Reproductive toxicology (Elmsford, N.Y.) · 2025
Impact of the environmental endocrine disruptor flutamide on cryptorchidism: Molecular mechanisms involving connexin-43 and p38-MAPK signaling.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Zhou Yu, Hong Yifan, Wang Shengwen, He Luna, Cui Yan, Wu Yinghua, Yan Fuli, Long Chunlan, Gao Jing
Аннотация
Cryptorchidism, a condition associated with male infertility, is exacerbated by exposure to environmental endocrine disruptors such as flutamide. This study investigates the molecular mechanisms of cryptorchidism and potential interventions targeting endocrine disruptor-induced testicular damage. A rat model of congenital cryptorchidism was established via prenatal flutamide exposure, and testes were harvested at postnatal day 90. Testicular histology, transcriptome sequencing, bioinformatic analysis, sperm analysis, immunohistochemistry, and lentiviral vector transfection were conducted. Cryptorchid testes exhibited impaired seminiferous tubule development, significant reductions in sperm count, and increased sperm abnormalities. Tight and gap junction proteins essential for blood-testis barrier (BTB) integrity, including Claudin-11, Occludin, and Connexin-43, were markedly downregulated. Transcriptomic analysis revealed activation of the p38 MAPK signaling pathway and excessive apoptosis in cryptorchid testes. Overexpression of Connexin-43 restored BTB integrity and suppressed the p38 MAPK pathway, rescuing spermatogenesis. These findings underscore the role of environmental anti-androgens in cryptorchidism pathogenesis and highlight Connexin-43 as a potential therapeutic target for mitigating testicular damage caused by endocrine disruptors.