Literature DB >> 620459

Myotonic dystrophy: studies on the lipid composition and metabolism of erythrocytes and skin fibroblasts.

N S Thomas, P S Harper.   

Abstract

With the aim of establishing the underlying biochemical lesion in myotonic dystrophy, the lipids of plasma and of the membranes of erythrocytes and cultured skin fibroblasts were investigated in patients with this disorder and normal age- and sex-matched controls. No qualitative or quantitative differences could be detected in the lipid constituents of either plasma or erythrocytes from patients and controls. Similar growth characteristics and levels of sodium [1-14C]acetate incorporation were found in skin fibroblasts from both groups when grown in medium supplemented with either normal serum or delipidated serum. It is concluded that despite the previous evidence that drug induced myotonia results from a primary disturbance of membrane lipids, and suggestions that myotonic dystrophy might have a similar basis, our results did not support this hypothesis. They do not however exclude a primary membrane enzyme abnormality as the basic defect for the disorder.

Entities:  

Mesh:

Substances:

Year:  1978        PMID: 620459     DOI: 10.1016/0009-8981(78)90201-2

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  2 in total

Review 1.  Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders: Thematic Review Series: Genetics of Human Lipid Diseases.

Authors:  Harjot K Saini-Chohan; Ryan W Mitchell; Frédéric M Vaz; Teresa Zelinski; Grant M Hatch
Journal:  J Lipid Res       Date:  2011-11-07       Impact factor: 5.922

Review 2.  Cells of Matter-In Vitro Models for Myotonic Dystrophy.

Authors:  Magdalena Matloka; Arnaud F Klein; Frédérique Rau; Denis Furling
Journal:  Front Neurol       Date:  2018-05-23       Impact factor: 4.003

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.