Literature DB >> 7118133

Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiency.

C J Rebouche, A G Engel.   

Abstract

L-Carnitine transport was studied in cultured muscle cells and skin fibroblasts of patients with primary systemic carnitine deficiency and control subjects. In both cell culture types, two systems for carnitine transport were identified. The kinetic parameters for carnitine transport were remarkably similar in cultured muscle cells and skin fibroblasts. Normal rates and kinetic properties of carnitine transport were observed for both cell lines from patients with systemic carnitine deficiency. These studies do not rule out a defect in carnitine transport in vivo.

Entities:  

Mesh:

Substances:

Year:  1982        PMID: 7118133     DOI: 10.1007/bf02796479

Source DB:  PubMed          Journal:  In Vitro        ISSN: 0073-5655


  20 in total

1.  Growth of human muscle in tissue culture. An improved technique.

Authors:  J A Witkowski; M Durbidge; V Dubowitz
Journal:  In Vitro       Date:  1976-02

2.  Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease.

Authors:  K Sato; F Imai; I Hatayama; R I Roelofs
Journal:  Biochem Biophys Res Commun       Date:  1977-09-23       Impact factor: 3.575

3.  Analysis of Michaelis kinetics for two independent, saturable membrane transport functions.

Authors:  J L Neal
Journal:  J Theor Biol       Date:  1972-04       Impact factor: 2.691

4.  Muscle-type phosphorylase activity present in muscle cells cultured from three patients with myophosphorylase deficiency.

Authors:  M C Meienhofer; V Askanas; D Proux-Daegelen; J C Dreyfus; W K Engel
Journal:  Arch Neurol       Date:  1977-12

5.  Systemic carnitine deficiency simulating recurrent Reye syndrome.

Authors:  A M Glasgow; G Eng; A G Engel
Journal:  J Pediatr       Date:  1980-05       Impact factor: 4.406

6.  AMP deaminase: stage-specific isozymes in differentiating chick muscle.

Authors:  D W Sammons; O P Chilson
Journal:  Arch Biochem Biophys       Date:  1978-12       Impact factor: 4.013

7.  McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme.

Authors:  S DiMauro; S Arnold; A Miranda; L P Rowland
Journal:  Ann Neurol       Date:  1978-01       Impact factor: 10.422

8.  Adult-onset acid maltase deficiency. Morphologic and biochemical abnormalities reproduced in in cultured muscle.

Authors:  V Askanas; W K Engel; S DiMauro; B R Brooks; M Mehler
Journal:  N Engl J Med       Date:  1976-03-11       Impact factor: 91.245

9.  In vitro analysis of hepatic carnitine biosynthesis in human systemic carnitine deficiency.

Authors:  C J Rebouche; A G Engel
Journal:  Clin Chim Acta       Date:  1980-10-09       Impact factor: 3.786

10.  Glycogen debrancher deficiency is reproduced in muscle culture.

Authors:  A F Miranda; S DiMauro; A Antler; L Z Stern; L P Rowland
Journal:  Ann Neurol       Date:  1981-03       Impact factor: 10.422

View more
  11 in total

Review 1.  Role of plasma membrane transporters in muscle metabolism.

Authors:  A Zorzano; C Fandos; M Palacín
Journal:  Biochem J       Date:  2000-08-01       Impact factor: 3.857

Review 2.  Carnitine biosynthesis in mammals.

Authors:  Frédéric M Vaz; Ronald J A Wanders
Journal:  Biochem J       Date:  2002-02-01       Impact factor: 3.857

Review 3.  Carnitine and acylcarnitines: pharmacokinetic, pharmacological and clinical aspects.

Authors:  Stephanie E Reuter; Allan M Evans
Journal:  Clin Pharmacokinet       Date:  2012-09-01       Impact factor: 6.447

4.  Six years' experience with carnitine supplementation in a patient with an inherited defective carnitine transport system.

Authors:  E Christensen; J Vikre-Jørgensen
Journal:  J Inherit Metab Dis       Date:  1995       Impact factor: 4.982

5.  Transport of carnitine into cells in hereditary carnitine deficiency.

Authors:  B O Eriksson; B Gustafson; S Lindstedt; I Nordin
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

6.  Kinetic compartmental analysis of carnitine metabolism in the human carnitine deficiency syndromes. Evidence for alterations in tissue carnitine transport.

Authors:  C J Rebouche; A G Engel
Journal:  J Clin Invest       Date:  1984-03       Impact factor: 14.808

7.  Carnitine metabolism and inborn errors.

Authors:  A G Engel; C J Rebouche
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

Review 8.  Carnitine transport: pathophysiology and metabolism of known molecular defects.

Authors:  I Tein
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

9.  Oral carnitine therapy in children with cystinosis and renal Fanconi syndrome.

Authors:  W A Gahl; I Bernardini; M Dalakas; W B Rizzo; G S Harper; J M Hoeg; O Hurko; J Bernar
Journal:  J Clin Invest       Date:  1988-02       Impact factor: 14.808

Review 10.  Hereditary human myopathies in muscle culture.

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

北京卡尤迪生物科技股份有限公司 © 2022-2023.