多种低剂量链脲佐菌素诱导的糖尿病作为研究人类自身免疫性糖尿病的模型

Q1 Health Professions
Ivan Koprivica, Suzana Stanisavljević, Dragica Mićanović, Ivana Stojanović, Đorđe Miljković
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引用次数: 0

摘要

针对胰腺β细胞的自身免疫反应是人类1型糖尿病(T1D)最重要的致病过程。自发性T1D动物模型极大地促进了我们对疾病发病机制和治疗选择的理解。在众多疾病模型中,相当大比例的T1D研究是对多种低剂量链脲佐菌素诱导的实验动物糖尿病并行进行的。在此,我们讨论了该模型对当代T1D研究的优势。此外,还提出了进一步改进该模型的挑战和前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple low dose streptozotocin-induced diabetes as a model for studying autoimmune diabetes in humans.

The autoimmune response directed against pancreatic β cells is the most essential pathogenic process in type 1 diabetes (T1D) in humans. Spontaneous animal models of T1D greatly contribute to our understanding of the disease pathogenesis and therapeutic options. Amongst many disease models, a significant proportion of T1D research is performed on multiple low dose streptozotocin induced diabetes in experimental animals, in parallel. Here, we discuss advantages of this model for contemporary T1D research. Additionally, challenges and perspectives for further improvement of the model are presented.

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来源期刊
CiteScore
5.50
自引率
0.00%
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审稿时长
12 weeks
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