Paolisso G, Gambardella A, Amato L, Tortoriello R, D'Amore A, Varricchio M, D'Onofrio F
Department of Geriatric Medicine and Metabolic Diseases, II University of Naples, Italy.
Diabetologia. 1995 Nov;38(11):1295-9. doi: 10.1007/BF00401761.
Our study investigates short- and long-term effects of infusion of non-esterified fatty acids (NEFA) on insulin secretion in healthy subjects. Twelve healthy individuals underwent a 24-h Intralipid (10% triglyceride emulsion) infusion at a rate of 0.4 ml/min with a simultaneous infusion of heparin (a bolus of 200 U followed by 0.2 U/min per kg body weight). After an overnight fast (baseline), at 6 and at 24 h of Intralipid infusion and 24 h after Intralipid discontinuation (recovery test), all subjects underwent an intravenous glucose tolerance test (iv-GTT) (25 g of glucose/min). Intralipid infusion caused a threefold rise in plasma NEFA concentrations with no difference between the 6- and the 24-h concentrations. Compared to baseline acute insulin response (AIR) (AIR = 63 +/- 8 mU/l), short-term (6-h) Intralipid infusion was associated with a significant increase in AIR (86 +/- 12 mU/l p < 0.01); in contrast, long-term (24-h) Intralipid delivery was associated with inhibition of AIR (31 +/- 5 mU/l) compared to baseline (p < 0.001) and to the 6-h (p < 0.03) triglyceride emulsion infusion. Intralipid infusion was associated with a progressive and significant decline in respiratory quotient (RQ). A positive correlation between changes in fasting plasma NEFA concentrations and AIR at the 6-h infusion (r = 0.89 p < 0.001) was found. In contrast, at the end of the Intralipid infusion period, changes in plasma NEFA concentrations and AIR were negatively correlated (r = -0.87 p < 0.001). The recovery test showed that fasting plasma NEFA concentrations, RQ and AIR had returned to baseline values. In the control study (n = 8) 0.9% NaCl infusion did not mimick the effect of Intralipid. In conclusion, our study demonstrates that short- and long-term exposures of beta cells to high plasma NEFA concentrations have opposite effects on glucose-induced insulin secretion.
我们的研究调查了输注非酯化脂肪酸(NEFA)对健康受试者胰岛素分泌的短期和长期影响。12名健康个体以0.4毫升/分钟的速率接受了24小时的英脱利匹特(10%甘油三酯乳剂)输注,同时输注肝素(先推注200单位,随后以每公斤体重0.2单位/分钟的速度输注)。在过夜禁食(基线)后,在英脱利匹特输注6小时和24小时时以及英脱利匹特输注停止后24小时(恢复试验),所有受试者均接受了静脉葡萄糖耐量试验(iv-GTT)(25克葡萄糖/分钟)。英脱利匹特输注使血浆NEFA浓度升高了三倍,6小时和24小时的浓度之间无差异。与基线急性胰岛素反应(AIR)(AIR = 63±8 mU/l)相比,短期(6小时)英脱利匹特输注使AIR显著增加(86±12 mU/l,p < 0.01);相反,与基线(p < 0.001)以及6小时(p < 0.03)甘油三酯乳剂输注相比,长期(24小时)英脱利匹特输注与AIR受到抑制(31±5 mU/l)有关。英脱利匹特输注与呼吸商(RQ)的逐渐且显著下降有关。发现在6小时输注时,空腹血浆NEFA浓度变化与AIR之间存在正相关(r = 0.89,p < 0.001)。相反,在英脱利匹特输注期结束时,血浆NEFA浓度变化与AIR呈负相关(r = -0.87,p < 0.001)。恢复试验表明,空腹血浆NEFA浓度、RQ和AIR已恢复至基线值。在对照研究(n = 8)中,输注0.9%氯化钠未模拟英脱利匹特的作用。总之,我们的研究表明,β细胞短期和长期暴露于高血浆NEFA浓度对葡萄糖诱导的胰岛素分泌具有相反的影响。