Townsend Raymond R, Zhao Huawei
Department of Medicine, University of Pennsylvania, Philadelphia, PA; and the Department of Medicine, Michigan State University, East Lansing, MI.
Metabolism. 2002 Jun;51(6):779-82. doi: 10.1053/meta.2002.31344.
Fatty acids fulfill important roles in physiology. The plasma concentrations of fatty acids are principally regulated by insulin, which suppresses the release of fatty acids from lipid stores, and catecholamines, which increase their release from lipid stores. Although insulin regulates the concentration of plasma free fatty acids (FFAs), little is known about the relative effects of insulin on the saturated compared with the unsaturated plasma fatty acids. In the current study, we specifically measured the plasma concentration of 3 saturated and 4 unsaturated fatty acids along with an estimate of lipolytic activity using a stable isotope of glycerol during a 3-hour, 1-step, euglycemic clamp study in humans. The data showed the expected decline in plasma fatty acids from 0.26 +/- 0.02 to 0.06 +/- 0.01 micromol/mL. Saturated fatty acids were reduced from 0.12 +/- 0.01 to 0.05 +/- 0.005 micromol/mL and unsaturated fatty acids were reduced from 0.11 +/- 0.01 to 0.01 +/- 0.001 micromol/mL after 3 hours of insulin infusion. At baseline, the ratio of saturated to unsaturated fatty acid was 55:45, which increased to 82:18 by the end of study. The changes in fatty acids were evident within 1 hour. Whole body lipolytic rates were measured with deuterated glycerol and decreased from 1.48 +/- 0.56 micromol x kg(-1) x min(-1) to 0.75 +/- 0.34 micromol x kg(-1) x min(-1). Baseline postabsorptive plasma fatty acid concentrations were significantly correlated to insulin sensitivity (M value) as measured during the euglycemic clamp. There were no significant differences between the more insulin-sensitive subjects when compared with the more insulin-resistant subjects with respect to the relative decreases in saturated and unsaturated fatty acids during insulin infusion. These data demonstrate a sustained differential effect of insulin on the plasma fatty acid profile.
脂肪酸在生理学中发挥着重要作用。血浆中脂肪酸的浓度主要受胰岛素调节,胰岛素会抑制脂肪酸从脂质储存中释放;儿茶酚胺也会调节其浓度,儿茶酚胺会增加脂肪酸从脂质储存中的释放。尽管胰岛素可调节血浆游离脂肪酸(FFA)的浓度,但与不饱和血浆脂肪酸相比,胰岛素对饱和血浆脂肪酸的相对影响却鲜为人知。在当前的研究中,我们在一项针对人类的3小时、单步、正常血糖钳夹研究中,使用甘油稳定同位素,专门测量了3种饱和脂肪酸和4种不饱和脂肪酸的血浆浓度,并估算了脂解活性。数据显示,血浆脂肪酸浓度如预期的那样从0.26±0.02微摩尔/毫升降至0.06±0.01微摩尔/毫升。胰岛素输注3小时后,饱和脂肪酸从0.12±0.01微摩尔/毫升降至0.05±0.005微摩尔/毫升,不饱和脂肪酸从0.11±0.01微摩尔/毫升降至0.01±0.001微摩尔/毫升。在基线时,饱和脂肪酸与不饱和脂肪酸的比例为55:45,到研究结束时增至82:18。脂肪酸的变化在1小时内就很明显。用氘代甘油测量的全身脂解率从1.48±0.56微摩尔·千克⁻¹·分钟⁻¹降至0.75±0.34微摩尔·千克⁻¹·分钟⁻¹。空腹状态下的基线血浆脂肪酸浓度与正常血糖钳夹期间测量的胰岛素敏感性(M值)显著相关。在胰岛素输注期间,与胰岛素抵抗较强的受试者相比,胰岛素敏感性较强的受试者在饱和脂肪酸和不饱和脂肪酸的相对降低方面没有显著差异。这些数据表明胰岛素对血浆脂肪酸谱具有持续的差异作用。