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脂肪乳剂/肝素输注可抑制人体血清瘦素水平。

Intralipid/heparin infusion suppresses serum leptin in humans.

作者信息

Garcia-Lorda P, Nash Wendy, Roche Ansley, Pi-Sunyer F-X, Laferrere B

机构信息

Obesity Research Center, St Luke's/Roosevelt Hospital Center, Columbia University College of Physicians and Surgeons, 1111 Amsterdam Avenue, New York, NY 10025, USA.

出版信息

Eur J Endocrinol. 2003 Jun;148(6):669-76. doi: 10.1530/eje.0.1480669.

Abstract

BACKGROUND/AIM: Our previous studies showed that administration of dexamethasone plus food increased serum leptin levels 100% more than dexamethasone alone. We hypothesized that this increase in leptin from the meal could result directly from the provision of fuel metabolites rather than from the meal-induced rise in insulin. In the current study, we tested the effect of an i.v. lipid fuel source (Intralipid 20%/heparin) that would incur only a modest increase in insulin. This study was undertaken because the role of lipid in the regulation of human leptin levels has been controversial, with differing effects reported: stimulatory, inhibitory, or no effect at all.

METHODS

In order to evaluate how lipids affect serum leptin in humans, we administered the following to seven lean, healthy, fasting subjects: (i) Intralipid 20% at 0.83 ml/kg.h plus heparin (800 IE/h) infused i.v. for 7 h (LIPID), (ii) LIPID with one initial pulse of insulin (0.09 U/kg) given s.c. (LIPID+INS), (iii) LIPID with dexamethasone (2 mg i.v. push) given at the start of the infusion (LIPID+DEX), and (iv) LIPID with insulin plus dexamethasone (LIPID+INS+DEX). Control trials in another 14 subjects matched hormonal conditions but lacked the LIPID infusion. Blood levels were collected over 8 h for determination of free fatty acids (FFA), glucose, insulin, and leptin under each experimental condition.

RESULTS

Over the 420 min of LIPID infusion, FFA levels rose four-fold from 0.28+/-0.05 mmol/l to 0.99+/-0.05 mmol/l. Serum leptin levels were suppressed by 10-20% in the LIPID condition as compared with control (no LIPID) between 90 min (P=0.008) and 360 min (P=0.045). LIPID+DEX did not increase leptin. A pulse of insulin (INS) increased serum insulin levels to 49.9+/-6.1 U/ml at 90 min and increased serum leptin by 21.3+/-6.6% at 480 min (P=0.054). LIPID decreased leptin in the face of this insulin-induced increase (LIPID+INS), between 360 min (P=0.017) and 420 min (P=0.003), with a 23% suppressive effect at 420 min. LIPID+DEX elevated leptin levels by 112.5+/-35.8% at 480 min (P=0.037), however, the Intralipid/heparin infusion did not blunt the rise of leptin under these conditions.

CONCLUSIONS

These data showed that Intralipid/heparin: (i) are not sufficient to trigger the effect of dexamethasone on leptin, (ii) have an acute inhibitory effect on both fasting and insulin-stimulated leptin levels, and (iii) that this inhibitory effect cannot reverse the strong stimulatory effect of dexamethasone and insulin on serum leptin.

摘要

背景/目的:我们之前的研究表明,给予地塞米松并同时进食比单独给予地塞米松使血清瘦素水平升高了100%。我们推测,进食引起的瘦素升高可能直接源于提供的燃料代谢产物,而非进食诱导的胰岛素升高。在本研究中,我们测试了静脉注射脂质燃料源(20%英脱利匹特/肝素)的效果,该燃料源只会使胰岛素有适度升高。开展本研究是因为脂质在调节人类瘦素水平中的作用一直存在争议,报道的影响各不相同:刺激作用、抑制作用或无作用。

方法

为了评估脂质如何影响人类血清瘦素,我们对7名瘦的、健康的、禁食的受试者给予以下处理:(i)以0.83 ml/kg·h的速度静脉输注20%英脱利匹特加肝素(800 IE/h),持续7小时(脂质组),(ii)脂质组加一次皮下注射初始剂量的胰岛素(0.09 U/kg)(脂质+胰岛素组),(iii)脂质组在输注开始时静脉推注地塞米松(2 mg)(脂质+地塞米松组),以及(iv)脂质组加胰岛素和地塞米松(脂质+胰岛素+地塞米松组)。另外14名受试者进行对照试验,其激素状况匹配,但未进行脂质输注。在每种实验条件下,于8小时内采集血样,以测定游离脂肪酸(FFA)、葡萄糖、胰岛素和瘦素水平。

结果

在脂质输注的420分钟内,FFA水平从0.28±0.05 mmol/L升高至0.99±0.05 mmol/L,升高了四倍。与对照组(无脂质输注)相比,在90分钟(P = 0.008)至360分钟(P = 0.045)期间,脂质组的血清瘦素水平被抑制了10 - 20%。脂质+地塞米松组并未使瘦素升高。一次胰岛素注射(胰岛素组)在90分钟时使血清胰岛素水平升高至49.9±6.1 U/ml,并在480分钟时使血清瘦素升高21.3±6.6%(P = 0.054)。在这种胰岛素诱导的升高情况下(脂质+胰岛素组),脂质在360分钟(P = 0.017)至420分钟(P = 0.003)期间降低了瘦素,在420分钟时具有23%的抑制作用。脂质+地塞米松组在480分钟时使瘦素水平升高了112.5±35.8%(P = 0.037),然而,在这些条件下,英脱利匹特/肝素输注并未减弱瘦素的升高。

结论

这些数据表明,英脱利匹特/肝素:(i)不足以引发地塞米松对瘦素的作用,(ii)对空腹和胰岛素刺激的瘦素水平均有急性抑制作用,以及(iii)这种抑制作用无法逆转地塞米松和胰岛素对血清瘦素的强烈刺激作用。

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