Rasmussen U F, Rasmussen H N, Andersen A J, Fogd Jørgensen P, Quistorff B
Copenhagen Muscle Research Centre, Department of Biochemistry, August Krogh Institute, University of Copenhagen, Denmark.
Biochem J. 1996 Apr 15;315 ( Pt 2)(Pt 2):659-63. doi: 10.1042/bj3150659.
Mitochondria were isolated from biopsies of the biceps femoris muscle of Danish landrace pigs. Three groups of animals were compared: (1) normal pigs; (2) pigs that were homozygous with respect to the gene Hal(n)/Hal(n) coding for the porcine malignant hyperthermia syndrome; and (3) heterozygote animals. A newly developed micro-method for preparation and assaying of small quantities of intact mitochondria was employed. With this technique mitochondria from biopsies weighing less than 100 mg were examined with respect to cytochrome content as well as phosphorylating and respiratory activities, including the nonphosphorylating exo-NADH oxidase activity. The mitochondria, prepared in a yield of 48%, showed high respiratory activities with tricarboxylic acid-cycle intermediates and pyruvate, and somewhat lower activity with palmitoyl-carnitine as substrate. The ATP synthase activity was about 1000 micromol ATP/min per g of protein and the maximal respiratory activity approx. 700 micromol of O2/min per g of protein. No differences among the three groups of animals were detected, except for the exo-NADH oxidase activities, which were 43, 78 and 107 micromol of O2/min per g of protein in the groups of normal, heterozygous and homozygous animals respectively. It is concluded that the exo-NADH oxidase activity may be a genetic manifestation of malignant hyperthermia and may play a significant role in the heat production characteristic of the syndrome.
从丹麦长白猪股二头肌活检组织中分离出线粒体。比较了三组动物:(1)正常猪;(2)对于编码猪恶性高热综合征的基因Hal(n)/Hal(n)纯合的猪;(3)杂合子动物。采用了一种新开发的用于制备和检测少量完整线粒体的微量方法。利用该技术,对重量小于100mg的活检组织中的线粒体进行了细胞色素含量以及磷酸化和呼吸活性的检测,包括非磷酸化的胞外NADH氧化酶活性。制备的线粒体产率为48%,对三羧酸循环中间产物和丙酮酸表现出高呼吸活性,以棕榈酰肉碱为底物时活性略低。ATP合酶活性约为每克蛋白质1000微摩尔ATP/分钟,最大呼吸活性约为每克蛋白质700微摩尔O2/分钟。除了胞外NADH氧化酶活性外,三组动物之间未检测到差异,正常、杂合和纯合动物组中该酶活性分别为每克蛋白质43、78和107微摩尔O2/分钟。结论是,胞外NADH氧化酶活性可能是恶性高热的一种遗传表现,可能在该综合征的产热特征中起重要作用。