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病变肌肉中胶原蛋白代谢的变化。II. 免疫组织化学研究。

Changes in collagen metabolism in diseased muscle. II. Immunohistochemical studies.

作者信息

Peltonen L, Myllylä R, Tolonen U, Myllylä V V

出版信息

Arch Neurol. 1982 Dec;39(12):756-9. doi: 10.1001/archneur.1982.00510240018005.

Abstract

Immunofluorescence studies using specific antibodies against collagen of types I, III, IV, and V were carried out on muscle biopsy specimens from 22 patients with various neuromuscular disorders and seven controls. Increased staining with all antibodies was seen in the patients with polymyositis and muscular dystrophy. Increased staining with types I and III antibodies was found in the samples from the patients with amyotrophic lateral sclerosis in cases with an elevated concentration of muscular hydroxyproline. Two patients with amyotrophic lateral sclerosis showed no accumulation of collagen, and this was similarly true of the polyneuropathy cases. An accumulation of types IV and V collagen was typical for the myotonia congenita samples. The immunohistochemical results were in good agreement with the biochemical findings from the same patients.

摘要

使用针对I型、III型、IV型和V型胶原蛋白的特异性抗体,对22例患有各种神经肌肉疾病的患者和7例对照的肌肉活检标本进行了免疫荧光研究。在多发性肌炎和肌肉营养不良患者中,所有抗体的染色均增加。在肌萎缩侧索硬化症患者样本中,当肌肉羟脯氨酸浓度升高时,发现I型和III型抗体染色增加。两名肌萎缩侧索硬化症患者未显示胶原蛋白积累,多神经病病例也是如此。IV型和V型胶原蛋白的积累是先天性肌强直样本的典型特征。免疫组织化学结果与同一患者的生化结果高度一致。

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