Piquet Marie-Astrid, Roulet Michel, Nogueira Véronique, Filippi Céline, Sibille Brigitte, Hourmand-Ollivier Isabelle, Pilet Marianne, Rouleau Vincent, Leverve Xavier M
Département d'Hépatologie et Nutrition, CHU, F-14033 Caen cedex, France.
J Hepatol. 2004 Nov;41(5):721-9. doi: 10.1016/j.jhep.2004.07.002.
BACKGROUND/AIMS: Polyunsaturated fatty acids (PUFA) deficiency is common in patients with alcoholic liver disease. The suitability of reversing such deficiency remains controversial. The aim was to investigate the role played by PUFA deficiency in the occurrence of alcohol-related mitochondrial dysfunction.
Wistar rats were fed either a control diet with or without alcohol (control and ethanol groups) or a PUFA deficient diet with or without alcohol (PUFA deficient and PUFA deficient+ethanol groups). After 6 weeks, liver mitochondria were isolated for energetic studies and fatty acid analysis.
Mitochondria from ethanol fed rats showed a dramatic decrease in oxygen consumption rates and in cytochrome oxidase activity. PUFA deficiency showed an opposite picture. PUFA deficient+ethanol group roughly reach control values, regarding cytochrome oxidase activity and respiratory rates. The relationship between ATP synthesis and respiratory rate was shifted to the left in ethanol group and to the right in PUFA-deficient group. The plots of control and PUFA deficient+ethanol groups were overlapping. Phospholipid arachidonic over linoleic ratio closely correlated to cytochrome oxidase and oxygen uptake.
PUFA deficiency reverses alcohol-related mitochondrial dysfunction via an increase in phospholipid arachidonic over linoleic ratio, which raises cytochrome oxidase activity. Such deficiency may be an adaptive mechanism.
背景/目的:多不饱和脂肪酸(PUFA)缺乏在酒精性肝病患者中很常见。逆转这种缺乏的适宜性仍存在争议。目的是研究PUFA缺乏在酒精相关线粒体功能障碍发生中所起的作用。
将Wistar大鼠分为喂食含或不含酒精的对照饮食组(对照组和乙醇组)或含或不含酒精的PUFA缺乏饮食组(PUFA缺乏组和PUFA缺乏+乙醇组)。6周后,分离肝脏线粒体进行能量研究和脂肪酸分析。
喂食乙醇的大鼠的线粒体显示氧消耗率和细胞色素氧化酶活性显著降低。PUFA缺乏则呈现相反的情况。就细胞色素氧化酶活性和呼吸速率而言,PUFA缺乏+乙醇组大致达到对照组值。乙醇组中ATP合成与呼吸速率之间的关系向左移动,而PUFA缺乏组则向右移动。对照组和PUFA缺乏+乙醇组的曲线重叠。磷脂花生四烯酸与亚油酸的比例与细胞色素氧化酶和氧摄取密切相关。
PUFA缺乏通过增加磷脂花生四烯酸与亚油酸的比例来逆转酒精相关的线粒体功能障碍,这会提高细胞色素氧化酶活性。这种缺乏可能是一种适应性机制。