Levinson D J, Chalker D
Arthritis Rheum. 1980 Jan;23(1):77-82. doi: 10.1002/art.1780230113.
The effect of maturation, castration, and sex hormonal treatment on hepatic xanthine oxidase activity (XOA) was evaluated in Sprague-Dawley rats. In mature rats XOA was 59% greater in males than in females, whereas in the immature animal the differences between sexes were insignificant. Pubescence resulted in a twofold increase in activity in the male which was prevented by prepubertal orchiectomy. Conversely, prepubertal oophorectomy caused a twofold increase in XOA in females. Urinary uric acid excretion paralleled XOA in rats fed 1% oxonic acid. XOA was significantly elevated in females after postpubertal castration or testosterone treatment while orchiectomy or estradiol-17 beta treatment in the mature male showed no effect. In summary, these data suggest that androgens are required during puberty for full expression of hepatic XOA, and furthermore, an ovarian suppressive effect is evident. In the adult rat only the female responds appreciably to hormonal manipulation.
在斯普拉格-道利大鼠中评估了成熟、去势和性激素治疗对肝脏黄嘌呤氧化酶活性(XOA)的影响。在成熟大鼠中,雄性的XOA比雌性高59%,而在未成熟动物中,两性之间的差异不显著。青春期导致雄性动物的活性增加两倍,而青春期前睾丸切除术可阻止这种增加。相反,青春期前卵巢切除术导致雌性动物的XOA增加两倍。在喂食1%氧嗪酸的大鼠中,尿尿酸排泄与XOA平行。青春期后去势或睾酮治疗后,雌性动物的XOA显著升高,而成熟雄性动物的睾丸切除术或雌二醇-17β治疗则无效果。总之,这些数据表明,青春期期间需要雄激素来充分表达肝脏XOA,此外,卵巢的抑制作用也很明显。在成年大鼠中,只有雌性对激素操作有明显反应。