Petrichenko I E, Chepurnenko N V, Perova N V, Oganov R G
USSR Research Center for Preventive Medicine, Moscow.
Biochem Int. 1989 May;18(5):913-22.
It has been found that lymphocytes of hypercholesterolemic (HCh) subjects are characterized by a reduced number of glucocorticoid receptors (GcR) as compared with the cells of normolipidemics (N). Addition of HCh-sera or very low density lipoproteins, or low density lipoproteins isolated both from HCh-sera and N-sera to cultured human skin fibroblasts brought about a fall in the number of GcR in the cells. High density lipoproteins had no effect on GcR level. Dexamethasone was less effective in inhibiting cholesterol synthesis from [14C]acetate in the lymphocytes and fibroblasts with a reduced number of GcR. In the presence of dexamethasone (I x 10(-8)M) in fibroblast growth medium, reduced number of GcR (due to preincubation with very low density lipoproteins) led to a substantial increase in cholesterol synthesis. These findings indicate that the sensitivity of peripheral cells to glucocorticoids is decreased in HCh which might be one of the trigger mechanisms of atherogenesis.
已发现,与血脂正常者(N)的细胞相比,高胆固醇血症(HCh)患者的淋巴细胞具有糖皮质激素受体(GcR)数量减少的特征。将HCh血清或极低密度脂蛋白,或从HCh血清和N血清中分离出的低密度脂蛋白添加到培养的人皮肤成纤维细胞中,会导致细胞中GcR数量下降。高密度脂蛋白对GcR水平无影响。地塞米松在抑制GcR数量减少的淋巴细胞和成纤维细胞中由[14C]乙酸盐合成胆固醇方面效果较差。在成纤维细胞生长培养基中存在地塞米松(1×10(-8)M)的情况下,GcR数量减少(由于与极低密度脂蛋白预孵育)导致胆固醇合成大幅增加。这些发现表明,HCh患者外周细胞对糖皮质激素的敏感性降低,这可能是动脉粥样硬化发生的触发机制之一。