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PIN1抑制对糖尿病的有益作用:简要综述

Beneficial Effects of PIN1 Inhibition on Diabetes Mellitus: A Concise Review.

作者信息

Chellappan Meeramol C, Vasu Soumya, Mahadevan Shriraam, Kathiravan Muthu Kumaradoss, Jayaraman Saravanan, Naik Soniya

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Sri Ramachandra Institute of Higher Education and Research, (DU) Porur-600 116, Chennai, India.

Department of Endocrinology, Sri Ramachandra Institute of Higher Education and Research, (DU) Porur-600 116, Chennai, India.

出版信息

Endocr Metab Immune Disord Drug Targets. 2025;25(1):2-7. doi: 10.2174/0118715303297663240307060019.

Abstract

Type 2 diabetes mellitus is a long-term medical illness in which the body either becomes resistant to insulin or fails to produce it sufficiently. Mostly, combinatorial therapy is required to control blood glucose levels. However, combinatorial therapy has detrimental side effects. The prevalence of the cases and subsequent increases in medical costs of the same intimidate human health globally. While there have been a lot of studies focused on developing diabetic regimens that work to lower blood glucose levels, their effectiveness is short-lived because of unfavorable side effects, such as weight gain and hypoglycemia. In recent years, the PIN1 (protein interacting with NIMA) enzyme has attracted the attention of researchers. Previous studies suggested that PIN1 may act on the various substrates that are involved in the progression of T2DM and also help in the management of diabetes-related disorders. Thus, the focus of the current review is to examine the correlation between PIN1, T2DM and its related disorders and explore the possibility of developing novel therapeutic targets through PIN1 inhibition.

摘要

2型糖尿病是一种长期的医学疾病,在这种疾病中,身体要么对胰岛素产生抵抗,要么无法产生足够的胰岛素。大多数情况下,需要联合治疗来控制血糖水平。然而,联合治疗有有害的副作用。这些病例的患病率以及随之而来的医疗费用增加对全球人类健康构成威胁。虽然已经有很多研究致力于开发能降低血糖水平的糖尿病治疗方案,但由于体重增加和低血糖等不良副作用,它们的有效性是短暂的。近年来,PIN1(与NIMA相互作用的蛋白质)酶引起了研究人员的关注。先前的研究表明,PIN1可能作用于参与2型糖尿病进展的各种底物,也有助于管理与糖尿病相关的疾病。因此,本综述的重点是研究PIN1、2型糖尿病及其相关疾病之间的相关性,并探索通过抑制PIN1开发新型治疗靶点的可能性。

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