Cristina Romeo Teodor, Hanganu Flavia, Brezovan Diana, Dumitrescu Eugenia, Muselin Florin, Chiurciu Viorica, Stancu Adrian Constantin, Pentea Marius Cristian, Motoc Andrei Gheorghe Marius
Department of Pharmacology and Pharmacy, Faculty of Veterinary Medicine, Banat's University of Agriculture and Veterinary Medicine, Timisoara, Romania;
Rom J Morphol Embryol. 2014;55(3 Suppl):1143-8.
The objective was the cytoarchitecture evaluation of known steroid dependent target tissues after administering of testosterone, compared to action of its more active ester, nortestosterone (nandrolone decanoate) in castrated rat males in the aim of Hershberger bio test. Study was performed on 30 castrated male Wistar rats, aged between 35 and 39 days, in peripubertal period, divided into five groups. Androgen doses administration begun at the rats' age of 49 days. Animals were injected i.m., daily, for 10 consecutive days as follows: Aquatest (Balkan Pharmaceuticals Ltd., Moldova) testosterone aqueous solution: Testosterone I group (0.4 mg/animal); Testosterone II (0.8 mg/animal); (Deca-Durabolin, Balkan Pharmaceuticals); nandrolone decanoate oily solution: Nortestosterone I (1.5 mg/kg body weight); Nortestosterone II (7.5 mg/kg body weight) and Control (White sesame oil, Manicos, Romania, 0.1 mL/animal). Gonadectomy (GDX) induced modifications of target tissues wet weight accompanied by important modifications in cytoarchitecture. Changes following exogenous administration of testosterone and nortestosterone decanoate were found in: liver (granular dystrophy, mega-mitochondria, tubular intumescences), prostate (increasing of the structural elements), seminal vesicles (hyalinosis, thickening of cell walls and the hyaline presence), levator ani-bulbo-cavernosus muscle (muscle fibbers dilacerations), bulbourethral glands (muscular fibbers rarefaction by fluid accumulation) demonstrating the disruptor activity especially for overdosed nandrolone decanoate.
目的是在赫什伯格生物试验中,对去势雄性大鼠给予睾酮后,与其活性更高的酯诺龙(癸酸诺龙)的作用相比较,对已知的类固醇依赖性靶组织进行细胞结构评估。研究选取了30只35至39日龄处于青春期前期的去势雄性Wistar大鼠,分为五组。雄激素剂量在大鼠49日龄时开始给予。动物每天肌肉注射,连续注射10天,具体如下:水睾酮(摩尔多瓦巴尔干制药有限公司)水溶液:睾酮I组(0.4毫克/只动物);睾酮II组(0.8毫克/只动物);(癸酸诺龙,巴尔干制药);癸酸诺龙油溶液:诺龙I组(1.5毫克/千克体重);诺龙II组(7.5毫克/千克体重)以及对照组(罗马尼亚马尼科斯的白芝麻油,0.1毫升/只动物)。性腺切除术(GDX)导致靶组织湿重改变,并伴有细胞结构的重要改变。在外源性给予睾酮和癸酸诺龙后,在以下组织中发现了变化:肝脏(颗粒性营养不良、巨型线粒体、肾小管肿大)、前列腺(结构成分增加)、精囊(透明变性、细胞壁增厚和透明物质存在)、提肛肌-球海绵体肌(肌纤维撕裂)、尿道球腺(因液体蓄积导致肌纤维稀疏),表明尤其是过量的癸酸诺龙具有破坏活性。