Literature DB >> 4507604

3-hydroxypropionate: significance of -oxidation of propionate in patients with propionic acidemia and methylmalonic acidemia.

T Ando, K Rasmussen, W L Nyhan, D Hull.   

Abstract

[l-(14)C]Propionate administered intravenously was metabolized to methylmalonate, to 3-hydroxypropionate, and to methylcitrate in the urine of a patient with methylmalonic acidemia. L-[U-(14)C]Isoleucine and L-[U-(14)C]valine were also converted to urinary methylmalonate and to 3-hydroxypropionate in the patient. Two patients with propionic acidemia due to a defect in propionyl-CoA carboxylase metabolized [l-(14)C]propionate to uninary methylcitrate and 3-hydroxypropionate. The appearance of radioactive 3-hydroxypropionate in the urine after the administration of these compounds indicates that beta-oxidation of propionyl-CoA through acryloyl-CoA was functioning in these patients. The conversion of valine to 3-hydroxypropionate suggests that valine is oxidized by way of propionate and propionyl-CoA in man.

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Year:  1972        PMID: 4507604      PMCID: PMC389649          DOI: 10.1073/pnas.69.10.2807

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  25 in total

1.  Cerebral gigantism: concentrations of amino acids in plasma and muscle.

Authors:  R L Bejar; G F Smith; S Park; W N Spellacy; S L Wolfson; W L Nyhan
Journal:  J Pediatr       Date:  1970-01       Impact factor: 4.406

2.  Localisation of enzymic defect in propionicacidaemia.

Authors:  D Gompertz; C N Storrs; D C Bau; T J Peters; E A Hughes
Journal:  Lancet       Date:  1970-05-30       Impact factor: 79.321

3.  Biotin-responsive propionicacidaemia.

Authors:  N D Barnes; D Hull; L Balgobin; D Gompertz
Journal:  Lancet       Date:  1970-08-01       Impact factor: 79.321

4.  Defective propionate carboxylation in ketotic hyperglycinaemia.

Authors:  Y E Hsia; K J Scully; L E Rosenberg
Journal:  Lancet       Date:  1969-04-12       Impact factor: 79.321

5.  Observations on the coexistence of methylmalonic acidemia and glycinemia.

Authors:  G Morrow; L A Barness; V H Auerbach; A M DiGeorge; T Ando; W L Nyhan
Journal:  J Pediatr       Date:  1969-05       Impact factor: 4.406

6.  Propionicacidemia, a new inborn error of metabolism.

Authors:  F A Hommes; J R Kuipers; J D Elema; J F Jansen; J H Jonxis
Journal:  Pediatr Res       Date:  1968-11       Impact factor: 3.756

7.  alpha-Methyl-cis-aconitic acid. Aconitase substrate. II. Substrate properties and aconitase mechanism.

Authors:  O Gawron; K P Mahajan
Journal:  Biochemistry       Date:  1966-07       Impact factor: 3.162

8.  Automatic determination of weak organic acids by partition column chromatography and indicator titration.

Authors:  L Kesner; E Muntwyler
Journal:  Anal Chem       Date:  1966-08       Impact factor: 6.986

9.  Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.

Authors:  V G Oberholzer; B Levin; E A Burgess; W F Young
Journal:  Arch Dis Child       Date:  1967-10       Impact factor: 3.791

10.  Congenital methylmalonic acidemia: enzymatic evidence for two forms of the disease.

Authors:  G Morrow; L A Barness; G J Cardinale; R H Abeles; J G Flaks
Journal:  Proc Natl Acad Sci U S A       Date:  1969-05       Impact factor: 11.205

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  28 in total

1.  Glutaric aciduria in two brothers.

Authors:  N J Brandt; N Gregersen; E Christensen; K Rasmussen
Journal:  J Inherit Metab Dis       Date:  1978       Impact factor: 4.982

2.  Integrated Omic Analysis of a Guinea Pig Model of Heart Failure and Sudden Cardiac Death.

Authors:  D Brian Foster; Ting Liu; Kai Kammers; Robert O'Meally; Ni Yang; Kyriakos N Papanicolaou; C Conover Talbot; Robert N Cole; Brian O'Rourke
Journal:  J Proteome Res       Date:  2016-08-03       Impact factor: 4.466

3.  Inter-relations between 3-hydroxypropionate and propionate metabolism in rat liver: relevance to disorders of propionyl-CoA metabolism.

Authors:  Kirkland A Wilson; Yong Han; Miaoqi Zhang; Jeremy P Hess; Kimberly A Chapman; Gary W Cline; Gregory P Tochtrop; Henri Brunengraber; Guo-Fang Zhang
Journal:  Am J Physiol Endocrinol Metab       Date:  2017-06-20       Impact factor: 4.310

4.  Mild form of methylmalonic aciduria misdiagnosed as propionic acidaemia during a ketotic crisis.

Authors:  I T de Almeida; M Duran; M F Silva; R Portela; A Cabral; T Tasso; F Eusébio; C Silveira
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

5.  Propionic acidaemia: clinical, biochemical and therapeutic aspects. Experience in 30 patients.

Authors:  W Lehnert; W Sperl; T Suormala; E R Baumgartner
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

Review 6.  [Methylmalonic aciduria. Classification, diagnosis and therapy (author's transl)].

Authors:  D Leupold
Journal:  Klin Wochenschr       Date:  1977-01-15

7.  Enamel defects and salivary methylmalonate in methylmalonic acidemia.

Authors:  C W Bassim; J T Wright; J P Guadagnini; R Muralidharan; J Sloan; D L Domingo; C P Venditti; T C Hart
Journal:  Oral Dis       Date:  2009-01-09       Impact factor: 3.511

8.  Hudson memorial lecture. Neonatal management of organic acidurias. Clinical update.

Authors:  J M Saudubray; H Ogier; C Charpentier; E Depondt; F X Coudé; A Munnich; G Mitchell; F Rey; J Rey; J Frézal
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

9.  Metabolism of malonic semialdehyde in man.

Authors:  R D Scholem; G K Brown
Journal:  Biochem J       Date:  1983-10-15       Impact factor: 3.857

10.  Mitochondrial dysfunction in mut methylmalonic acidemia.

Authors:  Randy J Chandler; Patricia M Zerfas; Sara Shanske; Jennifer Sloan; Victoria Hoffmann; Salvatore DiMauro; Charles P Venditti
Journal:  FASEB J       Date:  2008-12-16       Impact factor: 5.191

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