Ma A, Kamp M, Bird D, Howlett V, Cameron D P
Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Queensland, Australia.
Aust N Z J Med. 1989 Feb;19(1):44-9. doi: 10.1111/j.1445-5994.1989.tb01674.x.
Gliclazide (80 mg bd) was administered to nine subjects with type 2 (non insulin dependent) diabetes inadequately controlled on diet only. Twenty-four hour glucose, insulin and c-peptide profiles were obtained before and after one week and four months of therapy. Insulin sensitivity was assessed by euglycemic hyperinsulinemic clamp before and after four months of treatment. Twenty-four hour glucose levels were significantly lowered after one week and four months. Insulin secretion, as assessed by the areas under the insulin and c-peptide curves, was enhanced after one week. The increase was most noted during the day in response to meals. The enhancement was maintained after four months of treatment with the increase in the postabsorptive phase becoming significant. Glucose utilisation rate was significantly increased at four months. It is concluded that both acute and prolonged gliclazide therapy directly or indirectly 1) enhances both meal stimulated and post absorptive insulin secretion and 2) increases insulin sensitivity. The relative contribution of each to improved diabetic control has not been established.
给9名仅通过饮食控制但血糖控制不佳的2型(非胰岛素依赖型)糖尿病患者服用格列齐特(80毫克,每日两次)。在治疗1周和4个月前后获取24小时血糖、胰岛素和C肽曲线。在治疗4个月前后通过正常血糖高胰岛素钳夹法评估胰岛素敏感性。1周和4个月后24小时血糖水平显著降低。通过胰岛素和C肽曲线下面积评估的胰岛素分泌在1周后增强。这种增加在白天对进餐的反应中最为明显。治疗4个月后这种增强得以维持,吸收后阶段的增加变得显著。4个月时葡萄糖利用率显著增加。结论是,格列齐特的急性和长期治疗直接或间接1)增强进餐刺激的和吸收后的胰岛素分泌,以及2)增加胰岛素敏感性。它们各自对改善糖尿病控制的相对贡献尚未确定。