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低强度耐力运动加癸酸诺龙可调节心脏脂联素及其受体。

Low-intensity endurance exercise plus nandrolone decanoate modulates cardiac adiponectin and its receptors.

作者信息

Karimi A, Joukar S, Najafipour H, Masoumi-Ardakani Y, Shahouzehi B

机构信息

Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.

Cardiovascular Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran.

出版信息

Auton Autacoid Pharmacol. 2017 Mar;37(2):29-33. doi: 10.1111/aap.12056.

Abstract

Vast adverse effects of anabolic-androgenic steroids (AASs) on athletes' cardiovascular systems have been reported. However, there is still a lack of adequate information regarding the pathways and mechanisms involved. We tested the hypothesis that adiponectin and its receptors in the heart may be affected by long-term use of AASs alongside exercising. Male Wistar rats were randomized into the control (CTL), exercise (EX), nandrolone (Nan), arachis (Arach) group which treated with arachis as vehicle, trained vehicle (EX+Arach) and trained nandrolone (EX+Nan) groups that were treated for 8 weeks. One day after the end of the protocol, animals were sacrificed and their hearts were frozen. TNF-α and adiponectin proteins of hearts were evaluated quantitatively by ELISA kits, and Western blot analysis was used for measuring adiponectin receptor protein expression. TNF-α protein increased significantly in the EX+Nan group (P<.05 vs CTL group). The AdipoR1 protein was significantly higher in the presence of nandrolone alongside exercise (P<.05 vs Nan and EX+Arach groups, P<.01 vs CTL and Arach groups). In addition, AdipoR2 protein enhanced in the EX+Nan group when compared with the other groups (P<.05 vs EX and EX+Arach groups, P<.01 vs CTL, Arach and Nan groups). Chronic nandrolone plus mild endurance exercise may be associated with imbalance in pro-/anti-inflammatory cytokines and may induce a positive modulatory effect on cardiac adiporeceptors in rat. Further studies are required before these findings can be generalized to humans.

摘要

已有报道指出合成代谢雄激素类固醇(AASs)对运动员心血管系统有巨大的不良影响。然而,关于其中涉及的途径和机制仍缺乏足够信息。我们检验了这样一个假设:长期使用AASs并同时进行锻炼可能会影响心脏中的脂联素及其受体。将雄性Wistar大鼠随机分为对照组(CTL)、运动组(EX)、诺龙组(Nan)、花生油组(Arach)(用花生油作为赋形剂处理)、训练赋形剂组(EX + Arach)和训练诺龙组(EX + Nan),所有组均处理8周。在实验方案结束一天后,处死动物并将其心脏冷冻。通过酶联免疫吸附测定试剂盒定量评估心脏中的肿瘤坏死因子-α(TNF-α)和脂联素蛋白,并使用蛋白质印迹分析来测量脂联素受体蛋白表达。EX + Nan组中的TNF-α蛋白显著增加(与CTL组相比,P <.05)。在运动同时使用诺龙的情况下,AdipoR1蛋白显著更高(与Nan组和EX + Arach组相比,P <.05;与CTL组和Arach组相比,P <.01)。此外,与其他组相比,EX + Nan组中的AdipoR2蛋白有所增强(与EX组和EX + Arach组相比,P <.05;与CTL组、Arach组和Nan组相比,P <.01)。长期使用诺龙并进行轻度耐力运动可能与促炎/抗炎细胞因子失衡有关,并可能对大鼠心脏脂联素受体产生正向调节作用。在将这些发现推广到人类之前,还需要进一步研究。

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