Zirkin B R, Santulli R, Strandberg J D, Wright W W, Ewing L L
Department of Population Dynamics, Johns Hopkins University, School of Hygiene and Public Health, Baltimore, Maryland 21205.
J Androl. 1993 Mar-Apr;14(2):118-23.
In seeking an animal model of age-associated changes in the male reproductive tract, we examined the effects of age on the health and testicular steroidogenic activity of the Brown Norway rat, with comparisons made to the Sprague-Dawley rat. When perfused in vitro under conditions of maximally stimulating luteinizing hormone significant age-associated reductions were seen in testosterone production by testes of Sprague-Dawley rats of 21-24 months of age and by testes of Brown Norway rats of 18-30 months of age. Decreases in the capacity of the testes to produce testosterone were reflected in age-associated decreases in both serum testosterone and in testosterone concentration within the seminiferous tubule fluid. In contrast to the Sprague-Dawley rat, changes in steroidogenic activity in the Brown Norway rat were not accompanied by the occurrence of pituitary adenomas, obesity, or testicular tumors. This along with its longevity, make the Brown Norway strain a highly promising model for testicular aging.
在寻找雄性生殖道年龄相关变化的动物模型时,我们研究了年龄对棕色挪威大鼠健康和睾丸类固醇生成活性的影响,并与斯普拉格-道利大鼠进行了比较。当在体外以最大刺激促黄体生成素的条件下灌注时,21 - 24月龄的斯普拉格-道利大鼠以及18 - 30月龄的棕色挪威大鼠的睾丸产生睾酮的量出现了显著的年龄相关减少。睾丸产生睾酮能力的下降反映在血清睾酮和生精小管液中睾酮浓度的年龄相关降低上。与斯普拉格-道利大鼠不同,棕色挪威大鼠的类固醇生成活性变化并未伴有垂体腺瘤、肥胖或睾丸肿瘤的发生。这连同其长寿特性,使棕色挪威品系成为睾丸衰老的极有前景的模型。