Melatonin ameliorates testicular damages induced by nicotine in mice

Fahimeh Mohammadghasemi1, Sina Khajeh Jahromi1

  • 1Cellular & Molecular Research Center, Guilan University of Medical Sciences, Rasht, Iran.

Abstract

Insights

Melatonin supplementation improved male reproductive health in nicotine-exposed mice. It enhanced sperm quality, spermatogenesis, and DNA integrity by reducing apoptosis and modulating testosterone levels.

Area of Science:

  • Reproductive Biology
  • Toxicology
  • Endocrinology

Background:

  • Nicotine exposure negatively impacts male reproductive function, leading to testicular damage and impaired sperm parameters.
  • Melatonin, a potent antioxidant, is investigated for its potential protective effects against toxicant-induced reproductive dysfunction.

Purpose of the Study:

  • To investigate the protective effects of melatonin against nicotine-induced testicular toxicity in male mice.
  • To evaluate the impact of melatonin on sperm nuclear integrity, epididymal sperm parameters, and reproductive hormone levels.

Main Methods:

  • Male mice were administered nicotine, melatonin, or a combination thereof.
  • Histology, Johnson's score, immunostaining, sperm chromatin dispersion (SCD) test, and ELISA were employed for evaluation.
  • Spermatogenesis, apoptosis, sperm chromatin integrity, testosterone, and luteinizing hormone (LH) levels were assessed.

Main Results:

  • Nicotine significantly reduced spermatogenesis, sperm parameters, and sex hormone levels.
  • Melatonin treatment improved spermatogenesis, sperm chromatin integrity, and sperm parameters, while reducing apoptosis.
  • Melatonin significantly increased serum testosterone levels, showing a negative correlation with DNA fragmentation.

Conclusions:

  • Melatonin administration mitigates nicotine-induced damage to the male reproductive system.
  • Melatonin enhances spermatogenesis quality and quantity and improves sperm chromatin integrity.
  • The protective effects of melatonin are linked to reduced apoptosis and modulation of testosterone levels.

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