Dietary regulation of glycolytic enzymes: XI. Effect of inhibitors of protein synthesis on the adaptation of certain jejunal glycolytic and folate-metabolizing enzymes to diet and sex steroids

1. 1. The effects of oral sex hormones, dietary fructose and casein without and with actinomycin D or ethionine and fasting upon the activities of two folate-metabolizing enzymes (serine hydroxymethyltransferase ( L-Serine: tetrahydrofolate 5,10-hydroxymethyltransferase, E.C. 2.1.2.1) and methylenet...

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Published inBiochimica et biophysica acta Vol. 237; no. 3; pp. 484 - 489
Main Authors Stifel, Fred B., Herman, Robert H., Rosensweig, Norton S.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 22.06.1971
Subjects
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ISSN0304-4165
0006-3002
1872-8006
DOI10.1016/0304-4165(71)90267-4

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Abstract 1. 1. The effects of oral sex hormones, dietary fructose and casein without and with actinomycin D or ethionine and fasting upon the activities of two folate-metabolizing enzymes (serine hydroxymethyltransferase ( L-Serine: tetrahydrofolate 5,10-hydroxymethyltransferase, E.C. 2.1.2.1) and methylenetetrahydrofolate dehydrogenase (5,10-methylenetetrahydrofolate: NADP oxidoreductase, E.C. 1.5.1.5)) and two glycolytic enzymes (pyruvate kinase (ATP: pyruvate phosphotransferase, E.C. 2.7.1.40) and fructose diphosphate aldolase (fructose-1,6-diphosphate D-glyceraldehyde-3-phosphate lyase, E.C. 4.1.2.13)) were studied in the jejunum of female and male rats. 2. 2. Actinomycin, an inhibitor of DNA-dependent RNA synthesis, and ethionine, an inhibitor of protein synthesis, both effectively decreased the adaptive responses of jejunal glycolytic and folate-metabolizing enzymes to diet and oral sex hormones. These findings lend support to the hypothesis that stimulation of synthesis of certain RNA species is probably one of the primary mechanisms by which sex hormones (17β -estradiol and testosteron) and diet produce adaptive increases in the activities of certain jejunal glycolytic and folate-metabolizing enzymes.
AbstractList 1. 1. The effects of oral sex hormones, dietary fructose and casein without and with actinomycin D or ethionine and fasting upon the activities of two folate-metabolizing enzymes (serine hydroxymethyltransferase ( L-Serine: tetrahydrofolate 5,10-hydroxymethyltransferase, E.C. 2.1.2.1) and methylenetetrahydrofolate dehydrogenase (5,10-methylenetetrahydrofolate: NADP oxidoreductase, E.C. 1.5.1.5)) and two glycolytic enzymes (pyruvate kinase (ATP: pyruvate phosphotransferase, E.C. 2.7.1.40) and fructose diphosphate aldolase (fructose-1,6-diphosphate D-glyceraldehyde-3-phosphate lyase, E.C. 4.1.2.13)) were studied in the jejunum of female and male rats. 2. 2. Actinomycin, an inhibitor of DNA-dependent RNA synthesis, and ethionine, an inhibitor of protein synthesis, both effectively decreased the adaptive responses of jejunal glycolytic and folate-metabolizing enzymes to diet and oral sex hormones. These findings lend support to the hypothesis that stimulation of synthesis of certain RNA species is probably one of the primary mechanisms by which sex hormones (17β -estradiol and testosteron) and diet produce adaptive increases in the activities of certain jejunal glycolytic and folate-metabolizing enzymes.
Author Rosensweig, Norton S.
Stifel, Fred B.
Herman, Robert H.
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SubjectTerms Aldehyde-Lyases - biosynthesis
Animals
Caseins - pharmacology
Dactinomycin - pharmacology
Dietary Carbohydrates
Dietary Proteins
Enzyme Induction
Estradiol - pharmacology
Ethionine - pharmacology
Fasting
Female
Folic Acid
Fructose - pharmacology
Fructosephosphates
Glycolysis - drug effects
Jejunum - drug effects
Jejunum - enzymology
Male
Metabolism - drug effects
NAD
Oxidoreductases - biosynthesis
Pyruvate Kinase - biosynthesis
Rats
RNA - biosynthesis
Serine
Testosterone - pharmacology
Time Factors
Transferases - biosynthesis
Title Dietary regulation of glycolytic enzymes: XI. Effect of inhibitors of protein synthesis on the adaptation of certain jejunal glycolytic and folate-metabolizing enzymes to diet and sex steroids
URI https://dx.doi.org/10.1016/0304-4165(71)90267-4
https://www.ncbi.nlm.nih.gov/pubmed/4330268
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Volume 237
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