SIRT-1作为治疗和预防糖尿病肾病的靶点的作用:综述

IF 2.4 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anita Kumari, Nalini Sodum, V Ravichandiran, Nitesh Kumar
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引用次数: 0

摘要

2型糖尿病是糖尿病肾病(DN)发展的主要因素,影响重要器官即肾脏,并进一步改变肾元系统的功能。由于其药物的高度普遍性和复杂性,DN正成为当今世界科学家面临的一个挑战。致病性DN的发生涉及多种危险因素,这些因素与不同的抗药物活性途径有关。由于这种DN成为研究人员无法预测的查询。SIRT1是一种沉默信息调节因子2相关酶1 (SIRT1)是烟酰胺腺嘌呤二核苷酸(NAD+)依赖的去乙酰化酶,作为细胞内转录活性的调节因子。SIRT-1的激活版本改善了与其他分子途径相关的代谢疾病状况。在含有足细胞、系膜细胞和肾近端小管细胞的糖尿病体外和体内实验模型中,SIRT1可减轻糖尿病肾病。SIRT1在DN中表现出肾保护作用,部分是通过转录因子的去乙酰化,如p53、PTP1B、FOXO、RelA、NF- kβ、STAT-3和PGC-1α/ PPARγ。研究表明,一些天然产物,如白藜芦醇和合成化合物,可以激活SIRT1,这进一步涉及级联途径,以防止DN。这一综述将有助于了解sirt1作为靶点在预防和治疗DN中的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of SIRT-1 as a Target for Treatment and Prevention of Diabetic Nephropathy: A Review.

Type-2 diabetes mellitus is a prime factor for the development of Diabetic Nephropathy (DN) that affects the vital organ namely the kidneys, and further alters the functions of the nephron system. DN is nowadays becoming a challenge for scientists towards the world because of its high pervasiveness and complexity of medication. Various risk factors are involved in the initiation of pathogenic DN, which are associated with different pathways against drug activity. Due to this DN becomes an unpredictable query to the researchers. SIRT1 is a silent information regulator factor 2 related enzyme 1 (SIRT1) is nicotinamide adenine dinucleotide (NAD+) dependent deacetylase that functions as an intracellular regulator of transcriptional activity. An activated version of SIRT-1 improves the metabolic diseased conditions associated with other molecular pathways. SIRT1 attenuates diabetic nephropathy in in vitro and in vivo experimental models of diabetes containing Podocytes, Mesangial cells, and Renal proximal tubular cells. SIRT1 shows nephroprotective effects in DN in part through deacetylation of transcription factors i.e., imply in the disease like p53, PTP1B, FOXO, RelA, NF- kβ, STAT-3, and PGC-1α/ PPARγ. It has been shown that some natural products like resveratrol and synthetic compounds are activating the SIRT1, this further involved the cascade pathways to prevent the DN. This review will help regarding the effectiveness of SIRT1as target in the prevention and treatment of DN.

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来源期刊
Current molecular pharmacology
Current molecular pharmacology Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
4.90
自引率
3.70%
发文量
112
期刊介绍: Current Molecular Pharmacology aims to publish the latest developments in cellular and molecular pharmacology with a major emphasis on the mechanism of action of novel drugs under development, innovative pharmacological technologies, cell signaling, transduction pathway analysis, genomics, proteomics, and metabonomics applications to drug action. An additional focus will be the way in which normal biological function is illuminated by knowledge of the action of drugs at the cellular and molecular level. The journal publishes full-length/mini reviews, original research articles and thematic issues on molecular pharmacology. Current Molecular Pharmacology is an essential journal for every scientist who is involved in drug design and discovery, target identification, target validation, preclinical and clinical development of drugs therapeutically useful in human disease.
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