Department of Orthopedics, Shanghai General Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 201620, China.
School of Medicine, Shanghai University, Shanghai 200444, China.
Biomolecules. 2021 Dec 28;12(1):41. doi: 10.3390/biom12010041.
Postmenopausal osteoporosis (PMOP) and sarcopenia are common diseases that predominantly affect postmenopausal women. In the occurrence and development of these two diseases, they are potentially pathologically connected with each other at various molecular levels. However, the application of metabolomics in sarco-osteoporosis and the metabolic rewiring happening throughout the estrogen loss-replenish process have not been reported. To investigate the metabolic alteration of sarco-osteoporosis and the possible therapeutical effects of estradiol, 24 mice were randomly divided into sham surgery, ovariectomy (OVX), and estradiol-treated groups. Three-dimensional reconstructions and histopathology examination showed significant bone loss after ovariectomy. Estrogen can well protect against OVX-induced bone loss deterioration. UHPLC-Q-TOF/MS was preformed to profile semi- polar metabolites of skeletal muscle samples from all groups. Metabolomics analysis revealed metabolic rewiring occurred in OVX group, most of which can be reversed by estrogen supplementation. In total, 65 differential metabolites were identified, and pathway analysis revealed that sarco-osteoporosis was related to the alterations in purine metabolism, glycerophospholipid metabolism, arginine biosynthesis, tryptophan metabolism, histidine metabolism, oxidative phosphorylation, and thermogenesis, which provided possible explanations for the metabolic mechanism of sarco-osteoporosis. This study indicates that an UHPLC-Q-TOF/MS-based metabolomics approach can elucidate the metabolic reprogramming mechanisms of sarco-osteoporosis and provide biological evidence of the therapeutical effects of estrogen on sarco-osteoporosis.
绝经后骨质疏松症 (PMOP) 和肌肉减少症是常见疾病,主要影响绝经后妇女。在这两种疾病的发生和发展过程中,它们在各种分子水平上可能存在潜在的病理联系。然而,代谢组学在肌-骨质疏松症中的应用以及贯穿雌激素缺失-补充过程中的代谢重排尚未被报道。为了研究肌-骨质疏松症的代谢变化以及雌二醇的可能治疗作用,将 24 只小鼠随机分为假手术、卵巢切除术 (OVX) 和雌二醇治疗组。三维重建和组织病理学检查显示卵巢切除后出现明显的骨丢失。雌激素能很好地防止 OVX 引起的骨丢失恶化。对所有组的骨骼肌样本进行了超高效液相色谱-四极杆飞行时间/质谱 (UHPLC-Q-TOF/MS) 进行半极性代谢物分析。代谢组学分析显示 OVX 组发生了代谢重排,其中大部分可通过雌激素补充得到逆转。总共鉴定出 65 种差异代谢物,通路分析显示肌-骨质疏松症与嘌呤代谢、甘油磷脂代谢、精氨酸生物合成、色氨酸代谢、组氨酸代谢、氧化磷酸化和产热的改变有关,这为肌-骨质疏松症的代谢机制提供了可能的解释。这项研究表明,基于 UHPLC-Q-TOF/MS 的代谢组学方法可以阐明肌-骨质疏松症的代谢重编程机制,并为雌激素对肌-骨质疏松症的治疗作用提供生物学证据。