Funke P J, Tunn U W, Senge T, Neumann F
Acta Endocrinol (Copenh). 1982 Jul;100(3):462-72. doi: 10.1530/acta.0.1000462.
The effect of the antioestrogen tamoxifen (TA) was investigated in different types of steroid-induced benign prostatic hyperplasia (BPH) in the castrated dog by histological, histochemical and biochemical analysis. A 6 months treatment with oestradiol-17 beta (E2) alone resulted in cystic and stromal hyperplasia and squamous epithelial metaplasia with a striking prostatic weight increase DNA and RNA content of the total glands increased significantly. The histochemical results and zinc values indicated the loss of normal epithelial function due to metaplatic transformation. The E2 induced cystic and metaplastic hyperplasia was prevented by TA while the stromal proliferation was significantly decreased but not abolished. Biochemical determinations revealed an effect similar to castration. After combined treatment with E2 and 3 alpha-androstanediol (3 alpha-diol) TA completely suppressed squamous metaplasia. A 3 alpha-diol induced glandular proliferation, monitored by a positive histochemical reaction, and significantly elevated zinc, DNA and RNA contents prevailed. A partial stromal stimulation indicates stimulating effects of 3 alpha-diol too on the stroma. The antioestrogenic effects of tamoxifen on experimentally induced BPH mainly manifest at the E2 induced epithelial alterations. The abolishing effects at the stromal level are distinct but not so impressive.
通过组织学、组织化学和生物化学分析,研究了抗雌激素他莫昔芬(TA)对去势犬不同类型类固醇诱导的良性前列腺增生(BPH)的影响。单独使用17β-雌二醇(E2)进行6个月的治疗导致囊性和间质增生以及鳞状上皮化生,前列腺重量显著增加,总腺体的DNA和RNA含量显著增加。组织化学结果和锌值表明由于化生转化导致正常上皮功能丧失。TA可预防E2诱导的囊性和化生增生,而间质增殖显著降低但未消除。生化测定显示出与去势相似的效果。与E2和3α-雄甾二醇(3α-二醇)联合治疗后,TA完全抑制了鳞状化生。通过阳性组织化学反应监测,3α-二醇诱导的腺体增殖以及显著升高的锌、DNA和RNA含量依然存在。部分间质刺激表明3α-二醇对间质也有刺激作用。他莫昔芬对实验性诱导的BPH的抗雌激素作用主要表现在E2诱导的上皮改变上。在间质水平的消除作用明显但不太显著。