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艾塞那肽-4可降低健康志愿者的空腹血糖和餐后血糖,并减少能量摄入。

Exendin-4 reduces fasting and postprandial glucose and decreases energy intake in healthy volunteers.

作者信息

Edwards C M, Stanley S A, Davis R, Brynes A E, Frost G S, Seal L J, Ghatei M A, Bloom S R

机构信息

Endocrine Unit, Imperial College of Science, Technology and Medicine, Hammersmith Hospital, London W12 0NN, United Kingdom.

出版信息

Am J Physiol Endocrinol Metab. 2001 Jul;281(1):E155-61. doi: 10.1152/ajpendo.2001.281.1.E155.

Abstract

Exendin-4 is a long-acting potent agonist of the glucagon-like peptide 1 (GLP-1) receptor and may be useful in the treatment of type 2 diabetes and obesity. We examined the effects of an intravenous infusion of exendin-4 (0.05 pmol. kg(-1). min(-1)) compared with a control saline infusion in healthy volunteers. Exendin-4 reduced fasting plasma glucose levels and reduced the peak change of postprandial glucose from baseline (exendin-4, 1.5 +/- 0.3 vs. saline, 2.2 +/- 0.3 mmol/l, P < 0.05). Gastric emptying was delayed, as measured by the paracetamol absorption method. Volunteers consumed 19% fewer calories at a free-choice buffet lunch with exendin-4 (exendin-4, 867 +/- 79 vs. saline 1,075 +/- 93 kcal, P = 0.012), without reported side effects. Thus our results are in accord with the possibility that exendin-4 may be a potential treatment for type 2 diabetes, particularly for obese patients, because it acts to reduce plasma glucose at least partly by a delay in gastric emptying, as well as by reducing calorie intake.

摘要

艾塞那肽-4是胰高血糖素样肽1(GLP-1)受体的长效强效激动剂,可能对2型糖尿病和肥胖症的治疗有用。我们在健康志愿者中比较了静脉输注艾塞那肽-4(0.05 pmol·kg⁻¹·min⁻¹)与对照生理盐水输注的效果。艾塞那肽-4降低了空腹血糖水平,并降低了餐后血糖相对于基线的峰值变化(艾塞那肽-4组为1.5±0.3 mmol/L,生理盐水组为2.2±0.3 mmol/L,P<0.05)。通过对乙酰氨基酚吸收法测量,胃排空延迟。在自由选择的自助午餐中,使用艾塞那肽-4的志愿者摄入的热量减少了19%(艾塞那肽-4组为867±79千卡,生理盐水组为1075±93千卡,P=0.012),且无不良反应报告。因此,我们的结果符合艾塞那肽-4可能是2型糖尿病潜在治疗方法的可能性,特别是对于肥胖患者,因为它至少部分通过延迟胃排空以及减少热量摄入来降低血糖。

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