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非肥胖糖尿病(NOD)小鼠中糖尿病的急性发作与渐进性发作:对1型糖尿病治疗干预的潜在影响

Acute Versus Progressive Onset of Diabetes in NOD Mice: Potential Implications for Therapeutic Interventions in Type 1 Diabetes.

作者信息

Mathews Clayton E, Xue Song, Posgai Amanda, Lightfoot Yaima L, Li Xia, Lin Andrea, Wasserfall Clive, Haller Michael J, Schatz Desmond, Atkinson Mark A

机构信息

Department of Pathology, University of Florida, Gainesville, FL.

Institute of Metabolism and Endocrinology, The Second Xiangya Hospital and the Diabetes Center, Metabolic Syndrome Research Center, Key Laboratory of Diabetes Immunology, Ministry of Education, Central South University, National Clinical Research Center for Metabolic Diseases, Changsha, Hunan, China.

出版信息

Diabetes. 2015 Nov;64(11):3885-90. doi: 10.2337/db15-0449. Epub 2015 Jul 27.

Abstract

Most natural history models for type 1 diabetes (T1D) propose that overt hyperglycemia results after a progressive loss of insulin-secreting β-cell mass and/or function. To experimentally address this concept, we prospectively determined morning blood glucose measurements every other day in multiple cohorts (total n = 660) of female NOD/ShiLtJ mice starting at 8 weeks of age until diabetes onset or 26 weeks of age. Consistent with this notion, a majority of mice that developed diabetes (354 of 489 [72%]) displayed a progressive increase in blood glucose with transient excursions >200 mg/dL, followed by acute and persistent hyperglycemia at diabetes onset. However, 135 of the 489 (28%) diabetic animals demonstrated normal glucose values followed by acute (i.e., sudden) hyperglycemia. Interestingly, diabetes onset occurred earlier in mice with acute versus progressive disease onset (15.37 ± 0.3207 vs. 17.44 ± 0.2073 weeks of age, P < 0.0001). Moreover, the pattern of onset (i.e., progressive vs. acute) dramatically influenced the ability to achieve reversal of T1D by immunotherapeutic intervention, with increased effectiveness observed in situations of a progressive deterioration in euglycemia. These studies highlight a novel natural history aspect in this animal model, one that may provide important guidance for the selection of subjects participating in human trials seeking disease reversal.

摘要

大多数1型糖尿病(T1D)的自然史模型认为,胰岛素分泌β细胞量和/或功能逐渐丧失后会出现明显的高血糖。为了通过实验验证这一概念,我们前瞻性地每隔一天测定多组(总共n = 660)8周龄雌性NOD/ShiLtJ小鼠的晨起血糖,直至糖尿病发病或26周龄。与此观点一致,大多数发生糖尿病的小鼠(489只中的354只[72%])血糖逐渐升高,短暂波动超过200 mg/dL,随后在糖尿病发病时出现急性持续性高血糖。然而,489只糖尿病动物中有135只(28%)血糖值正常,随后出现急性(即突然)高血糖。有趣的是,急性发病的小鼠比渐进性发病的小鼠糖尿病发病更早(分别为15.37 ± 0.3207周龄和17.44 ± 0.2073周龄,P < 0.0001)。此外,发病模式(即渐进性与急性)极大地影响了通过免疫治疗干预实现T1D逆转的能力,在血糖正常逐渐恶化的情况下观察到有效性增加。这些研究突出了该动物模型中一个新的自然史方面,这可能为选择参与寻求疾病逆转的人体试验的受试者提供重要指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb0/4613974/5226c63fda1b/db150449f1.jpg

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