Nephrology and Kidney Transplant Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran; Department of Physiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Nephrology and Kidney Transplant Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran; Department of Physiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Steroids. 2024 Nov;211:109503. doi: 10.1016/j.steroids.2024.109503. Epub 2024 Aug 27.
Anabolic-androgenic steroids (AAS) abuse is linked to some abnormalities in several tissues including the kidney. However, the precise molecular mediators involved in AAS-induced kidney disorder remain elusive. The main objective of the present study was to investigate the effect of Nandrolone decanoate on kidney injury alone or in combination with moderate exercise and its related mechanisms. Thirty-two male Wistar rats were subdivided randomly into four groups. control (Con), Nandrolone (10 mg/kg)(N), Exercise (Exe), Nandrolone + Exercise (N+Exe). RESULTS: After 6 weeks, nandrolone treatment led to a significant increase in functional parameters such as serum cystatin c, urea, creatinine, albuminuria and Albumin/ creatinine ratio indicating kidney dysfunction. Moreover, nandrolone treatment increased vacuolization, focal inflammation, hemorragia, cast formation fibrosis in the renal tissue of rats. miRNA-146a increased in kidney tissue after nandrolone exposure by using RT-PCR which may be considered idealtheranomiRNAcandidates for diagnosis and treatment. Western blotting indicated that IRAK1, TRAF6, TNF-α, NF-κB, iNOS and TGF-β protein expressions were considerably elevated in the kidneys of nandrolone treated rats. Moderate exercise could alleviate the renal dysfunction, histological abnormalities and aforementioned proteins. Our findings suggested that nandrolone consumption can cause damage to kidney tissue probably through miRNA-146a targeting IRAK1 and TRAF6 via activation of the NF-κB and TGF-β pathway. These results provide future lines of research in the identification of theranoMiRNAs related to nandrolone treatment, which can be ameliorated by moderate exercise.
合成代谢雄激素类固醇(AAS)滥用与包括肾脏在内的几种组织的一些异常有关。然而,与 AAS 诱导的肾脏疾病相关的确切分子介质仍不清楚。本研究的主要目的是研究癸酸诺龙单独或与中等强度运动联合对肾脏损伤的影响及其相关机制。32 只雄性 Wistar 大鼠随机分为四组。对照组(Con)、癸酸诺龙(10mg/kg)(N)、运动组(Exe)、癸酸诺龙+运动组(N+Exe)。结果:6 周后,诺龙治疗导致血清胱抑素 C、尿素、肌酐、蛋白尿和白蛋白/肌酐比值等功能参数显著增加,表明肾功能障碍。此外,诺龙治疗增加了大鼠肾脏组织中的空泡化、局灶性炎症、出血、铸型形成和纤维化。通过 RT-PCR 发现,诺龙暴露后肾脏组织中 miRNA-146a 增加,这可能被认为是诊断和治疗的理想治疗性 miRNA 候选物。Western blot 表明,诺龙处理大鼠肾脏中 IRAK1、TRAF6、TNF-α、NF-κB、iNOS 和 TGF-β 蛋白表达显著升高。中等强度运动可减轻肾功能障碍、组织学异常和上述蛋白。我们的研究结果表明,诺龙的摄入可能会导致肾脏组织损伤,可能是通过 miRNA-146a 靶向 IRAK1 和 TRAF6,从而激活 NF-κB 和 TGF-β 通路。这些结果为识别与诺龙治疗相关的治疗性 miRNA 提供了未来的研究方向,适度运动可以改善这些 miRNA。