AI Article Synopsis

  • Pregnant Wistar rats were divided into five groups for a 21-day treatment to study the effects of NP (a chemical) and the potential protective role of MLT (melatonin) on learning, memory, and testicular health.
  • The results indicated that NP did not impair learning and memory in the first generation of rats but did cause significant damage to testicular tissues, reducing the size and number of critical structures involved in sperm production.
  • MLT showed potential in reversing the damage caused by NP, improving antioxidant activity, and supporting better testicular health and learning abilities in the rats.

Article Abstract

Methods: Pregnant Wistar rats were randomly assigned into five groups: control, NP (25 mg/kg), NP (25 mg/kg)+MLT (10 mg/kg), NP (25 mg/kg)+MLT (20 mg/kg), and MLT (20 mg/kg). The duration of treatment was 21 days from gestation time. Morris water maze was used to assess learning and memory. NP concentrations of serum and testicular tissue were measured by HPLC. Histological analysis of testicular tissues was done by H&E staining.

Results: Behavioral study showed that NP does not impair learning and memory in first-generation rats. Histomorphometric results showed that NP can significantly reduce the cross-sectional area of the seminiferous tubules and the epithelium, the diameter and number of seminiferous tubules, the thickness of the epithelium, and the number of spermatocytes and spermatogonia compared to other groups. MLT reversed the NP-induced histomorphometric. Also, it changes and increased the activity of superoxide dismutase (SOD), total antioxidant capacity (TAC), and catalase (CAT). The level of malondialdehyde (MDA) significantly decreased in MLT-treated groups compared with the NP group.

Conclusion: Our finding showed that MLT enhanced the learning process and reduced NP-induced testicular tissue damage through its antioxidants and cytoprotective effects.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072055PMC
http://dx.doi.org/10.1155/2022/1877761DOI Listing

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