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Ferroptosis: a potential bridge linking gut microbiota and chronic kidney disease.
Mao, Zi-Hui; Gao, Zhong-Xiuzi; Pan, Shao-Kang; Liu, Dong-Wei; Liu, Zhang-Suo; Wu, Peng.
Afiliação
  • Mao ZH; Traditional Chinese Medicine Integrated Department of Nephrology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, PR China.
  • Gao ZX; Institute of Nephrology, Zhengzhou University, Zhengzhou, PR China.
  • Pan SK; Henan Province Research Center for Kidney Disease, Zhengzhou, PR China.
  • Liu DW; Key Laboratory of Precision Diagnosis and Treatment for Chronic Kidney Disease in Henan Province, Zhengzhou, PR China.
  • Liu ZS; Traditional Chinese Medicine Integrated Department of Nephrology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, PR China.
  • Wu P; Institute of Nephrology, Zhengzhou University, Zhengzhou, PR China.
Cell Death Discov ; 10(1): 234, 2024 May 15.
Article em En | MEDLINE | ID: mdl-38750055
ABSTRACT
Ferroptosis is a novel form of lipid peroxidation-driven, iron-dependent programmed cell death. Various metabolic pathways, including those involved in lipid and iron metabolism, contribute to ferroptosis regulation. The gut microbiota not only supplies nutrients and energy to the host, but also plays a crucial role in immune modulation and metabolic balance. In this review, we explore the metabolic pathways associated with ferroptosis and the impact of the gut microbiota on host metabolism. We subsequently summarize recent studies on the influence and regulation of ferroptosis by the gut microbiota and discuss potential mechanisms through which the gut microbiota affects ferroptosis. Additionally, we conduct a bibliometric analysis of the relationship between the gut microbiota and ferroptosis in the context of chronic kidney disease. This analysis can provide new insights into the current research status and future of ferroptosis and the gut microbiota.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Cell Death Discov Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Cell Death Discov Ano de publicação: 2024 Tipo de documento: Article