ISSN 1518 0557
Potentiating response of D- Ribose-L-Cysteine on Sodium arsenate- induced hormonal imbalance, spermatogenesis impairments and histomorphometric alterations in adult male Wistar rat

2021; 25
Babatunde Ogunlade, Sunday Aderemi Adelakun, V.O. Ukwenya, T.T. Elemoso
JBRA Assist. Reprod. 2021; 25 (3):358-367

Received July 27, 2020
Accepted January 27, 2021
Abstract

Introduction: Reproductive toxicity is an important health challenge mostly associated with exposure to several environmental toxicants. Arsenic is a ubiquitous toxic compound present in the environment naturally. This study was conducted to evaluate the dietary supplements of D-Ribose-L-Cysteine against sodium arsenate-induced testicular toxicity in adult male Wistar rats. Materials and Methods: A total of 32 male rats (150-250g) were randomly divided into four (4) groups (n=8). Group A received normal saline as placebo; Group B received 8mg/kg BW of Sodium arsenate only; Group C received 8mg/kg BW of Sodium arsenate and 10 mg/kg BW of D-Ribose- L-cysteine; Group D received 8mg/kg BW of Sodium arsenate and 30 mg/kg BW of D-Ribose- L-cysteine. All administration was done via oral gavage for 28 days, thereafter animals were sedated with pentobarbital sodium (intraperitoneally); testes and blood serum were obtained for analysis. Results: The results showed abnormal testicular morphology with degeneration and decrease in spermatogonia, vacuolation and empty lumen, intense necrosis, spermatogenesis disruption (decrease sperm count, motility, viability) and degraded germinal epithelium of the seminiferous tubules, reduction in hormone profile (FSH, LH, and TT) and oxidative stress parameters (CAT, GSH, and SOD) with a corresponding increase in MDA level in arsenic only treated rats (group B) compared to control (group A) but was ameliorated after DRLC administration both in low and high doses respectively. Conclusion: D-Ribose-L-Cysteine attenuated distorted testicular morphology, altered semen characteristics, hormone profile, and oxidative stress markers by preventing the deleterious toxicity of sodium arsenate.


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doi: 10.5935/1518-0557.20200109

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