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游离脂肪酸(FFA)的急性变化不会改变血清瘦素水平。

Acute changes in free-fatty acids (FFA) do not alter serum leptin levels.

作者信息

Peinò R, Fernández Alvarez J, Peñalva A, Considine R V, Rodriguez-Segade S, Rodriguez-Garcia J, Cordido F, Casanueva F F, Dieguez C

机构信息

Department of Medicine, Complejo Hospitalario Universitario de Santiago, Spain.

出版信息

J Endocrinol Invest. 1998 Sep;21(8):526-30. doi: 10.1007/BF03347339.

Abstract

Leptin, the product of the ob gene, is a recently discovered hormone secreted by adipocytes. Serum leptin concentrations increase in correlation with the percentage of body fat, but besides that little is known about the physiological actions of leptin in humans. The aim of this study was to assess the influence of changes in circulating free-fatty acids on serum leptin levels. Increases in plasma FFA levels (p < 0.02) were obtained in a group of normal subjects following the administration of intralipid plus heparin (250 ml 10% Intralipid plus 5000 U heparin). FFA reduction was achieved through the administration of acipimox (250 mg, orally, at 0 min and at 210 min), a lipid-lowering drug devoid of side effects, to a group of normal (p < 0.02) and obese subjects (p < 0.05). An increase in circulating FFA levels in normal subjects (n = 6), following administration of a lipid-heparin infusion, failed to modify plasma leptin levels as assessed by the area under the curve (AUC; mean +/- SE 892 +/- 168 for placebo vs 896 +/- 260 following intralipid plus heparin). Similarly, whereas acipimox pretreatment induced a reduction in FFA levels compared to placebo in normal (n = 6) and obese subjects (n = 8), it also failed to modify plasma leptin levels at any time-point studied. The results indicate that short-term reduction or increase in circulating FFA are not associated to changes in plasma leptin levels.

摘要

瘦素是ob基因的产物,是一种最近发现的由脂肪细胞分泌的激素。血清瘦素浓度与体脂百分比呈正相关,但除此之外,人们对瘦素在人体内的生理作用知之甚少。本研究的目的是评估循环游离脂肪酸变化对血清瘦素水平的影响。一组正常受试者在输注脂肪乳剂加肝素(250ml 10%脂肪乳剂加5000U肝素)后,血浆游离脂肪酸水平升高(p<0.02)。通过对一组正常受试者(p<0.02)和肥胖受试者(p<0.05)口服阿西莫司(250mg,分别在0分钟和210分钟时服用)来降低游离脂肪酸水平,阿西莫司是一种无副作用的降脂药物。在正常受试者(n=6)中,输注脂肪乳剂加肝素后循环游离脂肪酸水平升高,但通过曲线下面积评估(AUC;安慰剂组平均±标准误为892±168,脂肪乳剂加肝素组为896±260),血浆瘦素水平未发生改变。同样,在正常受试者(n=6)和肥胖受试者(n=8)中,与安慰剂相比,阿西莫司预处理可降低游离脂肪酸水平,但在任何研究时间点均未改变血浆瘦素水平。结果表明,循环游离脂肪酸的短期降低或升高与血浆瘦素水平的变化无关。

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