Second Department of Internal Medicine, Aristotle University of Thessaloniki, Greece.
Angiology. 2011 Jan;62(1):38-45. doi: 10.1177/0003319710371616. Epub 2010 Aug 3.
We assessed the effect of epinephrine on human monocytes. Monocytes were isolated from 16 healthy obese and 10 lean healthy subjects. Insulin sensitivity was assessed by euglycemic hyperinsulinemic clamp. Obese subjects were subdivided into 2 sub-groups, insulin sensitive (IS) and insulin resistant (IR). Monocyte properties [attachment to laminin 1, migration through laminin 1, oxidized-low density lipoprotein (oxLDL) phagocytosis] were assessed pre- and post-stimulation in vitro with epinephrine. Experiments were repeated after incubation with a Na(+)/H( +) exchanger-1 inhibitor (NHE-1) (cariporide). Epinephrine increased monocyte attachment to laminin in lean and obese IR subjects through involvement of NHE-1, PKC, NO synthase, NADPH oxidase and actin polymerization. In contrast, epinephrine did not affect monocyte migration. Epinephrine increased oxLDL phagocytosis in all groups studied. Incubation with cariporide attenuated oxLDL phagocytosis. Epinephrine induces monocyte dysfunction which may be atherogenic.
我们评估了肾上腺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。将肥胖者分为胰岛素敏感(IS)和胰岛素抵抗(IR)两组。在体外,用肾上腺素预先和刺激后评估单核细胞的特性[附着在层粘连蛋白 1 上、穿过层粘连蛋白 1 迁移、氧化低密度脂蛋白(oxLDL)吞噬]。实验在与 Na(+)/H( +)交换体-1 抑制剂(NHE-1)(cariporide)孵育后重复。肾上腺素通过 NHE-1、PKC、NOS、NADPH 氧化酶和肌动蛋白聚合作用增加瘦人和肥胖 IR 受试者单核细胞附着在层粘连蛋白上。相比之下,肾上腺素不影响单核细胞迁移。肾上腺素增加了所有研究组的 oxLDL 吞噬作用。cariporide 的孵育减弱了 oxLDL 的吞噬作用。肾上腺素诱导单核细胞功能障碍,可能具有动脉粥样硬化作用。