Výsledky vyhledávání - "Ignac, Ovari"

Akademický článek

The influence of the way of regression on the results obtained by the receptorial responsiveness method (RRM), a procedure to estimate a change in the concentration of a pharmacological agonist near the receptor

Autor: Ignac Ovari, Gabor Viczjan, Tamas Erdei, Barbara Takacs, Vera Tarjanyi, Judit Zsuga, Miklos Szucs, Zoltan Szilvassy, Bela Juhasz, Rudolf Gesztelyi

Publikováno v: Frontiers in Pharmacology, Vol 15 (2024)

The receptorial responsiveness method (RRM) enables the estimation of a change in concentration of an (even degradable) agonist, near its receptor, via curve fitting to (at least) two concentration-effect (E/c) curves of a stable agonist. One curve s

Externí odkaz: https://doaj.org/article/972b6fd40489411ea1af45c47d01b30c

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Akademický článek

The effect of a long-term treatment with cannabidiol-rich hemp extract oil on the adenosinergic system of the zucker diabetic fatty (ZDF) rat atrium

Autor: Gabor Viczjan, Anna Szilagyi, Barbara Takacs, Ignac Ovari, Reka Szekeres, Vera Tarjanyi, Tamas Erdei, Vanda Teleki, Judit Zsuga, Zoltan Szilvassy, Bela Juhasz, Balazs Varga, Rudolf Gesztelyi

Publikováno v: Frontiers in Pharmacology, Vol 13 (2022)

Cannabidiol (CBD), the most extensively studied non-intoxicating phytocannabinoid, has been attracting a lot of interest worldwide owing to its numerous beneficial effects. The aim of this study was to explore the effect that CBD exerts on the adenos

Externí odkaz: https://doaj.org/article/bcba8b436b4d4d11859545dfaf32956f

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A Body of Circumstantial Evidence for the Irreversible Ectonucleotidase Inhibitory Action of FSCPX, an Agent Known as a Selective Irreversible A

Autor: Gabor, Viczjan, Tamas, Erdei, Ignac, Ovari, Nora, Lampe, Reka, Szekeres, Mariann, Bombicz, Barbara, Takacs, Anna, Szilagyi, Judit, Zsuga, Zoltan, Szilvassy, Bela, Juhasz, Rudolf, Gesztelyi

Publikováno v: International Journal of Molecular Sciences

In previous studies using isolated, paced guinea pig left atria, we observed that FSCPX, known as a selective A1 adenosine receptor antagonist, paradoxically increased the direct negative inotropic response to A1 adenosine receptor agonists (determin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0179d17b56005f3515196df0dbd60201
https://pubmed.ncbi.nlm.nih.gov/34575993

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