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游离脂肪酸水平的急性升高会导致肥胖受试者出现肝脏胰岛素抵抗。

Acute elevation of free fatty acid levels leads to hepatic insulin resistance in obese subjects.

作者信息

Bevilacqua S, Bonadonna R, Buzzigoli G, Boni C, Ciociaro D, Maccari F, Giorico M A, Ferrannini E

出版信息

Metabolism. 1987 May;36(5):502-6. doi: 10.1016/0026-0495(87)90051-5.

DOI:10.1016/0026-0495(87)90051-5
PMID:3553852
Abstract

Raised levels of free fatty acids (FFA) compete with glucose for utilization by insulin-sensitive tissues, and, therefore, they may induce insulin resistance in the normal subject. The influence of experimental elevations in FFA levels on glucose metabolism in native insulin-resistant states is not known. We studied seven women with moderate obesity (63% above their ideal body weight) but normal glucose tolerance with the use of the insulin clamp technique with or without an infusion of Intralipid + heparin. Upon raising plasma insulin levels to approximately 60 microU/mL while maintaining euglycemia, whole body glucose utilization (3H-3-glucose) rose similarly without (from 66 +/- 7 to 113 +/- 11 mg/min m2, P less than .02) or with (from 70 +/- 7 to 137 +/- 19 mg/min m2, P less than .02) concomitant lipid infusion. In contrast, endogenous glucose production was considerably (73%) suppressed (from 66 +/- 7 to 15 +/- 8 mg/min m2, P less than .001) during the clamp without lipid, but declined only marginally (from 70 +/- 7 to 48 +/- 7 mg/min m2, NS) with lipid administration. The difference between the control and the lipid study was highly significant (P less than .02), and amounted to an average of 3.8 g of relative glucose overproduction during the second hour of the clamp. Blood levels of lactate rose by 34 +/- 15% (.1 greater than P greater than .05) in the control study but only by 17 +/- 10% (NS) during lipid infusion. Blood pyruvate concentrations fell in both sets of experiments (by approximately 45% at the end of the study) with similar time courses.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

游离脂肪酸(FFA)水平升高会与葡萄糖竞争胰岛素敏感组织的利用,因此,它们可能在正常受试者中诱导胰岛素抵抗。FFA水平的实验性升高对天然胰岛素抵抗状态下葡萄糖代谢的影响尚不清楚。我们使用胰岛素钳夹技术,在有或没有输注英脱利匹特+肝素的情况下,研究了7名中度肥胖(比理想体重高63%)但糖耐量正常的女性。在将血浆胰岛素水平提高到约60微单位/毫升并维持血糖正常的情况下,无论有无(从66±7至113±11毫克/分钟·平方米,P<0.02)同时输注脂质,全身葡萄糖利用(3H-3-葡萄糖)的升高相似。相比之下,在无脂质钳夹期间,内源性葡萄糖生成受到显著抑制(73%)(从66±7至15±8毫克/分钟·平方米,P<0.001),但在给予脂质时仅略有下降(从70±7至48±7毫克/分钟·平方米,无显著性差异)。对照研究与脂质研究之间的差异非常显著(P<0.02),在钳夹的第二个小时内,平均相对葡萄糖过量生成量为3.8克。在对照研究中,血乳酸水平升高了34±15%(0.1>P>0.05),但在脂质输注期间仅升高了17±10%(无显著性差异)。在两组实验中,血丙酮酸浓度均下降(研究结束时下降约45%),且时间进程相似。(摘要截短于250字)

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