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去势犬中良性前列腺增生(BPH)的剂量依赖性激素诱导

Dose-dependent hormonal induction of benign prostatic hyperplasia (BPH) in castrated dogs.

作者信息

Juniewicz P E, Lemp B M, Barbolt T A, LaBrie T K, Batzold F H, Reel J R

机构信息

Department of Pharmacology, Sterling Research Group, Rensselaer, New York 12144.

出版信息

Prostate. 1989;14(4):341-52. doi: 10.1002/pros.2990140406.

DOI:10.1002/pros.2990140406
PMID:2473460
Abstract

A model for the dose-dependent hormonal induction of benign prostatic hyperplasia (BPH) in castrated dogs has been established using subcutaneously implanted Silastic capsules containing 5 alpha-androstane-3 alpha, 17 beta-diol (3 alpha-diol) and estradiol-17 beta. In vivo release rates per capsule approximated 122.0 +/- 4.2 micrograms 3 alpha-diol and 22.7 +/- 0.8 micrograms estradiol per day based on in vitro studies and resulted in dose-dependent increases in serum 3 alpha-diol and dihydrotestosterone concentrations. The implantation of castrated dogs with either 10 or 20 Silastic capsules containing 3 alpha-diol and one capsule containing estradiol or the intramuscular injection of 3 alpha-diol (75 mg/week) and estradiol (0.75 mg/week) for 99 days significantly increased (P less than .01) prostatic weights and total prostatic DNA over intact controls. These treatments also resulted in a histomorphological pattern similar to that observed in dogs with the glandular form of spontaneous BPH. In addition, normal prostatic secretory function as determined by semen volume was maintained in these dogs. Although subcutaneous implantation of five Silastic capsules containing 3 alpha-diol and one capsule containing estradiol into castrated dogs resulted in prostatic weights and total prostatic DNA that were similar (P less than .10) to intact controls, these prostates were characterized histomorphologically by glandular atrophy and squamous metaplasia. Furthermore, prostatic secretory function was decreased (P less than .05) in these animals compared with intact controls at 3 months of treatment. This study has led to the development of a model of steroid-induced BPH that will facilitate the evaluation of competitive androgen-receptor antagonists in the dog.

摘要

通过皮下植入含有5α-雄烷-3α,17β-二醇(3α-二醇)和雌二醇-17β的硅橡胶胶囊,已建立了去势犬良性前列腺增生(BPH)剂量依赖性激素诱导模型。基于体外研究,每个胶囊的体内释放率约为每天122.0±4.2微克3α-二醇和22.7±0.8微克雌二醇,导致血清3α-二醇和双氢睾酮浓度呈剂量依赖性增加。给去势犬植入10或20个含3α-二醇的硅橡胶胶囊和1个含雌二醇的胶囊,或肌肉注射3α-二醇(75毫克/周)和雌二醇(0.75毫克/周)99天,与完整对照组相比,前列腺重量和前列腺总DNA显著增加(P<0.01)。这些处理还导致了与自发性腺型BPH犬相似的组织形态学模式。此外,这些犬的精液量所测定的正常前列腺分泌功能得以维持。虽然给去势犬皮下植入5个含3α-二醇的硅橡胶胶囊和1个含雌二醇的胶囊,其前列腺重量和前列腺总DNA与完整对照组相似(P<0.10),但这些前列腺在组织形态学上的特征是腺萎缩和鳞状化生。此外,与完整对照组相比,在治疗3个月时这些动物的前列腺分泌功能降低(P<0.05)。本研究已促成了一种类固醇诱导的BPH模型的建立,这将有助于评估犬体内竞争性雄激素受体拮抗剂。

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