Pumpkin seed oil lessens the colchicine-induced altered sex male hormone balance, testicular oxidative status, sperm abnormalities, and collagen deposition in male rats via Caspase3/Desmin/PCNA modulation

• Published in: Food and chemical toxicology 2024-11, Vol.193, p.115029, Article 115029
• Main Authors: Abd-Elhakim, Yasmina M., El-Fatah, Samaa Salah Abd, Behairy, Amany, Saber, Taghred M., El-Sharkawy, Nabela I., Moustafa, Gihan G., Abdelgawad, Fathy Elsayed, Saber, Taisir, Samaha, Mariam M., El Euony, Omnia I.
• Format: Article
• Language: English
• Subjects: Animals; Caspase 3 - genetics; Caspase 3 - metabolism; Caspase-3; Colchicine; Colchicine - pharmacology; Collagen - metabolism; Cucurbita - chemistry; Desmin; Gonadal Steroid Hormones - metabolism; Male; Male sex hormones; Oxidative Stress - drug effects; Plant Oils - pharmacology; Proliferating cell nuclear antigen; Proliferating Cell Nuclear Antigen - metabolism; Pumpkin seed oil; Rats; Rats, Sprague-Dawley; Seeds - chemistry; Sperm Motility - drug effects; Spermatozoa - drug effects; Testis - drug effects; Testis - metabolism; Testosterone
• ISSN: 0278-6915; 1873-6351; 1873-6351
• DOI: 10.1016/j.fct.2024.115029

This study examined the efficiency of pumpkin seed oil (PSO) to rescue the colchicine (CHC)-induced adverse impacts on sperm characteristics, male sex hormones, testicular architecture, oxidative status, DNA content, collagen deposition, and immune expression of desmin and PCNA. Male Sprague Dawley rats were divided into four experimental groups (n = 10 each): control (distilled water), CHC (0.6 mg/kg b.wt), PSO (4 mL/kg b.wt), and CHC + PSO. After 60 days of dosing, CHC significantly reduced sperm motility (19%), sperm concentration (38%), estradiol (52%), testosterone (37%), luteinizing hormone (54%), and follicle-stimulating hormone (29%) compared to the control. Yet, the testicular tissues of CHC-administered rats exhibited elevated abnormal sperms (156%), malondialdehyde (354%), lactate dehydrogenase (73%), Caspase-3 (66%), and 8-hydroxyguanosine (65%) but lower reduced glutathione (74%), catalase (73%), and superoxide dismutase (78%) compared to the control group. Moreover, CHC induced testicular degeneration, distorted seminiferous tubules, apoptotic cells, exfoliated spermatogenic cells, reduced DNA content, decreased PCNA and desmin immune-expression, and increased collagen deposition. PSO effectively reversed the CHC-induced alterations in sperm quality and testicular function and architecture, likely through its antioxidant, antifibrotic, anti-apoptotic, and DNA-protective properties. These results suggest that PSO may be a beneficial intervention for long-term CHC users and may protect against CHC-induced male reproductive toxicity.