Tuzcu Mehmet, Özdemir Oğuzhan, Orhan Cemal, Şahin Nurhan, Morde Abhijeet, Padigaru Muralidhara, Bhanuse Prakash, Şahin Kazım
Department of Biology, Faculty of Science, Firat University, Elazığ, Turkiye.
Department of Veterinary Science, Technical Sciences Vocational School, Batman University, Batman, Turkiye.
Turk J Biol. 2023 Dec 14;48(1):59-69. doi: 10.55730/1300-0152.2682. eCollection 2024.
BACKGROUND/AIM: Exhausting exercise can damage muscle tissue due to free radical interactions. It is hypothesized that the increase in free radicals following muscle injury, either due to oxidative damage to biomolecules or the activation of inflammatory cytokines, may lead to secondary muscle damage. This study investigated the effects of a novel joint health formula (JHF) containing bisdemethoxycurcumin-enriched curcumin, 3-O-Acetyl-11-keto-beta-boswellic acid-enriched Boswellia (AKBA), and Ashwagandha on exhaustion time, grip strength, antioxidant status, and muscle-signaling proteins in exhaustively exercised rats.
Twenty-eight rats were divided into four groups: Control (C), exercise (E), E + JHF 100 (100 mg/kg), and E + JHF 200 (200 mg/kg).
An increase in time to exhaustion and grip strength was recorded with JHF supplementation in a dose-dependent manner (p < 0.0001). In addition, serum and muscle lactate dehydrogenase, malondialdehyde, myoglobin, creatine kinase, and lactic acid concentrations were decreased in the groups supplemented with JHF, particularly at the high dose of JHF (200 mg/kg) (p < 0.0001 for all). JHF supplementation also increased antioxidant enzyme activities and suppressed the production of inflammatory cytokines compared to the exercise group (p < 0.0001). Moreover, JHF reduced the levels of PGC-1α, p-70S6K1, MAFbx, MuRF1, and p-mTOR proteins in muscle tissue compared to the exercise group (p < 0.05), being more effective at high doses.
These findings show that JHF might reduce muscle damage by modulating antiinflammatory, antioxidant, and muscle mass regulatory pathways in exhausted training rats. At the same time, JHF improved exercise performance and grip strength.
背景/目的:力竭运动可因自由基相互作用而损伤肌肉组织。据推测,肌肉损伤后自由基增加,这可能是由于生物分子的氧化损伤或炎性细胞因子的激活,进而可能导致继发性肌肉损伤。本研究调查了一种新型关节健康配方(JHF),其含有富含双去甲氧基姜黄素的姜黄素、富含3-O-乙酰-11-酮-β-乳香酸的乳香(AKBA)以及南非醉茄,对力竭运动大鼠的力竭时间、握力、抗氧化状态和肌肉信号蛋白的影响。
28只大鼠分为四组:对照组(C)、运动组(E)、E + JHF 100(100毫克/千克)组和E + JHF 200(200毫克/千克)组。
补充JHF后,力竭时间和握力呈剂量依赖性增加(p < 0.0001)。此外,补充JHF的组中,血清和肌肉中的乳酸脱氢酶、丙二醛、肌红蛋白、肌酸激酶和乳酸浓度降低,尤其是高剂量JHF(200毫克/千克)组(所有p < 0.0001)。与运动组相比,补充JHF还增加了抗氧化酶活性并抑制了炎性细胞因子的产生(p < 0.0001)。此外,与运动组相比,JHF降低了肌肉组织中PGC-1α、p-70S6K1、MAFbx、MuRF1和p-mTOR蛋白的水平(p < 0.05),高剂量时更有效。
这些发现表明,JHF可能通过调节力竭训练大鼠的抗炎、抗氧化和肌肉质量调节途径来减少肌肉损伤。同时,JHF改善了运动表现和握力。