Avaliação da atividade antinociceptiva espinhal da toxina Tx3-4 do veneno da aranha Phoneutria nigriventer em camundongos
Existing medicines for the treatment of pain are often associated withserious side effects and rapid development of tolerance, thus, there is a need for new, more selective molecules. The inhibition of voltage-gated calcium channels (VGCCs) in the dorsal horn of the spinal cord has been shown an imp...
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| Tipo de recurso: | tesis de maestría |
| Estado: | Versión publicada |
| Fecha de publicación: | 2009 |
| País: | Brasil |
| Institución: | Universidade Federal de Minas Gerais (UFMG) |
| Repositorio: | Repositório Institucional da UFMG |
| Idioma: | portugués |
| OAI Identifier: | oai:repositorio.ufmg.br:1843/BUOS-92PM5V |
| Acceso en línea: | http://hdl.handle.net/1843/BUOS-92PM5V |
| Access Level: | acceso abierto |
| Palabra clave: | Farmacologia Bioquímica e Molecular Gânglios espinhais Veneno Toxinas Analgésicos/farmacologia Farmacologia Aranha Analgésicos Analgésicos não entorpecentes/uso terapêutico Camundongos |
| Sumario: | Existing medicines for the treatment of pain are often associated withserious side effects and rapid development of tolerance, thus, there is a need for new, more selective molecules. The inhibition of voltage-gated calcium channels (VGCCs) in the dorsal horn of the spinal cord has been shown an important target, once the reduction of intracellular levels of calcium is a mechanism of nociceptive transmission modulation. The objective of the present study was to investigate the possible antinociceptive activity of the toxin Tx3-4, purified from Phoneutria nigriventers venom, since affinity for N-, P/Q and R-type VGCCs wasestablished and compares activity with the -conotoxins MVIIC and MVIIA. The phonotoxin was intratecally injected and demonstrate an antinociceptive effect in behavioral response and inflammatory nociceptive models. The Tx3-4 was able to inhibit formalin induced nociception both pre- and pos-treatment in inflammatory phase, but -conotoxin-MVIIA actuated only in pre-treatmen and -conotoxina-MVIIC only in pos-treatment. In addition, Tx3-4 inhibited behavioral response NMDA-induced and postoperative mechanical allodynia, and as so, ithas been more powerfull and effective in clinic model and did not affect the response induced by hot-plate, without disturbing the reflexes that areresponsible to protect the skin and body tissues. Furthermore, there was a rise of therapeutic potential in a central sensitization model, postoperative nociception, and Tx3-4 did not affect the motor coordination or motor locomotion when administered in naive animals. Thus, more studies are necessary to better clarify the mechanisms involved both, Tx3-4 toxins antinociceptive effect, and toxicity in mice. |
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