Moffat M P, Dhalla N S
Can J Cardiol. 1985 May-Jun;1(3):194-200.
ATPase and calcium binding activities were studied in sarcolemmal membranes from hearts of male rats fed either a control or 2% cholesterol diet for different time periods. Studies with isolated membrane revealed a significant increase in Na+-K+ ATPase activity, sialic acid content and ATP-independent calcium binding capacity in the presence of 1.25 mM CaCl2 in the 6 week cholesterol fed group. By 12 weeks, Na+-K+ ATPase, Mg2+-ATPase and Ca2+-ATPase activities as well as ATP-independent calcium binding in the presence of 0.05 mM CaCl2 were increased in membranes from cholesterol fed rats. A significant increase (P less than 0.05) in the sarcolemmal cholesterol/phospholipid molar ratio, which is an indicator of a decrease in membrane fluidity, was also noted in the 12 week cholesterol fed group. Concanavalin A, which is believed to decrease membrane fluidity, stimulated both Mg2+ and Ca2+-dependent ATPase activities and increased ATP-independent calcium binding in control sarcolemmal preparations and these changes resembled those observed in the sarcolemma from cholesterol fed rats. Since concanavalin A did not alter the activity of Na+-K+ ATPase, it appears that some of the observed differences in sarcolemmal activities upon cholesterol feeding did not correlate well with changes in membrane order. At 24 weeks, there was a generalized depression in the sarcolemmal ATPase activities of the cholesterol group; both Mg2+ ATPase and Ca2+ ATPase were significantly less than in control.(ABSTRACT TRUNCATED AT 250 WORDS)
在不同时间段,对喂食对照饮食或2%胆固醇饮食的雄性大鼠心脏肌膜中的ATP酶和钙结合活性进行了研究。对分离膜的研究表明,在喂食胆固醇6周的组中,当存在1.25 mM氯化钙时,Na+-K+ ATP酶活性、唾液酸含量和不依赖ATP的钙结合能力显著增加。到12周时,喂食胆固醇大鼠的膜中,Na+-K+ ATP酶、Mg2+-ATP酶和Ca2+-ATP酶活性以及在0.05 mM氯化钙存在下不依赖ATP的钙结合能力均增加。在喂食胆固醇12周的组中,还观察到肌膜胆固醇/磷脂摩尔比显著增加(P小于0.05),这是膜流动性降低的一个指标。刀豆球蛋白A被认为会降低膜流动性,它刺激了对照肌膜制剂中Mg2+和Ca2+依赖的ATP酶活性,并增加了不依赖ATP的钙结合,这些变化与喂食胆固醇大鼠的肌膜中观察到的变化相似。由于刀豆球蛋白A没有改变Na+-K+ ATP酶的活性,因此看来喂食胆固醇后肌膜活性中观察到的一些差异与膜有序性的变化没有很好的相关性。在24周时,胆固醇组的肌膜ATP酶活性普遍降低;Mg2+ ATP酶和Ca2+ ATP酶均显著低于对照组。(摘要截短至250字)