Department of Nutrition, Dietetics, and Hospitality Management, Auburn University, Auburn, AL 36849, USA.
Department of Nutrition, Dietetics, and Hospitality Management, Auburn University, Auburn, AL 36849, USA; Boshell Metabolic Diseases and Diabetes Program, Auburn University, Auburn, AL 36849, USA.
Pharmacol Res. 2021 Sep;171:105783. doi: 10.1016/j.phrs.2021.105783. Epub 2021 Jul 22.
Diabetes and Alzheimer's disease are common chronic illnesses in the United States and lack clearly demonstrated therapeutics. Mitochondria, the "powerhouse of the cell", is involved in the homeostatic regulation of glucose, energy, and reduction/oxidation reactions. The mitochondria has been associated with the etiology of metabolic and neurological disorders through a dysfunction of regulation of reactive oxygen species. Mitochondria-targeted chemicals, such as the Szeto-Schiller-31 peptide, have advanced therapeutic potential through the inhibition of oxidative stress and the restoration of normal mitochondrial function as compared to traditional antioxidants, such as vitamin E. In this article, we summarize the pathophysiological relevance of the mitochondria and the beneficial effects of Szeto-Schiller-31 peptide in the treatment of Diabetes and Alzheimer's disease.
糖尿病和老年痴呆症是美国常见的慢性疾病,缺乏明确的治疗方法。线粒体是“细胞的动力源”,参与葡萄糖、能量和氧化还原反应的体内平衡调节。线粒体通过调节活性氧的功能障碍与代谢和神经紊乱的病因有关。与传统抗氧化剂如维生素 E 相比,线粒体靶向化学物质,如 Szeto-Schiller-31 肽,通过抑制氧化应激和恢复正常线粒体功能,具有更先进的治疗潜力。本文总结了线粒体的病理生理学相关性以及 Szeto-Schiller-31 肽在治疗糖尿病和老年痴呆症中的有益作用。
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