments / Mood / Morbidity / Mucosa / Myenteric plexus / Myenteric Plexus - metabolism / Myenteric Plexus - pathology / Nervous system / Neurobiology / Neuroglia - metabolism / Neuroglia - pathology / Neurology / Neuronal-glial interactions / Neurons / Neurons - metabolism / Neurons - pathology / Neuropathology / Neurosciences / Nodose ganglion / Nodose Ganglion - metabolism / Nodose Ganglion - pathology / Obesity / Organic mental disorder / Phenotypes / Physiological aspects / Risk factors / Small intestine / Toll-like receptors