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康力龙和/或滥用大麻对雄性白化大鼠心肌肥厚机制和氧化应激的影响与运动的关系:运动滥用的实践。

Effect of Stanozolol and/or Cannabis Abuse on Hypertrophic Mechanism and Oxidative Stress of Male Albino Rat Cardiac Tissue in Relation to Exercise: A Sport Abuse Practice.

机构信息

Narcotics, Ergogenics and Poisons Department, Medical Research and Clinical Studies Institute, National Research Centre, Dokki, P.O. 12622, Giza, Egypt.

出版信息

Cardiovasc Toxicol. 2024 Jun;24(6):527-538. doi: 10.1007/s12012-024-09859-0. Epub 2024 May 8.

Abstract

Adolescents commonly co-abuse many drugs including anabolic androgenic steroids either they are athletes or non-athletes. Stanozolol is the major anabolic used in recent years and was reported grouped with cannabis. The current study aimed at evaluating the biochemical and histopathological changes related to the hypertrophic effects of stanozolol and/or cannabis whether in condition of exercise practice or sedentary conditions. Adult male Wistar albino rats received either stanozolol (5 mg/kg, s.c), cannabis (10 mg/kg, i.p.), and a combination of both once daily for two months. Swimming exercise protocol was applied as a training model. Relative heart weight, oxidative stress biomarkers, cardiac tissue fibrotic markers were evaluated. Left ventricular morphometric analysis and collagen quantification was done. The combined treatment exhibited serious detrimental effects on the heart tissues. It increased heart tissue fibrotic markers (Masson's trichrome stain (p < 0.001), cardiac COL3 (p < 0.0001), and VEGF-A (p < 0.05)), lowered heart glutathione levels (p < 0.05) and dramatically elevated oxidative stress (increased malondialdehyde (p < 0.0001) and 8-OHDG (p < 0.0001)). Training was not ameliorating for the observed effects. Misuse of cannabis and stanozolol resulted in more hypertrophic consequences of the heart than either drug alone, which were at least largely assigned to oxidative stress, heart tissue fibrotic indicators, histological alterations, and morphometric changes.

摘要

青少年通常会滥用多种药物,包括合成代谢雄激素类固醇,无论他们是否是运动员。司坦唑醇是近年来主要使用的合成代谢药物,据报道与大麻一起使用。本研究旨在评估与司坦唑醇和/或大麻的肥大效应相关的生化和组织病理学变化,无论是否在运动实践或久坐条件下。成年雄性 Wistar 白化大鼠每天接受一次 5mg/kg 的司坦唑醇(皮下注射)、10mg/kg 的大麻(腹腔注射)和两者的组合,持续两个月。游泳运动方案被用作训练模型。评估相对心脏重量、氧化应激生物标志物、心脏组织纤维化标志物。进行左心室形态计量分析和胶原定量。联合治疗对心脏组织表现出严重的不良影响。它增加了心脏组织纤维化标志物(马松三色染色(p<0.001)、心脏 COL3(p<0.0001)和 VEGF-A(p<0.05)),降低了心脏谷胱甘肽水平(p<0.05),并显著增加了氧化应激(增加了丙二醛(p<0.0001)和 8-OHDG(p<0.0001))。训练并不能改善观察到的效果。大麻和司坦唑醇的滥用导致心脏的肥大后果比单独使用任何一种药物都更严重,这些后果至少在很大程度上归因于氧化应激、心脏组织纤维化指标、组织学改变和形态计量变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/35c8/11102414/efbda38b1d0d/12012_2024_9859_Fig1_HTML.jpg

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