Melatonin protects kidney against apoptosis induced by acute unilateral ureteral obstruction in rats

Mehmet Erol Yildirim1, Hüseyin Badem2, Muzaffer Cakmak3

  • 1Turgut Özal University School of Medicine, Department of Urology, Ankara, Turkey.

Abstract

Insights

Melatonin treatment reduced kidney apoptosis after unilateral ureteral obstruction. However, renal histology did not return to normal levels, indicating incomplete protection against kidney injury.

Area of Science:

  • Nephrology
  • Endocrinology
  • Cell Biology

Background:

  • Acute unilateral ureteral obstruction (UUO) can lead to significant kidney damage.
  • Apoptosis plays a critical role in the pathogenesis of UUO-induced renal injury.
  • Melatonin, a hormone with antioxidant and anti-inflammatory properties, is investigated for its potential renoprotective effects.

Purpose of the Study:

  • To determine if melatonin administration can mitigate apoptotic mechanisms in the kidney following acute UUO.
  • To evaluate the timing of melatonin administration (immediate vs. delayed) on its protective efficacy.

Main Methods:

  • A rat model of acute UUO was established.
  • Five experimental groups were included: control, sham, UUO with saline, UUO with immediate melatonin, and UUO with delayed melatonin.
  • Kidney tissues were analyzed for apoptotic index and Ki-67 scores.

Main Results:

  • UUO significantly increased the apoptotic index compared to control and sham groups.
  • Melatonin treatment (both immediate and delayed) reduced the apoptotic index in UUO kidneys.
  • However, melatonin did not fully restore the apoptotic index to control levels, and there was no significant difference between immediate and delayed melatonin administration.

Conclusions:

  • Melatonin demonstrates a protective effect by reducing apoptosis in kidneys subjected to acute UUO.
  • Despite apoptosis reduction, melatonin administration did not normalize renal histology, suggesting limited efficacy in complete renoprotection.
  • The timing of melatonin administration did not significantly impact its apoptotic-reducing effect in this model.