Search Results - "Beirão, Paulo Sérgio Lacerda"

N‐Salicyloyltryptamine, a new anticonvulsant drug, acts on voltage‐dependent Na+, Ca2+, and K+ ion channels by Araújo, Demétrius Antonio Machado, Mafra, Roberta Amaral, Rodrigues, Andréia Laura Prates, Miguel‐Silva, Válter, Beirão, Paulo Sérgio Lacerda, De Almeida, Reinaldo Nóbrega, Quintans, Lucindo, Souza, Maria Fátima Vanderlei de, Cruz, Jader Santos

“…The aim of this work was to study the effects of N‐salicyloyltryptamine (STP), a novel anticonvulsant agent, on voltage‐gated ion channels in GH3 cells. In…”
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Angiotensin 1–7 increases quantal content and facilitation at the frog neuromuscular junction by Ricardo Bevilaqua, Enéias, Kushmerick, Christopher, Sérgio Lacerda Beirão, Paulo, Araujo Naves, Lı́gia

“…At the neuromuscular junction, several endogenous substances have been shown to act presynaptically to modify transmitter release. Here we show that…”
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Characterization of the first two toxins isolated from the venom of the ancient scorpion Tityus (Archaeotityus) mattogrossensis (Borelli, 1901) by de Oliveira, Natiela Beatriz, Magalhães, Ana Carolina Martins, Bloch, Jr, Carlos, Beirão, Paulo Sérgio Lacerda, Silva, Anita de Oliveira, Melani, Rafael D, Barbosa, Eder Alves, Pires, Osmindo Rodrigues, Schwartz, Carlos Alberto

“…Almost all characterized toxins are from subgenera and , there are only a few data about toxins produced by , an ancient group in genus. crude venom was…”
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Carvacrol Decreases Neuronal Excitability by Inhibition of Voltage-Gated Sodium Channels by Joca, Humberto Cavalcante, Cruz-Mendes, Yuri, Oliveira-Abreu, Klausen, Maia-Joca, Rebeca Peres Moreno, Barbosa, Roseli, Lemos, Telma Leda, Lacerda Beirão, Paulo Sergio, Leal-Cardoso, José Henrique

“…The monoterpenoid carvacrol (1) is present in many essential oils of plants and has attracted attention because of its beneficial biological activities,…”
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Action of the saliva of Triatoma infestans (Heteroptera: Reduviidae) on sodium channels by Dan, A, Pereira, M.H, Pesquero, J.L, Diotaiuti, L, Beirao, P.S.L

“…Saliva of Triatoma infestans (Klug) produced a progressive reduction in the amplitude of the compound action potential recorded from rat sciatic nerve. The…”
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BcIV, a new paralyzing peptide obtained from the venom of the sea anemone Bunodosoma caissarum. A comparison with the Na + channel toxin BcIII by Oliveira, Joacir Stolarz, Zaharenko, André Junqueira, Ferreira, Wilson Alves, Konno, Katsuhiro, Shida, Cláudio Saburo, Richardson, Michael, Lúcio, Aline Duarte, Beirão, Paulo Sérgio Lacerda, de Freitas, José Carlos

“…Sea anemones produce a wide variety of biologically active compounds, such as the proteinaceous neurotoxins and cytolysins. Herein we report a new peptide,…”
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N ‐Salicyloyltryptamine, a new anticonvulsant drug, acts on voltage‐dependent Na + , Ca 2+ , and K + ion channels by Araújo, Demétrius Antonio Machado, Mafra, Roberta Amaral, Rodrigues, Andréia Laura Prates, Miguel‐Silva, Válter, Beirão, Paulo Sérgio Lacerda, De Almeida, Reinaldo Nóbrega, Quintans, Lucindo, Souza, Maria Fátima Vanderlei de, Cruz, Jader Santos

“…The aim of this work was to study the effects of N ‐salicyloyltryptamine (STP), a novel anticonvulsant agent, on voltage‐gated ion channels in GH3 cells. In…”
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Veratridine modifies the TTX-resistant Na + channels in rat vagal afferent neurons by Campos, Fabiana Vasconcelos, Moreira, Thaı́s Helena, Beirão, Paulo Sérgio Lacerda, Cruz, Jader Santos

“…A number of neurotoxins from venoms of invertebrates and plants are ligands for voltage-gated Na + channels and are useful tools for studying Na + channel…”
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BcIV, a new paralyzing peptide obtained from the venom of the sea anemone Bunodosoma caissarum. A comparison with the Na+ channel toxin BcIII by Oliveira, Joacir Stolarz, Zaharenko, André Junqueira, Ferreira, Jr, Wilson Alves, Konno, Katsuhiro, Shida, Cláudio Saburo, Richardson, Michael, Lúcio, Aline Duarte, Beirão, Paulo Sérgio Lacerda, de Freitas, José Carlos

“…Sea anemones produce a wide variety of biologically active compounds, such as the proteinaceous neurotoxins and cytolysins. Herein we report a new peptide,…”
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