Reducing Oxidative Stress and Inflammation by Pyruvate Dehydrogenase Kinase 4 Inhibition Is Important in Prevention of Renal Ischemia-Reperfusion Injury in Diabetic Mice

Diabetes Metab J. 2024 May;48(3):405-417. doi: 10.4093/dmj.2023.0196. Epub 2024 Feb 1.

Abstract

Backgruound: Reactive oxygen species (ROS) and inflammation are reported to have a fundamental role in the pathogenesis of ischemia-reperfusion (IR) injury, a leading cause of acute kidney injury. The present study investigated the role of pyruvate dehydrogenase kinase 4 (PDK4) in ROS production and inflammation following IR injury.

Methods: We used a streptozotocin-induced diabetic C57BL6/J mouse model, which was subjected to IR by clamping both renal pedicles. Cellular apoptosis and inflammatory markers were evaluated in NRK-52E cells and mouse primary tubular cells after hypoxia and reoxygenation using a hypoxia work station.

Results: Following IR injury in diabetic mice, the expression of PDK4, rather than the other PDK isoforms, was induced with a marked increase in pyruvate dehydrogenase E1α (PDHE1α) phosphorylation. This was accompanied by a pronounced ROS activation, as well as tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), interleukin-1β (IL-1β), and monocyte chemoattractant protein-1 (MCP-1) production. Notably, sodium dichloroacetate (DCA) attenuated renal IR injury-induced apoptosis which can be attributed to reducing PDK4 expression and PDHE1α phosphorylation levels. DCA or shPdk4 treatment reduced oxidative stress and decreased TNF-α, IL-6, IL-1β, and MCP-1 production after IR or hypoxia-reoxygenation injury.

Conclusion: PDK4 inhibition alleviated renal injury with decreased ROS production and inflammation, supporting a critical role for PDK4 in IR mediated damage. This result indicates another potential target for reno-protection during IR injury; accordingly, the role of PDK4 inhibition needs to be comprehensively elucidated in terms of mitochondrial function during renal IR injury.

Keywords: Acute kidney injury; Diabetes mellitus; Inflammation; Ischemia; Pyruvate dehydrogenase kinase 4; Reactive oxygen species; Reperfusion.

MeSH terms

  • Acute Kidney Injury / etiology
  • Acute Kidney Injury / metabolism
  • Acute Kidney Injury / prevention & control
  • Animals
  • Apoptosis* / drug effects
  • Diabetes Mellitus, Experimental* / complications
  • Diabetes Mellitus, Experimental* / metabolism
  • Diabetic Nephropathies / metabolism
  • Dichloroacetic Acid / pharmacology
  • Inflammation* / metabolism
  • Kidney / metabolism
  • Kidney / pathology
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Oxidative Stress* / drug effects
  • Phosphorylation / drug effects
  • Pyruvate Dehydrogenase (Lipoamide) / metabolism
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase* / antagonists & inhibitors
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase* / metabolism
  • Reactive Oxygen Species* / metabolism
  • Reperfusion Injury* / metabolism
  • Reperfusion Injury* / prevention & control

Substances

  • Reactive Oxygen Species
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase
  • Pyruvate Dehydrogenase (Lipoamide)
  • Dichloroacetic Acid
  • Pdk4 protein, mouse
  • pyruvate dehydrogenase E1alpha subunit