Osama Eman, Khowailed Effat, Rashed L, Fawzy A, Hassan Rokia Mohamad, Harb Inas, Maher Muhammad
Department of Medical Physiology, Faculty of Medicine, Cairo University, Giza, Egypt.
Department of Medical Biochemistry, Faculty of Medicine, Cairo University, Giza, Egypt.
Pflugers Arch. 2024 May;476(5):797-808. doi: 10.1007/s00424-024-02922-3. Epub 2024 Feb 17.
A common anthracycline antibiotic used to treat cancer patients is doxorubicin (DOX). One of the effects of DOX therapy is skeletal muscle fatigue. Our goal in this research was to study the beneficial effect of exercise on DOX-induced damaged muscle fibers and compare the effect of different exercise strategies (prophylactic, post- toxicity and combined) on DOX toxicity. Five groups were created from 40 male rats: group I, control group; group II, DOX was administered intraperitoneally for 2 weeks over 6 equal injections (each 2.5 mg/kg); group III, rats trained for 3 weeks before DOX; group IV, rats trained for 8 weeks after DOX; and group V, rats were trained for 3 weeks before DOX followed by 8 weeks after. Measures of oxidative damage (HO, catalase), inflammation (TNF-α), and glucose transporter 4 (GLUT4) expression on skeletal muscle were assessed. Also, Homeostatic Model Assessment for Insulin Resistance (HOMA-IR) was estimated. Skeletal performance was evaluated by contraction time (CT), half relaxation time (1/2 RT), and force-frequency relationship by the end of this research. The current study demonstrated a detrimental effect of DOX on skeletal performance as evidenced by a significant increase in CT and 1/2 RT compared to control; in addition, HO, TNF-α, and HOMA-IR were significantly increased with a significant decrease in GLUT4 expression and catalase activity. Combined exercise therapy showed a remarkable improvement in skeletal muscle performance, compared to DOX, CT, and 1/2 RT which were significantly decreased; HO and TNF-α were significantly decreased unlike catalase antioxidant activity that significantly increased; in addition, skeletal muscle glucose metabolism was significantly improved as GLUT4 expression significantly increased and HOMA-IR was significantly decreased. Exercise therapy showed significant improvement in all measured parameters relative to DOX. However, combined exercise therapy showed the best improvement relative to both pre-exercise and post-exercise groups.
一种用于治疗癌症患者的常见蒽环类抗生素是阿霉素(DOX)。DOX治疗的其中一个影响是骨骼肌疲劳。本研究的目的是研究运动对DOX诱导的受损肌纤维的有益作用,并比较不同运动策略(预防性、毒性发作后和联合性)对DOX毒性的影响。从40只雄性大鼠中分为五组:第一组为对照组;第二组,通过6次等量注射(每次2.5mg/kg)腹腔注射DOX,持续2周;第三组,在给予DOX前训练3周的大鼠;第四组,在给予DOX后训练8周的大鼠;第五组,在给予DOX前训练3周,随后在给予DOX后训练8周的大鼠。评估骨骼肌上氧化损伤(HO、过氧化氢酶)、炎症(肿瘤坏死因子-α)和葡萄糖转运蛋白4(GLUT4)表达的指标。此外,还评估了胰岛素抵抗的稳态模型评估(HOMA-IR)。在本研究结束时,通过收缩时间(CT)、半松弛时间(1/2 RT)和力-频率关系评估骨骼性能。当前研究表明,与对照组相比,CT和1/2 RT显著增加,证明DOX对骨骼性能有有害影响;此外,HO、肿瘤坏死因子-α和HOMA-IR显著增加,而GLUT4表达和过氧化氢酶活性显著降低。与DOX相比,联合运动疗法使骨骼肌性能有显著改善,CT和1/2 RT显著降低;HO和肿瘤坏死因子-α显著降低,而过氧化氢酶抗氧化活性显著增加;此外,随着GLUT4表达显著增加和HOMA-IR显著降低,骨骼肌葡萄糖代谢显著改善。相对于DOX,运动疗法在所有测量参数上均有显著改善。然而,相对于运动前和运动后组,联合运动疗法显示出最佳改善效果。