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Vasodilatory effects of catechol derivatives ex vivo
Šmídová, Kristýna ; Pourová, Jana (advisor) ; Carazo Fernández, Alejandro (referee)
Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmacology & Toxicology Student: Kristýna Šmídová Supervisor: doc. PharmDr. Jana Pourová, Ph.D. Title of diploma thesis: Vasodilatory effects of catechol derivatives ex vivo Polyphenols, including flavonoids, are a broad group of natural substances with significant effects on human health, including the prevention of cardiovascular diseases. Their metabolites can also be active, with clinical effects which may even exceed those of the parent compounds. The aim of this diploma thesis was to verify vasodilatory effects of one flavonoid metabolite type, a series of catechol derivatives and elucidate the mechanism of action of the most potent substance. The established ex vivo method of isolated aortic rings of Wistar rats with isotonic registration of tissue contraction and dilation (software S.P.E.L. Advanced Kymograph Software) was used. In the experiments with the rat aorta precontracted by norepinephrin, 3-methoxycatechol was the most effective vasodilator (EC50 = 7,6 µmol.l-1). In the mechanistic study, we found out that its effect is endothelium-independent, and that 3-methoxycatechol enhances the vasodilatory effect of sodium nitropruside. However, the specific mechanism responsible for vasodilation was not identified and...
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UV-Vis and IR Spectroelectrocbemistry of Copper Complexes and Bioactive Compounds
Sokolová, Romana ; Obluková, Michaela ; Sýs, M. ; Mikysek, T. ; Wantulok, J. ; Nycz, J. E. ; Degano, I.
The interpretation of the change of absorption spectrum of an oxidized and reduced molecule\nrecorded during the electron transfer is an efficient tool for the determination of oxidation or\nreduction mechanism. This technique provides the information about the electroactive\nchromophore and is performed in two regimes of electrochemical measurement, cyclic\nvoltammetry and chronoamperometry, respectively. This approach was successfully applied to\nstudy the fundamental electrochemical behavior of recently synthesized copper complexes\nproviding biomimetic activity, ofpolyphenolic bioactive compounds, and also for the reduction\nof halogenated phenanthrolines. The identification of redox products was done by\nchromatographic techniques as HPLC-DAD and HPLC-ESI-MS/MS.
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Vasodilatory effects of catechol derivatives ex vivo
Šmídová, Kristýna ; Pourová, Jana (advisor) ; Carazo Fernández, Alejandro (referee)
Charles University Faculty of Pharmacy in Hradec Králové Department of Pharmacology & Toxicology Student: Kristýna Šmídová Supervisor: doc. PharmDr. Jana Pourová, Ph.D. Title of diploma thesis: Vasodilatory effects of catechol derivatives ex vivo Polyphenols, including flavonoids, are a broad group of natural substances with significant effects on human health, including the prevention of cardiovascular diseases. Their metabolites can also be active, with clinical effects which may even exceed those of the parent compounds. The aim of this diploma thesis was to verify vasodilatory effects of one flavonoid metabolite type, a series of catechol derivatives and elucidate the mechanism of action of the most potent substance. The established ex vivo method of isolated aortic rings of Wistar rats with isotonic registration of tissue contraction and dilation (software S.P.E.L. Advanced Kymograph Software) was used. In the experiments with the rat aorta precontracted by norepinephrin, 3-methoxycatechol was the most effective vasodilator (EC50 = 7,6 µmol.l-1). In the mechanistic study, we found out that its effect is endothelium-independent, and that 3-methoxycatechol enhances the vasodilatory effect of sodium nitropruside. However, the specific mechanism responsible for vasodilation was not identified and...
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Utilization of mass spectrometry and other analytical techniques for analysis of rhenium complexes
Vaňátková, Petra ; Jelínek, Ivan (advisor) ; Smrček, Stanislav (referee)
Rhenium complexes coordinated with suitable organic ligand gain increased interest in radiopharmaceutical medicine. Besides suitable radiological properties given by a metal ion itself, detailed knowledge of overall chemical properties of formed complexes, namely their exact structures, chemical stabilities and possible degradation pathways are essential pre-requisites for their clinical application. Selected rhenium complexes with pyrogallol 2,3-dihydroxynaphthalene and catechol as strongly bound ligands were prepared by a reaction of tetrabutylammonium tetrachlorooxorhenate with twofold molar excess of ligand in presence of various amount of triethylamine. The structures of formed complexes and their consequent reaction products were estimated by means of mass spectrometry with electrospray ionization. The kinetics of reactions in course of complex formation and consequent decomposition were primarily followed by UV- Vis absorption spectra measurement, complemented by single or continuous electrospray mass spectrometry analyses. Optimized HPLC and CZE procedures were utilized for monitoring of the composition of reaction mixtures in course of Re complex formation and for purity check of prepared complexes. Semi-preparative HPLC mode was succesfully utilized for isolation and final purification of...
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