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首页> 外文期刊>Life sciences >Comparison of therapeutic regimens in the amelioration of alterations in rat gastrointestinal mucosal DNA, RNA and protein induced by streptozotocin diabetes mellitus.
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Comparison of therapeutic regimens in the amelioration of alterations in rat gastrointestinal mucosal DNA, RNA and protein induced by streptozotocin diabetes mellitus.

机译:改善链脲佐菌素糖尿病所致大鼠胃肠道粘膜DNA,RNA和蛋白质改变的治疗方案比较。

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摘要

Type 1 diabetes mellitus is characterized by hyperglycemia, insulinopenia, and secondary neural, renal and vascular complications. Clinical manifestations in the gastrointestinal tract range from initial mild complications to more severe complications as the disease progresses, but as of yet, are poorly understood. The current study has two main foci 1) to monitor the alterations in gastrointestinal DNA, RNA and protein content induced by streptozotocin diabetes and 2) to use these parameters to monitor the efficacy of intensive insulin treatment versus pancreatic islet transplantation in the amelioration of the diabetes induced alterations. Female Wistar Furth rats were rendered diabetic by streptozotocin injection and measured for alterations in gastrointestinal DNA, RNA and protein content. Similarly, animals which had streptozotocin-induced diabetes were also treated by intensive insulin therapy or pancreatic islet transplant and monitored for alterations in gastrointestinal DNA, RNA and protein content. In general, diabetes induced increases in stomach, duodenal, jejunal and colonic macromolecular content. With few exceptions, treatment with either intensive insulin or pancreatic islet transplantation returned each variable measured back to control levels. In every case, pancreatic islet transplantation was comparable to intensive insulin therapy. In the short term the treatments are comparable, but long term analyses are needed to determine if the treatments offer any difference in their ability to prevent the long term complications related to diabetes mellitus.
机译:1型糖尿病的特征是高血糖,胰岛素缺乏症以及继发性神经,肾和血管并发症。胃肠道的临床表现范围从最初的轻度并发症到随着疾病的进展而更为严重的并发症,但迄今为止,人们对其了解甚少。当前的研究有两个主要重点:1)监测链脲佐菌素糖尿病诱导的胃肠道DNA,RNA和蛋白质含量的变化; 2)使用这些参数监测强化胰岛素治疗与胰岛移植改善糖尿病的疗效诱发的变化。通过注射链脲佐菌素使雌性Wistar Furth大鼠成为糖尿病,并测量其胃肠道DNA,RNA和蛋白质含量的变化。类似地,患有链脲佐菌素诱导的糖尿病的动物也通过强化胰岛素治疗或胰岛移植治疗,并监测胃肠道DNA,RNA和蛋白质含量的变化。通常,糖尿病引起的胃,十二指肠,空肠和结肠大分子含量增加。除少数例外,采用强化胰岛素或胰岛移植治疗后,每个测得的变量均恢复至对照水平。在每种情况下,胰岛移植均与强化胰岛素治疗相当。在短期内,治疗方法具有可比性,但需要进行长期分析,以确定治疗方法在预防与糖尿病相关的长期并发症方面是否有任何区别。

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