Gastaldi M, Lerique B, Boyer J
INSERM, U.260, UER de Médecine, Marseille, France.
Alcohol Alcohol. 1991;26(4):451-7. doi: 10.1093/oxfordjournals.alcalc.a045138.
Challenging intact erythrocytes from normal human subjects with ethanol resulted in dose-dependent decreases in rates of acylation of phosphatidylcholine (PC) and phosphatidylethanolamine (PE) while triacylglycerol (TAG) acylation was stimulated. In erythrocytes from alcoholic subjects, the responses were of lesser magnitude, indicating a lower sensitivity to ethanol. This in vitro resistance, typical of the state of tolerance, was associated in erythrocytes from alcoholic subjects with increased baseline rates of acylation of PC, PE and TAG, suggesting high levels of glycerolipid fatty acid turnover. These results suggest that (1) intact human erythrocytes are qualitatively and quantitatively valid for studying the adaptive response to ethanol; and (2) chronic alcoholism is associated with increases in turnover rates of the acyl moieties of lipid membrane components regardless of the pattern of initial sensitivity to ethanol. Increased acylation rates during chronic alcoholism might modify the remodeling of the lipid matrix and thereby the membrane function.
用乙醇刺激正常人体受试者的完整红细胞,会导致磷脂酰胆碱(PC)和磷脂酰乙醇胺(PE)的酰化速率呈剂量依赖性降低,而三酰甘油(TAG)的酰化受到刺激。在酒精性受试者的红细胞中,反应程度较小,表明对乙醇的敏感性较低。这种体外抗性是耐受性状态的典型表现,在酒精性受试者的红细胞中,与PC、PE和TAG酰化的基线速率增加有关,表明甘油olipid脂肪酸周转水平较高。这些结果表明:(1)完整的人红细胞在定性和定量方面对于研究对乙醇的适应性反应是有效的;(2)慢性酒精中毒与脂质膜成分酰基部分的周转速率增加有关,而与对乙醇的初始敏感性模式无关。慢性酒精中毒期间酰化速率的增加可能会改变脂质基质的重塑,从而改变膜功能。