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瘦素和胰岛素抵抗对瘦素和肥胖健康参与者人单核细胞特性的影响。

Effect of leptin and insulin resistance on properties of human monocytes in lean and obese healthy participants.

机构信息

Metabolic Diseases Unit, Second Department of Internal Medicine, Medical School, Aristotle University of Thessaloniki, Greece.

出版信息

Angiology. 2010 Nov;61(8):768-74. doi: 10.1177/0003319710369104. Epub 2010 May 12.

Abstract

We assessed the effect of leptin on human monocytes. Monocytes were isolated from 16 healthy obese and 10 lean healthy participants. Insulin sensitivity was assessed by euglycemic hyperinsulinemic clamp. Obese participants were subdivided into 2 subgroups, insulin sensitive (IS) and insulin resistant (IR). Monocyte properties (attachment to laminin 1, migration through laminin 1, surface expression of CD36, oxidized low-density lipoprotein [oxLDL] phagocytosis) were assessed pre- and poststimulation in vitro with leptin. Experiments were repeated after incubation with rosiglitazone and a Na(+)/H(+) exchanger-1 inhibitor (cariporide). We found a significant correlation between insulin resistance and monocyte attachment to laminin and oxLDL phagocytosis. Leptin increased the atherosclerosis-related properties of monocytes in all groups, apart from surface expression of CD36 in IS obese participants. Incubation with rosiglitazone or cariporide attenuated the observed effects. Leptin induces monocyte dysfunction which may be atherogenic. Correlation with insulin resistance suggests that atherosclerosis might be accelerated before the onset of diabetes.

摘要

我们评估了瘦素对人单核细胞的作用。从 16 名健康肥胖者和 10 名健康瘦者中分离出单核细胞。通过正葡萄糖高胰岛素钳夹评估胰岛素敏感性。将肥胖参与者分为 2 个亚组,胰岛素敏感(IS)和胰岛素抵抗(IR)。体外用瘦素预先和刺激后评估单核细胞特性(附着于层粘连蛋白 1、穿过层粘连蛋白 1迁移、表面表达 CD36、氧化型低密度脂蛋白[oxLDL]吞噬)。在孵育罗格列酮和 Na(+)/H(+)交换体-1 抑制剂(cariporide)后重复实验。我们发现胰岛素抵抗与单核细胞附着于层粘连蛋白和 oxLDL 吞噬之间存在显著相关性。瘦素增加了所有组中与动脉粥样硬化相关的单核细胞特性,除了 IS 肥胖参与者表面表达 CD36 之外。用罗格列酮或 cariporide 孵育可减弱观察到的作用。瘦素诱导单核细胞功能障碍,可能具有致动脉粥样硬化作用。与胰岛素抵抗相关表明,在糖尿病发病之前,动脉粥样硬化可能会加速。

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