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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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 |
doi_str_mv | 10.1007/s00210-015-1208-0 |
format | Article |
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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><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 & 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 & purification</subject><subject>Mannosides - pharmacology</subject><subject>Methanol - chemistry</subject><subject>Mice</subject><subject>Neurosciences</subject><subject>Original Article</subject><subject>Pharmacology/Toxicology</subject><subject>Phytotherapy</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - isolation & purification</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Leaves</subject><subject>Plants, Medicinal</subject><subject>Proanthocyanidins - chemistry</subject><subject>Proanthocyanidins - isolation & purification</subject><subject>Proanthocyanidins - pharmacology</subject><subject>Proton Pump Inhibitors - pharmacology</subject><subject>Quercetin - analogs & derivatives</subject><subject>Quercetin - chemistry</subject><subject>Quercetin - isolation & purification</subject><subject>Quercetin - pharmacology</subject><subject>Rabbits</subject><subject>Rats, Wistar</subject><subject>Solidago - chemistry</subject><subject>Solvents - chemistry</subject><subject>Stomach Ulcer - chemically induced</subject><subject>Stomach Ulcer - metabolism</subject><subject>Stomach Ulcer - pathology</subject><subject>Stomach Ulcer - prevention & control</subject><subject>Tumor Necrosis Factor-alpha - metabolism</subject><subject>Wound Healing - drug effects</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kd2KFDEQhYMo7rj6AN5IwJv1ojXpSTrdl-7iHywoqNehJl09kyWdjEl60X0wn8-anVVEEBJScL46VeQw9lSKl1II86oI0UrRCKkb2Yq-EffYSqp128hBtvfZiuSelKE_YY9KuRJCdFLrh-yk7YzuRdet2M9PO8gzuBTS1jsIPOM-5Vo4bNJS-RZKzWmfU0VX_TVynCaqCk8Tn7HuIKbgHcfvNYOrfMpp5gHhGm-JzySOsE3c7XzAWHzhZ-cZbnzwEDnkSBNfcIgj92Tp0rxPESOV3xbMztfs460K0w0GqunkNB6Ix-zBBKHgk7v3lH19--bLxfvm8uO7DxevLxunVFubzdp0cjK9Vg6FMZru2AmjR9BOKGWcHiWgNtK4XmtQg2l71KNo1QCbQbr1KTs7-tIX0FKl2tkXhyFAxLQUKw11rI1RA6HP_0Gv0pIjbXegpKH_1oooeaRcTqVknOw--xnyDyuFPYRqj6FaCtUeQrWCep7dOS-bGcc_Hb9TJKA9AoWkuMX81-j_uv4C_yiv1w</recordid><startdate>20160401</startdate><enddate>20160401</enddate><creator>de Barros, Mariel</creator><creator>Mota da Silva, Luisa</creator><creator>Boeing, Thaise</creator><creator>Somensi, Lincon Bordignon</creator><creator>Cury, Benhur Judah</creator><creator>de Moura Burci, Ligia</creator><creator>Santin, José Roberto</creator><creator>de Andrade, Sérgio Faloni</creator><creator>Monache, Franco Delle</creator><creator>Cechinel-Filho, Valdir</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20160401</creationdate><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><author>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</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 & 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 & purification</topic><topic>Mannosides - pharmacology</topic><topic>Methanol - chemistry</topic><topic>Mice</topic><topic>Neurosciences</topic><topic>Original Article</topic><topic>Pharmacology/Toxicology</topic><topic>Phytotherapy</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - isolation & purification</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Leaves</topic><topic>Plants, Medicinal</topic><topic>Proanthocyanidins - chemistry</topic><topic>Proanthocyanidins - isolation & purification</topic><topic>Proanthocyanidins - pharmacology</topic><topic>Proton Pump Inhibitors - pharmacology</topic><topic>Quercetin - analogs & derivatives</topic><topic>Quercetin - chemistry</topic><topic>Quercetin - isolation & purification</topic><topic>Quercetin - pharmacology</topic><topic>Rabbits</topic><topic>Rats, Wistar</topic><topic>Solidago - chemistry</topic><topic>Solvents - chemistry</topic><topic>Stomach Ulcer - chemically induced</topic><topic>Stomach Ulcer - metabolism</topic><topic>Stomach Ulcer - pathology</topic><topic>Stomach Ulcer - prevention & control</topic><topic>Tumor Necrosis Factor-alpha - metabolism</topic><topic>Wound Healing - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & 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 & Medical Complete (Alumni)</collection><collection>Health & 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> |
fulltext | fulltext |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T00%3A45%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pharmacological%20reports%20about%20gastroprotective%20effects%20of%20methanolic%20extract%20from%20leaves%20of%20Solidago%20chilensis%20(Brazilian%20arnica)%20and%20its%20components%20quercitrin%20and%20afzelin%20in%20rodents&rft.jtitle=Naunyn-Schmiedeberg's%20archives%20of%20pharmacology&rft.au=de%20Barros,%20Mariel&rft.date=2016-04-01&rft.volume=389&rft.issue=4&rft.spage=403&rft.epage=417&rft.pages=403-417&rft.issn=0028-1298&rft.eissn=1432-1912&rft_id=info:doi/10.1007/s00210-015-1208-0&rft_dat=%3Cproquest_cross%3E1772837749%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1771780654&rft_id=info:pmid/26758066&rfr_iscdi=true |