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氧化-炎症相互作用与多靶点天然药物:解读糖尿病血管并发症

Oxidative-Inflammatory Crosstalk and Multi-Target Natural Agents: Decoding Diabetic Vascular Complications.

作者信息

Liu Jingwen, Li Kexin, Yi Zixin, Wang Changshan, Yang Rui

机构信息

School of Life Science, Inner Mongolia University, Hohhot 010020, China.

Department of Pharmacology, School of Basic Medicine, Inner Mongolia Medical University, Hohhot 010110, China.

出版信息

Curr Issues Mol Biol. 2025 Aug 4;47(8):614. doi: 10.3390/cimb47080614.

Abstract

Diabetes mellitus (DM) is one of the leading causes of death and disability worldwide and its prevalence continues to rise. Chronic hyperglycemia exposes patients to severe complications. Among these, diabetic vascular lesions are the most destructive. Their primary driver is the synergistic interaction between hyperglycemia-induced oxidative stress and chronic inflammation. This review systematically elucidates how multiple pathological pathways-namely, metabolic dysregulation, mitochondrial dysfunction, endoplasmic reticulum stress, and epigenetic reprogramming-cooperate to drive oxidative stress and inflammatory cascades. Confronting this complex pathological network, natural products, unlike conventional single-target synthetic drugs, exert multi-target synergistic effects, simultaneously modulating several key pathogenic networks. This enables the restoration of redox homeostasis and the suppression of inflammatory responses, thereby improving vascular function and delaying both microvascular and macrovascular disease progression. However, the clinical translation of natural products still faces multiple challenges and requires comprehensive mechanistic studies and rigorous validation to fully realize their therapeutic potential.

摘要

糖尿病(DM)是全球范围内主要的死亡和致残原因之一,其患病率持续上升。慢性高血糖会使患者面临严重并发症。其中,糖尿病血管病变最具破坏性。其主要驱动因素是高血糖诱导的氧化应激与慢性炎症之间的协同相互作用。本综述系统阐述了多种病理途径,即代谢失调、线粒体功能障碍、内质网应激和表观遗传重编程,如何协同驱动氧化应激和炎症级联反应。与传统的单靶点合成药物不同,天然产物面对这种复杂的病理网络时,发挥多靶点协同作用,同时调节多个关键致病网络。这能够恢复氧化还原稳态并抑制炎症反应,从而改善血管功能,延缓微血管和大血管疾病进展。然而,天然产物的临床转化仍面临多重挑战,需要全面的机制研究和严格验证,以充分实现其治疗潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d351/12384710/ed1d3abeb84f/cimb-47-00614-g001.jpg

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