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运用形式化建模方法破译与胰岛素抵抗相关的 ANGPTL8 调控网络的表达动态。

Deciphering the expression dynamics of ANGPTL8 associated regulatory network in insulin resistance using formal modelling approaches.

机构信息

Research Center for Modelling and Simulation (RCMS), National university of Sciences and Technology (NUST), Sector H-12, Islamabad 46000, Pakistan.

Department of Computer Science and Information Technology, University of Malakand, Chakdara, Dir Lower, Khyber Pakhtunkhwa 18800, Pakistan.

出版信息

IET Syst Biol. 2020 Apr;14(2):47-58. doi: 10.1049/iet-syb.2019.0032.

Abstract

ANGPTL8 is a recently identified novel hormone which regulates both glucose and lipid metabolism. The increase in ANGPTL8 during compensatory insulin resistance has been recently reported to improve glucose tolerance and a part of cytoprotective metabolic circuit. However, the exact signalling entities and dynamics involved in this process have remained elusive. Therefore, the current study was conducted with a specific aim to model the regulation of ANGPTL8 with emphasis on its role in improving glucose tolerance during insulin resistance. The main contribution of this study is the construction of a discrete model (based on kinetic logic of René Thomas) and its equivalent Stochastic Petri Net model of ANGPTL8 associated Biological Regulatory Network (BRN) which can predict its dynamic behaviours. The predicted results of these models are in-line with the previous experimental observations and provide comprehensive insights into the signalling dynamics of ANGPTL8 associated BRN. The authors' results support the hypothesis that ANGPTL8 plays an important role in supplementing the insulin signalling pathway during insulin resistance and its loss can aggravate the pathogenic process by quickly leading towards Diabetes Mellitus. The results of this study have potential therapeutic implications for treatment of Diabetes Mellitus and are suggestive of its potential as a glucose-lowering agent.

摘要

ANGPTL8 是一种新发现的激素,可调节葡萄糖和脂质代谢。最近有报道称,代偿性胰岛素抵抗期间 ANGPTL8 的增加可改善葡萄糖耐量,并作为细胞保护代谢回路的一部分。然而,该过程中涉及的确切信号实体和动态仍不明确。因此,本研究的目的是建立一个离散模型(基于 René Thomas 的动力学逻辑)及其 ANGPTL8 相关生物调节网络(BRN)的等效随机 Petri 网模型,以重点研究其在胰岛素抵抗期间改善葡萄糖耐量的作用。该模型的预测结果与之前的实验观察结果一致,为 ANGPTL8 相关 BRN 的信号动态提供了全面的见解。作者的结果支持 ANGPTL8 在胰岛素抵抗期间补充胰岛素信号通路中起重要作用的假设,其缺失可通过迅速导致糖尿病而使疾病进程恶化。该研究的结果对糖尿病的治疗具有潜在的治疗意义,并提示其作为降血糖剂的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4cc/8687251/c883dede209f/SYB2-14-47-g001.jpg

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