Pierart Z Camila, Serrano L Valentina
Departamento de Nutrición, Facultad de Medicina, Universidad de Chile, Chile.
Rev Med Chil. 2012 Mar;140(3):373-8. doi: 10.4067/S0034-98872012000300015.
Endothelial lipase (EL) is synthetized by endothelial cells and its main substrates are lipoprotein phospholipids. Over expression of EL reduces high density lipoprotein (HDL) cholesterol and phospholipids, in vivo and in vitro. Inhibition of the enzyme achieves the opposite effects. The synthesis of the enzyme is regulated by interleukin 1 and tumor necrosis factor a. These inflammatory cytokines play a role in diabetes and vascular disease. An increase in vascular mechanical forces, that play a role in atherogenesis, also increase the synthesis of EL. There is expression of EL in endothelial cells, macrophages and muscle cells of atherosclerotic lesions of coronary arteries of humans. This evidence leads to the suspicion that EL plays a role in atherogenesis. There are also higher plasma levels of EL in subjects with type 2 diabetes, who are especially susceptible to the development of vascular lesions. Therefore the inhibition of EL could play an important role in HDL metabolism and could be a new therapeutic strategy for the prevention of atherosclerosis.
内皮脂肪酶(EL)由内皮细胞合成,其主要底物是脂蛋白磷脂。在体内和体外,EL的过度表达都会降低高密度脂蛋白(HDL)胆固醇和磷脂水平。抑制该酶则会产生相反的效果。该酶的合成受白细胞介素1和肿瘤坏死因子α调节。这些炎性细胞因子在糖尿病和血管疾病中起作用。在动脉粥样硬化形成中起作用的血管机械力增加也会增加EL的合成。在人类冠状动脉粥样硬化病变的内皮细胞、巨噬细胞和肌肉细胞中存在EL表达。这一证据使人怀疑EL在动脉粥样硬化形成中起作用。在2型糖尿病患者中,EL的血浆水平也较高,这些患者尤其易发生血管病变。因此,抑制EL可能在HDL代谢中起重要作用,并且可能成为预防动脉粥样硬化的一种新的治疗策略。