Jourabchi Amirreza, Abdi Morteza, Roshanghar Leila, Ghavifekr Homa Aminzadeh
Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Anatomical Sciences, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Sep 1. doi: 10.1007/s00210-025-04551-8.
This study aimed to evaluate the effects of bone marrow-derived mesenchymal stem cell (BMMSC) transplantation and quercetin treatment on the testes of immature mice exposed to cyclophosphamide. Twenty-five prepubertal mice were divided into five groups: control; cyclophosphamide (CTX) group (150 mg/kg); quercetin + CTX group (quercetin 75 mg/kg/day intraperitoneally for 14 days plus CTX); CTX + BMMSC group (CTX followed by injection of 1 × 10 BMMSCs into each testis 24 h after CTX administration); and quercetin + CTX + BMMSC group (combination of quercetin, CTX, and BMMSC injection as described). At the end of the study, serum testosterone levels, biochemical markers, and histopathological and immunohistochemical analyses of testicular tissue were performed. CTX treatment significantly decreased serum testosterone levels and antioxidant enzymes such as superoxide dismutase (SOD) and catalase (CAT) in testicular tissue. CTX also caused tissue damage and increased expression of NF-κB protein (p < 0.05). Treatment with quercetin and BMMSCs improved testicular tissue damage and oxidative stress markers. The findings suggest that quercetin and BMMSC therapy provide protective effects against cyclophosphamide-induced testicular injury in prepubertal mice through molecular and cellular mechanisms.
本研究旨在评估骨髓间充质干细胞(BMMSC)移植和槲皮素治疗对暴露于环磷酰胺的未成熟小鼠睾丸的影响。将25只青春期前小鼠分为五组:对照组;环磷酰胺(CTX)组(150 mg/kg);槲皮素+CTX组(槲皮素75 mg/kg/天腹腔注射14天加CTX);CTX+BMMSC组(CTX给药后24小时,向每个睾丸注射1×10个BMMSC);以及槲皮素+CTX+BMMSC组(如上述槲皮素、CTX和BMMSC注射联合使用)。在研究结束时,对血清睾酮水平、生化标志物以及睾丸组织进行了组织病理学和免疫组织化学分析。CTX治疗显著降低了血清睾酮水平以及睾丸组织中抗氧化酶如超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的水平。CTX还导致组织损伤并增加了NF-κB蛋白的表达(p<0.05)。槲皮素和BMMSC治疗改善了睾丸组织损伤和氧化应激标志物。研究结果表明,槲皮素和BMMSC疗法通过分子和细胞机制对青春期前小鼠环磷酰胺诱导的睾丸损伤具有保护作用。