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dc.contributor.advisor1Matos, Ione Maria de-
dc.contributor.advisor1Latteshttp://lattes.cnpq.br/5831392312967216pt_BR
dc.contributor.advisor-co1Silva, Maisa-
dc.contributor.advisor-co1Latteshttp://lattes.cnpq.br/7455078028049054pt_BR
dc.contributor.referee1Amaro, Bolivar Ralisson-
dc.contributor.referee1Latteshttp://lattes.cnpq.br/0499407882277672pt_BR
dc.contributor.referee2Lautner, Roberto Queiroga-
dc.contributor.referee2Latteshttp://lattes.cnpq.br/3518763240483624pt_BR
dc.creatorSantos, Filipe Ferreira-
dc.creator.Latteshttp://lattes.cnpq.br/1487928983217630pt_BR
dc.date.accessioned2024-12-18T15:53:12Z-
dc.date.available2024-12-17-
dc.date.available2024-12-18T15:53:12Z-
dc.date.issued2024-08-09-
dc.identifier.urihttps://repositorio.ufjf.br/jspui/handle/ufjf/17949-
dc.description.abstractBackground Scorpions have evolved a highly efficient venom that serves both to capture prey and for self-defense. As a result, peptides isolated from the venom of various scorpion species show great potential for the development of new medicines. Purpose This systematic review provides an overview of the therapeutic potential of peptides isolated from scorpion venom that act on the cardiovascular system. Methods We systematically searched PubMed, Scopus, Web of Science, EMBASE, and the Virtual Health Library for relevant studies published until December 2023, using the terms “peptides,” “scorpion,” “bradykinin potentiating factor,” “effects on cardiovascular diseases,” and “antihypertensive effects.” Results The literature search yielded 240 references. After applying the inclusion criteria, 17 studies were selected for analy- sis. Our review yielded five key findings: First, the identification of canonical bradykinin-potentiating peptides, which act as inhibitors of the angiotensin-converting enzyme, and non-canonical bradykinin-potentiating peptides, which act as B2 recep- tor agonists, enhancing the physiological effects of bradykinin. Second, a peptide regulating cardiomyocyte proteins was discovered. Third, an inotropic peptide was identified. Fourth, a potent hERG blocker peptide was found. Finally, a peptide with significant sodium current blocking capabilities in ventricular myocytes was identified. Conclusion The high specificity and potency of these scorpion venom-derived molecules underscore their potential as novel therapeutic agents in the cardiovascular field. This research highlights the importance of exploring natural bioactive compounds for the development of innovative treatments for cardiovascular diseases.pt_BR
dc.description.resumo-pt_BR
dc.languageengpt_BR
dc.publisherUniversidade Federal de Juiz de Fora - Campus Avançado de Governador Valadarespt_BR
dc.publisher.countryBrasilpt_BR
dc.publisher.departmentICV - Instituto de Ciências da Vidapt_BR
dc.publisher.initialsUFJF/GVpt_BR
dc.rightsAcesso Abertopt_BR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/br/*
dc.subjectVenom peptidespt_BR
dc.subjectScorpion venompt_BR
dc.subjectCardiovascular diseasespt_BR
dc.subjectSystematic reviewpt_BR
dc.subject.cnpqCNPQ::CIENCIAS DA SAUDE::FARMACIApt_BR
dc.titleScorpion venom peptides as therapeutic agents in cardiovascular diseases: a systematic reviewpt_BR
dc.typeTrabalho de Conclusão de Cursopt_BR
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