Flanagan Daniel E, Evans Mark L, Monsod Teresa P, Rife Frances, Heptulla Rubina A, Tamborlane William V, Sherwin Robert S
Section of Endocrinology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
Am J Physiol Endocrinol Metab. 2003 Feb;284(2):E313-6. doi: 10.1152/ajpendo.00569.2001.
Ghrelin is a novel peptide that acts on the growth hormone (GH) secretagogue receptor in the pituitary and hypothalamus. It may function as a third physiological regulator of GH secretion, along with GH-releasing hormone and somatostatin. In addition to the action of ghrelin on the GH axis, it appears to have a role in the determination of energy homeostasis. Although feeding suppresses ghrelin production and fasting stimulates ghrelin release, the underlying mechanisms controlling this process remain unclear. The purpose of this study was to test the hypotheses, by use of a stepped hyperinsulinemic eu- hypo- hyperglycemic glucose clamp, that either hyperinsulinemia or hypoglycemia may influence ghrelin production. Having been stable in the period before the clamp, ghrelin levels rapidly fell in response to insulin infusion during euglycemia (baseline ghrelin 207 +/- 12 vs. 169 +/- 10 fmol/ml at t = 30 min, P < 0.001). Ghrelin remained suppressed during subsequent periods of hypoglycemia (mean glucose 53 +/- 2 mg/dl) and hyperglycemia (mean glucose 163 +/- 6 mg/dl). Despite suppression of ghrelin, GH showed a significant rise during hypoglycemia (baseline 4.1 +/- 1.3 vs. 28.2 +/- 3.9 microg/l at t = 120 min, P < 0.001). Our data suggest that insulin may suppress circulating ghrelin independently of glucose, although glucose may have an additional effect. We conclude that the GH response seen during hypoglycemia is not regulated by circulating ghrelin.
胃饥饿素是一种新型肽,作用于垂体和下丘脑的生长激素(GH)促分泌素受体。它可能作为生长激素分泌的第三种生理调节因子,与生长激素释放激素和生长抑素共同发挥作用。除了胃饥饿素对生长激素轴的作用外,它似乎在能量稳态的调节中也发挥作用。虽然进食会抑制胃饥饿素的产生,禁食会刺激胃饥饿素的释放,但控制这一过程的潜在机制仍不清楚。本研究的目的是通过使用阶梯式高胰岛素-正常-低-高血糖葡萄糖钳夹技术来检验以下假设:高胰岛素血症或低血糖可能影响胃饥饿素的产生。在钳夹前的时间段内保持稳定后,在血糖正常期间(基础胃饥饿素水平为207±12,在t = 30分钟时为169±10 fmol/ml,P < 0.001),胃饥饿素水平随着胰岛素输注迅速下降。在随后的低血糖期(平均血糖53±2 mg/dl)和高血糖期(平均血糖163±6 mg/dl),胃饥饿素仍受到抑制。尽管胃饥饿素受到抑制,但在低血糖期间生长激素显著升高(基础值4.1±1.3,在t = 120分钟时为28.2±3.9 μg/l,P < 0.001)。我们的数据表明,胰岛素可能独立于葡萄糖抑制循环中的胃饥饿素,尽管葡萄糖可能有额外的作用。我们得出结论,低血糖期间观察到的生长激素反应不受循环胃饥饿素的调节。