Ji Yu, Wang Yujie, Liu Yuhang, Liu Yutong, Qin Jiao, Yuan Daohuan, Liu Quansheng
Guangdong Key Laboratory of Animal Conservation and Resource Utilization, Guangdong Public Laboratory of Wild Animal Conservation and Utilization, Institute of Zoology, Guangdong Academy of Sciences, Guangzhou 050000, China.
Animals (Basel). 2024 Nov 12;14(22):3240. doi: 10.3390/ani14223240.
This study investigates whether ketoconazole, a CYP3A4 inhibitor, can enhance the suppressive effects of quinestrol on reproductive capacity, potentially allowing for a reduced quinestrol dosage while maintaining its efficacy. A total of 104 healthy adult male mice were divided into two groups, assessed at 10 and 30 days. Within each group, six treatment categories were tested: the control (CK), quinestrol alone (Q1, Q5), and quinestrol combined with varying doses of ketoconazole (Q1 + K0.4, Q1 + K2, Q5 + K0.4). The key parameters measured included internal and reproductive organ weights, sperm density, sperm motility, sperm abnormalities, and CYP3A4 enzyme content in intestinal and liver tissues. After 10 days, the combination of a low dose of quinestrol with ketoconazole (Q1 + K0.4) showed the most significant pronounced effects in reducing reproductive potential, with notable reductions in epididymal weight, sperm density, sperm abnormality rate and vitality, serum hormone levels, and CYP3A4 content in the small intestine and liver. Although some reproductive parameters returned to near-baseline levels after 30 days, the Q1 + K0.4 regimen continued to exhibit reduced seminal vesicle weight and testosterone levels. Importantly, the combination did not significantly increase CYP3A4 enzyme content, indicating effective metabolic inhibition. The combination of quinestrol and ketoconazole, especially the Q1 + K0.4 regimen, demonstrated the most noticeable impact on reducing reproductive capacity. This regimen significantly reduced key reproductive parameters and showed strong metabolic inhibition, suggesting that ketoconazole substantially enhances the efficacy of quinestrol in fertility control.
本研究调查了细胞色素P450 3A4(CYP3A4)抑制剂酮康唑是否能增强炔雌醚对生殖能力的抑制作用,从而有可能在维持炔雌醚疗效的同时降低其剂量。总共104只健康成年雄性小鼠被分为两组,在第10天和第30天进行评估。每组内测试了六个处理类别:对照组(CK)、单独使用炔雌醚组(Q1、Q5)以及炔雌醚与不同剂量酮康唑联合使用组(Q1 + K0.4、Q1 + K2、Q5 + K0.4)。所测量的关键参数包括体内和生殖器官重量、精子密度、精子活力、精子异常情况以及肠道和肝脏组织中的CYP3A4酶含量。10天后,低剂量炔雌醚与酮康唑联合使用组(Q1 + K0.4)在降低生殖潜能方面显示出最显著的效果,附睾重量、精子密度、精子异常率和活力、血清激素水平以及小肠和肝脏中的CYP3A4含量均有显著降低。尽管30天后一些生殖参数恢复到接近基线水平,但Q1 + K0.4方案的精囊重量和睾酮水平仍持续降低。重要的是,联合使用并未显著增加CYP3A4酶含量,表明代谢抑制有效。炔雌醚与酮康唑联合使用,尤其是Q1 + K0.4方案,对降低生殖能力的影响最为显著。该方案显著降低了关键生殖参数,并显示出强大的代谢抑制作用,表明酮康唑可显著增强炔雌醚在生育控制方面的疗效。