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Your search keyword '"Segarra G"' showing total 3 results
Start Over Author "Segarra G" Journal cardiovascular research
3 results on '"Segarra G"'

2. Oral abstract presentations

Author

Davidson, S. M., primary, Duchen, M. M., additional, Yellon, D. M., additional, Fields, L., additional, Zaccolo, M., additional, Laeremans, H., additional, Daskalopoulos, E. P., additional, Janssen, B. J. A., additional, Blankesteijn, W. M., additional, Tillmanns, J., additional, Hoffmann, D., additional, Habbaba, Y., additional, Fraccarollo, D., additional, Galuppo, P., additional, Bauersachs, J., additional, Novella, S., additional, Segarra, G., additional, Dantas, A. P., additional, Bueno-Beti, C., additional, Novensa, L., additional, Lazaro-Franco, M., additional, Martinez-Gil, N., additional, Medina, P., additional, Hermenegildo, C., additional, Ohanian, J., additional, Liao, A., additional, Trafford, A. W., additional, Ohanian, V., additional, Perez-Moreno, A., additional, Garcia-Canadilla, P., additional, Dominguez, J. M., additional, Crispi, F., additional, Gratacos, E., additional, Amat-Roldan, I., additional, Gotschy, A., additional, Herold, V., additional, Bauer, E., additional, Schrodt, C., additional, Lykowsky, G., additional, Rommel, E., additional, Jakob, P., additional, Bauer, W., additional, Shah, M., additional, Sikkel, M. B., additional, Desplantez, T., additional, Collins, T. P., additional, O'Gara, P., additional, Harding, S. E., additional, Lyon, A. R., additional, Macleod, K. T., additional, Ferrantini, C., additional, Sacconi, L., additional, Lotti, I., additional, Coppini, R., additional, Tesi, C., additional, Yan, P., additional, Loew, L. M., additional, Cerbai, E., additional, Poggesi, C., additional, Pavone, F. S., additional, Franco, D., additional, Daimi, H., additional, Dominguez, J. N., additional, Hove-Madsen, L., additional, Cinca, J., additional, Vazquez, E., additional, Aranega, A. E., additional, Poon, K. L., additional, Kirchmaier, B. C., additional, Schwerte, T., additional, Huisken, J., additional, Winkler, C., additional, Jungblut, B. C., additional, Stainier, D. Y., additional, Brand, T., additional, Stuckey, D. J., additional, Tremoleda, J. L., additional, Mcsweeney, S., additional, Fiedler, L., additional, Harada, M., additional, Carr, C. A., additional, Tyler, D. J., additional, Gsell, W., additional, Clarke, K., additional, Schneider, M. D., additional, Sequeira, V., additional, Regan, J. A., additional, Michels, M., additional, Ten Cate, F. J., additional, Van Slegtenhorst, M. A., additional, Stienen, G. J. M., additional, Dos Remedios, C., additional, and Van Der Velden, J., additional

Published
2012
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3. U-46619-induced potentiation of noradrenergic constriction in the human saphenous vein: antagonism by thromboxane receptor blockade.

Author

Vila JM, Martínez-León JB, Medina P, Segarra G, Ballester RM, Otero E, and Lluch S

Subjects
Aged, Calcium Channel Blockers pharmacology, Dihydropyridines metabolism, Dose-Response Relationship, Drug, Drug Synergism, Electric Stimulation, Endothelium, Vascular metabolism, Female, Humans, In Vitro Techniques, Male, Middle Aged, Nifedipine pharmacology, Potassium Chloride pharmacology, Saphenous Vein, Stimulation, Chemical, 15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic Acid pharmacology, Endothelium, Vascular drug effects, Norepinephrine pharmacology, Receptors, Thromboxane antagonists & inhibitors, Thromboxane A2 analogs & derivatives, Thromboxane A2 pharmacology, Vasoconstrictor Agents pharmacology
Abstract

Objective: We investigated the potentiating effect of U-46619, a synthetic analogue of thromboxane A(2) (TXA(2)), on the adrenergic responses in human saphenous vein., Methods: Saphenous vein rings were obtained from 35 patients undergoing coronary artery bypass surgery. The rings were suspended in organ bath chambers for isometric recording of tension., Results: U-46619 (10(-10)-3 x 10(-7) mol/l) produced concentration-dependent and endothelium-independent contractile responses. U-46619 (10(-10) mol/l) potentiated the contractions elicited by electrical stimulation and potassium chloride, and produced leftward shifts of the concentration-response curve for noradrenaline. The TXA(2) receptor antagonist SQ-30741 (10(-8) mol/l) prevented the potentiation evoked by U-46619. The dihydropyridine calcium antagonist nifedipine (10(-6) mol/l) did not affect the potentiation of electrical stimulation and noradrenaline induced by U-46619, but abolished the potentiation of U-46619 on KCl-induced contractions., Conclusions: U-46619 facilitates sympathetic neurotransmission and potentiates constrictor effects of noradrenaline in human saphenous veins through stimulation of TXA(2) receptors. These effects are independent of calcium entry through dihydropyridine calcium channels.

Published
2001
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