[Aortic development and ageing in the rat aorta -- Comparative histochemical and histoenzymological study (author's transl)]. 1975

P Hadjiisky, and J Renais, and L Scebat

A comparative study was made of 36 aortic enzyme activities (E.A.) and 6 macromelecular substances at different stages of ontogenesis in 49 male rats. In the foetal aorta (19th day) the E.Z. were moderate or weak and restricted to a few metabolic pathways: glycolysis, diaphorases, esterolysis of some nucleotides and glucosaminoglycan (GAG) metabolism. During the neonatal period (1st-3rd day), the pre-existing E.A. increased; some aerobic and lipolytic activities became histochemically detectable; longitudinal and radial gradients became established. These changes seemed to provide evidence of increased morphogenic activities and metabolic exchanges. During the prepuberty and puberty period (10-20th day-2nd month) all the E.A., as well as metachromasis and pyroniophilia increased, and new E.A. appeared (GluDH, GPDH, 5/Nase, Ac.Pase-Ca++, Mg++, pH 7.2). These changes appeared to be related to cell proliferation and connective tissue increase during the period of fast aortic growth. The increase of some E.A. (Est/ase, Ch. est, ATPase-Ca++, Mg++, 5/Nase, Alk. Pase) suggested a correlation between enzymatic differentiation and hormonal maturation. During adulthood (6-12th month), the E.A. were stable except for 5/Nase, lysosomal and lipolytic activities which increased. Some E.A. were found to be high (diaphorases, glycolytic and esterolytic enzymes), or moderate (aerobic oxidoreductases, lysosome, lipolysis and GAG-linked E.A.), while others were weak or absent (glycogen pathway E.A.). These observations seemed to correlate with synthetic processes and defence mechanisms. Ageing (17th month) was characterized by an increase of metachromatic GAG and acid lipids and by a decrease of pyroninophillia. Lysosome, glycolysis and phospholipogenesis-linked E.A. increased. In some animals (individual reactivity) kreb's cycle and lypolysis-E.A. decreased.

UI MeSH Term Description Entries
D008297 Male Males
D010084 Oxidation-Reduction A chemical reaction in which an electron is transferred from one molecule to another. The electron-donating molecule is the reducing agent or reductant; the electron-accepting molecule is the oxidizing agent or oxidant. Reducing and oxidizing agents function as conjugate reductant-oxidant pairs or redox pairs (Lehninger, Principles of Biochemistry, 1982, p471). Redox,Oxidation Reduction
D010088 Oxidoreductases The class of all enzymes catalyzing oxidoreduction reactions. The substrate that is oxidized is regarded as a hydrogen donor. The systematic name is based on donor:acceptor oxidoreductase. The recommended name will be dehydrogenase, wherever this is possible; as an alternative, reductase can be used. Oxidase is only used in cases where O2 is the acceptor. (Enzyme Nomenclature, 1992, p9) Dehydrogenases,Oxidases,Oxidoreductase,Reductases,Dehydrogenase,Oxidase,Reductase
D010744 Phosphoric Monoester Hydrolases A group of hydrolases which catalyze the hydrolysis of monophosphoric esters with the production of one mole of orthophosphate. Phosphatase,Phosphatases,Phosphohydrolase,Phosphohydrolases,Phosphomonoesterase,Phosphomonoesterases,Phosphoric Monoester Hydrolase,Hydrolase, Phosphoric Monoester,Hydrolases, Phosphoric Monoester,Monoester Hydrolase, Phosphoric
D002802 Cholinesterases Acylcholineacylhydrolase,Cholase,Cholinesterase
D004950 Esterases Any member of the class of enzymes that catalyze the cleavage of an ester bond and result in the addition of water to the resulting molecules. Esterase
D006003 Glycogen
D006019 Glycolysis A metabolic process that converts GLUCOSE into two molecules of PYRUVIC ACID through a series of enzymatic reactions. Energy generated by this process is conserved in two molecules of ATP. Glycolysis is the universal catabolic pathway for glucose, free glucose, or glucose derived from complex CARBOHYDRATES, such as GLYCOGEN and STARCH. Embden-Meyerhof Pathway,Embden-Meyerhof-Parnas Pathway,Embden Meyerhof Parnas Pathway,Embden Meyerhof Pathway,Embden-Meyerhof Pathways,Pathway, Embden-Meyerhof,Pathway, Embden-Meyerhof-Parnas,Pathways, Embden-Meyerhof
D006025 Glycosaminoglycans Heteropolysaccharides which contain an N-acetylated hexosamine in a characteristic repeating disaccharide unit. The repeating structure of each disaccharide involves alternate 1,4- and 1,3-linkages consisting of either N-acetylglucosamine (see ACETYLGLUCOSAMINE) or N-acetylgalactosamine (see ACETYLGALACTOSAMINE). Glycosaminoglycan,Mucopolysaccharides
D006651 Histocytochemistry Study of intracellular distribution of chemicals, reaction sites, enzymes, etc., by means of staining reactions, radioactive isotope uptake, selective metal distribution in electron microscopy, or other methods. Cytochemistry

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