Analgesic and side effects of intravenous recombinant Phα1β.

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Autor(es): dc.creatorRigo, Flavia Karine-
Autor(es): dc.creatorRossato, Mateus Fortes-
Autor(es): dc.creatorBorges, Vanessa-
Autor(es): dc.creatorSilva, Juliana Figueira da-
Autor(es): dc.creatorPereira, Elizete Maria Rita-
Autor(es): dc.creatorÁvila, Ricardo Andrez Machado de-
Autor(es): dc.creatorTrevisan, Gabriela-
Autor(es): dc.creatorAstoni, Duana Carvalho dos Santos-
Autor(es): dc.creatorDiniz, Danuza Montijo-
Autor(es): dc.creatorSilva, Marco Aurélio Romano-
Autor(es): dc.creatorCastro Junior, Célio José de-
Autor(es): dc.creatorCunha, Thiago Mattar-
Autor(es): dc.creatorFerreira, Juliano-
Autor(es): dc.creatorGomez, Marcus Vinicius-
Data de aceite: dc.date.accessioned2025-08-21T15:14:20Z-
Data de disponibilização: dc.date.available2025-08-21T15:14:20Z-
Data de envio: dc.date.issued2022-11-03-
Data de envio: dc.date.issued2022-11-03-
Data de envio: dc.date.issued2019-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/jspui/handle/123456789/15751-
Fonte completa do material: dc.identifierhttps://doi.org/10.1590/1678-9199-JVATITD-2019-0070-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1007467-
Descrição: dc.descriptionBackground: Intrathecal injection of voltage-sensitive calcium channel blocker peptide toxins exerts analgesic effect in several animal models of pain. Upon intrathecal administration, recombinant Phα1β exerts the same analgesic effects as the those of the native toxin. However, from a clinical perspective, the intrathecal administration limits the use of anesthetic drugs in patients. Therefore, this study aimed to investigate the possible antinociceptive effect of intravenous recombinant Phα1β in rat models of neuropathic pain, as well as its side effects on motor, cardiac (heart rate and blood pressure), and biochemical parameters. Methods: Male Wistar rats and male Balb-C mice were used in this study. Giotto Biotech® synthesized the recombinant version of Phα1β using Escherichia coli expression. In rats, neuropathic pain was induced by chronic constriction of the sciatic nerve and paclitaxel-induced acute and chronic pain. Mechanical sensitivity was evaluated using von Frey filaments. A radiotelemeter transmitter (TA11PA-C10; Data Sciences, St. Paul, MN, USA) was placed on the left carotid of mice for investigation of cardiovascular side effects. Locomotor activity data were evaluated using the open-field paradigm, and serum CKMB, TGO, TGP, LDH, lactate, creatinine, and urea levels were examined. Results: Intravenous administration of recombinant Phα1β toxin induced analgesia for up to 4 h, with ED50 of 0.02 (0.01-0.03) mg/kg, and reached the maximal effect (Emax = 100% antinociception) at a dose of 0.2 mg/kg. No significant changes were observed in any of the evaluated motor, cardiac or biochemical parameters. Conclusion: Our data suggest that intravenous administration of recombinant Phα1β may be feasible for drug-induced analgesia, without causing any severe side effects.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Direitos: dc.rightsaberto-
Direitos: dc.rightsThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http:// creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/ publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Fonte: o PDF do artigo.-
Palavras-chave: dc.subjectAnalgesia-
Palavras-chave: dc.subjectNeuropathic pain-
Palavras-chave: dc.subjectIntravenous drug delivery system-
Palavras-chave: dc.subjectCardiac function-
Palavras-chave: dc.subjectMotor activity-
Título: dc.titleAnalgesic and side effects of intravenous recombinant Phα1β.-
Aparece nas coleções:Repositório Institucional - UFOP

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