Mistry D, Buchanan L, Dattani G, Weaver P, Riches A
Prostate. 1982;3(3):291-9. doi: 10.1002/pros.2990030310.
The proliferative responses of rat prostate and human benign prostatic hyperplasia have been followed in organ culture using [125I] iododeoxyuridine uptake to monitor DNA synthesis. In serum-free cultures, testosterone induced a marked increase in DNA synthesis (three-fold) in 4- to 6-month-old rat prostates at concentrations of 4 x 10(-9) to 4 x 10(-6) M, whereas in greater than 12-month-old rat prostates the response was less marked. Human benign prostatic hyperplasia also showed an increased uptake at similar testosterone concentrations and of a similar magnitude to the response of greater than 12-month-old rat prostates. At 10(-5) M DNA synthesis was markedly suppressed in cultures of both rat and human prostate. The proliferative response of human benign prostatic hyperplasia increases up to days 3 to 4 in culture and then declines in both control and hormone-treated groups and may represent repair processes which appear to be hormone dependent.
利用[125I]碘脱氧尿苷摄取来监测DNA合成,在器官培养中追踪了大鼠前列腺和人良性前列腺增生的增殖反应。在无血清培养中,睾酮在4×10(-9)至4×10(-6)M浓度下,使4至6月龄大鼠前列腺中的DNA合成显著增加(三倍),而在大于12月龄的大鼠前列腺中,反应则不那么明显。人良性前列腺增生在相似的睾酮浓度下也显示出摄取增加,且幅度与大于12月龄大鼠前列腺的反应相似。在10(-5)M时,大鼠和人前列腺培养物中的DNA合成均被显著抑制。人良性前列腺增生的增殖反应在培养至第3至4天时增加,然后在对照组和激素处理组中均下降,这可能代表了似乎依赖激素的修复过程。