Direct Evidence that Protein Kinase C Mediates the Acute Inhibitory Effect of Oxidised Low Density Lipoprotein on Acetylcholine-induced Endothelium-dependent Relaxation of Rabbit Aorta

J. Smith, Nicola J. Turner, M. Evans, R. A. Evans, R. Babuji
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引用次数: 2

Abstract

This study further examines the involvement of protein kinase C and superoxide anions in the inhibition of agonist-induced endothelium-dependent relaxation by oxidised low density lipoprotein (LDL). Pretreatment of rabbit aorta rings with either oxidised low density lipoprotein or phorbol dibutyrate (PDB) inhibited acetylcholine-induced endothelium-dependent relaxation, but not endothelium-independent relaxations to glyceryl trinitrate. Prior exposure of the rings to either of the specific protein kinase C inhibitors Ro 31-8220 or Ro 31-7549 prevented or reduced respectively the inhibition of acetylcholine-induced relaxation by oxidised LDL or PDB. Neither inhibitor alone affected acetylcholine-induced relaxation. We directly demonstrate for the first time that oxidised, but not native, LDL produces a prolonged activation of protein kinase C in endothelial cells, which was prevented by pretreatment with Ro 31-8220. Oxidised or native LDL, or Ro 31-8220 increased superoxide anion production by rabbit aorta...
蛋白激酶C介导氧化低密度脂蛋白对乙酰胆碱诱导的兔主动脉内皮依赖性舒张急性抑制作用的直接证据
本研究进一步探讨了蛋白激酶C和超氧阴离子在氧化低密度脂蛋白(LDL)抑制激动剂诱导的内皮依赖性松弛中的作用。用氧化低密度脂蛋白或二丁酸磷(PDB)预处理兔主动脉环可抑制乙酰胆碱诱导的内皮依赖性舒张,但对三硝酸甘油无内皮依赖性舒张作用。事先将这些环暴露于特定的蛋白激酶C抑制剂Ro 31-8220或Ro 31-7549中,分别阻止或减少氧化LDL或PDB对乙酰胆碱诱导的松弛的抑制。没有一种抑制剂单独影响乙酰胆碱诱导的松弛。我们首次直接证明氧化的LDL(而非天然的)在内皮细胞中产生蛋白激酶C的延长激活,这可以通过Ro 31-8220预处理来阻止。氧化或天然LDL,或Ro 31-8220增加了兔主动脉超氧阴离子的产生。
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