1. Academic Validation
  2. Circadian light/dark cycle reversal exacerbates the progression of chronic kidney disease in mice

Circadian light/dark cycle reversal exacerbates the progression of chronic kidney disease in mice

  • J Pineal Res. 2024 May;76(4):e12964. doi: 10.1111/jpi.12964.
Jiayang Zhang 1 2 Lejia Qiu 2 Zhaiyi Liu 3 Jiaxin Liu 3 Bo Yu 4 Chengcheng Liu 2 Baoyin Ren 1 2 Jiaqi Zhang 2 Shuyao Li 2 Youfei Guan 3 Feng Zheng 1 2 Guangrui Yang 4 Lihong Chen 1 2
Affiliations

Affiliations

  • 1 WuHu Hospital, East China Normal University (The Second People's Hospital, Wuhu), Wuhu, China.
  • 2 Health Science Center, East China Normal University, Shanghai, China.
  • 3 Advanced Institute for Medical Sciences, Dalian Medical University, Dalian, China.
  • 4 School of Clinical Medicine, Shanghai University of Medicine and Health Sciences, Shanghai, China.
Abstract

Circadian disruption such as shift work, jet lag, has gradually become a global health issue and is closely associated with various metabolic disorders. The influence and mechanism of circadian disruption on renal injury in chronic kidney disease (CKD) remains inadequately understood. Here, we evaluated the impact of environmental light disruption on the progression of chronic renal injury in CKD mice. By using two abnormal light exposure models to induce circadian disruption, we found that circadian disruption induced by weekly light/dark cycle reversal (LDDL) significantly exacerbated renal dysfunction, accelerated renal injury, and promoted renal fibrosis in mice with 5/6 nephrectomy and unilateral ureteral obstruction (UUO). Mechanistically, RNA-seq analysis revealed significant immune and metabolic disorder in the LDDL-conditioned CKD kidneys. Consistently, renal content of ATP was decreased and ROS production was increased in the kidney tissues of the LDDL-challenged CKD mice. Untargeted metabolomics revealed a significant buildup of lipids in the kidney affected by LDDL. Notably, the level of β-NMN, a crucial intermediate in the NAD+ pathway, was found to be particularly reduced. Moreover, we demonstrated that both β-NMN and melatonin administration could significantly rescue the light-disruption associated kidney dysfunction. In conclusion, environmental circadian disruption may exacerbate chronic kidney injury by facilitating inflammatory responses and disturbing metabolic homeostasis. β-NMN and melatonin treatments may hold potential as promising approaches for preventing and treating light-disruption associated CKD.

Keywords

chronic kidney disease; circadian disruption; light/dark cycle reversal; melatonin; β‐NMN.

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