Literature DB >> 1128236

Labile methyl balances for normal humans on various dietary regimens.

S H Mudd, J R Poole.   

Abstract

Normal young adult male and female subjects were maintained on fixed dietary regimens which were either essentially normal or were semisynthetic and curtailed in methionine and choline intakes and virtually free of cystine. The subjects maintained stable weights and remained in positive nitrogen balance or within the zone of sulfur equilibrium. Choline intakes were calculated, and urinary excretions of creatinine, creatine, and sacrosine were measured. Creatinine excretions of male subjects on essentially normal diets outweighed the total intakes of labile methyl groups. Taking into account the excretions of additional methylated compounds, as judged from published values, it appears that methyl neogenesis must normally play a role in both males and females. When labile methyl intake is curtailed, de novo formation of methyl groups is quantitatively more significant than ingestion of preformed methyl moieties. On the normal diets used in these experiments, the average homocysteinyl moiety in males cycled between methionine and homocysteine at least 1.9 times before being converted to cystathionine. For females, the average number of cycles was at least 1.5. When labile methyl intake was curtailed, the average number of cycles rose to 3.9 for males and 3.0 for females under the conditions employed.

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Year:  1975        PMID: 1128236     DOI: 10.1016/0026-0495(75)90040-2

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  95 in total

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2.  Methionine adenosyltransferase alpha-helix structure unfolds at lower temperatures than beta-sheet: a 2D-IR study.

Authors:  Ibon Iloro; Rosana Chehín; Félix M Goñi; María A Pajares; José-Luis R Arrondo
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

Review 3.  Mechanisms and consequences of the impaired trans-sulphuration pathway in liver disease: Part I. Biochemical implications.

Authors:  J M Mato; F Corrales; A Martin-Duce; P Ortiz; M A Pajares; C Cabrero
Journal:  Drugs       Date:  1990       Impact factor: 9.546

4.  Probing the S-adenosylmethionine-binding site of rat guanidinoacetate methyltransferase. Effect of site-directed mutagenesis of residues that are conserved across mammalian non-nucleic acid methyltransferases.

Authors:  A Hamahata; Y Takata; T Gomi; M Fujioka
Journal:  Biochem J       Date:  1996-07-01       Impact factor: 3.857

5.  Proteomic analysis of human hepatoma cells expressing methionine adenosyltransferase I/III: Characterization of DDX3X as a target of S-adenosylmethionine.

Authors:  Paul C Schröder; Joaquín Fernández-Irigoyen; Emilie Bigaud; Antonio Serna; Rubén Renández-Alcoceba; Shelly C Lu; José M Mato; Jesús Prieto; Fernando J Corrales
Journal:  J Proteomics       Date:  2012-01-16       Impact factor: 4.044

6.  Evaluation of total plasma homocysteine in Indian newborns using heel-prick samples.

Authors:  A Radha Rama Devi; S M Naushad; Krishna C Prasad
Journal:  Indian J Pediatr       Date:  2006-06       Impact factor: 1.967

7.  Guanidinoacetate methyltransferase deficiency: the first inborn error of creatine metabolism in man.

Authors:  S Stöckler; D Isbrandt; F Hanefeld; B Schmidt; K von Figura
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

8.  Betaine in the treatment of homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency.

Authors:  U Wendel; H J Bremer
Journal:  Eur J Pediatr       Date:  1984-06       Impact factor: 3.183

9.  Folate deficiency disturbs hepatic methionine metabolism and promotes liver injury in the ethanol-fed micropig.

Authors:  Charles H Halsted; Jesus A Villanueva; Angela M Devlin; Onni Niemelä; Seppo Parkkila; Timothy A Garrow; Lynn M Wallock; Mark K Shigenaga; Stepan Melnyk; S Jill James
Journal:  Proc Natl Acad Sci U S A       Date:  2002-07-16       Impact factor: 11.205

10.  Diethyl maleate, an in vivo chemical depletor of glutathione, affects the response of male and female rats to arsenic deprivation.

Authors:  E O Uthus
Journal:  Biol Trace Elem Res       Date:  1994-12       Impact factor: 3.738

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