• 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

Increased ammonia production during forearm ischemic work test in McArdle's disease.

作者信息

Rumpf K W, Wagner H, Kaiser H, Meinck H M, Goebel H H, Scheler F

出版信息

Klin Wochenschr. 1981 Dec 1;59(23):1319-20. doi: 10.1007/BF01711182.

DOI:10.1007/BF01711182
PMID:6947119
Abstract

A patient with typical features of late onset McArdle's disease is described. During forearm ischemic work test the patient exhibited an exaggerated increase in ammonia release, largely exceeding normal values. It is suggested, that this is due to an activation of the myokinase/myoadenylate deaminase pathway. Besides lack of lactate release increased ammonia release during ischemia may be a typical feature of McArdle's disease.

摘要

相似文献

1
Increased ammonia production during forearm ischemic work test in McArdle's disease.
Klin Wochenschr. 1981 Dec 1;59(23):1319-20. doi: 10.1007/BF01711182.
2
Skeletal muscle adenosine, inosine and hypoxanthine release following ischaemic forearm exercise in myoadenylate deaminase deficiency and McArdle's disease.肌腺苷酸脱氨酶缺乏症和麦克尔憩室病患者前臂缺血运动后骨骼肌中腺苷、肌苷和次黄嘌呤的释放情况。
Adv Exp Med Biol. 1986;195 Pt B:517-23. doi: 10.1007/978-1-4684-1248-2_80.
3
Metabolism of branched-chain amino acids and ammonia during exercise: clues from McArdle's disease.运动期间支链氨基酸和氨的代谢:来自麦克尔憩室病的线索。
Int J Sports Med. 1990 May;11 Suppl 2:S101-13. doi: 10.1055/s-2007-1024861.
4
ATP degradation products after ischemic exercise: hereditary lack of phosphorylase or carnitine palmityltransferase.
Neurology. 1985 Sep;35(9):1355-7. doi: 10.1212/wnl.35.9.1355.
5
The exercise metaboreflex is maintained in the absence of muscle acidosis: insights from muscle microdialysis in humans with McArdle's disease.在不存在肌肉酸中毒的情况下运动代谢反射仍得以维持:来自对患有麦克尔迪氏病的人类进行肌肉微透析的见解。
J Physiol. 2001 Dec 1;537(Pt 2):641-9. doi: 10.1111/j.1469-7793.2001.00641.x.
6
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.糖原贮积病V型和VII型患者运动肌肉中嘌呤降解过多。
J Clin Invest. 1985 Aug;76(2):556-60. doi: 10.1172/JCI112006.
7
[Glucose metabolism during muscular exercise in McArdle's disease].
Acta Clin Belg. 1979;34(3):151-7. doi: 10.1080/22953337.1979.11718681.
8
McArdle's disease with myoadenylate deaminase deficiency: observations in a combined enzyme deficiency.伴有肌腺苷酸脱氨酶缺乏的麦克尔氏病:一种复合酶缺乏症的观察
Neurology. 1987 Jun;37(6):1039-42. doi: 10.1212/wnl.37.6.1039.
9
Lactate production in McArdle's disease.麦克尔憩室病中的乳酸生成
Postgrad Med J. 1977 Mar;53(617):161-4. doi: 10.1136/pgmj.53.617.161.
10
McArdle's disease diagnosed following statin-induced myositis.
Ann Clin Biochem. 2004 Jul;41(Pt 4):338-40. doi: 10.1258/0004563041201554.

引用本文的文献

1
McArdle Disease: Clinical, Biochemical, Histological and Molecular Genetic Analysis of 60 Patients.麦克尔迪氏病:60例患者的临床、生化、组织学及分子遗传学分析
Biomedicines. 2020 Feb 15;8(2):33. doi: 10.3390/biomedicines8020033.
2
Metabolic profiles of exercise in patients with McArdle disease or mitochondrial myopathy.麦卡德尔病或线粒体肌病患者运动的代谢特征。
Proc Natl Acad Sci U S A. 2017 Aug 1;114(31):8402-8407. doi: 10.1073/pnas.1703338114. Epub 2017 Jul 17.
3
The exercise metaboreflex is maintained in the absence of muscle acidosis: insights from muscle microdialysis in humans with McArdle's disease.

本文引用的文献

1
Myopathy due to a defect in muscle glycogen breakdown.由于肌肉糖原分解缺陷导致的肌病。
Clin Sci. 1951 Feb;10(1):13-35.
2
A metabolic myopathy due to absence of muscle phosphorylase.一种由于肌肉磷酸化酶缺乏引起的代谢性肌病。
Am J Med. 1961 Apr;30:502-17. doi: 10.1016/0002-9343(61)90075-4.
3
Disruption of the purine nucleotide cycle. A potential explanation for muscle dysfunction in myoadenylate deaminase deficiency.嘌呤核苷酸循环的破坏。对肌腺苷酸脱氨酶缺乏症中肌肉功能障碍的一种潜在解释。
在不存在肌肉酸中毒的情况下运动代谢反射仍得以维持:来自对患有麦克尔迪氏病的人类进行肌肉微透析的见解。
J Physiol. 2001 Dec 1;537(Pt 2):641-9. doi: 10.1111/j.1469-7793.2001.00641.x.
4
Myoadenylate deaminase deficiency. Functional and metabolic abnormalities associated with disruption of the purine nucleotide cycle.肌腺苷酸脱氨酶缺乏症。与嘌呤核苷酸循环中断相关的功能和代谢异常。
J Clin Invest. 1984 Mar;73(3):720-30. doi: 10.1172/JCI111265.
5
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.糖原贮积病V型和VII型患者运动肌肉中嘌呤降解过多。
J Clin Invest. 1985 Aug;76(2):556-60. doi: 10.1172/JCI112006.
6
Myoadenylate deaminase deficiency.肌腺苷酸脱氨酶缺乏症
Klin Wochenschr. 1986 Apr 1;64(7):342-7. doi: 10.1007/BF01711958.
7
Myoadenylate deaminase deficiency.肌腺苷酸脱氨酶缺乏症
Klin Wochenschr. 1987 Nov 2;65(21):1023-33. doi: 10.1007/BF01726321.
8
McArdle's disease with late-onset symptoms: case report and review of the literature.伴有迟发症状的麦克尔迪氏病:病例报告及文献综述
J Neurol Neurosurg Psychiatry. 1992 May;55(5):407-8. doi: 10.1136/jnnp.55.5.407.
J Clin Invest. 1980 Dec;66(6):1419-23. doi: 10.1172/JCI109995.
4
The second wind phenomenon in McArdle's syndrome.麦克尔迪氏综合征中的第二次呼吸现象。
Acta Med Scand Suppl. 1967;472:294-307. doi: 10.1111/j.0954-6820.1967.tb12635.x.
5
Ammonia production in muscle and other tissues: the purine nucleotide cycle.肌肉及其他组织中的氨生成:嘌呤核苷酸循环
Physiol Rev. 1972 Apr;52(2):382-414. doi: 10.1152/physrev.1972.52.2.382.
6
A kinetic determination of ammonia in plasma.
Clin Chim Acta. 1974 Oct 30;56(2):151-7. doi: 10.1016/0009-8981(74)90223-x.
7
Myoadenylate deaminase deficiency: a new disease of muscle.肌腺苷酸脱氨酶缺乏症:一种新的肌肉疾病。
Science. 1978 May 5;200(4341):545-8. doi: 10.1126/science.644316.
8
Adenylate deaminase from rat muscle. Regulation by purine nucleotides and orthophosphate in the presence of 150 mM KCl.大鼠肌肉中的腺苷酸脱氨酶。在150 mM氯化钾存在下,嘌呤核苷酸和正磷酸盐的调节作用。
J Biol Chem. 1979 Sep 25;254(18):8994-9.