Carvalho Fabiano B, Bueno Andressa, Lhamas Cibele L, Gutierres Jessié M, Carvalho Mariana B, Brusco Indiara, Oliveira Sara M, Bottari Nathieli B, Silva Aniélen D, Miron Vanessa V, Alves Mariana S, Leitemperger Jossiele W, Loro Vânia L, Schetinger Maria Rosa C, Morsch Vera M, de Andrade Cinthia M
Graduate Program in Veterinary Medicine, Veterinary Hospital, Federal University of Santa Maria, Av. Roraima, 1000, Santa Maria 97105-900, RS, Brazil; Graduate Program in Biological Sciences: Biochemical Toxicology, Center for Natural and Exact Sciences, Federal University of Santa Maria, Av. Roraima, 1000, Santa Maria 97105-900, RS, Brazil.
Graduate Program in Veterinary Medicine, Veterinary Hospital, Federal University of Santa Maria, Av. Roraima, 1000, Santa Maria 97105-900, RS, Brazil.
Steroids. 2020 Sep;161:108670. doi: 10.1016/j.steroids.2020.108670. Epub 2020 May 27.
We investigated the adverse effects of the anabolic androgenic steroids (AAS) boldenone (BOL) and stanazolol (ST) on the enzymatic antioxidant systems of the rat liver. Male Wistar rats were divided in three protocols (P): PI, 5 mg/kg BOL or ST once a week for 4 weeks; PII, 2.5 mg/kg BOL or ST once a week for 8 weeks; PIII, 1.25 mg/kg BOL or ST once a week for 12 weeks. AAS were administered intramuscularly (0.2 ml, olive oil vehicle) once a week in all protocols. Activities of the enzymes glutathione peroxidase (GPx), glutathione S-transferase (GST), and glutathione reductase (GR), superoxide dismutase (SOD), catalase (CAT), were investigated. We assessed the content of hydrogen peroxide (HO), glycogen and lactate; and enzyme markers of neutrophils (myeloperoxidase, MPO) and macrophages (NAGase). PI and PII altered the SOD and CAT activities and increased the HO content. PI led to increases in the MPO and NAGase activities. In contrast, changes in GPx, GST and, GR were observed under PII and, to a greater extend, under PIII. Following PIII, GPx, GR, and GST exhibited reduced activities. All protocols altered the glycogen and lactate content. The use of high doses of AAS for a short duration first alters SOD/CAT activity. In contrast, at lower doses of AAS for long periods is associated with changes in the glutathione system. Protocols with high doses of AAS for a short duration exert the most deleterious effects on redox status, markers of cellular infiltration, and the metabolic functioning of hepatic tissues.
我们研究了合成代谢雄激素类固醇(AAS)苯丙酸诺龙(BOL)和司坦唑醇(ST)对大鼠肝脏酶促抗氧化系统的不良影响。将雄性Wistar大鼠分为三个方案组(P):PI组,每周一次注射5mg/kg的BOL或ST,共4周;PII组,每周一次注射2.5mg/kg的BOL或ST,共8周;PIII组,每周一次注射1.25mg/kg的BOL或ST,共12周。在所有方案组中,每周一次肌肉注射AAS(0.2ml,橄榄油载体)。研究了谷胱甘肽过氧化物酶(GPx)、谷胱甘肽S-转移酶(GST)、谷胱甘肽还原酶(GR)、超氧化物歧化酶(SOD)、过氧化氢酶(CAT)的活性。我们评估了过氧化氢(HO)、糖原和乳酸的含量;以及中性粒细胞(髓过氧化物酶,MPO)和巨噬细胞(NAGase)的酶标志物。PI组和PII组改变了SOD和CAT的活性,并增加了HO的含量。PI组导致MPO和NAGase活性增加。相比之下,在PII组观察到GPx、GST和GR的变化,在PIII组变化更大。在PIII组之后,GPx、GR和GST的活性降低。所有方案组都改变了糖原和乳酸的含量。短时间使用高剂量的AAS首先会改变SOD/CAT的活性。相比之下,长时间使用低剂量的AAS与谷胱甘肽系统的变化有关。短时间使用高剂量AAS的方案对氧化还原状态、细胞浸润标志物和肝组织的代谢功能产生最有害的影响。