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Some Dietary Phenolic Compounds Can Activate Thyroid Peroxidase and Inhibit Lipoxygenase-Preliminary Study in the Model Systems.
Habza-Kowalska, Ewa; Kaczor, Agnieszka A; Bartuzi, Damian; Pilat, Jacek; Gawlik-Dziki, Urszula.
Afiliação
  • Habza-Kowalska E; Department of Biochemistry and Food Chemistry, University of Life Sciences, Skromna Str. 8, 20-704 Lublin, Poland.
  • Kaczor AA; Department of Synthesis and Chemical Technology of Pharmaceutical Substances with Computer Modeling Laboratory, Faculty of Pharmacy, Medical University of Lublin, 4A Chodzki St., 20-093 Lublin, Poland.
  • Bartuzi D; School of Pharmacy, University of Eastern Finland, Yliopistonranta 1, P.O. Box 1627, FI-70211 Kuopio, Finland.
  • Pilat J; Department of Synthesis and Chemical Technology of Pharmaceutical Substances with Computer Modeling Laboratory, Faculty of Pharmacy, Medical University of Lublin, 4A Chodzki St., 20-093 Lublin, Poland.
  • Gawlik-Dziki U; Department of General Surgery, Transplantology and Clinical Nutrition, Medical University of Lublin, Jaczewskiego Str. 8, 20-090 Lublin, Poland.
Int J Mol Sci ; 22(10)2021 May 12.
Article em En | MEDLINE | ID: mdl-34065957
The presented research concerns the triple activity of trans-cinnamic (tCA), ferulic (FA) and syringic acids (SA). They act as thyroid peroxidase (TPO) activators, lipoxygenase (LOX) inhibitors and show antiradical activity. All compounds showed a dose-dependent TPO activatory effect, thus the AC50 value (the concentration resulting in 50% activation) was determined. The tested compounds can be ranked as follows: tCA > FA > SA with AC50 = 0.10, 0.39, 0.69 mM, respectively. Strong synergism was found between FA and SA. The activatory effects of all tested compounds may result from interaction with the TPO allosteric site. It was proposed that conformational change resulting from activator binding to TPO allosteric pocket results from the flexibility of a nearby loop formed by residues Val352-Tyr363. All compounds act as uncompetitive LOX inhibitors. The most effective were tCA and SA, whereas the weakest was FA (IC50 = 0.009 mM and IC50 0.027 mM, respectively). In all cases, an interaction between the inhibitors carboxylic groups and side-chain atoms of Arg102 and Arg139 in an allosteric pocket of LOX was suggested. FA/tCA and FA/SA acted synergistically, whereas tCA/SA demonstrated antagonism. The highest antiradical activity was found in the case of SA (IC50 = 0.22 mM). FA/tCA and tCA/SA acted synergistically, whereas antagonism was found for the SA/FA mixture.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autoantígenos / Inibidores de Lipoxigenase / Ativadores de Enzimas / Proteínas de Ligação ao Ferro / Compostos Fitoquímicos / Iodeto Peroxidase / Proteína-Lisina 6-Oxidase Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Autoantígenos / Inibidores de Lipoxigenase / Ativadores de Enzimas / Proteínas de Ligação ao Ferro / Compostos Fitoquímicos / Iodeto Peroxidase / Proteína-Lisina 6-Oxidase Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article