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α7nAChR-mediated cholinergic anti-inflammatory pathway of immune cells in sepsis induced cardiac injury

  • Yufan Yang1,2,†
  • Yueqi He1,†
  • Jiaotian Huang1,2
  • Xiulan Lu1,2
  • Zhenghui Xiao1,2,*,

1Department of Intensive Care Unit, the School of Pediatrics, Hengyang Medical School, University of South China (Hunan Children’s Hospital), 410007 Changsha, Hunan, China

2Department of Intensive Care Unit, the Affiliated Children’s Hospital of Xiangya School of Medicine, Central South University (Hunan Children’s Hospital), 410007 Changsha, Hunan, China

DOI: 10.22514/sv.2025.003 Vol.21,Issue 1,January 2025 pp.21-24

Submitted: 01 April 2024 Accepted: 10 May 2024

Published: 08 January 2025

*Corresponding Author(s): Zhenghui Xiao E-mail: xiaozh@hnetyy.net

† These authors contributed equally.

Abstract

Sepsis is a systemic syndrome characterized by widespread inflammatory responses induced by pathogenic microorganism invasion into the body, with increased suscep-tibility to major organs. Sepsis-induced cardiomyopathy is characterized by reversible myocardial depression or injury, primarily presenting as acute heart failure and/or arrhythmias triggered by sepsis. The mortality rate substantially increases when septic patients develop sepsis-induced cardiomyopathy. The cholinergic anti-inflammatory pathway (CAP) regulates inflammatory responses through the release of acetylcholine (ACh) via the vagus nerve and acts upon α7 nicotinic acetylcholine receptors (α7nAChR) on immune cells to suppress pro-inflammatory sytokines synthesis. In this review, we provide a concise overview of the current understanding of the α7nAChR-mediated CAP in sepsis-induced cardiac injury, with a primary focus on α7nAChR involvement in immune regulation.


Keywords

α7nAChR; Mediated cholinergic anti-inflammatory pathway; Immune cells; Sepsis; Cardiac injury


Cite and Share

Yufan Yang,Yueqi He,Jiaotian Huang,Xiulan Lu,Zhenghui Xiao. α7nAChR-mediated cholinergic anti-inflammatory pathway of immune cells in sepsis induced cardiac injury. Signa Vitae. 2025. 21(1);21-24.

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