Research Institute of Sport and Exercise Science, Liverpool John Moores University, Liverpool, UK.
Faculty of Science, Liverpool Hope University, Liverpool, UK.
Rev Endocr Metab Disord. 2021 Jun;22(2):389-405. doi: 10.1007/s11154-020-09616-y. Epub 2020 Dec 2.
It is estimated 6.4% of males and 1.6% of females globally use anabolic-androgenic steroids (AAS), mostly for appearance and performance enhancing reasons. In combination with resistance exercise, AAS use increases muscle protein synthesis resulting in skeletal muscle hypertrophy and increased performance. Primarily through binding to the androgen receptor, AAS exert their hypertrophic effects via genomic, non-genomic and anti-catabolic mechanisms. However, chronic AAS use also has a detrimental effect on metabolism ultimately increasing the risk of cardiovascular disease (CVD). Much research has focused on AAS effects on blood lipids and lipoproteins, with abnormal concentrations of these associated with insulin resistance, hypertension and increased visceral adipose tissue (VAT). This clustering of interconnected abnormalities is often referred as metabolic syndrome (MetS). Therefore, the aim of this review is to explore the impact of AAS use on mechanisms of muscle hypertrophy and markers of MetS. AAS use markedly decreases high-density lipoprotein cholesterol (HDL-C) and increases low-density lipoprotein cholesterol (LDL-C). Chronic AAS use also appears to cause higher fasting insulin levels and impaired glucose tolerance and possibly higher levels of VAT; however, research is currently lacking on the effects of AAS use on glucose metabolism. While cessation of AAS use can restore normal lipid levels, it may lead to withdrawal symptoms such as depression and hypogonadism that can increase CVD risk. Research is currently lacking on effective treatments for withdrawal symptoms and further long-term research is warranted on the effects of AAS use on metabolic health in males and females.
据估计,全球有 6.4%的男性和 1.6%的女性使用合成代谢雄激素类固醇(AAS),主要是出于改善外貌和提高运动表现的目的。与阻力运动相结合,AAS 的使用会增加肌肉蛋白质的合成,从而导致骨骼肌肥大和运动表现的提高。AAS 主要通过与雄激素受体结合,通过基因组、非基因组和抗分解代谢机制发挥其肥大作用。然而,慢性 AAS 使用也会对代谢产生不利影响,最终增加心血管疾病(CVD)的风险。许多研究都集中在 AAS 对血液脂质和脂蛋白的影响上,这些异常与胰岛素抵抗、高血压和内脏脂肪组织(VAT)增加有关。这种相互关联的异常的聚集通常被称为代谢综合征(MetS)。因此,本综述的目的是探讨 AAS 使用对肌肉肥大机制和 MetS 标志物的影响。AAS 使用显著降低高密度脂蛋白胆固醇(HDL-C)并增加低密度脂蛋白胆固醇(LDL-C)。慢性 AAS 使用似乎还会导致更高的空腹胰岛素水平、糖耐量受损和可能更高的 VAT 水平;然而,目前关于 AAS 使用对葡萄糖代谢影响的研究还很缺乏。虽然停止 AAS 使用可以恢复正常的血脂水平,但它可能导致停药症状,如抑郁和性腺功能减退,这会增加 CVD 的风险。目前缺乏有效的停药症状治疗方法,需要对男性和女性 AAS 使用对代谢健康的长期影响进行进一步的研究。