Suppr超能文献

重复小剂量链脲佐菌素和阿霉素诱导比格犬长期稳定的 1 型糖尿病模型。

Repeated Low-Dose Streptozotocin and Alloxan Induced Long-Term and Stable Type 1 Diabetes Model in Beagle Dogs.

机构信息

College of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642 Guangdong, China.

出版信息

Biomed Res Int. 2022 Aug 8;2022:5422287. doi: 10.1155/2022/5422287. eCollection 2022.

Abstract

Type 1 diabetes mellitus (T1DM) is a chronic disease represented by insulin-causing pancreatic -cell disruption and hyperglycemia. Therefore, it is necessary to establish a variety of animal models of diabetes to study the pathogenesis and pathophysiology of it. However, there are few reports on the use of beagle dogs to establish an animal model of type 1 diabetes. This study aimed to explore a simple and feasible modeling method to establish a long-term and stable type 1 diabetes model in beagle dogs. Forty adult beagle dogs were randomly divided into control group and model group. After 24 h of fasting, streptozotocin (20 mg/kg) and alloxan (20 mg/kg) were injected through the cephalic vein. The second intravenous injection was given on the 4th day after the first injection. Insulin release testing was performed on the 7th day after the last intravenous injection. Fasting blood glucose and body weight were recorded monthly. Four months after the last injection, the serum fructosamine content and the ratio of glycated hemoglobin were detected. Then, the pancreatic tissue was harvested for histopathological examination. The results showed that the level of fasting blood glucose of the 16 dogs in the model group was consistently higher than 11.1 mmol/L for 4 consecutive months. Moreover, compared with the control group, the insulin release curve of the model group was flat with no increase. The body weight of the model group was significantly reduced, and the ratios of blood glucose, fructosamine, and glycosylated hemoglobin were significantly higher than those in the control group. Meanwhile, histopathological examination of the pancreas showed that the islet beta cells appeared to have vacuoles or even necrosis. In the model group, pancreatic -cells were damaged and insulin release was reduced. These results suggest that the above modeling methods can induce long-term and stable type 1 diabetes models in beagle dogs.

摘要

1 型糖尿病(T1DM)是一种以胰岛素引起的胰腺β细胞破坏和高血糖为特征的慢性疾病。因此,有必要建立各种糖尿病动物模型来研究其发病机制和病理生理学。然而,关于使用比格犬建立 1 型糖尿病动物模型的报道较少。本研究旨在探索一种简单可行的建模方法,以建立比格犬长期稳定的 1 型糖尿病模型。40 只成年比格犬随机分为对照组和模型组。禁食 24 h 后,经头静脉注射链脲佐菌素(20 mg/kg)和三氧嘧啶(20 mg/kg)。首次注射后第 4 天进行第二次静脉注射。末次静脉注射后第 7 天进行胰岛素释放试验。每月记录空腹血糖和体重。末次注射后 4 个月,检测血清果糖胺含量和糖化血红蛋白比值。然后采集胰腺组织进行组织病理学检查。结果显示,模型组 16 只犬的空腹血糖水平连续 4 个月持续高于 11.1mmol/L。此外,与对照组相比,模型组的胰岛素释放曲线平坦,没有增加。模型组体重明显减轻,血糖、果糖胺和糖化血红蛋白比值明显高于对照组。同时,胰腺组织学检查显示胰岛β细胞出现空泡甚至坏死。模型组胰腺β细胞受损,胰岛素释放减少。这些结果表明,上述建模方法可诱导比格犬产生长期稳定的 1 型糖尿病模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4821/9377912/0f50a964108d/BMRI2022-5422287.001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验