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Journal Abstract Search

159 related items for PubMed ID: 9037574

  • 21. Ro 40-7592: inhibition of COMT in rat brain and extracerebral tissues.
    Zürcher G, Colzi A, Da Prada M.
    J Neural Transm Suppl; 1990; 32():375-80. PubMed ID: 2089102
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  • 22. Chronic Alcohol Exposure Differentially Alters One-Carbon Metabolism in Rat Liver and Brain.
    Auta J, Zhang H, Pandey SC, Guidotti A.
    Alcohol Clin Exp Res; 2017 Jun; 41(6):1105-1111. PubMed ID: 28369960
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  • 23. Catechol-O-methyltransferase inhibition in erythrocytes and liver by BIA 3-202 (1-[3,4-dibydroxy-5-nitrophenyl]-2-phenyl-ethanone).
    Soares-da-Silva P, Vieira-Coelho MA, Parada A.
    Pharmacol Toxicol; 2003 Jun; 92(6):272-8. PubMed ID: 12787259
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  • 24. Phospholipid methylase activity, [3H]S-adenosyl-L-homocysteine binding, and S-adenosyl-L-methionine and S-adenosyl-L-homocysteine levels in rat brain during maturation.
    Gharib A, Rey C, Fonlupt P, Sarda N, Pacheco H.
    J Neurochem; 1985 Jul; 45(1):32-6. PubMed ID: 3998730
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  • 25. High-performance liquid chromatographic analysis of S-adenosylmethionine and its metabolites in rat tissues: interrelationship with changes in biogenic catechol levels following treatment with L-dopa.
    Wagner J, Danzin C, Huot-Olivier S, Claverie N, Palfreyman MG.
    J Chromatogr; 1984 May 04; 290():247-62. PubMed ID: 6736164
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  • 30. No change of brain extracellular catecholamine levels after acute catechol-O-methyltransferase inhibition: a microdialysis study in anaesthetized rats.
    Li YH, Wirth T, Huotari M, Laitinen K, MacDonald E, Männistö PT.
    Eur J Pharmacol; 1998 Sep 04; 356(2-3):127-37. PubMed ID: 9774242
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  • 32. BIA 3-202, a novel catechol-O-methyltransferase inhibitor, reduces the peripheral O-methylation of L-DOPA and enhances its availability to the brain.
    Parada A, Soares-da-Silva P.
    Pharmacology; 2003 May 04; 68(1):29-37. PubMed ID: 12660477
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  • 33. Methionine Metabolites in Patients With Sepsis.
    Wexler O, Gough MS, Morgan MAM, Mack CM, Apostolakos MJ, Doolin KP, Mooney RA, Arning E, Bottiglieri T, Pietropaoli AP.
    J Intensive Care Med; 2018 Jan 04; 33(1):37-47. PubMed ID: 27591199
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  • 35. Effect of catechol-O-methyl transferase inhibition on peripheral and central metabolism of 6-[18F]fluoro-L-dopa.
    Pauwels T, Dethy S, Goldman S, Monclus M, Luxen A.
    Eur J Pharmacol; 1994 May 12; 257(1-2):53-8. PubMed ID: 8082707
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  • 36. Coadministration of β-asarone and levodopa increases dopamine in rat brain by accelerating transformation of levodopa: a different mechanism from Madopar.
    Huang L, Deng M, Zhang S, Fang Y, Li L.
    Clin Exp Pharmacol Physiol; 2014 Sep 12; 41(9):685-90. PubMed ID: 24910244
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  • 37. The COMT inhibitor, entacapone, reduces levodopa-induced elevations in plasma homocysteine in healthy adult rats.
    Nissinen E, Nissinen H, Larjonmaa H, Väänänen A, Helkamaa T, Reenilä I, Rauhala P.
    J Neural Transm (Vienna); 2005 Sep 12; 112(9):1213-21. PubMed ID: 15614425
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  • 40. Acute administration of L-DOPA induces changes in methylation metabolites, reduced protein phosphatase 2A methylation, and hyperphosphorylation of Tau protein in mouse brain.
    Bottiglieri T, Arning E, Wasek B, Nunbhakdi-Craig V, Sontag JM, Sontag E.
    J Neurosci; 2012 Jul 04; 32(27):9173-81. PubMed ID: 22764226
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