胰高血糖素样肽1受体
兴奋剂
内分泌学
受体
肠促胰岛素
内科学
医学
2型糖尿病
药理学
不利影响
糖尿病
减肥
中止
2型糖尿病
艾塞那肽
胰岛素样生长因子1受体
胰岛素
化学
黑素皮质素4受体
胰岛素受体
胰高血糖素样肽-1
酶联受体
利拉鲁肽
雌激素相关受体α
胰高血糖素受体
作者
Clifford J. Rosen,Julie R. Ingelfinger
标识
DOI:10.1056/nejmra2500106
摘要
Glucagon-like peptide-1 (GLP-1) receptor agonists are incretin analogues that promote glucose-mediated insulin release and are used to treat type 2 diabetes mellitus and obesity. GLP-1 receptor agonists and GLP-1 and glucose-dependent insulinotropic peptide agonists have several mechanisms of action, including reduction of gastric emptying, inhibition of glucagon secretion, beneficial changes in the intestinal microbiome, and direct effects on hypothalamic nuclei to enhance satiety (which promotes weight loss). Beyond the impressive effects of GLP-1 receptor agonists on blood glucose levels and body weight, large-scale randomized, controlled trials have shown that GLP-1 receptor agonists reduce cardiovascular risk and slow progression to renal failure in persons at high risk and those with type 2 diabetes. Adverse side effects from GLP-1 receptor agonists are mostly gastrointestinal but may also include loss of muscle and bone mass. Questions remain about long-term adherence, weight regain after discontinuation of treatment, and the functional implications of the loss of muscle and bone mass. Recent and ongoing targeted studies suggest the possibility of additional uses for GLP-1 receptor agonists.
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