Inhibition of the pyroptosis-associated inflammasome pathway: The important potential mechanism of ginsenosides in ameliorating diabetes and its complications

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL
Pan Liu , Zhengdong Zhang , Yichen Cai , Yunjiao Yang , Jun Yuan , Qiu Chen
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引用次数: 3

Abstract

Diabetes mellitus (DM) and its complications have become an important global public health issue, affecting human health and negatively impacting life and lifespan. Pyroptosis is a recently discovered form of pro-inflammatory programmed cell death (PCD). To date, pyroptosis-associated inflammasome pathways have been identified primarily in the canonical and non-canonical inflammasome pathway, apoptotic caspase-mediated pathway, granzyme-mediated pathway, and streptococcal pyrogenic exotoxin B (SpeB)-mediated pathway. The activation of diabetes-mediated pyroptosis-associated factors play an important role in the pathophysiology of DM and its complications. Studies have shown that ginsenosides exert significant protective effects on DM and its complications. Through inhibiting the activation of pyroptosis-associated inflammasome pathways, and then the DM and its complications are improved. This review summarizes the subtypes of ginsenosides and their chemical characteristics, pharmacokinetics and side effects, the main pyroptosis-associated inflammasome pathways that have been discovered to date, and the potential mechanism of different subtypes of ginsenosides in the treatment of DM and its complications (such as diabetic cardiomyopathy, diabetic nephropathy, diabetic liver injury, diabetic retinopathy, and diabetic ischemic stroke) via anti-pyroptosis-associated inflammasome pathways. These findings may provide ideas for further research to explore ginsenoside mechanism in improving DM and its complications. However, many pyroptosis-associated inflammasome pathways and targets involved in the occurrence and development of DM and its complications are still unknown. In the future, further studies using in vitro cell models, in vivo animal models, and human disease models can be used to further elucidate the mechanism of ginsenosides in the treatment of DM and its complications.

Abstract Image

抑制焦热相关炎性体通路:人参皂苷改善糖尿病及其并发症的重要潜在机制
糖尿病(DM)及其并发症已成为一个重要的全球公共卫生问题,影响着人类健康并对生命和寿命产生负面影响。焦亡是最近发现的一种促炎性程序性细胞死亡(PCD)。迄今为止,已确定的与热原相关的炎性小体途径主要有典型和非典型炎性小体途径、凋亡性caspase介导途径、颗粒酶介导途径和链球菌热原性外毒素B (SpeB)介导途径。糖尿病介导的焦热相关因子的激活在糖尿病及其并发症的病理生理中起重要作用。研究表明,人参皂苷对糖尿病及其并发症具有显著的保护作用。通过抑制焦热相关炎性体通路的激活,进而改善糖尿病及其并发症。本文综述了人参皂苷的亚型及其化学特性、药代动力学、毒副作用、迄今为止发现的主要焦热相关炎性体途径,以及不同亚型人参皂苷治疗糖尿病及其并发症(如糖尿病心肌病、糖尿病肾病、糖尿病肝损伤、糖尿病视网膜病变、糖尿病肾损伤、糖尿病肾损伤等)的潜在机制。和糖尿病缺血性中风)通过抗焦热相关的炎性体途径。这些发现可能为进一步研究人参皂苷改善糖尿病及其并发症的机制提供思路。然而,许多与焦热相关的炎性体途径和靶点参与糖尿病及其并发症的发生和发展仍然是未知的。未来,通过体外细胞模型、体内动物模型和人体疾病模型的进一步研究,可以进一步阐明人参皂苷治疗糖尿病及其并发症的机制。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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