链脲佐菌素比四氧嘧啶更容易诱导2型糖尿病

Manik Islam, M. Rupeshkumar, K. Reddy
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引用次数: 14

摘要

四氧嘧啶和链脲佐菌素往往是有毒的葡萄糖类似物,它们优先通过实际的GLUT2葡萄糖转运蛋白在胰腺组织中积累。四氧嘧啶和链脲佐菌素是糖尿病研究中最值得注意的致糖尿病化学物质。两者都是细胞毒性葡萄糖类似物。尽管它们的细胞毒性实际上是通过不同的途径实现的,但它们的细胞选择运动系统是相似的。1838年,维勒和李比希合成了嘧啶型,这些人后来称之为四氧嘧啶。1943年,四氧嘧啶引起了人们对糖尿病研究的兴趣,Dunn和McLetchie报告说,由于胰腺组织的特殊坏死,四氧嘧啶可以刺激动物体内的糖尿病。随之而来的胰岛素缺乏导致一种新的糖尿病,称为四氧嘧啶糖尿病。链脲佐菌素(STZ)是在1960年通过消色链霉菌分离得到的,它是一种抗菌药物,也已被用作化学治疗的烷基化剂。1963年,rakietenting。哪些链脲佐菌素实际上会导致糖尿病再一次,这种胰岛素减少的痛苦,被称为链脲佐菌素糖尿病是由胰腺组织的特定坏死引起的链脲佐菌素可能是动物体内与糖尿病相关的实际诱导的首选药物。与四氧嘧啶相比,STZ在诱导糖尿病大鼠方面具有更高的诱导价格和更低的毒性。特别是在诱导DM2时,STZ和烟酰胺可以在最近的功能中使用。与四氧嘧啶相关的死亡率实际上很高,并导致体重大幅下降。在这篇简短的文章中,我们可能会证明使用STZ实际上比使用四氧嘧啶更安全、更方便地诱导与糖尿病相关的2型糖尿病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Streptozotocin is more convenient than Alloxan for the induction of Type 2 diabetes
Alloxan as well as Streptozotocin tend to be toxic glucose analogues which preferentially build up in pancreatic beta tissue via the actual GLUT2 glucose transporter. Alloxan as well as Streptozotocin would be the most notable diabetogenic chemical substances in diabetes investigation. Both tend to be cytotoxic glucose analogues. Even though their cytotoxicity is actually achieved by way of different paths, their systems of beta cellular selective motion are similar. In 1838, Wohler as well as Liebig synthesized the pyrimidine type, which these people later known as alloxan. Within 1943, alloxan grew to become of curiosity about diabetes investigation when Dunn as well as McLetchie reported it could stimulate diabetes within animals due to the particular necrosis from the pancreatic beta tissue. The ensuing insulinopenia causes a situation of fresh diabetes mellitus known as alloxan diabetes. Streptozotocin (STZ) was isolated through Streptomyces achromogenes within 1960, Streptozotocin is definitely an antimicrobial agent and it has also already been used like a chemotherapeutic alkylating agent. In 1963, Rakieteneting. reported which Streptozotocin is actually diabetogenic. Once again, this insulinopenia affliction, called Streptozotocin diabetes is brought on by the particular necrosis from the pancreatic beta tissue and Streptozotocin may be the agent of preference for the actual induction associated with diabetes mellitus within animals since. STZ is actually preferred compared to Alloxan in order to induce diabetic rat because of its higher inductive price and reduce toxicity. STZ is much better especially whenever inducing DM2, STZ as well as nicotinamide may be used within recent functions. The fatality rate associated with alloxan is actually high and result in a high reduction in bodyweight. In this short article we may demonstrates using STZ is actually more security and handy than using Alloxan for that induction associated with diabetes mellitus 2.
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