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与机制相匹配的模型:用于研究糖尿病病理生理学各方面的合适啮齿动物模型。

Matching model with mechanism: Appropriate rodent models for studying various aspects of diabetes pathophysiology.

作者信息

Daniels Gatward Lydia F, King Aileen J F

机构信息

School of Cardiovascular and Metabolic Medicine & Sciences, King's College London, London, United Kingdom.

School of Cardiovascular and Metabolic Medicine & Sciences, King's College London, London, United Kingdom.

出版信息

Methods Cell Biol. 2025;192:39-68. doi: 10.1016/bs.mcb.2024.05.003. Epub 2024 Jun 19.

Abstract

Many rodent models are available for preclinical diabetes research making it a challenge for researchers to choose the most appropriate one for their experimental question. To aid in this, models have classically been categorized according to which type of diabetes they represent, and further into whether the model is induced, spontaneous or the result of genetic manipulation. This fails to capture the complexity of pathogenesis seen in diabetes in humans. This includes pathogenesis specifically involving the beta cell, which is no longer considered to be innocuous in the development and progression of diabetes. In this chapter we explore rodent models that incorporate the initiating factors believed to be involved in type 1 diabetes (autoimmunity) and type 2 diabetes (insulin resistance), before further discussing rodents that can be used to model specific mechanisms involved in a failure of functional beta cell mass (impaired beta cell function and beta cell apoptosis). We segregate models of beta cell pathogenesis based on the beta cell stressor predominantly associated with phenotype, but it is important to consider that most rodent models will exhibit more than one beta cell stressor. Similarly, many models exhibit more than one pathogenic mechanism, for example the same model may show insulin resistance, impaired beta cell function as well as beta cell loss. This can complicate interpretation of results and should be considered, and the model thoroughly researched, during the experimental planning stage.

摘要

有许多啮齿动物模型可用于临床前糖尿病研究,这使得研究人员难以选择最适合其实验问题的模型。为了辅助这一选择过程,传统上模型是根据它们所代表的糖尿病类型进行分类的,并且进一步分为模型是诱导型、自发型还是基因操作的结果。这未能涵盖人类糖尿病发病机制的复杂性。这包括特别涉及β细胞的发病机制,β细胞在糖尿病的发生和发展中不再被认为是无害的。在本章中,我们将探讨一些啮齿动物模型,这些模型纳入了被认为与1型糖尿病(自身免疫)和2型糖尿病(胰岛素抵抗)相关的起始因素,然后再进一步讨论可用于模拟功能性β细胞量衰竭(β细胞功能受损和β细胞凋亡)所涉及的特定机制的啮齿动物。我们根据主要与表型相关的β细胞应激源对β细胞发病机制模型进行分类,但重要的是要考虑到大多数啮齿动物模型将表现出不止一种β细胞应激源。同样,许多模型表现出不止一种致病机制,例如同一模型可能显示胰岛素抵抗、β细胞功能受损以及β细胞丢失。这可能会使结果的解释变得复杂,在实验规划阶段应该予以考虑,并对模型进行全面研究。

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