Melander A, Donnelly R, Rydberg T
NEPI Foundation, Malmö, Sweden.
Clin Pharmacokinet. 1998 Mar;34(3):181-8. doi: 10.2165/00003088-199834030-00001.
Sulphonylureas have remained the mainstay of oral therapy for type 2 (non-insulin-dependent) diabetes mellitus (NIDDM). They stimulate insulin release from pancreatic beta cells. Pharmacokinetic differences between the various sulphonylureas are of clinical importance in terms of the time to onset of action, timing of drug administration in relation to food intake, magnitude and duration of the glucose-lowering effect and the risk of serious hypoglycaemia. Recent studies with improved analytical sensitivity have shown that the elimination half-life of glibenclamide is longer than previously thought and that 2 metabolites of glibenclamide have significant hypoglycaemic activity. Furthermore, single dose studies in healthy volunteers using an integrated pharmacokinetic-pharmacodynamic model have identified clear concentration-effect relationships for both glibenclamide and its metabolites after oral and intravenous administration. Under multiple dose conditions, kinetic-dynamic relations have been identified with shorter-acting drugs in dosages that give discontinuous sulphonylurea exposure. However, at continuous exposure, i.e. sustained 24-hour therapeutic concentrations in plasma, there is evidence indicating the development of tolerance, which may be caused by downregulation of beta cell sensitivity. As more sophisticated concentration-effect studies appear, it has become evident that currently recommended maximum daily doses of many sulphonylureas are too high.
磺脲类药物一直是2型(非胰岛素依赖型)糖尿病(NIDDM)口服治疗的主要药物。它们刺激胰腺β细胞释放胰岛素。各种磺脲类药物之间的药代动力学差异在起效时间、与食物摄入相关的给药时间、降糖效果的幅度和持续时间以及严重低血糖风险方面具有临床重要性。近期分析灵敏度有所提高的研究表明,格列本脲的消除半衰期比之前认为的更长,且格列本脲的两种代谢产物具有显著的降糖活性。此外,在健康志愿者中使用综合药代动力学-药效学模型进行的单剂量研究已确定口服和静脉给药后格列本脲及其代谢产物均存在明确的浓度-效应关系。在多剂量条件下,已确定了使用导致磺脲类药物暴露不连续的剂量的短效药物的动力学-动态关系。然而,在持续暴露时,即血浆中持续24小时的治疗浓度,有证据表明会出现耐受性,这可能是由β细胞敏感性下调引起的。随着更复杂的浓度-效应研究的出现,很明显目前许多磺脲类药物推荐的最大日剂量过高。