V
Valeria Camarda
Researcher at University of Ferrara
Publications - 38
Citations - 1133
Valeria Camarda is an academic researcher from University of Ferrara. The author has contributed to research in topics: Receptor & Agonist. The author has an hindex of 22, co-authored 38 publications receiving 1099 citations. Previous affiliations of Valeria Camarda include University of California, Irvine & GlaxoSmithKline.
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Journal ArticleDOI
Effects of human urotensin II in isolated vessels of various species; comparison with other vasoactive agents
Valeria Camarda,Anna Rizzi,Girolamo Calo,Gabrielle Gendron,Stephan I. Perron,Evi Kostenis,Paolo Zamboni,Francesco Mascoli,Domenico Regoli +8 more
TL;DR: The hU-II/GPR14 is not a functional contractile system in vessels of several species, in contrast with NA/α1, Ang II/AT1, 5HT/5HT2 and ET-1/ETA-ETB; the rat aorta appears however to be a sensitive and reliable preparation for evaluating biological activities of h U-II and related peptides.
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Pharmacological profile of NOP receptors coupled with calcium signaling via the chimeric protein Gαqi5
Valeria Camarda,Carmela Fischetti,Nicholas Anzellotti,Paola Molinari,Caterina Ambrosio,Evi Kostenis,Domenico Regoli,Claudio Trapella,Remo Guerrini,Salvadori Severo,Girolamo Calo +10 more
TL;DR: The results demonstrated that the FlexStation II–Gαqi5–NOP receptor calcium assay represents an adequate and useful screening for NOP receptor ligands, particularly for antagonists.
Journal ArticleDOI
Urantide mimics urotensin-II induced calcium release in cells expressing recombinant UT receptors
Valeria Camarda,Wei Song,Erika Marzola,Martina Spagnol,Remo Guerrini,Severo Salvadori,Domenico Regoli,Jonathan P. Thompson,David J. Rowbotham,David J. Behm,Stephen A. Douglas,Girolamo Calo,David G. Lambert +12 more
TL;DR: Urantide behaves as a competitive, potent, and pure antagonist in the rat aorta bioassay, while as an agonist in a calcium mobilization assay performed in CHO(hUT) cells and should be considered a low efficacy partial agonist.
Journal ArticleDOI
In vitro and in vivo pharmacological characterization of the neuropeptide s receptor antagonist [D-Cys(tBu)5]neuropeptide S.
Valeria Camarda,Anna Rizzi,Chiara Ruzza,Silvia Zucchini,Giuliano Marzola,Erika Marzola,Remo Guerrini,Severo Salvadori,Rainer K. Reinscheid,Domenico Regoli,Girolamo Calo +10 more
TL;DR: It is demonstrated that the arousal-promoting action of NPS is because of the selective activation of the NPSR protein.
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Pharmacological profile of hemokinin 1: a novel member of the tachykinin family.
TL;DR: Pharmacologically characterised the effects of hemokinin 1 using three tachykinin monoreceptor systems and indicates that HK-1 behaves as a NK(1) preferring receptor agonist.