Dose- and time-related effects of caffeine on the testis in immature male rats

J. Bae, Hyeonhae Choi, Yuri Choi, J. Roh
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引用次数: 15

Abstract

We previously showed that prepubertal chronic caffeine exposure adversely affected the development of the testes in male rats. Here we investigated dose- and time-related effects of caffeine consumption on the testis throughout sexual maturation in prepubertal rats. A total of 80 male SD rats were randomly divided into four groups: controls and rats fed 20, 60, or 120 mg caffeine/kg/day, respectively, via gavage for 10, 20, 30, or 40 days. Preputial separation was monitored daily before the rats were sacrificed. Terminal blood samples were collected for hormone assay, and testes were grossly evaluated and weighed. One testis was processed for histological analysis, and the other was collected to isolate Leydig cells. Caffeine exposure significantly increased the relative weight of the testis in a dose-related manner after 30 days of exposure, whereas the absolute testis weight tended to decrease at the 120 mg dose of caffeine. The mean diameter of the seminiferous tubules and height of the germinal epithelium significantly decreased in the caffeine-fed groups after 40 days of caffeine exposure, which was accompanied by a reduced BrdU incorporation rate in germ cells. In addition, caffeine intake significantly reduced in vivo and ex vivo testosterone production in a dose-related manner. Our results demonstrate that caffeine exposure during sexual maturation alter the testicular microarchitecture and also slow germ cell proliferation even at the 20 mg dose level. Furthermore, caffeine may act directly on Leydig cells and interfere with testosterone production in a dose-related manner, consequently delaying onset of sexual maturation.
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咖啡因对未成熟雄性大鼠睾丸的剂量和时间相关影响
我们之前的研究表明,青春期前慢性咖啡因暴露对雄性大鼠睾丸的发育有不利影响。在这里,我们研究了咖啡因摄入对青春期前大鼠性成熟过程中睾丸的剂量和时间相关影响。将80只雄性SD大鼠随机分为4组:对照组和大鼠分别饲喂20、60、120 mg /kg/d咖啡因,灌胃10、20、30、40 d。在处死大鼠前每天监测包皮分离情况。收集晚期血液样本进行激素测定,并对睾丸进行粗略评估和称重。一个睾丸进行组织学分析,另一个收集来分离间质细胞。暴露于咖啡因30天后,睾丸的相对重量以剂量相关的方式显著增加,而在120 mg剂量下,睾丸的绝对重量有下降的趋势。在咖啡因暴露40天后,咖啡因喂养组的精管平均直径和生殖上皮高度显著降低,同时生殖细胞中BrdU掺入率降低。此外,咖啡因摄入显著降低体内和体外睾酮的产生,并以剂量相关的方式。我们的研究结果表明,性成熟期间的咖啡因暴露即使在20毫克的剂量水平下也会改变睾丸微结构并减慢生殖细胞增殖。此外,咖啡因可能直接作用于间质细胞,并以剂量相关的方式干扰睾丸激素的产生,从而延迟性成熟的发生。
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