Department of Clinical and Biological Sciences, University of Turin, 10125 Turin, Italy.
Nutrients. 2024 Apr 26;16(9):1302. doi: 10.3390/nu16091302.
Oleocanthal (OC) is a monophenol of extra-virgin olive oil (EVOO) endowed with antibiotic, cardioprotective and anticancer effects, among others, mainly in view of its antioxidant and anti-inflammatory properties. OC has been largely investigated in terms of its anticancer activity, in Alzheimer disease and in collagen-induced arthritis; however, the possibility that it can also affect muscle biology has been totally overlooked so far. This study is the first to describe that OC modulates alterations induced in C2C12 myotubes by stimuli known to induce muscle wasting in vivo, namely TNF-α, or in the medium conditioned by the C26 cachexia-inducing tumor (CM-C26). C2C12 myotubes were exposed to CM-C26 or TNF-α in the presence or absence of OC for 24 and 48 h and analyzed by immunofluorescence and Western blotting. In combination with TNF-α or CM-C26, OC was revealed to be able to restore both the myotube's original size and morphology and normal levels of both atrogin-1 and MuRF1. OC seems unable to impinge on the autophagic-lysosomal proteolytic system or protein synthesis. Modulations towards normal levels of the expression of molecules involved in myogenesis, such as Pax7, myogenin and MyHC, were also observed in the myotube cultures exposed to OC and TNF-α or CM-C26. In conclusion, the data presented here show that OC exerts a protective action in C2C12 myotubes exposed to TNF-α or CM-C26, with mechanisms likely involving the downregulation of ubiquitin-proteasome-dependent proteolysis and the partial relief of myogenic differentiation impairment.
油橄榄苦素 (OC) 是特级初榨橄榄油 (EVOO) 中的一种单酚,具有抗生素、心脏保护和抗癌等作用,主要归因于其抗氧化和抗炎特性。OC 的抗癌活性、阿尔茨海默病和胶原诱导性关节炎等方面已经进行了广泛研究,但迄今为止,人们完全忽略了它可能影响肌肉生物学的可能性。这项研究首次描述了 OC 可调节已知可在体内诱导肌肉消耗的刺激(即 TNF-α)或 C26 致恶病质肿瘤(CM-C26)条件培养基(CM-C26)诱导的 C2C12 肌管中的变化。C2C12 肌管在存在或不存在 OC 的情况下分别用 CM-C26 或 TNF-α孵育 24 和 48 小时,并通过免疫荧光和 Western blot 进行分析。与 TNF-α或 CM-C26 联合使用时,OC 被证明能够恢复肌管的原始大小和形态,以及 atrogin-1 和 MuRF1 的正常水平。OC 似乎无法影响自噬溶酶体蛋白水解系统或蛋白质合成。在暴露于 OC 和 TNF-α或 CM-C26 的肌管培养物中,还观察到与肌生成相关分子的表达水平向正常水平的调节,如 Pax7、myogenin 和 MyHC。总之,这里呈现的数据表明,OC 对暴露于 TNF-α或 CM-C26 的 C2C12 肌管发挥保护作用,其机制可能涉及下调泛素蛋白酶体依赖性蛋白水解和部分缓解肌生成分化受损。