葡萄糖激酶
内科学
内分泌学
胰岛素
糖尿病
胰高血糖素
碳水化合物代谢
激活剂(遗传学)
血糖调节
激素
医学
新陈代谢
化学
受体
出处
期刊:Molecular Interventions
[CLOCKSS Archive]
日期:2003-10-01
卷期号:3 (7): 367-370
被引量:30
摘要
The hormones glucagon and insulin delicately regulate the concentration of blood glucose. When patients become resistant to the effects of insulin or produce too little of it to properly regulate glucose concentrations, then diabetes can result. Unfortunately, not all patients with insulin-resistant, type 2 diabetes mellitus respond to drugs that improve insulin sensitivity. However, there is reason to be hopeful. A new molecule that targets glucokinase (GK), the enzyme responsible for phosphorylating glucose in pancreatic beta cells and hepatic cells, acts to significantly reduce blood glucose concentrations in rodents. The GK activator RO-28-1675 increased the glucose affinity and Vmax of GK, and rats treated with RO-28-1675 had improved glucose tolerance and elevated glucose uptake in liver. These results provide the basis for improved drug design that may alleviate diabetes mellitus and the disorders that accompany it in patients.
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