Literature DB >> 20564565

Thyroid hormones and D-aspartic acid, D-aspartate oxidase, D-aspartate racemase, H2O2, and ROS in rats and mice.

Enza Topo1, George Fisher, Andrea Sorricelli, Francesco Errico, Alessandro Usiello, Antimo D'Aniello.   

Abstract

Total concentrations of thyroid hormones T(3) and T(4), and of their free forms, FT(3) and FT(4), D-aspartic acid (D-Asp), D-aspartate oxidase (D-AspO), D-aspartate racemase, H(2)O(2), and ROS (reactive oxygen species) were determined in rats and mice. T(3) and T(4) were 1 and 50 ng/ml, respectively, in serum, and 750 and 40000 ng/g, respectively, in thyroid. Concentrations of the free forms FT(3) and FT(4) were ca. 250 times lower than their respective total concentrations. The endogenous content of D-Asp in thyroid gland was ca. 100 nmol/g tissue, whereas the activity of D-AspO was ca. 80 units/mg thyroid, and that of D-aspartate racemase was ca. 15 units/mg thyroid. H(2)O(2) Concentration in rat and mouse thyroid gland was ca. 290 pmol/g thyroid, and the concentration of ROS was ca. 10 pmol/DCF/min/mg protein. H(2)O(2) is essential for the iodination of the tyrosyl residues to produce mono- and diiodotyrosine that are the precursors for the synthesis of T(3) and T(4). Production of H(2)O(2) in thyroid glands occurs by oxidation of endogenous D-Asp by D-AspO (D-Asp+O(2)+H(2)O-->alpha-oxaloacetate+NH(3)+H(2)O(2)). D-Aspartate racemase catalyzes the in vivo production of D-Asp from L-Asp. Thus, interaction of endogenous D-Asp, D-AspO, and D-aspartate racemase in thyroid gland constitutes an additional biochemical pathway for the production of H(2)O(2) and consequently for the synthesis of thyroid hormones.

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Year:  2010        PMID: 20564565     DOI: 10.1002/cbdv.200900360

Source DB:  PubMed          Journal:  Chem Biodivers        ISSN: 1612-1872            Impact factor:   2.408


  10 in total

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4.  Olanzapine, but not clozapine, increases glutamate release in the prefrontal cortex of freely moving mice by inhibiting D-aspartate oxidase activity.

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Journal:  Sci Rep       Date:  2017-04-10       Impact factor: 4.379

5.  Biological Membrane-Packed Mesenchymal Stem Cells Treat Acute Kidney Disease by Ameliorating Mitochondrial-Related Apoptosis.

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6.  Simultaneous Measurement of Amino Acid Enantiomers in Aged Mouse Brain Samples by LC/MS/MS Combined with Derivatization Using Nzzm321990 α-(5-Fluoro-2,4-dinitrophenyl)-l-leucinamide (l-FDLA).

Authors:  Taiji Yamamoto; Keisuke Yaku; Takashi Nakagawa
Journal:  Metabolites       Date:  2021-01-15

7.  Human D-aspartate Oxidase: A Key Player in D-aspartate Metabolism.

Authors:  Loredano Pollegioni; Gianluca Molla; Silvia Sacchi; Giulia Murtas
Journal:  Front Mol Biosci       Date:  2021-06-23

8.  Decreased free d-aspartate levels are linked to enhanced d-aspartate oxidase activity in the dorsolateral prefrontal cortex of schizophrenia patients.

Authors:  Tommaso Nuzzo; Silvia Sacchi; Francesco Errico; Simona Keller; Orazio Palumbo; Ermanno Florio; Daniela Punzo; Francesco Napolitano; Massimiliano Copetti; Massimo Carella; Lorenzo Chiariotti; Alessandro Bertolino; Loredano Pollegioni; Alessandro Usiello
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9.  Selective demethylation of two CpG sites causes postnatal activation of the Dao gene and consequent removal of D-serine within the mouse cerebellum.

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Journal:  Clin Epigenetics       Date:  2019-10-28       Impact factor: 6.551

Review 10.  New Evidence on the Role of D-Aspartate Metabolism in Regulating Brain and Endocrine System Physiology: From Preclinical Observations to Clinical Applications.

Authors:  Alessandro Usiello; Maria Maddalena Di Fiore; Arianna De Rosa; Sara Falvo; Francesco Errico; Alessandra Santillo; Tommaso Nuzzo; Gabriella Chieffi Baccari
Journal:  Int J Mol Sci       Date:  2020-11-18       Impact factor: 5.923

  10 in total

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