合成代谢类固醇“十酸诺龙”对成年雄性白化大鼠心脏和骨骼肌的毒性作用与水飞蓟素和胡芦巴种子提取物的潜在改善作用。

IF 2.8 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Dalia Abd Elwahab Hassan, Sherien S Ghaleb, Amr Reda Zaki, Ahmed Abdelmenem, Shimaa Nabil, Mostafa Abdallah Abdel Alim
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引用次数: 2

摘要

背景:合成代谢类固醇(AS)通常被健身者和运动员滥用,目的是增加他们的力量和肌肉质量,但不幸的是,长期使用AS可能会导致严重的副作用。癸酸诺龙是一类合成代谢雄激素类固醇,在全球范围内迅速传播,临床上和非法使用。我们的研究旨在评估合成代谢类固醇对雄性白化大鼠心脏和骨骼肌的毒性作用,并评估胡芦巴种子提取物和水飞蓟素的潜在改善作用。方法:选取雄性白化大鼠120只,随机分为6组;第一组:对照组,第二组:口服合成代谢类固醇癸酸诺龙,第三组:口服水飞蓟素,第四组:口服胡芦巴籽提取物,第五组:口服合成代谢类固醇癸酸诺龙和水飞蓟素,第六组:服用合成代谢类固醇癸酸诺龙和胡芦巴籽提取物。实验结束时,处死大鼠,采集血样进行生化分析,解剖标本进行组织病理学检查。结果:合成代谢类固醇对大鼠的毒性作用表现为血清高密度脂蛋白(HDL)水平显著降低,胆固醇、甘油三酯和低密度脂蛋白(LDL)水平显著升高。心肌肌钙蛋白I水平显著升高。心肌和骨骼肌的组织病理学检查显示明显的退行性改变和坏死。水飞蓟素和葫芦巴籽提取物对大鼠的生化和组织病理学变化均有保护作用。研究了水飞蓟素和胡芦巴籽提取物对心脏和骨骼肌的抗氧化作用,结果表明,与对照组相比,AS治疗大鼠组织中超氧化物歧化酶(SOD)、过氧化氢酶(过氧化氢酶)和还原性谷胱甘肽(GSH)水平降低。另一方面,组织丙二醛(MDA)水平升高。结论:合成代谢类固醇对白化病大鼠的心脏和骨骼肌有毒性作用,葫芦巴籽提取物和水飞蓟素对其有改善作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The toxic effects of anabolic steroids "nandrolone decanoate" on cardiac and skeletal muscles with the potential ameliorative effects of silymarin and fenugreek seeds extract in adult male albino rats.

The toxic effects of anabolic steroids "nandrolone decanoate" on cardiac and skeletal muscles with the potential ameliorative effects of silymarin and fenugreek seeds extract in adult male albino rats.

The toxic effects of anabolic steroids "nandrolone decanoate" on cardiac and skeletal muscles with the potential ameliorative effects of silymarin and fenugreek seeds extract in adult male albino rats.

Background: Anabolic steroids (AS) are commonly abused by body builders and athletes aiming to increase their strength and muscle mass but unfortunately, the long-term use of AS may lead to serious side effects. Nandrolone Decanoate is one of the Class II anabolic androgenic steroids which quickly spread globally and used clinically and illicitly. Our research was directed to assess the toxic effects of anabolic steroids on cardiac and skeletal muscles in male albino rats and to evaluate the potential ameliorative effects of fenugreek seeds extract and silymarin.

Methods: Our research was done on 120 male albino rats that were allocated into 6 groups; group I: Served as a control group, group II: Received the anabolic steroid Nandrolone Decanoate, group III: Received silymarin orally, group IV: Received fenugreek seeds extract orally, group (V): Received the anabolic steroid Nandrolone Decanoate and silymarin and group (VI): Received the anabolic steroid Nandrolone Decanoate and fenugreek seeds extract. By the end of the study, rats were sacrificed, and blood samples were collected for biochemical analysis and autopsy samples for histopathological examination.

Results: The anabolic steroids toxic effects on rats showed a significant decrease in serum High Density Lipoprotein (HDL) level and increase in cholesterol, triglycerides, and Low-Density Lipoprotein (LDL) levels. There was a significant elevation in cardiac troponin I level. As regards to histopathological examination of the cardiac and skeletal muscles, the study showed marked degenerative changes and necrosis. Both silymarin and fenugreek seeds extract provided a protective effect on the biochemical and histopathological changes. The antioxidant effects of silymarin and fenugreek seeds extract were evaluated on the heart, skeletal muscles and showed that, the tissue levels of Superoxide dismutase (SOD), Catalase and reduced glutathione (GSH) decreased in AS treated rats compared to the control group. On the other hand, the tissue Malondialdehyde (MDA) levels were elevated.

Conclusions: Anabolic steroids have a toxic effect on the cardiac and skeletal muscles of albino rats with improvement by treatment with fenugreek seeds extract and silymarin.

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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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