Chronic Low-Dose Lipid Infusion in Healthy Patients Induces Markers of Endothelial Activation Independent of Its Metabolic Effects

Sangeeta R. Kashyap MD, Renata Belfort MD, Eugenio Cersosimo MD, Shuko Lee PhD, Kenneth Cusi PhD
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引用次数: 24

Abstract

Elevated plasma triglyceride/free fatty acid (FFA) levels and insulin resistance may promote atherosclerosis through endothelial activation (ie, increased expression of intercellular adhesion molecule 1 [ICAM-1]/vascular adhesion molecule 1 [VCAM-1], and endothelin-1 [ET-1]) in patients with the metabolic syndrome, but this has never been directly tested. The authors measured endothelial activation and insulin sensitivity (euglycemic insulin clamp with [3- 3 H]-glucose) after a 4-day low-dose lipid infusion that elevated plasma FFA to levels observed in the metabolic syndrome in 20 lean, non-diabetic insulin-resistant subjects with a strong family history of type 2 diabetes mellitus (FH + ) and 10 insulin-sensitive volunteers without a family history of type 2 diabetes mellitus (FH ). Low-dose lipid infusion reduced insulin sensitivity by approximately 25% in insulin-sensitive FH controls but did not worsen preexisting insulin resistance in FH + . Low-dose lipid infusion elevated plasma ICAM and VCAM levels similarly in both groups (approximately 12%–18%; P<.01 vs baseline), while plasma ET-1 levels increased more in FH+vs FH(46% vs 10%; P=.005). Increased plasma FFA levels closely correlated with elevated ICAM (r=0.60; P<.01), VCAM, and ET-1 levels (r=0.39 and r=0.42, respectively; P<.05). Low-dose lipid infusion induces endothelial activation in both lean insulin-resistant (FH+) and insulin-sensitive (FH) healthy patients, regardless of changes in insulin sensitivity. These results prove that even a modest lipid oversupply may be sufficient to trigger a deleterious endothelial response.

健康患者的慢性低剂量脂质输注诱导内皮激活标志物,而不依赖于其代谢效应
代谢综合征患者血浆甘油三酯/游离脂肪酸(FFA)水平升高和胰岛素抵抗可能通过内皮激活(即细胞间粘附分子1[ICAM-1]/血管粘附分子1[VCAM-1]和内皮素-1[ET-1]的表达增加)促进动脉粥样硬化,但这从未被直接测试过。作者在4天的低剂量脂质输注后测量了内皮细胞活化和胰岛素敏感性([3-3H]-葡萄糖的正常血糖胰岛素钳),该输注将血浆FFA升高到20例瘦、中、重度肥胖的代谢综合征中观察到的水平,具有2型糖尿病(FH+)家族史的非糖尿病胰岛素抵抗受试者和10名没有2型糖尿病家族史的胰岛素敏感志愿者。低剂量脂质输注使胰岛素敏感性FH−对照组的胰岛素敏感性降低了约25%,但并未使FH+组先前存在的胰岛素抵抗恶化。低剂量脂质输注使两组的血浆ICAM和VCAM水平相似地升高(与基线相比约为12%-18%;P<;.01),而FH+组的血浆ET-1水平与FH-组相比增加更多(46%与10%;P=.005),和ET-1水平(分别为r=0.39和r=0.42;P<;.05)。低剂量脂质输注在瘦胰岛素抵抗(FH+)和胰岛素敏感(FH-)健康患者中诱导内皮细胞活化,而与胰岛素敏感性的变化无关。这些结果证明,即使是适度的脂质过量也可能足以引发有害的内皮反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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