Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris

Detalhes bibliográficos
Autor(a) principal: Pierri, Elaise G. [UNESP]
Data de Publicação: 2017
Outros Autores: Castro, Rogerio C. [UNESP], Vizioli, Ednir O. [UNESP], Ferreira, Carla M. R. [UNESP], Cavalheiro, Alberto J. [UNESP], Tininis, Aristeu G., Chin, Chung M. [UNESP], Santos, Andre G. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.bjp.2016.12.008
http://hdl.handle.net/11449/163098
Resumo: The present study aimed to investigate the anti-inflammatory activity of ethanolic extract from Casearia sylvestris Sw., Salicaceae, leaves and to identify the compounds responsible for this activity. The ethanolic extract from C. sylvestris leaves was fractionated by solid phase extraction and the chemical composition of extract and fractions were assessed by chromatographic techniques. Casearin-like clerodane diterpenes were quantified in ethanolic extract (27.4%, w/w) and in fraction 2 of solid phase extraction (50.6%, w/w). Carrageenan-induced paw edema and carrageenan-induced pleurisy assays (rats) were used to evaluate anti-inflammatory activity of ethanolic extract, its fractions and clerodane diterpenes from C. sylvestris caseargrewiin F and casearin B. The ethanolic extract was tested in the rat paw edema model and the doses tested (10 and 100 mg/kg) had no effect. In the pleurisy model, the extract doses of 300 and 500 mg/kg showed inhibitory effect. The fraction 2 of solid phase extraction (10 mg/kg), caseargrewiin F and casearin B (0.5 mg/kg) showed a significant reduction (p < 0.05) of the carrageenan-induced paw edema in rats compared to indomethacin. Gastric ulcers were not observed in animals treated with samples from C. sylvestris. In conclusion, the ethanolic extract from C. sylvestris, its enriched fraction of clerodane diterpenes, casearin B and caseargrewiin F exhibited anti-inflammatory activity on in vivo models in rats. Casearin-like clerodane diterpenes may be considered active chemical markers for C. sylvestris leaves. On the other hand, these diterpenes are promising compounds in the development of new drugs with anti-inflammatory action without gastric side effects. (c) 2017 Sociedade Brasileira de Farmacognosia. Published by Elsevier Editora Ltda.
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spelling Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestrisClerodane diterpeneCasearin BCaseargrewiin FAnti-inflammatory activityGastric side effectsThe present study aimed to investigate the anti-inflammatory activity of ethanolic extract from Casearia sylvestris Sw., Salicaceae, leaves and to identify the compounds responsible for this activity. The ethanolic extract from C. sylvestris leaves was fractionated by solid phase extraction and the chemical composition of extract and fractions were assessed by chromatographic techniques. Casearin-like clerodane diterpenes were quantified in ethanolic extract (27.4%, w/w) and in fraction 2 of solid phase extraction (50.6%, w/w). Carrageenan-induced paw edema and carrageenan-induced pleurisy assays (rats) were used to evaluate anti-inflammatory activity of ethanolic extract, its fractions and clerodane diterpenes from C. sylvestris caseargrewiin F and casearin B. The ethanolic extract was tested in the rat paw edema model and the doses tested (10 and 100 mg/kg) had no effect. In the pleurisy model, the extract doses of 300 and 500 mg/kg showed inhibitory effect. The fraction 2 of solid phase extraction (10 mg/kg), caseargrewiin F and casearin B (0.5 mg/kg) showed a significant reduction (p < 0.05) of the carrageenan-induced paw edema in rats compared to indomethacin. Gastric ulcers were not observed in animals treated with samples from C. sylvestris. In conclusion, the ethanolic extract from C. sylvestris, its enriched fraction of clerodane diterpenes, casearin B and caseargrewiin F exhibited anti-inflammatory activity on in vivo models in rats. Casearin-like clerodane diterpenes may be considered active chemical markers for C. sylvestris leaves. On the other hand, these diterpenes are promising compounds in the development of new drugs with anti-inflammatory action without gastric side effects. (c) 2017 Sociedade Brasileira de Farmacognosia. Published by Elsevier Editora Ltda.Univ Estadual Paulista, Fac Ciencias Farmaceut, Dept Principios Ativos Nat & Toxicol, Lab Farmacognosia, Araraquara, SP, BrazilUniv Estadual Paulista, Fac Ciencias Farmaceut, Dept Farm & Med, Lab Pesquisa Desenvolvimento Farm, Araraquara, SP, BrazilUniv Estadual Paulista, Inst Quim, Dept Quim Organ, Nucleo Bioensaios Biossintese & Ecofisiol Prod Na, Araraquara, SP, BrazilInst Fed Sao Paulo, Campus Avancado Matao, Matao, SP, BrazilUniv Estadual Paulista, Fac Ciencias Farmaceut, Dept Principios Ativos Nat & Toxicol, Lab Farmacognosia, Araraquara, SP, BrazilUniv Estadual Paulista, Fac Ciencias Farmaceut, Dept Farm & Med, Lab Pesquisa Desenvolvimento Farm, Araraquara, SP, BrazilUniv Estadual Paulista, Inst Quim, Dept Quim Organ, Nucleo Bioensaios Biossintese & Ecofisiol Prod Na, Araraquara, SP, BrazilSoc Brasileira FarmacognosiaUniversidade Estadual Paulista (Unesp)Inst Fed Sao PauloPierri, Elaise G. [UNESP]Castro, Rogerio C. [UNESP]Vizioli, Ednir O. [UNESP]Ferreira, Carla M. R. [UNESP]Cavalheiro, Alberto J. [UNESP]Tininis, Aristeu G.Chin, Chung M. [UNESP]Santos, Andre G. [UNESP]2018-11-26T17:40:05Z2018-11-26T17:40:05Z2017-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article495-501application/pdfhttp://dx.doi.org/10.1016/j.bjp.2016.12.008Revista Brasileira De Farmacognosia-brazilian Journal Of Pharmacognosy. Curitiba-pr: Soc Brasileira Farmacognosia, v. 27, n. 4, p. 495-501, 2017.0102-695Xhttp://hdl.handle.net/11449/16309810.1016/j.bjp.2016.12.008S0102-695X2017000400495WOS:000406961700015S0102-695X2017000400495.pdf97343336079754130000-0003-4141-0455Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista Brasileira De Farmacognosia-brazilian Journal Of Pharmacognosyinfo:eu-repo/semantics/openAccess2023-10-25T06:06:14Zoai:repositorio.unesp.br:11449/163098Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-10-25T06:06:14Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
title Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
spellingShingle Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
Pierri, Elaise G. [UNESP]
Clerodane diterpene
Casearin B
Caseargrewiin F
Anti-inflammatory activity
Gastric side effects
title_short Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
title_full Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
title_fullStr Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
title_full_unstemmed Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
title_sort Anti-inflammatory action of ethanolic extract and clerodane diterpenes from Casearia sylvestris
author Pierri, Elaise G. [UNESP]
author_facet Pierri, Elaise G. [UNESP]
Castro, Rogerio C. [UNESP]
Vizioli, Ednir O. [UNESP]
Ferreira, Carla M. R. [UNESP]
Cavalheiro, Alberto J. [UNESP]
Tininis, Aristeu G.
Chin, Chung M. [UNESP]
Santos, Andre G. [UNESP]
author_role author
author2 Castro, Rogerio C. [UNESP]
Vizioli, Ednir O. [UNESP]
Ferreira, Carla M. R. [UNESP]
Cavalheiro, Alberto J. [UNESP]
Tininis, Aristeu G.
Chin, Chung M. [UNESP]
Santos, Andre G. [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Inst Fed Sao Paulo
dc.contributor.author.fl_str_mv Pierri, Elaise G. [UNESP]
Castro, Rogerio C. [UNESP]
Vizioli, Ednir O. [UNESP]
Ferreira, Carla M. R. [UNESP]
Cavalheiro, Alberto J. [UNESP]
Tininis, Aristeu G.
Chin, Chung M. [UNESP]
Santos, Andre G. [UNESP]
dc.subject.por.fl_str_mv Clerodane diterpene
Casearin B
Caseargrewiin F
Anti-inflammatory activity
Gastric side effects
topic Clerodane diterpene
Casearin B
Caseargrewiin F
Anti-inflammatory activity
Gastric side effects
description The present study aimed to investigate the anti-inflammatory activity of ethanolic extract from Casearia sylvestris Sw., Salicaceae, leaves and to identify the compounds responsible for this activity. The ethanolic extract from C. sylvestris leaves was fractionated by solid phase extraction and the chemical composition of extract and fractions were assessed by chromatographic techniques. Casearin-like clerodane diterpenes were quantified in ethanolic extract (27.4%, w/w) and in fraction 2 of solid phase extraction (50.6%, w/w). Carrageenan-induced paw edema and carrageenan-induced pleurisy assays (rats) were used to evaluate anti-inflammatory activity of ethanolic extract, its fractions and clerodane diterpenes from C. sylvestris caseargrewiin F and casearin B. The ethanolic extract was tested in the rat paw edema model and the doses tested (10 and 100 mg/kg) had no effect. In the pleurisy model, the extract doses of 300 and 500 mg/kg showed inhibitory effect. The fraction 2 of solid phase extraction (10 mg/kg), caseargrewiin F and casearin B (0.5 mg/kg) showed a significant reduction (p < 0.05) of the carrageenan-induced paw edema in rats compared to indomethacin. Gastric ulcers were not observed in animals treated with samples from C. sylvestris. In conclusion, the ethanolic extract from C. sylvestris, its enriched fraction of clerodane diterpenes, casearin B and caseargrewiin F exhibited anti-inflammatory activity on in vivo models in rats. Casearin-like clerodane diterpenes may be considered active chemical markers for C. sylvestris leaves. On the other hand, these diterpenes are promising compounds in the development of new drugs with anti-inflammatory action without gastric side effects. (c) 2017 Sociedade Brasileira de Farmacognosia. Published by Elsevier Editora Ltda.
publishDate 2017
dc.date.none.fl_str_mv 2017-07-01
2018-11-26T17:40:05Z
2018-11-26T17:40:05Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.bjp.2016.12.008
Revista Brasileira De Farmacognosia-brazilian Journal Of Pharmacognosy. Curitiba-pr: Soc Brasileira Farmacognosia, v. 27, n. 4, p. 495-501, 2017.
0102-695X
http://hdl.handle.net/11449/163098
10.1016/j.bjp.2016.12.008
S0102-695X2017000400495
WOS:000406961700015
S0102-695X2017000400495.pdf
9734333607975413
0000-0003-4141-0455
url http://dx.doi.org/10.1016/j.bjp.2016.12.008
http://hdl.handle.net/11449/163098
identifier_str_mv Revista Brasileira De Farmacognosia-brazilian Journal Of Pharmacognosy. Curitiba-pr: Soc Brasileira Farmacognosia, v. 27, n. 4, p. 495-501, 2017.
0102-695X
10.1016/j.bjp.2016.12.008
S0102-695X2017000400495
WOS:000406961700015
S0102-695X2017000400495.pdf
9734333607975413
0000-0003-4141-0455
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista Brasileira De Farmacognosia-brazilian Journal Of Pharmacognosy
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 495-501
application/pdf
dc.publisher.none.fl_str_mv Soc Brasileira Farmacognosia
publisher.none.fl_str_mv Soc Brasileira Farmacognosia
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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