Diet-microbiome interactions promote enteric nervous system resilience following spinal cord injury

Spinal cord injury (SCI) results in numerous systemic dysfunctions, including intestinal dysmotility and enteric nervous system (ENS) atrophy. The ENS has capacity to recover following perturbation, yet intestinal pathologies persist. With emerging evidence demonstrating SCI-induced alterations to gut microbiome composition, we hypothesized that microbiome modulation contributes to post-injury enteric recovery. Here, we show that intervention with the dietary fiber, inulin, prevents SCI-induced ENS atrophy and dysmotility in mice. While SCI-associated microbiomes and specific injury-sensitive gut microbes are not sufficient to modulate intestinal dysmotility after injury, intervention with microbially-derived short-chain fatty acid (SCFA) metabolites prevents ENS dysfunctions in injured mice. Notably, inulin-mediated resilience is dependent on IL-10 signaling, highlighting a critical diet-microbiome-immune axis that promotes ENS resilience post-injury. Overall, we demonstrate that diet and microbially-derived signals distinctly impact ENS survival after traumatic spinal injury and represent a foundation to uncover etiological mechanisms and future therapeutics for SCI-induced neurogenic bowel.

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Institutions

Publication Details

Journal
npj Biofilms and Microbiomes
Published
2024-08-29
DOI
https://doi.org/10.1038/s41522-024-00556-y
Citations
12
Primary Topic
Spinal Dysraphism and Malformations
Type
article
Field-Weighted Citation Impact
6.52

Funders

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article

Diet-microbiome interactions promote enteric nervous system resilience following spinal cord injury

Jianjun Chang, Adam M. Hamilton, Anna E. Williams, Nardos Kebede et al.
12 citations
npj Biofilms and Microbiomes
Spinal Dysraphism and Malformations
6.52
article

Diet-microbiome interactions promote enteric nervous system resilience following spinal cord injury

Jianjun Chang, Adam M. Hamilton, Anna E. Williams, Nardos Kebede, Timothy R. Sampson, Sean D. Kelly, Sandra M. Garraway, Lisa Blackmer‐Raynolds, Shanthi Srinivasan, Yaqing Li
article en
12 citations

Abstract

Spinal cord injury (SCI) results in numerous systemic dysfunctions, including intestinal dysmotility and enteric nervous system (ENS) atrophy. The ENS has capacity to recover following perturbation, yet intestinal pathologies persist. With emerging evidence demonstrating SCI-induced alterations to gut microbiome composition, we hypothesized that microbiome modulation contributes to post-injury enteric recovery. Here, we show that intervention with the dietary fiber, inulin, prevents SCI-induced ENS atrophy and dysmotility in mice. While SCI-associated microbiomes and specific injury-sensitive gut microbes are not sufficient to modulate intestinal dysmotility after injury, intervention with microbially-derived short-chain fatty acid (SCFA) metabolites prevents ENS dysfunctions in injured mice. Notably, inulin-mediated resilience is dependent on IL-10 signaling, highlighting a critical diet-microbiome-immune axis that promotes ENS resilience post-injury. Overall, we demonstrate that diet and microbially-derived signals distinctly impact ENS survival after traumatic spinal injury and represent a foundation to uncover etiological mechanisms and future therapeutics for SCI-induced neurogenic bowel.

npj Biofilms and MicrobiomesVol. 10(1)
Emory University (US), Atlanta VA Health Care System (US)
Craig H. Neilsen Foundation, Emory University, National Institutes of Health, School of Medicine, Emory University, National Institute on Aging, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Neurological Disorders and Stroke, National Institute of Environmental Health Sciences
Openalex Percentile: Top 3%
Spinal Dysraphism and Malformations
6.52
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