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dc.contributor.authorAlves, Rafael dos Santos-
dc.date.accessioned2019-02-04T12:52:57Z-
dc.date.available2019-02-04T12:52:57Z-
dc.date.issued2016-11-09-
dc.identifier.citationALVES, Rafael dos Santos. Antinociceptive effect of Aristolochia trilobata stem essential oil and 6-methyl-5-hepten-2-yl acetate, its main compound, in rodents. São Cristóvão, SE, 2016. Monografia (Graduação em Farmácia) - Departamento de Farmácia, Centro de Ciências Biológicas e da Saúde, Universidade Federal de Sergipe, São Cristóvão, 2016pt_BR
dc.identifier.urihttp://ri.ufs.br/jspui/handle/riufs/10384-
dc.description.abstractAristolochia trilobata L. is an aromatic plant, popularly known as „mil-homens?, and its essential oil is generally used to treat colic, diarrhea, and dysentery disorders. We evaluated the antinociceptive effect of A. trilobata stem essential oil (EO) and of its major compound, the (R)-(-)-6-methyl-5-hepten-2-yl acetate (sulcatyl acetate: SA), using acetic acid (0.65%)-induced writhing response and formalin -induced (20 µl of 2,5%) nociceptive behavior in mice. We also evaluated the EO and SA effect on motor coordination, using the rota-rod apparatus. EO (25, 50 and 100 mg/kg) or SA (25 and 50 mg/kg) reduced nociceptive behavior in the writhing test (p < 0.001). EO (100 mg/kg) and SA (25 and 50 mg/kg) decreased the nociception on first phase of formalin test (p < 0.05). On second phase, EO(25: p < 0.01; 50: p < 0.05 and 100 mg/kg: p < 0.001) and SA (25 and 50 mg/kg; p < 0.001) reduced the nociceptive response induced by formalin. EO and SA were not able to cause changes in the motor coordination of animals. Together, our results suggest that the EO has an analgesic profile and SA seems to be one of the active compounds in this effectpor
dc.languageporpt_BR
dc.subjectFarmáciapor
dc.subjectEnsino de farmáciapor
dc.subjectAristoloquiáceapor
dc.subjectPlantas aromáticaspor
dc.subjectEssenciaspor
dc.subjectÓleos essenciaispor
dc.subjectDorpor
dc.titleAntinociceptive effect of Aristolochia trilobata stem essential oil and 6-methyl-5-hepten-2-yl acetate, its main compound, in rodentspt_BR
dc.typeMonografiapt_BR
dc.contributor.advisor1Guimarães, Adriana Gibara-
dc.publisher.departmentDFA - Departamento de Farmácia – São Cristóvão - Presencialpt_BR
dc.subject.cnpqCIENCIAS BIOLOGICAS::FARMACOLOGIA::FARMACOLOGIA CLINICApt_BR
dc.publisher.initialsUniversidade Federal de Sergipept_BR
dc.description.localSão Cristóvão, SEpt_BR
Aparece nas coleções:Farmácia

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