Sleeve gastrectomy ameliorates renal injury in obesity-combined hyperuricemic nephropathy mice by modulating the AMPK/Nrf2/ABCG2 pathway

Sci Rep. 2024 Oct 1;14(1):22834. doi: 10.1038/s41598-024-73807-9.

Abstract

Hyperuricemic nephropathy (HN) is renal injury caused by hyperuricemia (HUA). While sleeve gastrectomy (SG) has shown promise in improving renal injury in patients with obesity-related HN, the mechanisms are not fully understood. This study induced an obesity-combined HN model in male ob/ob mice and measured serum uric acid (SUA), creatinine, and other biochemical indicators 6 weeks post-surgery. Renal histological changes were evaluated through staining techniques, and the study also assessed renal adenosine monophosphate-activated protein kinase (AMPK) and nuclear factor erythroid 2-related factor 2 (Nrf2) phosphorylation levels and urate transporter ABCG2 expression. In vitro experiments involved Nrf2 knockdown in AMPK-activated HK-2 cells and ChIP to confirm Nrf2 binding to the ABCG2 promoter. Results showed that SG reduced SUA levels, serum creatinine, and blood urea nitrogen, increased p-AMPK, p-Nrf2 protein, and ABCG2 expression, and alleviated renal fibrosis and inflammation. In vitro, Nrf2 knockdown down-regulated ABCG2 expression, and ChIP confirmed Nrf2's role in ABCG2 transcription. The study suggests that SG may improve renal injury in HN mice by modulating the AMPK/Nrf2 pathway and upregulating ABCG2 transcription.

Keywords: ABCG2; AMPK; Hyperuricemic nephropathy; Nrf2; Sleeve gastrectomy.

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • ATP Binding Cassette Transporter, Subfamily G, Member 2* / genetics
  • ATP Binding Cassette Transporter, Subfamily G, Member 2* / metabolism
  • Animals
  • Disease Models, Animal
  • Gastrectomy* / methods
  • Humans
  • Hyperuricemia* / metabolism
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney Diseases / etiology
  • Kidney Diseases / metabolism
  • Kidney Diseases / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • NF-E2-Related Factor 2* / genetics
  • NF-E2-Related Factor 2* / metabolism
  • Obesity* / complications
  • Obesity* / metabolism
  • Obesity* / surgery
  • Signal Transduction

Substances

  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • NF-E2-Related Factor 2
  • AMP-Activated Protein Kinases
  • Abcg2 protein, mouse
  • Nfe2l2 protein, mouse