Gårevik Nina, Rane Anders, Björkhem-Bergman Linda, Ekström Lena
Division of Clinical Pharmacology, Department of Laboratory Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
Subst Abuse Rehabil. 2014 Dec 10;5:121-7. doi: 10.2147/SAR.S71285. eCollection 2014.
To study the effect and time profile of different doses of testosterone enanthate on the blood lipid profile and gonadotropins.
Twenty-five healthy male volunteers aged 27-43 years were given 500 mg, 250 mg, and 125 mg of testosterone enanthate as single intramuscular doses of Testoviron(®) Depot. Luteinizing hormone (LH), follicle-stimulating hormone (FSH), blood lipid profile (total cholesterol, plasma [p-] low-density lipoprotein, p-high-density lipoprotein [HDL], p-apolipoprotein A1 [ApoA1], p-apolipoprotein B, p-triglycerides, p-lipoprotein(a), serum [s-] testosterone, and 25-hydroxyvitamin D3) were analyzed prior to, and 4 and 14 days after dosing. Testosterone and epitestosterone in urine (testosterone/epitestosterone ratio) were analyzed prior to each dose after a washout period of 6-8 weeks.
All doses investigated suppressed the LH and FSH concentrations in serum. LH remained suppressed 6 weeks after the 500 mg dose. These results indicate that testosterone has a more profound endocrine effect on the hypothalamic-pituitary-gonadal axis than was previously thought. There was no alteration in 25-hydroxyvitamin D3 levels after testosterone administration compared to baseline levels. The 250 and 500 mg doses induced decreased concentrations of ApoA1 and HDL, whereas the lowest dose (125 mg) did not have any effect on the lipid profile.
The single doses of testosterone produced a dose-dependent increase in serum testosterone concentrations together with suppression of s-LH and s-FSH. Alterations in ApoA1 and HDL were observed after the two highest single doses. It is possible that long-time abuse of anabolic androgenic steroids will lead to alteration in vitamin D status. Knowledge and understanding of the side effects of anabolic androgenic steroids are important to the treatment and care of abusers of testosterone.
研究不同剂量庚酸睾酮对血脂谱和促性腺激素的影响及时间变化情况。
25名年龄在27 - 43岁的健康男性志愿者,分别单次肌肉注射500mg、250mg和125mg的庚酸睾酮(Testoviron® Depot)。在给药前、给药后4天和14天分析促黄体生成素(LH)、促卵泡生成素(FSH)、血脂谱(总胆固醇、血浆低密度脂蛋白、血浆高密度脂蛋白[HDL]、血浆载脂蛋白A1[ApoA1]、血浆载脂蛋白B、血浆甘油三酯、血浆脂蛋白(a)、血清睾酮和25 - 羟基维生素D3)。在6 - 8周的洗脱期后,每次给药前分析尿液中的睾酮和表睾酮(睾酮/表睾酮比值)。
所有研究剂量均抑制血清中LH和FSH浓度。500mg剂量给药后6周LH仍被抑制。这些结果表明,睾酮对下丘脑 - 垂体 - 性腺轴的内分泌作用比之前认为的更为显著。与基线水平相比,睾酮给药后25 - 羟基维生素D3水平没有变化。250mg和500mg剂量导致ApoA1和HDL浓度降低,而最低剂量(125mg)对血脂谱没有任何影响。
单次剂量的睾酮使血清睾酮浓度呈剂量依赖性增加,同时抑制血清LH和血清FSH。在两个最高单次剂量后观察到ApoA1和HDL的变化。长期滥用合成代谢雄激素类固醇可能会导致维生素D状态改变。了解合成代谢雄激素类固醇的副作用对于睾酮滥用者的治疗和护理很重要。