Amelioration of Type 2 Diabetes Mellitus by Plant-derived Natural Dipeptidyl Peptidase-4 Inhibitors through Incretin Degradation Lowering Effect: An Updated Review

Q4 Pharmacology, Toxicology and Pharmaceutics Current Enzyme Inhibition Pub Date : 2023-09-12 DOI:10.2174/1573408019666230912123312
Hari Kishan, Manjusha Choudhary, Sachin Sharma, Prabhjeet Kaur Bamrah, Nitesh Choudhary
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Abstract

Abstract: Glucagon-like peptide-1 and Glucose-dependent insulinotropic polypeptides are the most investigated gut peptides concerned with the biological glucose milieu. Early and late metabolism of incretin governs glucose homeostasis in diabetes mellitus. Dipeptidyl Peptidase-4, present in pancreatic alpha cells, is responsible for incretin degradation. Emerging biotechnological and molecular approaches established the pathophysiological role of Dipeptidyl Peptidase-4 and incretin in type 2 diabetes mellitus. Thus, various conventional synthetic Dipeptidyl Peptidase-4 inhibitors have been formulated, but they have serious adverse effects such as cancer, pancreatitis, cardiovascular risks, hepatic dysfunctions, etc. So, the concoction of a Dipeptidyl Peptidase-4 inhibitor entity with less or no severe adverse event becomes a need for society and medical corridor. Over the last two decades, natural or conventional herbal remedies have emerged as an alternate therapy for diabetes and treating its complications. This review summarized various plants (Emblica officinalis, Adenia viridiflora, Cleome droserifolia, Lens culinaris, Hedera nepalensis Melicope glabra, etc.) Dipeptidyl Peptidase-4 inhibitors, which have been preclinically proven for hyperglycemia treatment.
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植物源性天然二肽基肽酶-4抑制剂通过降低肠促胰岛素降解作用改善2型糖尿病:最新综述
摘要:胰高血糖素样肽-1和葡萄糖依赖性胰岛素多肽是研究最多的与生物葡萄糖环境有关的肠道肽。胰岛素的早期和晚期代谢控制糖尿病的葡萄糖稳态。二肽基肽酶-4存在于胰腺细胞中,负责肠促胰岛素的降解。新兴的生物技术和分子方法确定了二肽基肽酶-4和肠促胰岛素在2型糖尿病中的病理生理作用。因此,人们配制了各种常规合成的二肽基肽酶-4抑制剂,但它们具有严重的不良反应,如癌症、胰腺炎、心血管风险、肝功能障碍等。因此,研制一种少或无严重不良反应的二肽基肽酶-4抑制剂实体成为社会和医学界的需要。在过去的二十年里,自然或传统的草药疗法已经成为治疗糖尿病及其并发症的替代疗法。本文综述了几种经临床前证实可治疗高血糖的二肽基肽酶-4抑制剂(Emblica officinalis、Adenia viridiflora、Cleome droserifolia、Lens culinaris、Hedera nepalensis Melicope glabra等)。
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来源期刊
Current Enzyme Inhibition
Current Enzyme Inhibition Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.30
自引率
0.00%
发文量
30
期刊介绍: Current Enzyme Inhibition aims to publish all the latest and outstanding developments in enzyme inhibition studies with regards to the mechanisms of inhibitory processes of enzymes, recognition of active sites, and the discovery of agonists and antagonists, leading to the design and development of new drugs of significant therapeutic value. Each issue contains a series of timely, in-depth reviews written by leaders in the field, covering a range of enzymes that can be exploited for drug development. Current Enzyme Inhibition is an essential journal for every pharmaceutical and medicinal chemist who wishes to have up-to-date knowledge about each and every development in the study of enzyme inhibition.
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