Frontiers in Microbiology (Jul 2023)

Gut microbiota and transcriptome dynamics in every-other-day fasting are associated with neuroprotection in rats with spinal cord injury

  • Junyu Wang,
  • Xiaohua Zhao,
  • Xiaohua Zhao,
  • Ruihan Zhou,
  • Meiyu Wang,
  • Wu Xiang,
  • Zilong You,
  • Min Li,
  • Ruiling Tang,
  • Jingqi Zheng,
  • Jiayu Li,
  • Li Zhu,
  • Jiaxin Gao,
  • Huaqiang Li,
  • Rizhao Pang,
  • Anren Zhang

DOI
https://doi.org/10.3389/fmicb.2023.1206909
Journal volume & issue
Vol. 14

Abstract

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IntroductionEvery-other-day fasting (EODF) is a classical intermittent fasting (IF) mode with neuroprotective effects that promotes motor function recovery after spinal cord injury (SCI) in rats. However, its dynamic effects on the gut microbiota and spinal cord transcriptome remain unknown.MethodsIn this study, 16S rRNA sequencing and RNA-seq analysis were used to investigate the effects of ad libitum (AL) and EODF dietary modes on the structural characteristics of rat gut microbiota in rats and the spinal cord transcriptome at various time points after SCI induction.ResultsOur results showed that both dietary modes affected the bacterial community composition in SCI rats, with EODF treatment inducing and suppressing dynamic changes in the abundances of potentially anti-inflammatory and pro-inflammatory bacteria. Furthermore, the differentially expressed genes (DEGs) enriched after EODF intervention in SCI rats were associated with various biological events, including immune inflammatory response, cell differentiation, protein modification, neural growth, and apoptosis. In particular, significant spatiotemporal differences were apparent in the DEGs associated with neuroprotection between the EODF and AL interventions. These DGEs were mainly focused on days 1, 3, and 7 after SCI. The relative abundance of certain genera was significantly correlated with DEGs associated with neuroprotective effects in the EODF-SCI group.DiscussionOur results showed that EODF treatment may exert neuroprotective effects by modulating the transcriptome expression profile following SCI in rats. Furthermore, gut microbiota may be partially involved in mediating these effects.

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