Anti-nociceptive effects of Carpolobia lutea G. Don (Polygalaceae) leaf fractions in animal models

dc.contributor.authorNwidu, Lucky Lebgosi
dc.contributor.authorNwafor, Paul Alozie
dc.contributor.authorDa Silva, Viviane Cândida [UNESP]
dc.contributor.authorRodrigues, Clenilson Martins [UNESP]
dc.contributor.authorSantos, Lourdes Campaner dos [UNESP]
dc.contributor.authorVilegas, Wagner [UNESP]
dc.contributor.authorNunes-De-Souza, Ricardo Luiz [UNESP]
dc.contributor.institutionNiger Delta University
dc.contributor.institutionUniversity of Uyo
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:25:57Z
dc.date.available2014-05-27T11:25:57Z
dc.date.issued2011-08-01
dc.description.abstractLeaves from Carpolobia lutea (Polygalaceae) were screened to establish the antiulcer ethnomedicinal claim and to quantitatively isolate, elucidate the active compounds by semi-preparative HPLC. The anti-nociceptive effects of Carpolobia lutea (CL) G. Don (Polygalaceae) organic leaf extracts were tested in experimental models in mice. The anti-nociceptive mechanism was determined using tail-flick test, acetic acid-induced abdominal constrictions, formalin-induced hind paw licking and the hot plate test. The fractions (ethanol, ethyl acetate, chloroform, n-hexane) and crude ethyl acetate extract of CL (770 mg/kg, i.p.) produced significant inhibitions of both phases of the formalin-induced pain in mice, a reduction in acetic acid-induced writhing as well as and an elevation of the pain threshold in the hot plate test in mice. The inhibitions were greater to those produced by indomethacin (5 mg/kg, i.p.). Ethyl acetate fraction revealed cinnamic and coumaric acids derivatives, which are described for the first time in literature. These cinnamalglucosides polyphenols characterised from CL may in part account for the pharmacological activities. These findings confirm its ethnomedical use in anti-inflammatory pain and in pains from gastric ulcer-associated symptoms. © 2011 Springer Basel AG.en
dc.description.affiliationDepartment of Pharmacology and Toxicology Faculty of Pharmacy Niger Delta University, Wilberforce Island, Bayelsa State
dc.description.affiliation, P.O. Box 10935, Port Harcourt, Rivers State
dc.description.affiliationDepartment of Pharmacology and Toxicology Faculty of Pharmacy University of Uyo, Uyo, Akwa Ibom State
dc.description.affiliationDepartamento de Química Orgânica Instituto de Química UNESP, Univ. Estadual Paulista, CP 355, Araraquara, SP CEP 14801-970
dc.description.affiliationLab. Farmacologia Faculdade de Ciencias UNESP, Araraquara-jau, km 01, Araraquara, SP 14801-902
dc.description.affiliationUnespDepartamento de Química Orgânica Instituto de Química UNESP, Univ. Estadual Paulista, CP 355, Araraquara, SP CEP 14801-970
dc.description.affiliationUnespLab. Farmacologia Faculdade de Ciencias UNESP, Araraquara-jau, km 01, Araraquara, SP 14801-902
dc.format.extent215-225
dc.identifierhttp://dx.doi.org/10.1007/s10787-010-0076-y
dc.identifier.citationInflammopharmacology, v. 19, n. 4, p. 215-225, 2011.
dc.identifier.doi10.1007/s10787-010-0076-y
dc.identifier.issn0925-4692
dc.identifier.issn1568-5608
dc.identifier.lattes3538253640602977
dc.identifier.orcid0000-0003-3032-2556
dc.identifier.scopus2-s2.0-79960245702
dc.identifier.urihttp://hdl.handle.net/11449/72569
dc.language.isoeng
dc.relation.ispartofInflammopharmacology
dc.relation.ispartofjcr3.304
dc.relation.ispartofsjr0,925
dc.relation.ispartofsjr0,925
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.subjectAntinociceptive
dc.subjectCarpolobia lutea
dc.subjectHPLC isolation of cinnamalglucosides
dc.subjectPolygalaceae
dc.subject4 coumaroyl 1 deoxyglucopyranoside derivative
dc.subjectacetic acid
dc.subjectacetic acid ethyl ester
dc.subjectalcohol
dc.subjectantinociceptive agent
dc.subjectatropine
dc.subjectCarpolobia lutea extract
dc.subjectchloroform
dc.subjectcinnamic acid
dc.subjectcinnamic acid derivative
dc.subjectcinnamoyl 1 deoxyglucopyranoside derivative
dc.subjectcoumaric acid
dc.subjectdimorf
dc.subjectformaldehyde
dc.subjecthexane
dc.subjectindometacin
dc.subjectmorphine sulfate
dc.subjectnaltrexone
dc.subjectplant extract
dc.subjectunclassified drug
dc.subjectabdominal pain
dc.subjectanalgesic activity
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectantinociception
dc.subjectcontrolled study
dc.subjectdrug isolation
dc.subjectdrug screening
dc.subjectdrug structure
dc.subjectfemale
dc.subjectfoot pain
dc.subjecthot plate test
dc.subjectlicking
dc.subjectmale
dc.subjectmouse
dc.subjectnonhuman
dc.subjectpain
dc.subjectpain threshold
dc.subjectplant leaf
dc.subjectpriority journal
dc.subjecttail flick test
dc.subjectwrithing test
dc.subjectAbdominal Pain
dc.subjectAnalgesics, Non-Narcotic
dc.subjectAnimals
dc.subjectAnti-Inflammatory Agents, Non-Steroidal
dc.subjectBehavior, Animal
dc.subjectCinnamates
dc.subjectCoumaric Acids
dc.subjectDrug Discovery
dc.subjectFemale
dc.subjectGlucosides
dc.subjectHot Temperature
dc.subjectLethal Dose 50
dc.subjectMale
dc.subjectMedicine, African Traditional
dc.subjectMice
dc.subjectMolecular Structure
dc.subjectNigeria
dc.subjectPain Measurement
dc.subjectPlant Extracts
dc.subjectPlant Leaves
dc.titleAnti-nociceptive effects of Carpolobia lutea G. Don (Polygalaceae) leaf fractions in animal modelsen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights
unesp.author.lattes3538253640602977
unesp.author.orcid0000-0003-3032-2556[6]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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