Aloia R C, Paxton J, Daviau J S, van Gelb O, Mlekusch W, Truppe W, Meyer J A, Brauer F S
Life Sci. 1985 Mar 11;36(10):1003-17. doi: 10.1016/0024-3205(85)90398-4.
The present study reports differences in phospholipid classes, fatty acids of individual phospholipids, and changes in membrane fluidity and Na+-K+-ATPase activity in brain microsomes of rats maintained on an alcohol diet for 35 days compared to sex, age and weight-matched control rats maintained on a calorically-equivalent, non-alcohol diet. Although no difference in Na+-K+-ATPase activity was found in microsomes from alcohol vs control rats when measured in the absence of added alcohol, the presence of low concentrations of ethanol (less than 100 mM) stimulated, while high concentrations (greater than 100 mM) inhibited enzyme activity. The stimulation was differentially expressed in that the microsomal enzyme from alcohol rats was stimulated to a lesser extent than the enzyme from control rats. However, the inhibiting effect of high concentrations of alcohol was similar in microsomes from both alcohol and control rats. Also in membranes from alcohol rats, there was a lower quantity of phosphatidylethanolamine (PE) and higher quantities of phosphatidylserine (PS) and phosphatidylinositol (PI) compared to membranes from control rats. The major change in fatty acid composition was a reduction in the level of polyunsaturated fatty acids, which was particularly evident in PI and PS. The linoleic acid: arachidonic acid ratio (18:2/20:4) and the saturation:unsaturation ratio were also increased in PI and PS in membranes from alcohol animals. However, the ratio of n-6/n-3 fatty acids remained the same or was reduced in membranes from alcoholic animals. Although no difference in the inherent "fluidity" of membranes from alcohol vs control rats could be demonstrated by electron paramagnetic resonance, molecular tolerance to ethanol was demonstrated in the membranes from alcohol rats by the resistance to the disordering effects of added ethanol.
本研究报告了与性别、年龄和体重匹配的、食用热量相当的非酒精饮食的对照大鼠相比,食用酒精饮食35天的大鼠脑微粒体中磷脂类别、单个磷脂的脂肪酸、膜流动性变化以及钠钾ATP酶活性的差异。尽管在不添加酒精的情况下测量时,酒精喂养大鼠和对照大鼠的微粒体中钠钾ATP酶活性没有差异,但低浓度乙醇(低于100 mM)的存在会刺激该酶活性,而高浓度(高于100 mM)则会抑制酶活性。这种刺激存在差异,即酒精喂养大鼠的微粒体酶受到的刺激程度低于对照大鼠的酶。然而,高浓度酒精对酒精喂养大鼠和对照大鼠微粒体的抑制作用相似。与对照大鼠的膜相比,酒精喂养大鼠的膜中磷脂酰乙醇胺(PE)含量较低,磷脂酰丝氨酸(PS)和磷脂酰肌醇(PI)含量较高。脂肪酸组成的主要变化是多不饱和脂肪酸水平降低,这在PI和PS中尤为明显。酒精喂养动物的膜中PI和PS的亚油酸:花生四烯酸比率(18:2/20:4)以及饱和:不饱和比率也增加。然而,酒精喂养动物的膜中n-6/n-3脂肪酸比率保持不变或降低。尽管电子顺磁共振无法证明酒精喂养大鼠和对照大鼠膜的固有“流动性”存在差异,但酒精喂养大鼠的膜对添加乙醇的无序效应具有抗性,表明其对乙醇具有分子耐受性。