Oxidative stress/angiotensinogen/renin-angiotensin system axis in patients with diabetic nephropathy

Masumi Kamiyama1, Maki Urushihara, Takashi Morikawa

  • 1Department of Physiology, Tulane University Health Sciences Center, 1430 Tulane Avenue, New Orleans, LA 70112, USA. hkobori@tulane.edu.

Insights

Diabetic nephropathy progression involves increased oxidative stress and the renin-angiotensin system (RAS) in the kidneys. Targeting this axis may offer new therapeutic strategies for kidney protection in diabetes.

Area of Science:

  • Nephrology
  • Endocrinology
  • Pathophysiology

Background:

  • Diabetic nephropathy is a major complication of diabetes.
  • Renin-angiotensin system (RAS) blockade shows reno-protective effects, but mechanisms are unclear.
  • Reactive oxygen species (ROS) are implicated in diabetic kidney disease progression.

Purpose of the Study:

  • To investigate the role of oxidative stress and RAS factors in human diabetic nephropathy.
  • To determine if intrarenal angiotensinogen (AGT) expression is increased in diabetic kidneys.
  • To examine the relationship between ROS, AGT, and renal dysfunction.

Main Methods:

  • Analysis of kidney biopsy samples from diabetic patients and controls.
  • Quantification of AGT, angiotensin II (Ang II), 4-hydroxy-2-nonenal (4-HNE), and heme oxygenase-1 (HO-1) expression.
  • Utilized fluorescence in situ hybridization and immunohistochemistry.

Main Results:

  • Expression of AGT, Ang II, 4-HNE, and HO-1 was significantly higher in diabetic kidneys.
  • Increased intrarenal AGT mRNA levels correlated with renal dysfunction.
  • Evidence supports an activated oxidative stress/AGT/RAS axis in diabetic nephropathy pathogenesis.

Conclusions:

  • The study provides direct evidence of enhanced oxidative stress and AGT expression in human diabetic kidneys.
  • The activated oxidative stress/AGT/RAS axis is crucial in the pathogenesis of diabetic nephropathy.
  • Findings suggest potential therapeutic targets within this axis for diabetic kidney disease.

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