Therapeutic potential of pollen

Detalhes bibliográficos
Autor(a) principal: Amâncio, D.
Data de Publicação: 2014
Outros Autores: Serrano, M, Anjos, O., Campos, M.G.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.11/6506
Resumo: The aim of this study was to evaluate the potential of phenolic compounds of Portuguese flora as a source of flavonoids for use in research of new active molecules using a previous screening by HPLC/DAD. Some of these compounds have bioactive properties as antioxidant and will study in order to determine its anti-inflammatory action. On the other hand, for example, flavones are possible research targets with benzodiazepine-like activity and isoflavones as estrogen-like. When these molecules appear much methylated or hydroxylated, anti-redox potential and antibacterial ability can be assessed. The samples were collected directly into stamens of plants and served as the basis for identification of pollen material collected by bees. The samples analyzed were: Carpobrotus edulis (L.) N.E.Br., Tilia spp., Viburnum tinus L. and Opuntia spp. Approximately 10 mg of pollen sample are dried and extracted with 50% ethanol (1:1, v/v), after was assisted by ultrasonication (30 min), centrifuged at 5000 rpm during 10 min and the supernatant used for HPLC/DAD according Campos and Markham [1]. The compounds structures were determined by UV absorption spectroscopy according Campos and Markham [1]. The more flavonoids common structure in the samples was of 3-O-glycosides of quercetin and kaempferol, and phenolic polymers acids. The less common structure is a derivative of kaempferol that have derivatization at the ring in C6 or C8 alkyl, which makes evident for further evaluation of their therapeutic activity, for the ability to GABAa binding receptors may be one of the possibilities. The studied species present a probability of being able to establish a relationship with greater therapeutic potential (Figure 1).
id RCAP_57385d747faa0a73bb432577ce2cf090
oai_identifier_str oai:repositorio.ipcb.pt:10400.11/6506
network_acronym_str RCAP
network_name_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository_id_str 7160
spelling Therapeutic potential of pollenPollenPhenolic compoundsFlavonoidsHPLC/DADThe aim of this study was to evaluate the potential of phenolic compounds of Portuguese flora as a source of flavonoids for use in research of new active molecules using a previous screening by HPLC/DAD. Some of these compounds have bioactive properties as antioxidant and will study in order to determine its anti-inflammatory action. On the other hand, for example, flavones are possible research targets with benzodiazepine-like activity and isoflavones as estrogen-like. When these molecules appear much methylated or hydroxylated, anti-redox potential and antibacterial ability can be assessed. The samples were collected directly into stamens of plants and served as the basis for identification of pollen material collected by bees. The samples analyzed were: Carpobrotus edulis (L.) N.E.Br., Tilia spp., Viburnum tinus L. and Opuntia spp. Approximately 10 mg of pollen sample are dried and extracted with 50% ethanol (1:1, v/v), after was assisted by ultrasonication (30 min), centrifuged at 5000 rpm during 10 min and the supernatant used for HPLC/DAD according Campos and Markham [1]. The compounds structures were determined by UV absorption spectroscopy according Campos and Markham [1]. The more flavonoids common structure in the samples was of 3-O-glycosides of quercetin and kaempferol, and phenolic polymers acids. The less common structure is a derivative of kaempferol that have derivatization at the ring in C6 or C8 alkyl, which makes evident for further evaluation of their therapeutic activity, for the ability to GABAa binding receptors may be one of the possibilities. The studied species present a probability of being able to establish a relationship with greater therapeutic potential (Figure 1).Repositório Científico do Instituto Politécnico de Castelo BrancoAmâncio, D.Serrano, MAnjos, O.Campos, M.G.2019-05-12T21:20:14Z20142014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.11/6506eng10.1055/s-0034-1394914info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-12-30T01:49:57Zoai:repositorio.ipcb.pt:10400.11/6506Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T16:37:06.387647Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Therapeutic potential of pollen
title Therapeutic potential of pollen
spellingShingle Therapeutic potential of pollen
Amâncio, D.
Pollen
Phenolic compounds
Flavonoids
HPLC/DAD
title_short Therapeutic potential of pollen
title_full Therapeutic potential of pollen
title_fullStr Therapeutic potential of pollen
title_full_unstemmed Therapeutic potential of pollen
title_sort Therapeutic potential of pollen
author Amâncio, D.
author_facet Amâncio, D.
Serrano, M
Anjos, O.
Campos, M.G.
author_role author
author2 Serrano, M
Anjos, O.
Campos, M.G.
author2_role author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico de Castelo Branco
dc.contributor.author.fl_str_mv Amâncio, D.
Serrano, M
Anjos, O.
Campos, M.G.
dc.subject.por.fl_str_mv Pollen
Phenolic compounds
Flavonoids
HPLC/DAD
topic Pollen
Phenolic compounds
Flavonoids
HPLC/DAD
description The aim of this study was to evaluate the potential of phenolic compounds of Portuguese flora as a source of flavonoids for use in research of new active molecules using a previous screening by HPLC/DAD. Some of these compounds have bioactive properties as antioxidant and will study in order to determine its anti-inflammatory action. On the other hand, for example, flavones are possible research targets with benzodiazepine-like activity and isoflavones as estrogen-like. When these molecules appear much methylated or hydroxylated, anti-redox potential and antibacterial ability can be assessed. The samples were collected directly into stamens of plants and served as the basis for identification of pollen material collected by bees. The samples analyzed were: Carpobrotus edulis (L.) N.E.Br., Tilia spp., Viburnum tinus L. and Opuntia spp. Approximately 10 mg of pollen sample are dried and extracted with 50% ethanol (1:1, v/v), after was assisted by ultrasonication (30 min), centrifuged at 5000 rpm during 10 min and the supernatant used for HPLC/DAD according Campos and Markham [1]. The compounds structures were determined by UV absorption spectroscopy according Campos and Markham [1]. The more flavonoids common structure in the samples was of 3-O-glycosides of quercetin and kaempferol, and phenolic polymers acids. The less common structure is a derivative of kaempferol that have derivatization at the ring in C6 or C8 alkyl, which makes evident for further evaluation of their therapeutic activity, for the ability to GABAa binding receptors may be one of the possibilities. The studied species present a probability of being able to establish a relationship with greater therapeutic potential (Figure 1).
publishDate 2014
dc.date.none.fl_str_mv 2014
2014-01-01T00:00:00Z
2019-05-12T21:20:14Z
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://hdl.handle.net/10400.11/6506
url http://hdl.handle.net/10400.11/6506
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1055/s-0034-1394914
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1799130832627040256