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多发性对称性脂肪瘤病中的线粒体呼吸功能:两例报告

Mitochondrial respiratory function in multiple symmetrical lipomatosis: report of two cases.

作者信息

Wu T P, Tsai J G, Chan P H, Lee H C, Wei Y H

机构信息

Department of Otolaryngology, Cardinal Tien Hospital, Taipei, Taiwan, R.O.C.

出版信息

J Formos Med Assoc. 1994 Jun;93(6):513-8.

PMID:7858441
Abstract

Madelung's disease is a rare benign disorder characterized by symmetrical deposition of adipose tissue on the neck and shoulders. The cause of Madelung's disease is obscure and may be associated with mitochondrial dysfunction. In this communication, we report two cases encountered at Cardinal Tien Hospital during 1992. Besides physical check-up and laboratory examination, adipose tissue and muscle biopsies from the biceps brachii were performed. As lipid metabolism is closely related to mitochondrial respiration, biochemical studies may be of great value in clarifying the pathogenetic mechanism of Madelung's disease. We thus determined the activities of mitochondrial respiratory enzymes (NADH cytochrome c reductase, succinate cytochrome c reductase, cytochrome c oxidase) in muscle and blood cells and revealed that the electron transport functions were all elevated. Molecular analysis of mitochondrial DNA from the muscle and blood cells of both patients failed to find large-scale deletion or point mutations.

摘要

马德隆氏病是一种罕见的良性疾病,其特征为颈部和肩部脂肪组织的对称性沉积。马德隆氏病的病因不明,可能与线粒体功能障碍有关。在本报告中,我们汇报了1992年在慈济医院遇到的两例病例。除了体格检查和实验室检查外,还对肱二头肌进行了脂肪组织和肌肉活检。由于脂质代谢与线粒体呼吸密切相关,生化研究可能对阐明马德隆氏病的发病机制具有重要价值。因此,我们测定了肌肉和血细胞中线粒体呼吸酶(NADH细胞色素c还原酶、琥珀酸细胞色素c还原酶、细胞色素c氧化酶)的活性,结果显示电子传递功能均升高。对两名患者肌肉和血细胞中线粒体DNA的分子分析未发现大规模缺失或点突变。

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