Literature DB >> 6683796

Muscle carnitine deficiency: fatty acid metabolism in cultured fibroblasts and muscle cells.

J Avigan, V Askanas, W K Engel.   

Abstract

L-carnitine, as little as 25nM, greatly increased oxidation of palmitate by carnitine-depleted cultured human skin fibroblasts from normal subjects, and from two patients with muscle carnitine deficiency. Carnitine stimulated oxidation of labeled palmitate by cultured muscle cells from rat, normal humans, or patients with muscle carnitine deficiency. Carnitine reduced incorporation of palmitate into glycerides in normal fibroblasts, and it may thereby counteract cellular accumulation of glycerides in cells. Fibroblasts from patients with muscle carnitine deficiency took up labeled carnitine at a normal rate. Dexamethasone increased palmitate oxidation by normal human fibroblasts and muscle cells of rat, and normal and muscle carnitine-deficient humans. The results parallel the reported effectiveness of carnitine, glucocorticoids, or medium-chain triglycerides in treatment of these patients.

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Year:  1983        PMID: 6683796     DOI: 10.1212/wnl.33.8.1021

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  3 in total

1.  A case of mitochondrial myopathy, lactic acidosis and complex I deficiency.

Authors:  L Bet; N Bresolin; M Moggio; G Meola; A Prelle; A H Schapira; T Binzoni; A Chomyn; F Fortunato; P Cerretelli
Journal:  J Neurol       Date:  1990-11       Impact factor: 4.849

Review 2.  Hereditary human myopathies in muscle culture.

Authors:  G Meola
Journal:  Ital J Neurol Sci       Date:  1991-06

3.  Expression of muscle-gene-specific isozymes of phosphorylase and creatine kinase in innervated cultured human muscle.

Authors:  A Martinuzzi; V Askanas; T Kobayashi; W K Engel; S Di Mauro
Journal:  J Cell Biol       Date:  1986-10       Impact factor: 10.539

  3 in total

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