Gormsen L C, Jessen N, Gjedsted J, Gjedde S, Nørrelund H, Lund S, Christiansen J S, Nielsen S, Schmitz O, Møller N
Medical Department M, Aarhus University Hospital, Aarhus University, Nørrebrogade 42, DK-8000 Aarhus C, Denmark.
J Clin Endocrinol Metab. 2007 May;92(5):1834-42. doi: 10.1210/jc.2006-2659. Epub 2007 Mar 6.
GH and other stress hormones stimulate lipolysis, which may result in free fatty acid (FFA)-mediated insulin resistance. However, there are also indications that FFAs in the very low physiological range have the same effect.
The objective of the study was to address systematically the dose-response relations between FFAs and insulin sensitivity.
We therefore examined eight healthy men for 8 h (6 h basal and 2 h glucose clamp) on four occasions.
Intralipid was infused at varying rates (0, 3, 6, 12 microl.kg(-1).min(-1)); lipolysis was blocked by acipimox; and endogenous GH, insulin, and glucagon secretion was blocked by somatostatin and subsequently replaced at fixed rates.
This resulted in four different FFA levels between 50 and 2000 micromol/liter, with comparable levels of insulin and counterregulatory hormones. Both in the basal state and during insulin stimulation, we saw progressively decreased glucose disposal, nonoxidative glucose disposal, and forearm muscle glucose uptake at FFA levels above 500 micromol/liter. Apart from forearm glucose uptake, the very same parameters were decreased at low FFA levels (approximately 50 micromol/liter). FFA rate of disposal was linearly related to the level of FFAs, whereas lipid oxidation reached a maximum at FFA levels approximately 1000 micromol/liter.
In the presence of comparable levels of all major metabolic hormones, insulin sensitivity peaks at physiological levels of FFAs with a gradual decrease at elevated as well as suppressed FFA concentrations. These data constitute comprehensive dose-response curves for FFAs in the full physiological range from close to zero to above 2000 micromol/liter.
生长激素(GH)和其他应激激素会刺激脂肪分解,这可能导致游离脂肪酸(FFA)介导的胰岛素抵抗。然而,也有迹象表明,极低生理范围内的FFA也有同样的作用。
本研究的目的是系统地探讨FFA与胰岛素敏感性之间的剂量反应关系。
因此,我们对8名健康男性进行了4次为期8小时(基础状态6小时和葡萄糖钳夹2小时)的检查。
以不同速率(0、3、6、12微升·千克-1·分钟-1)输注脂肪乳剂;用阿昔莫司阻断脂肪分解;用生长抑素阻断内源性GH、胰岛素和胰高血糖素的分泌,随后以固定速率进行替代。
这导致FFA水平在50至2000微摩尔/升之间出现四种不同水平,胰岛素和对抗调节激素水平相当。在基础状态和胰岛素刺激期间,当FFA水平高于500微摩尔/升时,我们观察到葡萄糖处置、非氧化葡萄糖处置和前臂肌肉葡萄糖摄取逐渐减少。除了前臂葡萄糖摄取外,在低FFA水平(约50微摩尔/升)时,这些参数也同样降低。FFA处置速率与FFA水平呈线性相关,而脂质氧化在FFA水平约为1000微摩尔/升时达到最大值。
在所有主要代谢激素水平相当的情况下,胰岛素敏感性在生理水平的FFA时达到峰值,在FFA浓度升高和降低时均逐渐降低。这些数据构成了FFA在从零接近到高于2000微摩尔/升的完整生理范围内的综合剂量反应曲线。