Serveur d'exploration sur les récepteurs immunitaires végétaux

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Anti-Inflammatory and Chemopreventive Effects of Bryophyllum pinnatum (Lamarck) Leaf Extract in Experimental Colitis Models in Rodents.

Identifieur interne : 000213 ( Main/Exploration ); précédent : 000212; suivant : 000214

Anti-Inflammatory and Chemopreventive Effects of Bryophyllum pinnatum (Lamarck) Leaf Extract in Experimental Colitis Models in Rodents.

Auteurs : Anderson Wilbur Lopes Andrade [Brésil] ; Gerlane Coelho Bernardo Guerra [Brésil] ; Daline Fernandes De Souza Araújo [Brésil] ; Raimundo Fernandes De Araújo Júnior [Brésil] ; Aurigena Antunes De Araújo [Brésil] ; Thaís Gomes De Carvalho [Brésil] ; Júlia Morais Fernandes [Brésil] ; Patrícia Diez-Echave [Espagne] ; Laura Hidalgo-García [Espagne] ; Maria Elena Rodriguez-Cabezas [Espagne] ; Julio Gálvez [Espagne] ; Silvana Maria Zucolotto [Brésil]

Source :

RBID : pubmed:32848723

Abstract

Inflammatory bowel diseases, mainly ulcerative colitis and Crohn's disease are characterized by chronic inflammation in the intestine. Currently several therapeutic strategies available to treat inflammatory bowel diseases. Though, most treatments can be associated with serious adverse effects what justifies the search for new treatments. In this sense, we highlight the interest in herbal products rich in bioactive compounds which immunomodulatory and antioxidant properties as is the case of Bryophyllum pinnatum (Crassulaceae). This plant is used in traditional medicine in Brazil for treating inflammatory diseases. We hypothesized that hydroethanolic B. pinnatum leaf extract has intestinal anti-inflammatory effects on two experimental colitis models: 2.4-dinitrobenzene sulfonic acid (DNBS) in rats, and dextran sulfate sodium (DSS) in mice. Ultra-fast liquid chromatography method used for the quantification of the main compounds indicated good linearity, specificity, selectivity, precision, robustness and accuracy. The major flavonoids (mg/g of the extract) quantified were: quercetin 3-O-α-L-arabinopyranosyl-(1→2)-α-L-rhamnopyranoside (35.56 ± 0.086 mg/g), kaempferol 3-O-α-L-arabinopyranosyl-(1→2)-α-L-rhamnopyranoside (4.66 ± 0.076 mg/g) and quercetin-3-O-rhamnopyranoside (4.56 ± 0.026 mg/g). The results obtained in the DNBS and DSS models indicate that extract has both chemopreventive and anti-inflammatory effects, observing a significant reduction in the disease activity index score, and less macroscopic and microscopic damage. The extract promoted downregulation of Toll-like receptor and kappa B p65 nuclear factor gene expression, leading to a reduction in pro-inflammatory and oxidative mediators, chemokines, and cell adhesion molecules. This immunomodulatory property was proposed that one of the possible action mechanisms of extract. An improvement in intestinal damage was also associated with a reduction in oxidative stress and infiltration of leukocytes, as evidenced by the reduction in malonaldialdehyde and myeloperoxidase activity and increase in total glutathione in the colonic tissue. Moreover, the extract improved the cytoarchitecture of the colonic tissue and the integrity of the intestinal epithelial barrier by restoring the expression of the proteins associated with mucosa protection. In view of the beneficial effects showed by the B. pinnatum leaf extract in preclinical rodent models of colitis there is the potential to conduct some future clinical studies to ensure safe and effective development of a phytotherapeutic treatment for human inflammatory bowel diseases.

DOI: 10.3389/fphar.2020.00998
PubMed: 32848723
PubMed Central: PMC7403504


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<title xml:lang="en">Anti-Inflammatory and Chemopreventive Effects of
<i>Bryophyllum pinnatum</i>
(Lamarck) Leaf Extract in Experimental Colitis Models in Rodents.</title>
<author>
<name sortKey="Andrade, Anderson Wilbur Lopes" sort="Andrade, Anderson Wilbur Lopes" uniqKey="Andrade A" first="Anderson Wilbur Lopes" last="Andrade">Anderson Wilbur Lopes Andrade</name>
<affiliation wicri:level="1">
<nlm:affiliation>Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.</nlm:affiliation>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal</wicri:regionArea>
<wicri:noRegion>Natal</wicri:noRegion>
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<affiliation wicri:level="1">
<nlm:affiliation>Health Science Center, Postgraduate Program in Drug Development and Technological Innovation, Federal University of Rio Grande do Norte, Natal, Brazil.</nlm:affiliation>
<country xml:lang="fr">Brésil</country>
<wicri:regionArea>Health Science Center, Postgraduate Program in Drug Development and Technological Innovation, Federal University of Rio Grande do Norte, Natal</wicri:regionArea>
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<name sortKey="Guerra, Gerlane Coelho Bernardo" sort="Guerra, Gerlane Coelho Bernardo" uniqKey="Guerra G" first="Gerlane Coelho Bernardo" last="Guerra">Gerlane Coelho Bernardo Guerra</name>
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<nlm:affiliation>Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.</nlm:affiliation>
<country xml:lang="fr">Brésil</country>
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<name sortKey="De Souza Araujo, Daline Fernandes" sort="De Souza Araujo, Daline Fernandes" uniqKey="De Souza Araujo D" first="Daline Fernandes" last="De Souza Araújo">Daline Fernandes De Souza Araújo</name>
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<nlm:affiliation>Health Sciences College of Trairi, Federal University of Rio Grande do Norte, Santa Cruz, Brazil.</nlm:affiliation>
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<name sortKey="De Araujo Junior, Raimundo Fernandes" sort="De Araujo Junior, Raimundo Fernandes" uniqKey="De Araujo Junior R" first="Raimundo Fernandes" last="De Araújo Júnior">Raimundo Fernandes De Araújo Júnior</name>
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<name sortKey="De Carvalho, Thais Gomes" sort="De Carvalho, Thais Gomes" uniqKey="De Carvalho T" first="Thaís Gomes" last="De Carvalho">Thaís Gomes De Carvalho</name>
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<wicri:regionArea>Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), University of Granada, Granada</wicri:regionArea>
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<nlm:affiliation>CIBER-EHD, Department of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, Granada, Spain.</nlm:affiliation>
<country xml:lang="fr">Espagne</country>
<wicri:regionArea>CIBER-EHD, Department of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, Granada</wicri:regionArea>
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<name sortKey="Rodriguez Cabezas, Maria Elena" sort="Rodriguez Cabezas, Maria Elena" uniqKey="Rodriguez Cabezas M" first="Maria Elena" last="Rodriguez-Cabezas">Maria Elena Rodriguez-Cabezas</name>
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<wicri:regionArea>Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), University of Granada, Granada</wicri:regionArea>
<orgName type="university">Université de Grenade</orgName>
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<settlement type="city">Grenade (Espagne)</settlement>
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<nlm:affiliation>CIBER-EHD, Department of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, Granada, Spain.</nlm:affiliation>
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<name sortKey="Galvez, Julio" sort="Galvez, Julio" uniqKey="Galvez J" first="Julio" last="Gálvez">Julio Gálvez</name>
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<name sortKey="Zucolotto, Silvana Maria" sort="Zucolotto, Silvana Maria" uniqKey="Zucolotto S" first="Silvana Maria" last="Zucolotto">Silvana Maria Zucolotto</name>
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<nlm:affiliation>Health Science Center, Postgraduate Program in Drug Development and Technological Innovation, Federal University of Rio Grande do Norte, Natal, Brazil.</nlm:affiliation>
<country xml:lang="fr">Brésil</country>
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<title level="j">Frontiers in pharmacology</title>
<idno type="ISSN">1663-9812</idno>
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<div type="abstract" xml:lang="en">Inflammatory bowel diseases, mainly ulcerative colitis and Crohn's disease are characterized by chronic inflammation in the intestine. Currently several therapeutic strategies available to treat inflammatory bowel diseases. Though, most treatments can be associated with serious adverse effects what justifies the search for new treatments. In this sense, we highlight the interest in herbal products rich in bioactive compounds which immunomodulatory and antioxidant properties as is the case of
<i>Bryophyllum pinnatum</i>
(Crassulaceae). This plant is used in traditional medicine in Brazil for treating inflammatory diseases. We hypothesized that hydroethanolic
<i>B. pinnatum</i>
leaf extract has intestinal anti-inflammatory effects on two experimental colitis models: 2.4-dinitrobenzene sulfonic acid (DNBS) in rats, and dextran sulfate sodium (DSS) in mice. Ultra-fast liquid chromatography method used for the quantification of the main compounds indicated good linearity, specificity, selectivity, precision, robustness and accuracy. The major flavonoids (mg/g of the extract) quantified were: quercetin 3-
<i>O</i>
-α-L-arabinopyranosyl-(1→2)-α-L-rhamnopyranoside (35.56 ± 0.086 mg/g), kaempferol 3-
<i>O</i>
-α-L-arabinopyranosyl-(1→2)-α-L-rhamnopyranoside (4.66 ± 0.076 mg/g) and quercetin-3-
<i>O</i>
-rhamnopyranoside (4.56 ± 0.026 mg/g). The results obtained in the DNBS and DSS models indicate that extract has both chemopreventive and anti-inflammatory effects, observing a significant reduction in the disease activity index score, and less macroscopic and microscopic damage. The extract promoted downregulation of Toll-like receptor and
<i>kappa</i>
B p65 nuclear factor gene expression, leading to a reduction in pro-inflammatory and oxidative mediators, chemokines, and cell adhesion molecules. This immunomodulatory property was proposed that one of the possible action mechanisms of extract. An improvement in intestinal damage was also associated with a reduction in oxidative stress and infiltration of leukocytes, as evidenced by the reduction in malonaldialdehyde and myeloperoxidase activity and increase in total glutathione in the colonic tissue. Moreover, the extract improved the cytoarchitecture of the colonic tissue and the integrity of the intestinal epithelial barrier by restoring the expression of the proteins associated with mucosa protection. In view of the beneficial effects showed by the
<i>B. pinnatum</i>
leaf extract in preclinical rodent models of colitis there is the potential to conduct some future clinical studies to ensure safe and effective development of a phytotherapeutic treatment for human inflammatory bowel diseases.</div>
</front>
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<DateRevised>
<Year>2020</Year>
<Month>09</Month>
<Day>28</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Print">1663-9812</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>11</Volume>
<PubDate>
<Year>2020</Year>
</PubDate>
</JournalIssue>
<Title>Frontiers in pharmacology</Title>
<ISOAbbreviation>Front Pharmacol</ISOAbbreviation>
</Journal>
<ArticleTitle>Anti-Inflammatory and Chemopreventive Effects of
<i>Bryophyllum pinnatum</i>
(Lamarck) Leaf Extract in Experimental Colitis Models in Rodents.</ArticleTitle>
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<MedlinePgn>998</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.3389/fphar.2020.00998</ELocationID>
<Abstract>
<AbstractText>Inflammatory bowel diseases, mainly ulcerative colitis and Crohn's disease are characterized by chronic inflammation in the intestine. Currently several therapeutic strategies available to treat inflammatory bowel diseases. Though, most treatments can be associated with serious adverse effects what justifies the search for new treatments. In this sense, we highlight the interest in herbal products rich in bioactive compounds which immunomodulatory and antioxidant properties as is the case of
<i>Bryophyllum pinnatum</i>
(Crassulaceae). This plant is used in traditional medicine in Brazil for treating inflammatory diseases. We hypothesized that hydroethanolic
<i>B. pinnatum</i>
leaf extract has intestinal anti-inflammatory effects on two experimental colitis models: 2.4-dinitrobenzene sulfonic acid (DNBS) in rats, and dextran sulfate sodium (DSS) in mice. Ultra-fast liquid chromatography method used for the quantification of the main compounds indicated good linearity, specificity, selectivity, precision, robustness and accuracy. The major flavonoids (mg/g of the extract) quantified were: quercetin 3-
<i>O</i>
-α-L-arabinopyranosyl-(1→2)-α-L-rhamnopyranoside (35.56 ± 0.086 mg/g), kaempferol 3-
<i>O</i>
-α-L-arabinopyranosyl-(1→2)-α-L-rhamnopyranoside (4.66 ± 0.076 mg/g) and quercetin-3-
<i>O</i>
-rhamnopyranoside (4.56 ± 0.026 mg/g). The results obtained in the DNBS and DSS models indicate that extract has both chemopreventive and anti-inflammatory effects, observing a significant reduction in the disease activity index score, and less macroscopic and microscopic damage. The extract promoted downregulation of Toll-like receptor and
<i>kappa</i>
B p65 nuclear factor gene expression, leading to a reduction in pro-inflammatory and oxidative mediators, chemokines, and cell adhesion molecules. This immunomodulatory property was proposed that one of the possible action mechanisms of extract. An improvement in intestinal damage was also associated with a reduction in oxidative stress and infiltration of leukocytes, as evidenced by the reduction in malonaldialdehyde and myeloperoxidase activity and increase in total glutathione in the colonic tissue. Moreover, the extract improved the cytoarchitecture of the colonic tissue and the integrity of the intestinal epithelial barrier by restoring the expression of the proteins associated with mucosa protection. In view of the beneficial effects showed by the
<i>B. pinnatum</i>
leaf extract in preclinical rodent models of colitis there is the potential to conduct some future clinical studies to ensure safe and effective development of a phytotherapeutic treatment for human inflammatory bowel diseases.</AbstractText>
<CopyrightInformation>Copyright © 2020 Andrade, Guerra, de Souza Araújo, de Araújo Júnior, de Araújo, de Carvalho, Fernandes, Diez-Echave, Hidalgo-García, Rodriguez-Cabezas, Gálvez and Zucolotto.</CopyrightInformation>
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<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Andrade</LastName>
<ForeName>Anderson Wilbur Lopes</ForeName>
<Initials>AWL</Initials>
<AffiliationInfo>
<Affiliation>Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Health Science Center, Postgraduate Program in Drug Development and Technological Innovation, Federal University of Rio Grande do Norte, Natal, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Guerra</LastName>
<ForeName>Gerlane Coelho Bernardo</ForeName>
<Initials>GCB</Initials>
<AffiliationInfo>
<Affiliation>Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>de Souza Araújo</LastName>
<ForeName>Daline Fernandes</ForeName>
<Initials>DF</Initials>
<AffiliationInfo>
<Affiliation>Health Sciences College of Trairi, Federal University of Rio Grande do Norte, Santa Cruz, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>de Araújo Júnior</LastName>
<ForeName>Raimundo Fernandes</ForeName>
<Initials>RF</Initials>
<AffiliationInfo>
<Affiliation>Postgraduate Program in Health Science, Federal University of Rio Grande do Norte (UFRN), Natal, Brazil.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>Postgraduate Program in Functional and Structural Biology, Department of Morphology, Federal University of Rio Grande do Norte (UFRN), Natal, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>de Araújo</LastName>
<ForeName>Aurigena Antunes</ForeName>
<Initials>AA</Initials>
<AffiliationInfo>
<Affiliation>Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>de Carvalho</LastName>
<ForeName>Thaís Gomes</ForeName>
<Initials>TG</Initials>
<AffiliationInfo>
<Affiliation>Postgraduate Program in Health Science, Federal University of Rio Grande do Norte (UFRN), Natal, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fernandes</LastName>
<ForeName>Júlia Morais</ForeName>
<Initials>JM</Initials>
<AffiliationInfo>
<Affiliation>Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Diez-Echave</LastName>
<ForeName>Patrícia</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>CIBER-EHD, Department of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Hidalgo-García</LastName>
<ForeName>Laura</ForeName>
<Initials>L</Initials>
<AffiliationInfo>
<Affiliation>Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>CIBER-EHD, Department of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y">
<LastName>Rodriguez-Cabezas</LastName>
<ForeName>Maria Elena</ForeName>
<Initials>ME</Initials>
<AffiliationInfo>
<Affiliation>Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>CIBER-EHD, Department of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Gálvez</LastName>
<ForeName>Julio</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>CIBER-EHD, Department of Pharmacology, Center for Biomedical Research (CIBM), University of Granada, Granada, Spain.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zucolotto</LastName>
<ForeName>Silvana Maria</ForeName>
<Initials>SM</Initials>
<AffiliationInfo>
<Affiliation>Health Science Center, Postgraduate Program in Drug Development and Technological Innovation, Federal University of Rio Grande do Norte, Natal, Brazil.</Affiliation>
</AffiliationInfo>
</Author>
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<Year>2020</Year>
<Month>07</Month>
<Day>29</Day>
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<Keyword MajorTopicYN="N">dextran sulfate sodium</Keyword>
<Keyword MajorTopicYN="N">flavonoid</Keyword>
<Keyword MajorTopicYN="N">herbal drug</Keyword>
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