High-salt diet induces microbiome dysregulation, neuroinflammation and anxiety in the chronic period after mild repetitive closed head injury in adolescent mice

Saef Izzy(Brigham and Women's Hospital), Taha Yahya(Brigham and Women's Hospital), Omar Albastaki(Brigham and Women's Hospital), Tian Cao(Brigham and Women's Hospital), Luke Schwerdtfeger(Brigham and Women's Hospital), Hadi Abou‐El‐Hassan(Brigham and Women's Hospital), Kusha Chopra(Massachusetts General Hospital), Millicent N. Ekwudo(Brigham and Women's Hospital), Ugne Kurdeikaite(Brigham and Women's Hospital), Isabelly Moraes Verissimo(Brigham and Women's Hospital), Danielle S. LeServe(Brigham and Women's Hospital), Toby B. Lanser(Brigham and Women's Hospital), Michael Aronchik(Brigham and Women's Hospital), Marília Garcia de Oliveira(Brigham and Women's Hospital), Thaís G. Moreira(Brigham and Women's Hospital), Rafael M. Rezende(Brigham and Women's Hospital), Joseph El Khoury(Harvard University), Laura M. Cox(Brigham and Women's Hospital), Howard L. Weiner(Brigham and Women's Hospital), Ross Zafonte(Brigham and Women's Hospital), Michael J. Whalen(Harvard University)
Brain Communications
January 1, 2024
Cited by 6Open Access
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Abstract

Abstract The associations between human concussions and subsequent sequelae of chronic neuropsychiatric and cardiovascular diseases such as hypertension have been reported; however, little is known about the underlying biological processes. We hypothesized that dietary changes, including a high-salt diet, disrupt the bidirectional gut–brain axis, resulting in worsening neuroinflammation and emergence of cardiovascular and behavioural phenotypes in the chronic period after repetitive closed head injury in adolescent mice. Adolescent mice were subjected to three daily closed head injuries, recovered for 12 weeks and then maintained on a high-salt diet or a normal diet for an additional 12 weeks. Experimental endpoints were haemodynamics, behaviour, microglial gene expression (bulk RNA sequencing), brain inflammation (brain tissue quantitative PCR) and microbiome diversity (16S RNA sequencing). High-salt diet did not affect systemic blood pressure or heart rate in sham or injured mice. High-salt diet increased anxiety-like behaviour in injured mice compared to sham mice fed with high-salt diet and injured mice fed with normal diet. Increased anxiety in injured mice that received a high-salt diet was associated with microgliosis and a proinflammatory microglial transcriptomic signature, including upregulation in interferon-gamma, interferon-beta and oxidative stress–related pathways. Accordingly, we found upregulation of tumour necrosis factor-alpha and interferon-gamma mRNA in the brain tissue of high salt diet–fed injured mice. High-salt diet had a larger effect on the gut microbiome composition than repetitive closed head injury. Increases in gut microbes in the families Lachnospiraceae, Erysipelotrichaceae and Clostridiaceae were positively correlated with anxiety-like behaviours. In contrast, Muribaculaceae, Acholeplasmataceae and Lactobacillaceae were negatively correlated with anxiety in injured mice that received a high-salt diet, a time-dependent effect. The findings suggest that high-salt diet, administered after a recovery period, may affect neurologic outcomes following mild repetitive head injury, including the development of anxiety. This effect was linked to microbiome dysregulation and an exacerbation of microglial inflammation, which may be physiological targets to prevent behavioural sequelae in the chronic period after mild repetitive head injury. The data suggest an important contribution of diet in determining long-term outcomes after mild repetitive head injury.


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