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Increased acetylcholine sensitivity in Duchenne muscular dystrophy myotubes.

作者信息

Meola G, Mancinelli E, Geremia L, Scarlato G

机构信息

Istituto di Clinica Neurologica, Centro Dino Ferrari, Università degli Studi di Milano.

出版信息

Ital J Neurol Sci. 1991 Apr;12(2):181-5. doi: 10.1007/BF02337031.

DOI:10.1007/BF02337031
PMID:2071364
Abstract

Monolayer cultures were established from explants of muscle obtained from 6 patients with Duchenne muscular dystrophy (DMD) and 9 controls. Electrophysiological studies were made after 3-4 weeks in vitro, when many myotubes had formed. An intracellular electrode was used to record cell membrane potential, and acetylcholine was applied by ionophoresis. The myotubes grown from Duchenne muscle showed greater acetylcholine sensitivity than controls.

摘要

相似文献

1
Increased acetylcholine sensitivity in Duchenne muscular dystrophy myotubes.
Ital J Neurol Sci. 1991 Apr;12(2):181-5. doi: 10.1007/BF02337031.
2
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Comparison between the growth pattern of cell cultures from normal and Duchenne dystrophy muscle.正常肌肉与杜氏肌营养不良症肌肉细胞培养物生长模式的比较。
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引用本文的文献

1
Hereditary human myopathies in muscle culture.肌肉培养中的遗传性人类肌病。
Ital J Neurol Sci. 1991 Jun;12(3):257-68. doi: 10.1007/BF02337773.

本文引用的文献

1
Membrane acetylcholinesterase in murine muscular dystrophy In vivo and in cultured myotubes.
Int J Dev Neurosci. 1985;3(4):331-40. doi: 10.1016/0736-5748(85)90066-8.
2
The acetylcholine sensitivity of frog muscle fibres after complete or partial devervation.完全或部分去神经支配后青蛙肌肉纤维的乙酰胆碱敏感性
J Physiol. 1960 Apr;151(1):1-23.
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Denervation changes in normal and myasthenia gravis human muscle fibres during organ culture.器官培养过程中正常及重症肌无力患者肌纤维的去神经变化
J Physiol. 1982 Dec;333:227-49. doi: 10.1113/jphysiol.1982.sp014451.
4
Differentiation properties of pure populations of human dystrophic muscle cells.人类营养不良性肌细胞纯群体的分化特性。
Exp Cell Res. 1983 Apr 1;144(2):495-503. doi: 10.1016/0014-4827(83)90431-7.
5
Comparison between the growth pattern of cell cultures from normal and Duchenne dystrophy muscle.正常肌肉与杜氏肌营养不良症肌肉细胞培养物生长模式的比较。
J Neurol Sci. 1984 May;64(2):149-60. doi: 10.1016/0022-510x(84)90033-9.
6
Defective myoblasts identified in Duchenne muscular dystrophy.在杜兴氏肌肉营养不良症中发现的有缺陷的成肌细胞。
Proc Natl Acad Sci U S A. 1983 Aug;80(15):4856-60. doi: 10.1073/pnas.80.15.4856.
7
Mucolipidosis II (I-cell disease): studies of muscle biopsy and muscle cultures.黏脂贮积症II型(I型细胞病):肌肉活检与肌肉培养研究
Pediatr Res. 1981 Oct;15(10):1334-9. doi: 10.1203/00006450-198110000-00006.
8
Intracellular calcium and desensitization of acetylcholine receptors.细胞内钙与乙酰胆碱受体的脱敏作用
Proc R Soc Lond B Biol Sci. 1980 Sep 26;209(1176):447-52. doi: 10.1098/rspb.1980.0106.
9
Cytogenetic analysis and muscle differentiation in a girl with severe muscular dystrophy.
J Neurol. 1986 Jun;233(3):168-70. doi: 10.1007/BF00314426.
10
Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets.
J Neurol. 1987 Dec;235(2):74-9. doi: 10.1007/BF00718013.