Correlation Engine 2.0
Clear Search sequence regions


  • acid (4)
  • Aifm2 (2)
  • apoptosis (4)
  • biosynthesis (2)
  • blood (1)
  • electron (1)
  • heat stroke (4)
  • HMGB1 (4)
  • hmgb1 protein (3)
  • humans (1)
  • measure (1)
  • mice (4)
  • pathogenesis (1)
  • plasma (1)
  • positron (2)
  • products (6)
  • receptor (6)
  • serum (1)
  • signal (1)
  • western blot (1)
  • Sizes of these terms reflect their relevance to your search.

    Heat stroke can induce a systemic inflammatory response, which may lead to multi‑organ dysfunction including acute kidney injury (AKI) and electrolyte disturbances. To investigate the pathogenesis of heat stroke (HS)‑related AKI, a mouse model of HS was induced by increasing the animal's core temperature to 41˚C. Blood samples obtained from the tail vein were used to measure plasma glucose and creatinine levels. Micro‑positron emission tomography‑computed tomography (micro‑PET/CT), H&E staining and transmission electron microscopy were conducted to examine metabolic and morphological changes in the mouse kidneys. Immunohistochemistry (IHC) and western blot analyses were performed to investigate the expression of apoptosis‑inducing factor mitochondria‑associated 2 (Aifm2), high‑mobility group box 1 (HMGB1) and receptor for advanced glycosylation end products (RAGE). Liquid chromatography‑mass spectrometry analysis was conducted to find differential metabolites and signaling pathways. The HS mouse model was built successfully, with significantly increased creatinine levels detected in the serum of HS mice compared with controls, whereas micro‑PET/CT revealed active metabolism in the whole body of HS mice. H&E and TUNEL staining revealed that the kidneys of HS mice exhibited signs of hemorrhage and apoptosis. IHC and western blotting demonstrated significant upregulation of Aifm2, HMGB1 and RAGE in response to HS. Finally, 136 differential metabolites were screened out, and enrichment of the 'biosynthesis of unsaturated fatty acids' pathway was detected. HS‑associated AKI is the renal manifestation of systemic inflammatory response syndrome, and may be triggered by the HMGB1/RAGE pathway. Metabolomics indicated increased adrenic acid, docosahexaenoic acid and eicosapentaenoic acid may serve as metabolic biomarkers for AKI in HS. The findings suggested that a correlation between the HMGB1/RAGE pathway and biosynthesis of unsaturated fatty acids may contribute to the progression of HS‑related AKI.

    Citation

    Ling Xue, Wenli Guo, Li Li, Santao Ou, Tingting Zhu, Liang Cai, Wenfei Ding, Weihua Wu. Metabolomic profiling identifies a novel mechanism for heat stroke‑related acute kidney injury. Molecular medicine reports. 2021 Apr;23(4)

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 33655337

    View Full Text