小鼠对链脲佐菌素致糖尿病作用的长期耐受性

Y. Abramovici , M.K. Agarwal
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引用次数: 2

摘要

单次腹腔注射5mg (250 mg/kg体重)链脲霉素可在48小时内诱导C57BL6和C57BL10(敏感)株雄性6周龄小鼠发生显性糖尿病。C3HHeJ和C3Heb(耐药)菌株表现出进行性迟发性高血糖,需要6周才能达到敏感菌株仅48小时的水平。对sz诱导糖尿病的抵抗与体重变化或药物的不同药代动力学无关。与C57BL6(敏感)小鼠相比,在sz后第一周,C3HHeJ(抗性)小鼠在组织学检查中显示免疫反应性胰岛素胰腺含量下降较小,胰岛损伤较轻。这些结果表明,菌株对sz诱导的糖尿病的抗性可能是在β细胞对药物细胞毒性作用的反应性水平上介导的。这个非常简单的实验工具可能在监测明显的胰岛素缺乏型糖尿病发病前的一段时间,以及探索构成遗传抗性胰腺的因素的性质方面具有价值,了解这些因素有助于人类糖尿病的管理。
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Prolonged refractoriness to the diabetogenic action of streptozotocin in mice

A single intraperitoneal injection of 5 mg (250 mg/kg body wt) streptozotocin induced overt diabetes within 48 hr in male, 6-week-old mice of C57BL6 and C57BL10 (sensitive) strains. The C3HHeJ and C3Heb (resistant) strains exhibited a progressive delayed-onset hyperglycemia which required 6 weeks to reach the level seen within only 48 hr in sensitive strains. Resistance to SZ-induced diabetes was not related to changes in body weights or different pharmacokinetics of the drug. C3HHeJ (resistant) mice showed a smaller fall in immunoreactive insulin pancreatic content and less severe damage of pancreatic islets on histologic examination, when compared to C57BL6 (sensitive) mice during the first week post-SZ. These results suggest that strain-related resistance to SZ-induced diabetes may be mediated at the level of the β cell's responsiveness to the cytotoxic action of the drug. This very simple experimental tool may be of value in monitoring the period before the onset of overt insulin-deficient diabetes and for probing the nature of factors that constitute a genetically resistant pancreas, understanding of which could aid management of diabetes mellitus in humans.

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