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Plant origin authentication of Sonoran Desert propolis: an antiproliferative propolis from a semi-arid region.

Identifieur interne : 000778 ( Main/Exploration ); précédent : 000777; suivant : 000779

Plant origin authentication of Sonoran Desert propolis: an antiproliferative propolis from a semi-arid region.

Auteurs : Efrain Alday [Mexique] ; Dora Valencia [Mexique] ; Adriana Garibay-Escobar [Mexique] ; Zaira Domínguez-Esquivel [Mexique] ; Anna Lisa Piccinelli [Italie] ; Luca Rastrelli [Italie] ; Juan Monribot-Villanueva [Mexique] ; José A. Guerrero-Analco [Mexique] ; Ram N Enrique Robles-Zepeda [Mexique] ; Javier Hernandez [Mexique] ; Carlos Velazquez [Mexique]

Source :

RBID : pubmed:31069518

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English descriptors

Abstract

The main chemical composition of Sonoran propolis (SP), as well as its antiproliferative activity on cancer cells through apoptosis induction, has been reported. The chemical constitution of SP remained qualitatively similar throughout the year, whereas the antiproliferative effect on cancer cells exhibited significant differences amongst seasonal samples. The main goal of this study was to provide phytochemical and pharmacological evidence for the botanical source of SP and its antiproliferative constituents. A chemical comparative analysis of SP and plant resins of species found in the surrounding areas of the beehives was carried out by HPLC-UV-DAD, as well as by 1H NMR experiments. The antiproliferative activity on cancerous (M12.C3.F6, HeLa, A549, PC-3) and normal cell lines (L-929; ARPE-19) was assessed through MTT assays. Here, the main polyphenolic profile of SP resulted to be qualitatively similar to Populus fremontii resins (PFR). However, the antiproliferative activity of PFR on cancer cells did not consistently match that exhibited by SP throughout the year. Additionally, SP induced morphological modifications on treated cells characterised by elongation, similar to those induced by colchicine, and different to those observed with PFR treatment. These results suggest that P. fremontii is the main botanical source of SP along the year. Nevertheless, the antiproliferative constituents of SP that induce that characteristic morphological elongation on treated cells are not obtained from PFR. Moreover, the presence of kaempferol-3-methyl-ether in SP could point Ambrosia ambrosioides as a secondary plant source. In conclusion, SP is a bioactive poplar-type propolis from semi-arid zones, in which chemical compounds derived from other semi-arid plant sources than poplar contribute to its antiproliferative activity.

DOI: 10.1007/s00114-019-1620-2
PubMed: 31069518


Affiliations:


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Le document en format XML

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<term>A549 Cells (MeSH)</term>
<term>Cell Line, Tumor (MeSH)</term>
<term>Cell Proliferation (drug effects)</term>
<term>Desert Climate (MeSH)</term>
<term>HeLa Cells (MeSH)</term>
<term>Humans (MeSH)</term>
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<term>Propolis (pharmacology)</term>
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<term>Cellules A549 (MeSH)</term>
<term>Cellules HeLa (MeSH)</term>
<term>Climat désertique (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Lignée cellulaire tumorale (MeSH)</term>
<term>Populus (composition chimique)</term>
<term>Prolifération cellulaire (effets des médicaments et des substances chimiques)</term>
<term>Propolis (composition chimique)</term>
<term>Propolis (pharmacologie)</term>
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<term>Propolis</term>
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<term>Populus</term>
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<term>Populus</term>
<term>Propolis</term>
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<term>Cell Proliferation</term>
</keywords>
<keywords scheme="MESH" qualifier="effets des médicaments et des substances chimiques" xml:lang="fr">
<term>Prolifération cellulaire</term>
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<term>Propolis</term>
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<term>Propolis</term>
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<term>Cellules A549</term>
<term>Cellules HeLa</term>
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<div type="abstract" xml:lang="en">The main chemical composition of Sonoran propolis (SP), as well as its antiproliferative activity on cancer cells through apoptosis induction, has been reported. The chemical constitution of SP remained qualitatively similar throughout the year, whereas the antiproliferative effect on cancer cells exhibited significant differences amongst seasonal samples. The main goal of this study was to provide phytochemical and pharmacological evidence for the botanical source of SP and its antiproliferative constituents. A chemical comparative analysis of SP and plant resins of species found in the surrounding areas of the beehives was carried out by HPLC-UV-DAD, as well as by
<sup>1</sup>
H NMR experiments. The antiproliferative activity on cancerous (M12.C3.F6, HeLa, A549, PC-3) and normal cell lines (L-929; ARPE-19) was assessed through MTT assays. Here, the main polyphenolic profile of SP resulted to be qualitatively similar to Populus fremontii resins (PFR). However, the antiproliferative activity of PFR on cancer cells did not consistently match that exhibited by SP throughout the year. Additionally, SP induced morphological modifications on treated cells characterised by elongation, similar to those induced by colchicine, and different to those observed with PFR treatment. These results suggest that P. fremontii is the main botanical source of SP along the year. Nevertheless, the antiproliferative constituents of SP that induce that characteristic morphological elongation on treated cells are not obtained from PFR. Moreover, the presence of kaempferol-3-methyl-ether in SP could point Ambrosia ambrosioides as a secondary plant source. In conclusion, SP is a bioactive poplar-type propolis from semi-arid zones, in which chemical compounds derived from other semi-arid plant sources than poplar contribute to its antiproliferative activity.</div>
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<ISOAbbreviation>Naturwissenschaften</ISOAbbreviation>
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<ArticleTitle>Plant origin authentication of Sonoran Desert propolis: an antiproliferative propolis from a semi-arid region.</ArticleTitle>
<Pagination>
<MedlinePgn>25</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1007/s00114-019-1620-2</ELocationID>
<Abstract>
<AbstractText>The main chemical composition of Sonoran propolis (SP), as well as its antiproliferative activity on cancer cells through apoptosis induction, has been reported. The chemical constitution of SP remained qualitatively similar throughout the year, whereas the antiproliferative effect on cancer cells exhibited significant differences amongst seasonal samples. The main goal of this study was to provide phytochemical and pharmacological evidence for the botanical source of SP and its antiproliferative constituents. A chemical comparative analysis of SP and plant resins of species found in the surrounding areas of the beehives was carried out by HPLC-UV-DAD, as well as by
<sup>1</sup>
H NMR experiments. The antiproliferative activity on cancerous (M12.C3.F6, HeLa, A549, PC-3) and normal cell lines (L-929; ARPE-19) was assessed through MTT assays. Here, the main polyphenolic profile of SP resulted to be qualitatively similar to Populus fremontii resins (PFR). However, the antiproliferative activity of PFR on cancer cells did not consistently match that exhibited by SP throughout the year. Additionally, SP induced morphological modifications on treated cells characterised by elongation, similar to those induced by colchicine, and different to those observed with PFR treatment. These results suggest that P. fremontii is the main botanical source of SP along the year. Nevertheless, the antiproliferative constituents of SP that induce that characteristic morphological elongation on treated cells are not obtained from PFR. Moreover, the presence of kaempferol-3-methyl-ether in SP could point Ambrosia ambrosioides as a secondary plant source. In conclusion, SP is a bioactive poplar-type propolis from semi-arid zones, in which chemical compounds derived from other semi-arid plant sources than poplar contribute to its antiproliferative activity.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Alday</LastName>
<ForeName>Efrain</ForeName>
<Initials>E</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry-Biology, University of Sonora, Blvd. Luis Encinas y Rosales s/n, 83000, Hermosillo, Sonora, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Valencia</LastName>
<ForeName>Dora</ForeName>
<Initials>D</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemical Biological and Agropecuary Sciences, University of Sonora, Av. Universidad e Irigoyen, 83600, Caborca, Son., Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Garibay-Escobar</LastName>
<ForeName>Adriana</ForeName>
<Initials>A</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry-Biology, University of Sonora, Blvd. Luis Encinas y Rosales s/n, 83000, Hermosillo, Sonora, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Domínguez-Esquivel</LastName>
<ForeName>Zaira</ForeName>
<Initials>Z</Initials>
<AffiliationInfo>
<Affiliation>Laboratorio de Química de productos Naturales, Unidad de Servicios de Apoyo en Resolución Analítica, Universidad Veracruzana, Dr. Luis Castelazo Ayala S/N, 575, 91190, Xalapa, Veracruz, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Piccinelli</LastName>
<ForeName>Anna Lisa</ForeName>
<Initials>AL</Initials>
<AffiliationInfo>
<Affiliation>Dipartimento di Farmacia, University of Salerno, Via Giovanni Paolo II, 132, 84084, Fisciano, SA, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Rastrelli</LastName>
<ForeName>Luca</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Dipartimento di Farmacia, University of Salerno, Via Giovanni Paolo II, 132, 84084, Fisciano, SA, Italy.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Monribot-Villanueva</LastName>
<ForeName>Juan</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Red de Estudios Moleculares Avanzados, Instituto de Ecología (INECOL) A.C., Clúster Científico y Tecnológico Biomimic®, Carretera antigua a Coatepec 351, 91070, Xalapa, Veracruz, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Guerrero-Analco</LastName>
<ForeName>José A</ForeName>
<Initials>JA</Initials>
<AffiliationInfo>
<Affiliation>Red de Estudios Moleculares Avanzados, Instituto de Ecología (INECOL) A.C., Clúster Científico y Tecnológico Biomimic®, Carretera antigua a Coatepec 351, 91070, Xalapa, Veracruz, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Robles-Zepeda</LastName>
<ForeName>Ramón Enrique</ForeName>
<Initials>RE</Initials>
<AffiliationInfo>
<Affiliation>Department of Chemistry-Biology, University of Sonora, Blvd. Luis Encinas y Rosales s/n, 83000, Hermosillo, Sonora, Mexico.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hernandez</LastName>
<ForeName>Javier</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Laboratorio de Química de productos Naturales, Unidad de Servicios de Apoyo en Resolución Analítica, Universidad Veracruzana, Dr. Luis Castelazo Ayala S/N, 575, 91190, Xalapa, Veracruz, Mexico. javmartinez@uv.mx.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Velazquez</LastName>
<ForeName>Carlos</ForeName>
<Initials>C</Initials>
<Identifier Source="ORCID">http://orcid.org/0000-0002-3728-7848</Identifier>
<AffiliationInfo>
<Affiliation>Department of Chemistry-Biology, University of Sonora, Blvd. Luis Encinas y Rosales s/n, 83000, Hermosillo, Sonora, Mexico. velaz@guayacan.uson.mx.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList>
<PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2019</Year>
<Month>05</Month>
<Day>08</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>Germany</Country>
<MedlineTA>Naturwissenschaften</MedlineTA>
<NlmUniqueID>0400767</NlmUniqueID>
<ISSNLinking>0028-1042</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList>
<Chemical>
<RegistryNumber>9009-62-5</RegistryNumber>
<NameOfSubstance UI="D011429">Propolis</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D000072283" MajorTopicYN="N">A549 Cells</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D045744" MajorTopicYN="N">Cell Line, Tumor</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D049109" MajorTopicYN="N">Cell Proliferation</DescriptorName>
<QualifierName UI="Q000187" MajorTopicYN="N">drug effects</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D003889" MajorTopicYN="N">Desert Climate</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006367" MajorTopicYN="N">HeLa Cells</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D032107" MajorTopicYN="N">Populus</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D011429" MajorTopicYN="N">Propolis</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="Y">chemistry</QualifierName>
<QualifierName UI="Q000494" MajorTopicYN="Y">pharmacology</QualifierName>
</MeshHeading>
</MeshHeadingList>
<KeywordList Owner="NOTNLM">
<Keyword MajorTopicYN="N">Ambrosia ambrosioides (Cav.) Payne</Keyword>
<Keyword MajorTopicYN="N">Antiproliferative activity</Keyword>
<Keyword MajorTopicYN="N">Polyphenolic profile</Keyword>
<Keyword MajorTopicYN="N">Populus fremontii S. Watson</Keyword>
<Keyword MajorTopicYN="N">Sonoran Desert propolis</Keyword>
</KeywordList>
</MedlineCitation>
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<Year>2019</Year>
<Month>01</Month>
<Day>17</Day>
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<Year>2019</Year>
<Month>04</Month>
<Day>11</Day>
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<PubMedPubDate PubStatus="revised">
<Year>2019</Year>
<Month>04</Month>
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