Messeha Samia S, Fidudusola Fidara F, Gendy Sherif, Latinwo Lekan M, Odewumi Caroline O, Soliman Karam F A
College of Science and Technology, Florida A&M University, Tallahassee, FL 32307, USA.
College of Pharmacy and Pharmaceutical Sciences, Institute of Public Health, Florida A&M University, Tallahassee, FL 32307, USA.
Nutrients. 2025 Jan 13;17(2):267. doi: 10.3390/nu17020267.
Biological aging is a substantial change that leads to different diseases, including osteoporosis (OP), a condition involved in loss of bone density, deterioration of bone structure, and increased fracture risk. In old people, there is a natural decline in bone mineral density (BMD), exacerbated by hormonal changes, particularly during menopause, and it continues in the early postmenopausal years. During this transition time, hormonal alterations are linked to elevated oxidative stress (OS) and decreased antioxidant defenses, leading to a significant increase in OP. Aging is significantly associated with an abnormal ratio of oxidant/antioxidant and modified nuclear factor erythroid-derived two related factor2 (Nrf2)/Kelch-like ECH-associated protein 1 (Keap1) pathway. OS adversely affects bone health by promoting osteoclastic (bone resorbing) activity and impairing osteoblastic (bone-forming cells). Nrf2 is critical in controlling OS and various cellular processes. The expression of Nrf2 is linked to multiple age-related diseases, including OP, and Nrf2 deficiency leads to unbalanced bone formation/resorption and a consequent decline in bone mass. Various drugs are available for treating OP; however, long-term uses of these medicines are implicated in diverse illnesses such as cancer, cardiovascular, and stroke. At the same time, multiple categories of natural products, in particular flavonoids, were proposed as safe alternatives with antioxidant activity and substantial anti-osteoporotic effects.
生物衰老会引发巨大变化,进而导致包括骨质疏松症(OP)在内的各种疾病。骨质疏松症表现为骨密度降低、骨结构恶化以及骨折风险增加。在老年人中,骨矿物质密度(BMD)会自然下降,而激素变化会加剧这种下降,尤其是在更年期期间,并且在绝经后的早期仍会持续。在这个过渡时期,激素变化与氧化应激(OS)升高和抗氧化防御能力下降有关,从而导致骨质疏松症显著增加。衰老与氧化剂/抗氧化剂的异常比例以及修饰的核因子红细胞衍生 2 相关因子 2(Nrf2)/ Kelch 样 ECH 相关蛋白 1(Keap1)信号通路的改变密切相关。氧化应激通过促进破骨细胞(骨吸收)活性和损害成骨细胞(骨形成细胞)对骨骼健康产生不利影响。Nrf2 在控制氧化应激和各种细胞过程中起着关键作用。Nrf2 的表达与包括骨质疏松症在内的多种与年龄相关的疾病有关,Nrf2 缺乏会导致骨形成/吸收失衡,进而导致骨量下降。有多种药物可用于治疗骨质疏松症;然而,长期使用这些药物会引发多种疾病,如癌症、心血管疾病和中风。与此同时,多种天然产物,特别是黄酮类化合物,被认为是具有抗氧化活性和显著抗骨质疏松作用的安全替代品。