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多酚类化合物抗糖尿病活性的潜在机制:综述

Mechanisms Underlying the Antidiabetic Activities of Polyphenolic Compounds: A Review.

作者信息

Nie Tina, Cooper Garth J S

机构信息

School of Biological Sciences, Faculty of Science, the University of Auckland, Auckland, New Zealand.

The Maurice Wilkins Centre for Molecular Biodiscovery, Faculty of Science, the University of Auckland, Auckland, New Zealand.

出版信息

Front Pharmacol. 2021 Dec 14;12:798329. doi: 10.3389/fphar.2021.798329. eCollection 2021.

Abstract

Polyphenolic compounds are thought to show considerable promise for the treatment of various metabolic disorders, including type 2 diabetes mellitus (T2DM). This review addresses evidence from , , and clinical studies for the antidiabetic effects of certain polyphenolic compounds. We focus on the role of cytotoxic human amylin (hA) aggregates in the pathogenesis of T2DM, and how polyphenols can ameliorate this process by suppressing or modifying their formation. Small, soluble amylin oligomers elicit cytotoxicity in pancreatic islet β-cells and may thus cause β-cell disruption in T2DM. Amylin oligomers may also contribute to oxidative stress and inflammation that lead to the triggering of β-cell apoptosis. Polyphenols may exert antidiabetic effects via their ability to inhibit hA aggregation, and to modulate oxidative stress, inflammation, and other pathways that are β-cell-protective or insulin-sensitizing. There is evidence that their ability to inhibit and destabilize self-assembly by hA requires aromatic molecular structures that bind to misfolding monomers or oligomers, coupled with adjacent hydroxyl groups present on single phenyl rings. Thus, these multifunctional compounds have the potential to be effective against the pleiotropic mechanisms of T2DM. However, substantial further research will be required before it can be determined whether a polyphenol-based molecular entity can be used as a therapeutic for type 2 diabetes.

摘要

多酚类化合物被认为在治疗包括2型糖尿病(T2DM)在内的各种代谢紊乱方面具有巨大潜力。本综述阐述了细胞实验、动物实验及临床研究中某些多酚类化合物抗糖尿病作用的证据。我们重点关注细胞毒性人胰岛淀粉样多肽(hA)聚集体在T2DM发病机制中的作用,以及多酚如何通过抑制或改变其形成来改善这一过程。小的、可溶的胰岛淀粉样多肽寡聚体在胰岛β细胞中引发细胞毒性,因此可能在T2DM中导致β细胞破坏。胰岛淀粉样多肽寡聚体也可能导致氧化应激和炎症,从而引发β细胞凋亡。多酚可能通过抑制hA聚集以及调节氧化应激、炎症和其他对β细胞有保护作用或使胰岛素敏感的途径发挥抗糖尿病作用。有证据表明,它们抑制hA自组装并使其不稳定的能力需要芳香族分子结构,该结构可与错误折叠的单体或寡聚体结合,并与单个苯环上相邻的羟基相连。因此,这些多功能化合物有可能有效对抗T2DM的多效性机制。然而,在确定基于多酚的分子实体是否可用于治疗2型糖尿病之前,还需要大量进一步的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec89/8712966/2ca050fd78f6/fphar-12-798329-g001.jpg

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