Giugliano D, Torella R, Sgambato S
Acta Diabetol Lat. 1979 Jan-Mar;16(1):77-81. doi: 10.1007/BF02590766.
The aim of this study was to compare the metabolic and hormonal effects of somatostatin to those of propranolol, a beta-adrenergic blocking agent known to reduce basal insulin secretion. For this purpose, 6 normal subjects received somatostatin (4 microgram/min) per 60 min and 6 subjects were infused with propranolol (0.08 mg/min). Somatostatin resulted in a significant decrease of basal insulin (p less than 0.05) and glucagon (p less than 0.01) and raised plasma FFA levels from a mean basal value of 417 +/- 24 muEq/1 (x +/- SEM) to 600 +/- 46 muEq/1 at 60 min (p less than 0.01). Propranolol significantly decreased basal insulin (p less than 0.05) and glucagon (p less than 0.05); FFA levels rose slightly at the end of propranolol administration (p less than 0.05). The levels of FFA which were significantly higher (p less than 0.025) during somatostatin as compared to those observed during propranolol, seem to suggest a role for this tetradecapeptide in lipid metabolism independent of its inhibiting action on islet hormone release.
本研究的目的是比较生长抑素与普萘洛尔(一种已知可降低基础胰岛素分泌的β-肾上腺素能阻滞剂)的代谢和激素效应。为此,6名正常受试者每60分钟接受生长抑素(4微克/分钟),6名受试者输注普萘洛尔(0.08毫克/分钟)。生长抑素导致基础胰岛素(p<0.05)和胰高血糖素(p<0.01)显著降低,并使血浆游离脂肪酸水平从平均基础值417±24微当量/升(x±SEM)在60分钟时升高至600±46微当量/升(p<0.01)。普萘洛尔显著降低基础胰岛素(p<0.05)和胰高血糖素(p<0.05);在普萘洛尔给药结束时游离脂肪酸水平略有升高(p<0.05)。与普萘洛尔给药期间相比,生长抑素期间游离脂肪酸水平显著更高(p<0.025),这似乎表明这种十四肽在脂质代谢中发挥作用,与其对胰岛激素释放的抑制作用无关。