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阻力训练和癸酸诺龙给药对小鼠心脏组织的影响。

The effect of resistance training and nandrolone decanoate administration on cardiac tissue in mice.

作者信息

Atias Yechiel, Ben-Zeev Tavor, Levi Chagai, Binman Lior, Hoffman Jay R

机构信息

School of Health Sciences, Ariel University, Israel.

School of Health Sciences, Ariel University, Israel.

出版信息

Steroids. 2025 Feb;214:109559. doi: 10.1016/j.steroids.2024.109559. Epub 2024 Dec 30.

Abstract

PURPOSE

This study examined the effect of resistance training (RT) by itself and in combination with supraphysiological administration of nandrolone decanoate (ND) on the inflammatory, apoptotic, and oxidative stress response in cardiac tissue. The effect of the training and androgen intervention on adiponectin expression, a potential cardio protectant was also examined.

METHODS

Forty male C57Bl/6J mice, 3 months of age were randomized into four groups (n = 10 per group). Two groups of animals performed a 3-day per week RT program for 7-weeks, while the other two groups remained sedentary (SED). The RT and SED animals were further randomized into an androgen group (RTA and SEDA, respectively) or a sham group (RTS and SEDS, respectively). Animals in the RTA and SEDA groups received 38-mg·kg injected once per week. Mice from RTS and SEDS received sham injections.

RESULTS

Main effects for group indicated that RT resulted in significant elevations in NFκβ (p < 0.001), glutamine peroxidase (GPX) (p = 0.007) and adiponectin (p < 0.001). Main effects for treatment indicated that ND administration resulted in greater elevations in NFκβ (p = 0.01) and TNF-α (p = 0.017). In addition, TNF-α expression was greater in RTA compared to RETS (p = 0.006) and the adiponectin response in RTA was greater (p's < 0.05) than all other groups. A significant correlation was noted between average training volume during the RT program and GPX expression (r = 0.716, p < 0.001).

CONCLUSION

Results indicate that RT and ND administration can increase markers of apoptosis and inflammation. Elevations in adiponectin expression suggest that it may act as a compensatory mechanism supporting cardiovascular health.

摘要

目的

本研究考察了阻力训练(RT)单独作用以及与癸酸诺龙(ND)超生理剂量联合使用对心脏组织炎症、凋亡和氧化应激反应的影响。同时还考察了训练和雄激素干预对脂联素表达(一种潜在的心脏保护剂)的影响。

方法

将40只3月龄雄性C57Bl/6J小鼠随机分为四组(每组n = 10)。两组动物每周进行3天的阻力训练计划,持续7周,而另外两组保持 sedentary(SED)状态。将进行阻力训练和SED的动物进一步随机分为雄激素组(分别为RTA和SEDA)或假手术组(分别为RTS和SEDS)。RTA组和SEDA组的动物每周注射一次38 mg·kg。RTS组和SEDS组的小鼠接受假注射。

结果

组间主效应表明,阻力训练导致NFκβ(p < 0.001)、谷氨酰胺过氧化物酶(GPX)(p = 0.007)和脂联素(p < 0.001)显著升高。处理主效应表明,给予ND导致NFκβ(p = 0.01)和TNF-α(p = 0.017)升高幅度更大。此外,与RETS相比,RTA组中TNF-α表达更高(p = 0.006),且RTA组中脂联素反应比所有其他组更大(p < 0.05)。在阻力训练计划期间的平均训练量与GPX表达之间存在显著相关性(r = 0.716,p < 0.001)。

结论

结果表明,阻力训练和给予ND可增加凋亡和炎症标志物。脂联素表达升高表明它可能作为支持心血管健康的一种代偿机制。

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