Kytikova O Y, Novgorodtseva T P, Antonyuk M V, Gvozdenko T A
Vladivostok branch of the Far Eastern scientific center of physiology and pathology of breathing - Research Institute of Medical Climatology and Rehabilitation Treatment, 73 G Russkaya str., Vladivostok 690105, Russian Federation, e-mail:
Adv Gerontol. 2019;32(6):948-958.
The pathogenesis of age-related diseases such as metabolic syndrome, type 2 diabetes, Parkinson's disease and Alzheimer's disease is associated with oxidative stress and chronic inflammation. Violation of redox homeostasis is accompanied by the development of peroxisome dysfunction and impaired biosynthesis of plasmalogens, which can be closely related to the aging process and the development of age-dependent pathology. Reflecting the functional activity of peroxisomes, plasmalogens can serve not only as potential biomarkers of diseases associated with oxidative stress and aging, but also as an important therapeutic target. The purpose of this review is to analyze the current knowledge of little-studied biological and pathological aspects of plasmalogen participation in the pathophysiology of neurodegenerative and metabolic diseases of older persons. Understanding the role of plasmalogens in the pathophysiology of these diseases can lead to the development of effective diagnostic and prognostic biomarkers, as well as treatment methods for neurodegenerative and metabolic diseases of older people.
代谢综合征、2型糖尿病、帕金森病和阿尔茨海默病等与年龄相关疾病的发病机制与氧化应激和慢性炎症有关。氧化还原稳态的破坏伴随着过氧化物酶体功能障碍的发展和缩醛磷脂生物合成受损,这可能与衰老过程以及年龄依赖性病理学的发展密切相关。缩醛磷脂反映了过氧化物酶体的功能活性,不仅可以作为与氧化应激和衰老相关疾病的潜在生物标志物,还可以作为重要的治疗靶点。本综述的目的是分析目前关于缩醛磷脂参与老年人神经退行性疾病和代谢疾病病理生理学的鲜为人知的生物学和病理学方面的知识。了解缩醛磷脂在这些疾病病理生理学中的作用可以导致开发有效的诊断和预后生物标志物,以及针对老年人神经退行性疾病和代谢疾病的治疗方法。