학술논문

Vasoconstrictor and hemodynamic effects of a methanolic extract from Rhinella marina toad poison.
Document Type
Academic Journal
Author
Santos CVD; NUPADS - Health Education and Research Center, Institute of Health Sciences, Federal University of Mato Grosso, 78550-728, Sinop, MT, Brazil; Department of Pharmacology, Ribeirao Preto Medical School, University of São Paulo, 14049-900, Ribeirão Preto, SP, Brazil.; Kerkhoff J; Institute of Natural, Humanities and Social Sciences, Federal University of Mato Grosso, 78577-267, Sinop, MT, Brazil.; Tomazelli CA; Department of Physiology and Biophysics, Institute of Biomedical Sciences, University of São Paulo, 05508-000, São Paulo, SP, Brazil.; Wenceslau CF; Cardiovascular Translational Research Center, Department of Cell Biology and Anatomy, University of South Carolina School of Medicine, Columbia, SC, 29209, USA.; Sinhorin AP; Institute of Natural, Humanities and Social Sciences, Federal University of Mato Grosso, 78577-267, Sinop, MT, Brazil.; de Jesus Rodrigues D; Institute of Natural, Humanities and Social Sciences, Federal University of Mato Grosso, 78577-267, Sinop, MT, Brazil.; Carneiro FS; Department of Pharmacology, Ribeirao Preto Medical School, University of São Paulo, 14049-900, Ribeirão Preto, SP, Brazil.; Bomfim GF; NUPADS - Health Education and Research Center, Institute of Health Sciences, Federal University of Mato Grosso, 78550-728, Sinop, MT, Brazil. Electronic address: gisele.bomfim@ufmt.br.
Source
Publisher: Pergamon Press Country of Publication: England NLM ID: 1307333 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-3150 (Electronic) Linking ISSN: 00410101 NLM ISO Abbreviation: Toxicon Subsets: MEDLINE
Subject
Language
English
Abstract
Rhinella marina toad is abundant in Brazil. Its poison contains cardiac glycosides called bufadienolides, which are extensively investigated for their bioactivity. Our aim was to characterize the vasoactivity of Rhinella marina poison (RmP) on the aorta of male Wistar rats. For this, the RmP was first collected and processed to obtain an alcoholic extract. To determine cardiovascular effects of RmP, we performed in vivo tests by administering RmP intravenously in doses of 0.1-0.8 mg/kg. Vascular reactivity was also performed through concentration-response curves to RmP (10 ng/mL to 200 μg/mL) in aortic segments with and without endothelium. RmP induced a concentration-dependent contraction in rat aorta which was partly endothelium-mediated. Nitric oxide contributes with this response in view that incubation with L-NAME increased the contractile response. Additionally, treatment with indomethacin [cyclooxygenase, (COX) inhibitor], nifedipine (L-type voltage-gated calcium channels blocker), and BQ-123 (ET A receptors antagonist) decreased maximum response, and ketanserin (5-HT 2 receptors antagonist) decreased pEC 50 , suggesting active participation of these pathways in the contractile response. On the other hand, apocynin (NADPH oxidase inhibitor) did not alter contractility. Incubation with prazosin (α 1 -adrenergic receptor antagonist) abolished the contractile response, suggesting that the RmP-induced contraction is dependent on the adrenergic pathway. In the Na + /K + ATPase protocol, a higher Emax was observed in the RmP experimental group, suggesting that RmP potentiated Na + /K + ATPase hyperpolarizing response. When this extract was injected (i.v.) in vivo, increase in blood pressure and decrease in heart rate were observed. The results were immediate and transitory, and occurred in a dose-dependent manner. Overall, these data suggest that the poison extract of R. marina toad has an important vasoconstrictor action and subsequent vasopressor effects, and its use can be investigated to some cardiovascular disorders.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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