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乳酸酸中毒和线粒体肌病与呼吸链复合体III的几种成分缺乏相关。

Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain.

作者信息

Kennaway N G, Buist N R, Darley-Usmar V M, Papadimitriou A, Dimauro S, Kelley R I, Capaldi R A, Blank N K, D'Agostino A

出版信息

Pediatr Res. 1984 Oct;18(10):991-9. doi: 10.1203/00006450-198410000-00017.

Abstract

We have studied a 17-year-old girl with lactic acidosis (3-18 mEq/liter) and progressive muscle weakness since 9 years of age. Morphological findings in muscle were of a typical ragged red myopathy with multiple collections of bizarre mitochondria, some containing paracrystalline inclusions. The carnitine content of serum and muscle was normal, as were the activities of carnitine palmitoyltransferase, carnitine octanoyltransferase, and carnitine acetyltransferase in the patient's muscle. Measurement of the enzymes of oxidative phosphorylation in both crude muscle homogenates and mitochondrial fractions showed close to normal activities of cytochrome c oxidase, succinate dehydrogenase, and ATPase. In contrast, succinate cytochrome c reductase activity was greatly reduced in the patient, being 0.035 mumol/min/g tissue in whole muscle (controls 1.16 +/- 0.47 mumol/min/g tissue) and 8 nmol/min/mg protein in the mitochondria (control, 340 nmol/min/mg protein). Rotenonesensitive NADH-cytochrome c reductase was also undetectable in the patient's mitochondria. Spectral analysis of cytochromes showed decrease of reducible cytochrome b to 16% of the control. These results indicate a defect of ubiquinol-cytochrome c reductase or the cytochrome bc1 segment (complex III) of the electron transport chain. Antibody-binding studies of the individual components of complex III showed additional deficiencies of core proteins I and II and peptide VI, indicating a more widespread defect of complex III than was evident from spectral analysis and enzyme activity measurements alone. Urine organic acid analysis after fasting and following a medium chain triglyceride load showed unusually high levels of lactate and 3-hydroxybutyrate, lower than expected levels of acetoacetate and dicarboxylic acids, and the presence of several other metabolites suggesting a disturbed citric acid cycle and redox state.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们研究了一名17岁女孩,自9岁起就患有乳酸酸中毒(3 - 18毫当量/升)并伴有进行性肌无力。肌肉的形态学检查发现为典型的破碎红肌病,有多个奇异线粒体聚集,部分含有类晶体包涵体。患者血清和肌肉中的肉碱含量正常,肌肉中肉碱棕榈酰转移酶、肉碱辛酰转移酶和肉碱乙酰转移酶的活性也正常。对粗肌肉匀浆和线粒体部分的氧化磷酸化酶进行测量,结果显示细胞色素c氧化酶、琥珀酸脱氢酶和ATP酶的活性接近正常。相比之下,患者的琥珀酸细胞色素c还原酶活性大幅降低,全肌肉中为0.035微摩尔/分钟/克组织(对照组为1.16±0.47微摩尔/分钟/克组织),线粒体中为8纳摩尔/分钟/毫克蛋白(对照组为340纳摩尔/分钟/毫克蛋白)。在患者的线粒体中也未检测到对鱼藤酮敏感的NADH - 细胞色素c还原酶。细胞色素的光谱分析显示可还原的细胞色素b降至对照组的16%。这些结果表明泛醌 - 细胞色素c还原酶或电子传递链的细胞色素bc1片段(复合体III)存在缺陷。对复合体III各个组分的抗体结合研究显示核心蛋白I和II以及肽VI存在额外缺陷,表明复合体III的缺陷比仅从光谱分析和酶活性测量中所显示的更为广泛。空腹及给予中链甘油三酯负荷后进行的尿有机酸分析显示,乳酸和3 - 羟基丁酸水平异常高,乙酰乙酸和二羧酸水平低于预期,并且存在其他几种代谢产物,提示柠檬酸循环和氧化还原状态紊乱。(摘要截选至250字)

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