Pharmacological reports about gastroprotective effects of methanolic extract from leaves of Solidago chilensis (Brazilian arnica) and its components quercitrin and afzelin in rodents

Solidago chilensis Meyenmost (Asteraceae), popularly known as “Brazilian arnica” or “arnica-do-campo,” is widely used in the folk medicine to treat gastric disorders. Based on this, the gastroprotective activity of S. chilensis methanolic extract was investigated. Besides, a phytochemical study allo...

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Veröffentlicht in:Naunyn-Schmiedeberg's archives of pharmacology 2016-04, Vol.389 (4), p.403-417
Hauptverfasser: de Barros, Mariel, Mota da Silva, Luisa, Boeing, Thaise, Somensi, Lincon Bordignon, Cury, Benhur Judah, de Moura Burci, Ligia, Santin, José Roberto, de Andrade, Sérgio Faloni, Monache, Franco Delle, Cechinel-Filho, Valdir
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container_title Naunyn-Schmiedeberg's archives of pharmacology
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creator de Barros, Mariel
Mota da Silva, Luisa
Boeing, Thaise
Somensi, Lincon Bordignon
Cury, Benhur Judah
de Moura Burci, Ligia
Santin, José Roberto
de Andrade, Sérgio Faloni
Monache, Franco Delle
Cechinel-Filho, Valdir
description Solidago chilensis Meyenmost (Asteraceae), popularly known as “Brazilian arnica” or “arnica-do-campo,” is widely used in the folk medicine to treat gastric disorders. Based on this, the gastroprotective activity of S. chilensis methanolic extract was investigated. Besides, a phytochemical study allowed isolation of two flavonoids (quercitrin and afzelin). The gastroprotective effects were investigated in acute gastric ulcer models, and the antisecretory activity was assessed in vivo and in vitro. The adhered mucus levels, reduced glutathione (GSH) content and myeloperoxidase (MPO) activity were quantified in ulcerated tissues. The contribution of isolated compounds in extract effects was evaluated, and its doses were calculated according to its yield. To evaluate the in vivo healing properties of S. chilensis methanolic extract, a chronic gastric ulcer was induced in mice by 10 % acetic acid. Evaluation of tumor necrosis factor (TNF) levels was also performed at the site of the acetic acid-induced gastric ulcer. In parallel, effects on cell viability and cell proliferation of fibroblasts (L929 cells) were determined by in vitro trials. Firstly, the S. chilensis methanolic extract (100 or 300 mg/kg) reduced the ulcer area induced by ethanol/HCl in mice when compared to the vehicle group. Moreover, the S. chilensis extract (300 mg/kg) prevented the mucus depletion, the increase in MPO activity and the decrease in the GSH levels in the ulcerated gastric tissue. The S. chilensis extract also was able to decrease the indomethacin-induced gastric ulcer in rats at a dose of 100 mg/kg. The antisecretory effect of the extract (100 mg/kg, intraduodenal (i.d.)) was confirmed by the reduction in the volume and acidity in parallel to an increase in the pH of gastric content. In addition, quercitrin (1.38 mg/kg, but not 0.46 mg/kg) and afzelin (0.026 and 0.078 mg/kg) decreased the ethanol/HCl-induced gastric ulcer. In this model, quercitrin (1.38 mg/kg) prevented the depletion of gastric GSH content and both quercitrin (1.38 mg/kg) and afzelin (0.078 mg/kg) reduced the MPO activity. These compounds also inhibited the H + ,K + -ATPase activity at a concentration of 1–100 μg/ml. In addition, the participation of quercitrin and afzelin in these effects also was confirmed. Furthermore, after 4 days of the treatment, an oral administration of S. chilensis methanolic extract (100 mg/kg) reduced the area of the gastric ulcer induced by acetic acid and the regeneration of the g
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Based on this, the gastroprotective activity of S. chilensis methanolic extract was investigated. Besides, a phytochemical study allowed isolation of two flavonoids (quercitrin and afzelin). The gastroprotective effects were investigated in acute gastric ulcer models, and the antisecretory activity was assessed in vivo and in vitro. The adhered mucus levels, reduced glutathione (GSH) content and myeloperoxidase (MPO) activity were quantified in ulcerated tissues. The contribution of isolated compounds in extract effects was evaluated, and its doses were calculated according to its yield. To evaluate the in vivo healing properties of S. chilensis methanolic extract, a chronic gastric ulcer was induced in mice by 10 % acetic acid. Evaluation of tumor necrosis factor (TNF) levels was also performed at the site of the acetic acid-induced gastric ulcer. In parallel, effects on cell viability and cell proliferation of fibroblasts (L929 cells) were determined by in vitro trials. Firstly, the S. chilensis methanolic extract (100 or 300 mg/kg) reduced the ulcer area induced by ethanol/HCl in mice when compared to the vehicle group. Moreover, the S. chilensis extract (300 mg/kg) prevented the mucus depletion, the increase in MPO activity and the decrease in the GSH levels in the ulcerated gastric tissue. The S. chilensis extract also was able to decrease the indomethacin-induced gastric ulcer in rats at a dose of 100 mg/kg. The antisecretory effect of the extract (100 mg/kg, intraduodenal (i.d.)) was confirmed by the reduction in the volume and acidity in parallel to an increase in the pH of gastric content. In addition, quercitrin (1.38 mg/kg, but not 0.46 mg/kg) and afzelin (0.026 and 0.078 mg/kg) decreased the ethanol/HCl-induced gastric ulcer. In this model, quercitrin (1.38 mg/kg) prevented the depletion of gastric GSH content and both quercitrin (1.38 mg/kg) and afzelin (0.078 mg/kg) reduced the MPO activity. These compounds also inhibited the H + ,K + -ATPase activity at a concentration of 1–100 μg/ml. In addition, the participation of quercitrin and afzelin in these effects also was confirmed. Furthermore, after 4 days of the treatment, an oral administration of S. chilensis methanolic extract (100 mg/kg) reduced the area of the gastric ulcer induced by acetic acid and the regeneration of the gastric mucosa was accompanied by a reduction in gastric TNF levels. The healing properties of the extract also were confirmed by enhancement of proliferation and coverage of scratched wounds in a fibroblast monolayer. Together, our results confirmed the gastroprotective effect of S. chilensis methanolic extract as well as its gastric healing potential and provided some support to the traditional use of S. chilensis for prevention and treatment of gastric lesions in complementation to its known anti-inflammatory properties.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/s00210-015-1208-0</identifier><identifier>PMID: 26758066</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject><![CDATA[Animals ; Anti-Inflammatory Agents - pharmacology ; Anti-Ulcer Agents - chemistry ; Anti-Ulcer Agents - isolation & purification ; Anti-Ulcer Agents - pharmacology ; Biomedical and Life Sciences ; Biomedicine ; Cell Line ; Cell Proliferation - drug effects ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Female ; Fibroblasts - drug effects ; Fibroblasts - metabolism ; Fibroblasts - pathology ; Gastric Mucosa - drug effects ; Gastric Mucosa - metabolism ; Gastric Mucosa - pathology ; Glutathione - metabolism ; H(+)-K(+)-Exchanging ATPase - metabolism ; Hydrogen-Ion Concentration ; Mannosides - chemistry ; Mannosides - isolation & purification ; Mannosides - pharmacology ; Methanol - chemistry ; Mice ; Neurosciences ; Original Article ; Pharmacology/Toxicology ; Phytotherapy ; Plant Extracts - chemistry ; Plant Extracts - isolation & purification ; Plant Extracts - pharmacology ; Plant Leaves ; Plants, Medicinal ; Proanthocyanidins - chemistry ; Proanthocyanidins - isolation & purification ; Proanthocyanidins - pharmacology ; Proton Pump Inhibitors - pharmacology ; Quercetin - analogs & derivatives ; Quercetin - chemistry ; Quercetin - isolation & purification ; Quercetin - pharmacology ; Rabbits ; Rats, Wistar ; Solidago - chemistry ; Solvents - chemistry ; Stomach Ulcer - chemically induced ; Stomach Ulcer - metabolism ; Stomach Ulcer - pathology ; Stomach Ulcer - prevention & control ; Tumor Necrosis Factor-alpha - metabolism ; Wound Healing - drug effects]]></subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 2016-04, Vol.389 (4), p.403-417</ispartof><rights>Springer-Verlag Berlin Heidelberg 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-b3761f7854ce0775077d6075da5c0447c5d1ae5717c855a49728e5d0249ab91c3</citedby><cites>FETCH-LOGICAL-c442t-b3761f7854ce0775077d6075da5c0447c5d1ae5717c855a49728e5d0249ab91c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00210-015-1208-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00210-015-1208-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26758066$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Barros, Mariel</creatorcontrib><creatorcontrib>Mota da Silva, Luisa</creatorcontrib><creatorcontrib>Boeing, Thaise</creatorcontrib><creatorcontrib>Somensi, Lincon Bordignon</creatorcontrib><creatorcontrib>Cury, Benhur Judah</creatorcontrib><creatorcontrib>de Moura Burci, Ligia</creatorcontrib><creatorcontrib>Santin, José Roberto</creatorcontrib><creatorcontrib>de Andrade, Sérgio Faloni</creatorcontrib><creatorcontrib>Monache, Franco Delle</creatorcontrib><creatorcontrib>Cechinel-Filho, Valdir</creatorcontrib><title>Pharmacological reports about gastroprotective effects of methanolic extract from leaves of Solidago chilensis (Brazilian arnica) and its components quercitrin and afzelin in rodents</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn-Schmiedeberg's Arch Pharmacol</addtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>Solidago chilensis Meyenmost (Asteraceae), popularly known as “Brazilian arnica” or “arnica-do-campo,” is widely used in the folk medicine to treat gastric disorders. Based on this, the gastroprotective activity of S. chilensis methanolic extract was investigated. Besides, a phytochemical study allowed isolation of two flavonoids (quercitrin and afzelin). The gastroprotective effects were investigated in acute gastric ulcer models, and the antisecretory activity was assessed in vivo and in vitro. The adhered mucus levels, reduced glutathione (GSH) content and myeloperoxidase (MPO) activity were quantified in ulcerated tissues. The contribution of isolated compounds in extract effects was evaluated, and its doses were calculated according to its yield. To evaluate the in vivo healing properties of S. chilensis methanolic extract, a chronic gastric ulcer was induced in mice by 10 % acetic acid. Evaluation of tumor necrosis factor (TNF) levels was also performed at the site of the acetic acid-induced gastric ulcer. In parallel, effects on cell viability and cell proliferation of fibroblasts (L929 cells) were determined by in vitro trials. Firstly, the S. chilensis methanolic extract (100 or 300 mg/kg) reduced the ulcer area induced by ethanol/HCl in mice when compared to the vehicle group. Moreover, the S. chilensis extract (300 mg/kg) prevented the mucus depletion, the increase in MPO activity and the decrease in the GSH levels in the ulcerated gastric tissue. The S. chilensis extract also was able to decrease the indomethacin-induced gastric ulcer in rats at a dose of 100 mg/kg. The antisecretory effect of the extract (100 mg/kg, intraduodenal (i.d.)) was confirmed by the reduction in the volume and acidity in parallel to an increase in the pH of gastric content. In addition, quercitrin (1.38 mg/kg, but not 0.46 mg/kg) and afzelin (0.026 and 0.078 mg/kg) decreased the ethanol/HCl-induced gastric ulcer. In this model, quercitrin (1.38 mg/kg) prevented the depletion of gastric GSH content and both quercitrin (1.38 mg/kg) and afzelin (0.078 mg/kg) reduced the MPO activity. These compounds also inhibited the H + ,K + -ATPase activity at a concentration of 1–100 μg/ml. In addition, the participation of quercitrin and afzelin in these effects also was confirmed. Furthermore, after 4 days of the treatment, an oral administration of S. chilensis methanolic extract (100 mg/kg) reduced the area of the gastric ulcer induced by acetic acid and the regeneration of the gastric mucosa was accompanied by a reduction in gastric TNF levels. The healing properties of the extract also were confirmed by enhancement of proliferation and coverage of scratched wounds in a fibroblast monolayer. Together, our results confirmed the gastroprotective effect of S. chilensis methanolic extract as well as its gastric healing potential and provided some support to the traditional use of S. chilensis for prevention and treatment of gastric lesions in complementation to its known anti-inflammatory properties.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-Ulcer Agents - chemistry</subject><subject>Anti-Ulcer Agents - isolation &amp; purification</subject><subject>Anti-Ulcer Agents - pharmacology</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell Line</subject><subject>Cell Proliferation - drug effects</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>Female</subject><subject>Fibroblasts - drug effects</subject><subject>Fibroblasts - metabolism</subject><subject>Fibroblasts - pathology</subject><subject>Gastric Mucosa - drug effects</subject><subject>Gastric Mucosa - metabolism</subject><subject>Gastric Mucosa - pathology</subject><subject>Glutathione - metabolism</subject><subject>H(+)-K(+)-Exchanging ATPase - metabolism</subject><subject>Hydrogen-Ion Concentration</subject><subject>Mannosides - chemistry</subject><subject>Mannosides - isolation &amp; 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Mota da Silva, Luisa ; Boeing, Thaise ; Somensi, Lincon Bordignon ; Cury, Benhur Judah ; de Moura Burci, Ligia ; Santin, José Roberto ; de Andrade, Sérgio Faloni ; Monache, Franco Delle ; Cechinel-Filho, Valdir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-b3761f7854ce0775077d6075da5c0447c5d1ae5717c855a49728e5d0249ab91c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Anti-Ulcer Agents - chemistry</topic><topic>Anti-Ulcer Agents - isolation &amp; purification</topic><topic>Anti-Ulcer Agents - pharmacology</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cell Line</topic><topic>Cell Proliferation - drug effects</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>Female</topic><topic>Fibroblasts - drug effects</topic><topic>Fibroblasts - metabolism</topic><topic>Fibroblasts - pathology</topic><topic>Gastric Mucosa - drug effects</topic><topic>Gastric Mucosa - metabolism</topic><topic>Gastric Mucosa - pathology</topic><topic>Glutathione - metabolism</topic><topic>H(+)-K(+)-Exchanging ATPase - metabolism</topic><topic>Hydrogen-Ion Concentration</topic><topic>Mannosides - chemistry</topic><topic>Mannosides - isolation &amp; 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Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Barros, Mariel</au><au>Mota da Silva, Luisa</au><au>Boeing, Thaise</au><au>Somensi, Lincon Bordignon</au><au>Cury, Benhur Judah</au><au>de Moura Burci, Ligia</au><au>Santin, José Roberto</au><au>de Andrade, Sérgio Faloni</au><au>Monache, Franco Delle</au><au>Cechinel-Filho, Valdir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacological reports about gastroprotective effects of methanolic extract from leaves of Solidago chilensis (Brazilian arnica) and its components quercitrin and afzelin in rodents</atitle><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle><stitle>Naunyn-Schmiedeberg's Arch Pharmacol</stitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><date>2016-04-01</date><risdate>2016</risdate><volume>389</volume><issue>4</issue><spage>403</spage><epage>417</epage><pages>403-417</pages><issn>0028-1298</issn><eissn>1432-1912</eissn><abstract>Solidago chilensis Meyenmost (Asteraceae), popularly known as “Brazilian arnica” or “arnica-do-campo,” is widely used in the folk medicine to treat gastric disorders. Based on this, the gastroprotective activity of S. chilensis methanolic extract was investigated. Besides, a phytochemical study allowed isolation of two flavonoids (quercitrin and afzelin). The gastroprotective effects were investigated in acute gastric ulcer models, and the antisecretory activity was assessed in vivo and in vitro. The adhered mucus levels, reduced glutathione (GSH) content and myeloperoxidase (MPO) activity were quantified in ulcerated tissues. The contribution of isolated compounds in extract effects was evaluated, and its doses were calculated according to its yield. To evaluate the in vivo healing properties of S. chilensis methanolic extract, a chronic gastric ulcer was induced in mice by 10 % acetic acid. Evaluation of tumor necrosis factor (TNF) levels was also performed at the site of the acetic acid-induced gastric ulcer. In parallel, effects on cell viability and cell proliferation of fibroblasts (L929 cells) were determined by in vitro trials. Firstly, the S. chilensis methanolic extract (100 or 300 mg/kg) reduced the ulcer area induced by ethanol/HCl in mice when compared to the vehicle group. Moreover, the S. chilensis extract (300 mg/kg) prevented the mucus depletion, the increase in MPO activity and the decrease in the GSH levels in the ulcerated gastric tissue. The S. chilensis extract also was able to decrease the indomethacin-induced gastric ulcer in rats at a dose of 100 mg/kg. The antisecretory effect of the extract (100 mg/kg, intraduodenal (i.d.)) was confirmed by the reduction in the volume and acidity in parallel to an increase in the pH of gastric content. In addition, quercitrin (1.38 mg/kg, but not 0.46 mg/kg) and afzelin (0.026 and 0.078 mg/kg) decreased the ethanol/HCl-induced gastric ulcer. In this model, quercitrin (1.38 mg/kg) prevented the depletion of gastric GSH content and both quercitrin (1.38 mg/kg) and afzelin (0.078 mg/kg) reduced the MPO activity. These compounds also inhibited the H + ,K + -ATPase activity at a concentration of 1–100 μg/ml. In addition, the participation of quercitrin and afzelin in these effects also was confirmed. Furthermore, after 4 days of the treatment, an oral administration of S. chilensis methanolic extract (100 mg/kg) reduced the area of the gastric ulcer induced by acetic acid and the regeneration of the gastric mucosa was accompanied by a reduction in gastric TNF levels. The healing properties of the extract also were confirmed by enhancement of proliferation and coverage of scratched wounds in a fibroblast monolayer. Together, our results confirmed the gastroprotective effect of S. chilensis methanolic extract as well as its gastric healing potential and provided some support to the traditional use of S. chilensis for prevention and treatment of gastric lesions in complementation to its known anti-inflammatory properties.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>26758066</pmid><doi>10.1007/s00210-015-1208-0</doi><tpages>15</tpages></addata></record>
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identifier ISSN: 0028-1298
ispartof Naunyn-Schmiedeberg's archives of pharmacology, 2016-04, Vol.389 (4), p.403-417
issn 0028-1298
1432-1912
language eng
recordid cdi_proquest_miscellaneous_1772837749
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Animals
Anti-Inflammatory Agents - pharmacology
Anti-Ulcer Agents - chemistry
Anti-Ulcer Agents - isolation & purification
Anti-Ulcer Agents - pharmacology
Biomedical and Life Sciences
Biomedicine
Cell Line
Cell Proliferation - drug effects
Disease Models, Animal
Dose-Response Relationship, Drug
Female
Fibroblasts - drug effects
Fibroblasts - metabolism
Fibroblasts - pathology
Gastric Mucosa - drug effects
Gastric Mucosa - metabolism
Gastric Mucosa - pathology
Glutathione - metabolism
H(+)-K(+)-Exchanging ATPase - metabolism
Hydrogen-Ion Concentration
Mannosides - chemistry
Mannosides - isolation & purification
Mannosides - pharmacology
Methanol - chemistry
Mice
Neurosciences
Original Article
Pharmacology/Toxicology
Phytotherapy
Plant Extracts - chemistry
Plant Extracts - isolation & purification
Plant Extracts - pharmacology
Plant Leaves
Plants, Medicinal
Proanthocyanidins - chemistry
Proanthocyanidins - isolation & purification
Proanthocyanidins - pharmacology
Proton Pump Inhibitors - pharmacology
Quercetin - analogs & derivatives
Quercetin - chemistry
Quercetin - isolation & purification
Quercetin - pharmacology
Rabbits
Rats, Wistar
Solidago - chemistry
Solvents - chemistry
Stomach Ulcer - chemically induced
Stomach Ulcer - metabolism
Stomach Ulcer - pathology
Stomach Ulcer - prevention & control
Tumor Necrosis Factor-alpha - metabolism
Wound Healing - drug effects
title Pharmacological reports about gastroprotective effects of methanolic extract from leaves of Solidago chilensis (Brazilian arnica) and its components quercitrin and afzelin in rodents
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