Hamilton C A, Thorin E, McCulloch J, Dominiczak M H, Reid J L
Department of Medicine and Therapeutics, Western Infirmary, Glasgow, Scotland, UK.
Atherosclerosis. 1994 May;107(1):55-63. doi: 10.1016/0021-9150(94)90141-4.
The aim of this study was to investigate the effects of chronic exposure to low density lipoprotein (LDL) and oxidised LDL (OXLDL) on phosphatidylinositol metabolism in bovine aortic endothelial cells. Basal levels of total inositol phosphates and inositol 1,4,5-trisphosphate were increased after both 18 and 66 h exposure to OXLDL 20 micrograms/ml. Levels also tended to be increased after exposure to LDL but this only reached significance for LDL 20 micrograms/ml after 18 h exposure. Absolute levels of inositol phosphates after stimulation with ATP were unaffected by incubation with LDL or OXLDL. However, when expressed as a percentage of basal levels, stimulated levels of inositol phosphates were reduced for ATP 10(-3) and 10(-4)M. Uptake of [3H]inositol into the phosphatidylinositol cycle was reduced after incubation with LDL and OXLDL for either 18 or 66 h. The effect of OXLDL was greater than that of LDL. The antioxidants EDTA and N-acetylcysteine attenuated the effects of LDL but not OXLDL. In addition, catalase but not mannitol or superoxide dismutase modified the effect of LDL on [3H]inositol uptake. These studies show that chronic exposure to OXLDL and to a lesser extent LDL can modify phosphatidylinositol metabolism in bovine aortic endothelial cells and that the effects of LDL may be attenuated by antioxidants and free radical scavengers. We hypothesise that the decreased uptake of [3H]inositol could be related to an alteration in membrane structure and integrity and may reflect alteration in transport of a number of ions and molecules.
本研究的目的是调查长期暴露于低密度脂蛋白(LDL)和氧化型低密度脂蛋白(OX-LDL)对牛主动脉内皮细胞磷脂酰肌醇代谢的影响。在暴露于20微克/毫升的OX-LDL 18小时和66小时后,总肌醇磷酸酯和肌醇1,4,5-三磷酸的基础水平均升高。暴露于LDL后水平也有升高趋势,但仅在暴露18小时后,20微克/毫升的LDL才达到显著水平。用ATP刺激后的肌醇磷酸酯绝对水平不受与LDL或OX-LDL孵育的影响。然而,当以基础水平的百分比表示时,对于10⁻³和10⁻⁴M的ATP,刺激后的肌醇磷酸酯水平降低。与LDL和OX-LDL孵育18小时或66小时后,[³H]肌醇进入磷脂酰肌醇循环的摄取减少。OX-LDL的作用大于LDL。抗氧化剂乙二胺四乙酸(EDTA)和N-乙酰半胱氨酸减弱了LDL的作用,但未减弱OX-LDL的作用。此外,过氧化氢酶而非甘露醇或超氧化物歧化酶改变了LDL对[³H]肌醇摄取的作用。这些研究表明,长期暴露于OX-LDL以及程度较轻的LDL可改变牛主动脉内皮细胞的磷脂酰肌醇代谢,且LDL的作用可能被抗氧化剂和自由基清除剂减弱。我们推测,[³H]肌醇摄取减少可能与膜结构和完整性的改变有关,并且可能反映了多种离子和分子转运的改变。