Ahmad N, Warren D W, Haltmeyer G C
Anat Rec. 1978 Dec;192(4):543-54. doi: 10.1002/ar.1091920408.
The effects of 5alpha-androstane-3alpha, 17beta-diol (3alpha-diol) and 5alpha-androstane-3beta, 17beta-diol (3beta-diol) were studied in rats hypophysectomized and treated daily for 30 days with the steroids, starting on the day of surgery (hypophysectomized, H) or 30 days following the removal of pituitary (hypophysectomized regressed, HR). The ability of 3beta-diol to maintain and restimulate the prostate glands and seminal vesicles of castrated (C) and castrated regressed (CR) rats, respectively, was also studied. This androgen (3beta-diol) was able to maintain as well as rejuvenate to some degree the sexual accessory glands of all treatment groups. The prostate glands and seminal vesicles in both castrated experimental groups showed increased stimulation with progressively higher dosages of 3beta-diol. At all dose levels, stimulation of seminal vesicles of CR rats was comparable to that of non-regressed castrates. The prostate glands, on the other hand, showed better maintenance in the higher dosage group. In H rats, the stimulation of sexual accessory glands by both androgens was not significantly different than normal controls. The seminal vesicles and prostate glands of HR rats treated with 3alpha-diol were well stimulated and comparable to those of H rats treated with 3alpha-diol. The seminal vesicles of HR rats treated with 3beta-diol were also well stimulated, though not to the extent as those with 3alpha-diol treatment. The prostate glands of the 3beta-diol treated HR rats were significantly smaller than those of the 3alpha-diol treatment group. However, these miniature glands were morphologically stimulated as evidenced by mitosis of parenchymal cells and accumulation of secretory products in the alveoli. This study clearly indicates that 3beta-diol is biologically active and the degree of stimulation varies with the animal preparation in which the androgens were tested.
研究了5α-雄甾烷-3α,17β-二醇(3α-二醇)和5α-雄甾烷-3β,17β-二醇(3β-二醇)对大鼠的影响。这些大鼠在手术当天(去垂体,H组)或垂体切除30天后(去垂体衰退,HR组)接受垂体切除,并每天用这些类固醇治疗30天。还研究了3β-二醇分别维持和重新刺激去势(C组)和去势衰退(CR组)大鼠前列腺和精囊的能力。这种雄激素(3β-二醇)能够维持并在一定程度上使所有治疗组的性附属腺恢复活力。两个去势实验组的前列腺和精囊随着3β-二醇剂量的逐渐增加而受到更强的刺激。在所有剂量水平下,CR组大鼠精囊受到的刺激与未衰退的去势大鼠相当。另一方面,前列腺在较高剂量组中表现出更好的维持效果。在H组大鼠中,两种雄激素对性附属腺的刺激与正常对照组无显著差异。用3α-二醇治疗的HR组大鼠的精囊和前列腺受到良好刺激,与用3α-二醇治疗的H组大鼠相当。用3β-二醇治疗的HR组大鼠的精囊也受到良好刺激,尽管程度不如用3α-二醇治疗的大鼠。用3β-二醇治疗的HR组大鼠的前列腺明显小于3α-二醇治疗组。然而,这些微型腺体在形态上受到刺激,表现为实质细胞的有丝分裂和肺泡中分泌产物的积累。这项研究清楚地表明,3β-二醇具有生物活性,并且刺激程度随测试雄激素的动物模型不同而变化。