The protection afforded by kefir against cyclophosphamide induced testicular toxicity in rats by oxidant antioxidant and histopathological evaluations

• Published in: Scientific reports Vol. 14; no. 1; pp. 18463 - 7
• Main Authors: Cetik Yildiz, Songul, Demir, Cemil, Cengiz, Mustafa, Irmak, Halit, Peker Cengiz, Betul, Ayhanci, Adnan
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 09-08-2024; Nature Publishing Group; Nature Portfolio
• Subjects: 631/250/251; 692/699; 692/699/67/2195; Animals; Antineoplastic Agents, Alkylating - adverse effects; Antineoplastic Agents, Alkylating - toxicity; Antioxidant; Antioxidants; Antioxidants - metabolism; Antioxidants - pharmacology; Atrophy; Cancer therapies; Cyclophosphamide; Cyclophosphamide - adverse effects; Cyclophosphamide - toxicity; Humanities and Social Sciences; Kefir; Male; multidisciplinary; Oxidants; Oxidants - metabolism; Oxidative stress; Oxidative Stress - drug effects; Oxidizing agents; Rats; Rats, Wistar; Science; Science (multidisciplinary); Side effects; Spermatids; Testes; Testicular toxicity; Testis - drug effects; Testis - metabolism; Testis - pathology; Toxicity; Tubules; Rats; Oxidative stress; Cyclophosphamide; Antioxidant; Testicular toxicity; Kefir
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-67982-y

Cyclophosphamide (CTX) is the most commonly used effective alkylating drug in cancer treatment, but its use is restricted because its toxic side effect causes testicular toxicity. CTX disrupts the tissue redox and antioxidant balance and the resulting tissue damage causes oxidative stress. In our study based on this problem, kefir against CTX-induced oxidative stress and testicular toxicity were investigated. Rats were divided into 6 groups: control, 150 mg/kg CTX, 5 and 10 mg/kg kefir, 5 and 10 mg/kg kefir + 150 CTX. While the fermented kefirs were mixed and given to the rats for 12 days, CTX was given as a single dose on the 12th day of the experiment. Testis was scored according to spermatid density, giant cell formation, cells shed into tubules, maturation disorder, and atrophy. According to our biochemical findings, the high levels of total oxidant status (TOS), and the low levels of total antioxidant status (TAS) in the CTX group, which are oxidative stress markers, indicate the toxic effect of CTX, while the decrease in TOS levels and the increase in TAS levels in the kefir groups indicate the protective effect of kefir. In the CTX-administered group, tubules with impaired maturation and no spermatids were observed in the transverse section of the testicle, while in the kefir groups, the presence of near-normal tubule structures and tubule lumens despite CTX showed the protective effect of kefir. In our study, it was observed that kefir had a protective and curative effect on CTX-induced toxicity and oxidative stress and could be a strong protector.