Resistance Training and Resveratrol Supplementation Improve Cancer Cachexia and Tumor Volume in Muscle Tissue of Male Mice Bearing Colon Cancer CT26 Cell Tumors.

IF 1.8 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mahdi Samadi, Farhad Daryanoosh, Zahra Mojtahedi, Afrooz Samsamy Pour, Hadi Nobari, Amir Hossein Zarifkar, Kayvan Khoramipour
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引用次数: 0

Abstract

Losing muscle functions due to reducing muscle mass and quality is one of the main features of cancer cachexia that impairs patients' quality of life and decrease their survival. This study aimed to investigate the synergistic effects of resistance training and resveratrol supplementation on cachexia induced by CT26 tumors in male mice. Forty-eight mice were divided into eight groups randomly: healthy sedentary vehicle (HSV), healthy exercise vehicle (HEV), healthy sedentary resveratrol (HSR), healthy exercise resveratrol (HER), CT-26 tumor-bearing sedentary vehicle (TSV), CT-26 tumor-bearing exercise vehicle (TEV), CT-26 tumor-bearing sedentary resveratrol (TSR) and CT-26 tumor-bearing exercise resveratrol (TER). Training groups performed ladder climbing with weights tied to their tails, for six weeks. Resveratrol-treated groups received 50 mg/kg daily by gavage. The results showed muscle weight, and mTORC1 phosphorylation decreased in TSV compared to the HSV group. mTORC1 phosphorylation was increased in TER compared to TSV, TEV, and TSR. In addition, AMPK phosphorylation was more elevated in HER compared to HSV, HEV, and HSR. LC3BII/I ratio was higher in TSV than HSV group. Tumor volume was increased in all groups, with the lowest increase in TER group. In tumor tissue, mTORC1 phosphorylation was decreased in TER than in TSV, TEV, and TSR groups; AMPK phosphorylation and LC3BII/I ratio were increased in TSV than in TEV, TSR, and TER groups. In conclusion, the synergistic effect of resistance training and resveratrol supplementation is the most effective in reducing tumor volume. These advantages were mostly in line with molecular findings.

阻力训练和补充白藜芦醇可改善结肠癌 CT26 细胞瘤雄性小鼠肌肉组织的癌痛和肿瘤体积。
因肌肉质量和质量下降而丧失肌肉功能是癌症恶病质的主要特征之一,它会损害患者的生活质量并降低其生存率。本研究旨在探讨阻力训练和补充白藜芦醇对CT26肿瘤诱导的雄性小鼠恶病质的协同作用。48只小鼠被随机分为8组:健康静坐载体(HSV)、健康运动载体(HEV)、健康静坐白藜芦醇(HSR)、健康运动白藜芦醇(HER)、CT-26肿瘤携带者静坐载体(TSV)、CT-26肿瘤携带者运动载体(TEV)、CT-26肿瘤携带者静坐白藜芦醇(TSR)和CT-26肿瘤携带者运动白藜芦醇(TER)。训练组进行爬梯运动,在其尾巴上绑上重物,为期六周。白藜芦醇治疗组每天灌胃 50 毫克/千克白藜芦醇。结果表明,与 HSV 组相比,TSV 组的肌肉重量和 mTORC1 磷酸化降低;与 TSV、TEV 和 TSR 相比,TER 组的 mTORC1 磷酸化增加。此外,与 HSV、HEV 和 HSR 相比,HER 的 AMPK 磷酸化程度更高。TSV 组的 LC3BII/I 比率高于 HSV 组。所有组的肿瘤体积都有所增加,TER 组的肿瘤体积增加最少。在肿瘤组织中,TER 组的 mTORC1 磷酸化低于 TSV、TEV 和 TSR 组;TSV 组的 AMPK 磷酸化和 LC3BII/I 比率高于 TEV、TSR 和 TER 组。总之,阻力训练和补充白藜芦醇的协同作用对减少肿瘤体积最为有效。这些优势与分子研究结果基本一致。
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来源期刊
Cell Biochemistry and Biophysics
Cell Biochemistry and Biophysics 生物-生化与分子生物学
CiteScore
4.40
自引率
0.00%
发文量
72
审稿时长
7.5 months
期刊介绍: Cell Biochemistry and Biophysics (CBB) aims to publish papers on the nature of the biochemical and biophysical mechanisms underlying the structure, control and function of cellular systems The reports should be within the framework of modern biochemistry and chemistry, biophysics and cell physiology, physics and engineering, molecular and structural biology. The relationship between molecular structure and function under investigation is emphasized. Examples of subject areas that CBB publishes are: · biochemical and biophysical aspects of cell structure and function; · interactions of cells and their molecular/macromolecular constituents; · innovative developments in genetic and biomolecular engineering; · computer-based analysis of tissues, cells, cell networks, organelles, and molecular/macromolecular assemblies; · photometric, spectroscopic, microscopic, mechanical, and electrical methodologies/techniques in analytical cytology, cytometry and innovative instrument design For articles that focus on computational aspects, authors should be clear about which docking and molecular dynamics algorithms or software packages are being used as well as details on the system parameterization, simulations conditions etc. In addition, docking calculations (virtual screening, QSAR, etc.) should be validated either by experimental studies or one or more reliable theoretical cross-validation methods.
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