H2S alleviated sepsis-induced acute kidney injury by inhibiting PERK/Bax-Bcl2 pathway

Nitric Oxide. 2024 Nov 1:152:11-18. doi: 10.1016/j.niox.2024.09.003. Epub 2024 Sep 11.

Abstract

To investigate the protective mechanisms of hydrogen sulfide (H2S) in sepsis-induced acute kidney injury (SAKI), we conducted an in vivo study using a SAKI mouse model induced by intraperitoneal lipopolysaccharide (LPS) injection. Following 6 h of LPS injection, levels of tumor necrosis factor-alpha (TNF-α) and blood urea nitrogen (Bun) were significantly elevated in mouse plasma. In the kidneys of SAKI mice, expression of H2S-generating enzymes cysteinyl-tRNA synthetase (CARS), cystathionine γ-lyase (CSE) and cystathionine β-synthase (CBS) was markedly downregulated, while glucose-regulated protein 78 (GRP78), activating transcription factor 6 (ATF6), phosphorylated protein kinase R-like endoplasmic reticulum kinase/protein kinase R-like endoplasmic reticulum kinase (p-PERK/PERK), and B-cell lymphoma-2 recombinant protein X/B-cell lymphoma-2 (Bax/Bcl2) expression was significantly upregulated. H2S improved renal function and attenuated renal histopathological changes in SAKI mice, thereby alleviating LPS-induced endoplasmic reticulum stress (ERS). Additionally, it inhibited the expression of p-PERK/PERK and Bax/Bcl2. After inhibiting CSE activity with dl-propargylglycine (PPG i. p.), the renal tissue pathology in LPS-induced AKI mice was further exacerbated, leading to enhanced activation of the PERK/Bax-Bcl2 pathway. Our findings suggest that endogenous H2S influences the pathogenesis of SAKI, while exogenous H2S protects against LPS-induced AKI by inhibiting the PERK/Bax-Bcl2 pathway involved in ERS.

Keywords: Acute kidney injury; Endoplasmic reticulum stress; Hydrogen sulfide; Sepsis.

MeSH terms

  • Acute Kidney Injury* / drug therapy
  • Acute Kidney Injury* / metabolism
  • Animals
  • Endoplasmic Reticulum Chaperone BiP*
  • Endoplasmic Reticulum Stress / drug effects
  • Hydrogen Sulfide* / metabolism
  • Hydrogen Sulfide* / pharmacology
  • Kidney / metabolism
  • Kidney / pathology
  • Lipopolysaccharides*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Proto-Oncogene Proteins c-bcl-2* / metabolism
  • Sepsis* / complications
  • Sepsis* / drug therapy
  • Sepsis* / metabolism
  • Signal Transduction / drug effects
  • bcl-2-Associated X Protein* / metabolism
  • eIF-2 Kinase* / metabolism

Substances

  • Hydrogen Sulfide
  • Hspa5 protein, mouse
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
  • eIF-2 Kinase
  • Endoplasmic Reticulum Chaperone BiP
  • PERK kinase
  • Lipopolysaccharides
  • Bcl2 protein, mouse
  • Bax protein, mouse