• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second case.

作者信息

DiMauro S, Bonilla E, Lee C P, Schotland D L, Scarpa A, Conn H, Chance B

出版信息

J Neurol Sci. 1976 Feb;27(2):217-32. doi: 10.1016/0022-510x(76)90063-0.

DOI:10.1016/0022-510x(76)90063-0
PMID:1249587
Abstract

In the second known case of non-thyroidal hypermetabolism (Luft's disease), there were large areas of mitochondrial aggregates in all fibers. Many mitochondria were abnormally large and contained packed cristae. In isolated mitochondrial fractions, studies of oxidative phosphorylation showed defective respiratory control and normal phosphorylation capacity ("loose coupling"). Spectra and content of cytochromes were normal. Basal ATPase activity was seven times greater than normal and poorly stimulated by 2,4-dinitrophenol. The rate of energy-dependent calcium uptake by isolated mitochondria was normal, but the amount of calcium accumulated was much decreased. Calcium could not be retained and was spontaneously released into the medium within 30 seconds. "Recycling" of calcium between mitochondria and cytosol may take place in vivo and result in sustained stimulation of respiration and loose coupling.

摘要

相似文献

1
Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second case.
J Neurol Sci. 1976 Feb;27(2):217-32. doi: 10.1016/0022-510x(76)90063-0.
2
Distribution of the ATPase inhibitor proteins of mitochondria in mammalian tissues including fibroblasts from a patient with Luft's disease.
Biochim Biophys Acta. 1992 Jun 9;1139(1-2):143-7. doi: 10.1016/0925-4439(92)90093-3.
3
[Physiopathology of mitochondria. From Luft's disease to aging and diabetes].[线粒体的病理生理学。从 Luft 病到衰老与糖尿病]
Lakartidningen. 1993 Aug 25;90(34):2770-5.
4
Luft's syndrome: O2 cost of exercise and chemical control of breathing.吕夫特综合征:运动的氧耗与呼吸的化学控制
J Appl Physiol. 1975 Nov;39(5):857-9. doi: 10.1152/jappl.1975.39.5.857.
5
Ragged-red fibers. A biochemical and morphological study.破碎红纤维。一项生化与形态学研究。
J Neurol Sci. 1975 Dec;26(4):479-88. doi: 10.1016/0022-510x(75)90048-9.
6
Luft's disease revisited. Severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control.重温 Luft 病。非甲状腺源性的严重高代谢伴线粒体呼吸控制维持缺陷。
Mt Sinai J Med. 1992 Mar;59(2):140-5.
7
Neuromuscular disorder associated with a defect in mitochondrial energy supply.与线粒体能量供应缺陷相关的神经肌肉疾病。
Arch Neurol. 1976 Jul;33(7):475-9. doi: 10.1001/archneur.1976.00500070017003.
8
Mitochondrial myopathies.线粒体肌病
Ann Neurol. 1985 Jun;17(6):521-38. doi: 10.1002/ana.410170602.
9
Disorders of glycogen metabolism of muscle.肌肉糖原代谢紊乱
CRC Crit Rev Clin Neurobiol. 1984;1(2):83-116.
10
Ultrastructural study of globular inclusions in human skeletal muscle mitochondria.人类骨骼肌线粒体中球状包涵体的超微结构研究
Acta Neuropathol. 1980;52(1):35-40. doi: 10.1007/BF00687226.

引用本文的文献

1
Variability of Clinical Phenotypes Caused by Isolated Defects of Mitochondrial ATP Synthase.孤立性线粒体 ATP 合酶缺陷导致的临床表型变异性。
Physiol Res. 2024 Aug 31;73(Suppl 1):S243-S278. doi: 10.33549/physiolres.935407. Epub 2024 Jul 17.
2
Congenital Hypermetabolism and Uncoupled Oxidative Phosphorylation.先天性高代谢和氧化磷酸化解偶联。
N Engl J Med. 2022 Oct 13;387(15):1395-1403. doi: 10.1056/NEJMoa2202949.
3
The F1Fo-ATPase inhibitor protein IF1 in pathophysiology.病理生理学中的F1Fo - ATP酶抑制蛋白IF1
Front Physiol. 2022 Aug 4;13:917203. doi: 10.3389/fphys.2022.917203. eCollection 2022.
4
The new role of FF ATP synthase in mitochondria-mediated neurodegeneration and neuroprotection.FF ATP 合酶在线粒体介导的神经退行性变和神经保护中的新作用。
Exp Neurol. 2020 Oct;332:113400. doi: 10.1016/j.expneurol.2020.113400. Epub 2020 Jul 10.
5
Mitochondrial disorders as windows into an ancient organelle.线粒体疾病:揭示古老细胞器的窗口
Nature. 2012 Nov 15;491(7424):374-83. doi: 10.1038/nature11707.
6
Molecular Regulation of the Mitochondrial F(1)F(o)-ATPsynthase: Physiological and Pathological Significance of the Inhibitory Factor 1 (IF(1)).线粒体F(1)F(o)-ATP合酶的分子调控:抑制因子1(IF(1))的生理和病理意义
Int J Cell Biol. 2012;2012:367934. doi: 10.1155/2012/367934. Epub 2012 Aug 26.
7
Historical perspective on mitochondrial medicine.线粒体医学的历史视角。
Dev Disabil Res Rev. 2010;16(2):106-13. doi: 10.1002/ddrr.102.
8
A history of mitochondrial diseases.线粒体疾病简史。
J Inherit Metab Dis. 2011 Apr;34(2):261-76. doi: 10.1007/s10545-010-9082-x. Epub 2010 May 21.
9
Overexpression of peroxisome proliferator-activated receptor gamma co-activator-1alpha leads to muscle atrophy with depletion of ATP.过氧化物酶体增殖物激活受体γ辅激活因子-1α的过表达会导致肌肉萎缩并伴有三磷酸腺苷耗竭。
Am J Pathol. 2006 Oct;169(4):1129-39. doi: 10.2353/ajpath.2006.060034.
10
Mitochondrial disease: a historical, biochemical, and London perspective.线粒体疾病:历史、生物化学及伦敦视角
Neurochem Res. 2004 Mar;29(3):483-91. doi: 10.1023/b:nere.0000014819.53972.b0.