Airway smooth muscle relaxant activity of Cordia dodecandra A. DC. mainly by cAMP increase and calcium channel blockade
The fight against chronic respiratory diseases needs the exploration of new active compounds with properties that contribute to diminish the symptoms or resolve the disease alongside current therapy. Eight extracts obtained from the bark and leaves of a Mayan medicinal plant used to treat asthma, Co...
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creator | Sánchez-Recillas, Amanda Rivero-Medina, Laura Ortiz-Andrade, Rolffy Araujo-León, Jesus Alfredo Flores-Guido, J. Salvador |
description | The fight against chronic respiratory diseases needs the exploration of new active compounds with properties that contribute to diminish the symptoms or resolve the disease alongside current therapy.
Eight extracts obtained from the bark and leaves of a Mayan medicinal plant used to treat asthma, Cordia dodecandra A. DC., were investigated for their relaxant effect on rat isolated tracheal rings pre-contracted with carbachol [1 µM]. The underlying functional mode of action of the most effective extract was assessed and the chromatographic fingerprints of more active extracts were analyzed.
The dichloromethane bark extract (DECd-b) was the most effective and potent (Emax= 87.57 ± 1.32 %; EC50 = 392.7 ± 5.18 µg/mL). DECd-b relaxant effect was maximized in presence of isoproterenol (β-adrenergic agonist, [10 µM]) and theophylline (phosphodiesterase unspecific inhibitor, [10 µM]). DECd-b also showed efficient relaxation of KCl [80 mM]-induced contraction and inhibition of CaCl2-induced contraction. Pre-incubation with propranolol (non-selective β-adrenergic antagonist, [10 µM]), SQ22536 (adenylyl cyclase inhibitor; [100 µM]), ODQ (guanylyl cyclase inhibitor; [10 µM]), l-NAME (nitric oxide synthase inhibitor; [10 µM]), indomethacin (a cyclooxygenase unspecific inhibitor; [10 µM]), glibenclamide (ATP-sensitive potassium channel blocker; [10 µM]) and 2-aminopyridine (voltage-gated potassium channel blocker [100 µM]) did not modify the DECd-b relaxant-effect curve. The chromatographic analysis of DECd-b suggests the cordiaquinones presence with double conjugated bounds such as menaquinone.
Results suggest that DECd-b induces relaxation mainly by cAMP increase and Ca2+ channel blockade. The chromatographic profiles and UV spectrum of DECd-b and HECd-l suggest the presence of molecules with structure of meroterpenoid naphthoquinones. This work report scientific evidence of C. dodecandra medicinal specie, which contributes to the pharmacological and phytochemical background of C. dodecandra providing an added value to the traditional use of this specie.
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doi_str_mv | 10.1016/j.jep.2018.10.013 |
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Eight extracts obtained from the bark and leaves of a Mayan medicinal plant used to treat asthma, Cordia dodecandra A. DC., were investigated for their relaxant effect on rat isolated tracheal rings pre-contracted with carbachol [1 µM]. The underlying functional mode of action of the most effective extract was assessed and the chromatographic fingerprints of more active extracts were analyzed.
The dichloromethane bark extract (DECd-b) was the most effective and potent (Emax= 87.57 ± 1.32 %; EC50 = 392.7 ± 5.18 µg/mL). DECd-b relaxant effect was maximized in presence of isoproterenol (β-adrenergic agonist, [10 µM]) and theophylline (phosphodiesterase unspecific inhibitor, [10 µM]). DECd-b also showed efficient relaxation of KCl [80 mM]-induced contraction and inhibition of CaCl2-induced contraction. Pre-incubation with propranolol (non-selective β-adrenergic antagonist, [10 µM]), SQ22536 (adenylyl cyclase inhibitor; [100 µM]), ODQ (guanylyl cyclase inhibitor; [10 µM]), l-NAME (nitric oxide synthase inhibitor; [10 µM]), indomethacin (a cyclooxygenase unspecific inhibitor; [10 µM]), glibenclamide (ATP-sensitive potassium channel blocker; [10 µM]) and 2-aminopyridine (voltage-gated potassium channel blocker [100 µM]) did not modify the DECd-b relaxant-effect curve. The chromatographic analysis of DECd-b suggests the cordiaquinones presence with double conjugated bounds such as menaquinone.
Results suggest that DECd-b induces relaxation mainly by cAMP increase and Ca2+ channel blockade. The chromatographic profiles and UV spectrum of DECd-b and HECd-l suggest the presence of molecules with structure of meroterpenoid naphthoquinones. This work report scientific evidence of C. dodecandra medicinal specie, which contributes to the pharmacological and phytochemical background of C. dodecandra providing an added value to the traditional use of this specie.
[Display omitted]</description><identifier>ISSN: 0378-8741</identifier><identifier>EISSN: 1872-7573</identifier><identifier>DOI: 10.1016/j.jep.2018.10.013</identifier><identifier>PMID: 30342193</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Animals ; Calcium channel blockade ; Calcium Channel Blockers - pharmacology ; cAMP ; Chromatographic fingerprint ; Cordia ; Cordia dodecandra ; Cyclic AMP - metabolism ; In Vitro Techniques ; Male ; Muscle Relaxation - drug effects ; Muscle, Smooth - drug effects ; Muscle, Smooth - physiology ; Parasympatholytics - pharmacology ; Plant Bark ; Plant Extracts - pharmacology ; Plant Leaves ; Rats, Wistar ; Relaxant activity ; Smooth muscle ; Trachea - drug effects ; Trachea - physiology ; Trachea relaxation</subject><ispartof>Journal of ethnopharmacology, 2019-01, Vol.229, p.280-287</ispartof><rights>2018 Elsevier B.V.</rights><rights>Copyright © 2018 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-46d97d8f1d8190b7a8e907d8816ac1b69f832a211512477c161aea8cc46571b03</citedby><cites>FETCH-LOGICAL-c379t-46d97d8f1d8190b7a8e907d8816ac1b69f832a211512477c161aea8cc46571b03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S037887411831571X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30342193$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sánchez-Recillas, Amanda</creatorcontrib><creatorcontrib>Rivero-Medina, Laura</creatorcontrib><creatorcontrib>Ortiz-Andrade, Rolffy</creatorcontrib><creatorcontrib>Araujo-León, Jesus Alfredo</creatorcontrib><creatorcontrib>Flores-Guido, J. Salvador</creatorcontrib><title>Airway smooth muscle relaxant activity of Cordia dodecandra A. DC. mainly by cAMP increase and calcium channel blockade</title><title>Journal of ethnopharmacology</title><addtitle>J Ethnopharmacol</addtitle><description>The fight against chronic respiratory diseases needs the exploration of new active compounds with properties that contribute to diminish the symptoms or resolve the disease alongside current therapy.
Eight extracts obtained from the bark and leaves of a Mayan medicinal plant used to treat asthma, Cordia dodecandra A. DC., were investigated for their relaxant effect on rat isolated tracheal rings pre-contracted with carbachol [1 µM]. The underlying functional mode of action of the most effective extract was assessed and the chromatographic fingerprints of more active extracts were analyzed.
The dichloromethane bark extract (DECd-b) was the most effective and potent (Emax= 87.57 ± 1.32 %; EC50 = 392.7 ± 5.18 µg/mL). DECd-b relaxant effect was maximized in presence of isoproterenol (β-adrenergic agonist, [10 µM]) and theophylline (phosphodiesterase unspecific inhibitor, [10 µM]). DECd-b also showed efficient relaxation of KCl [80 mM]-induced contraction and inhibition of CaCl2-induced contraction. Pre-incubation with propranolol (non-selective β-adrenergic antagonist, [10 µM]), SQ22536 (adenylyl cyclase inhibitor; [100 µM]), ODQ (guanylyl cyclase inhibitor; [10 µM]), l-NAME (nitric oxide synthase inhibitor; [10 µM]), indomethacin (a cyclooxygenase unspecific inhibitor; [10 µM]), glibenclamide (ATP-sensitive potassium channel blocker; [10 µM]) and 2-aminopyridine (voltage-gated potassium channel blocker [100 µM]) did not modify the DECd-b relaxant-effect curve. The chromatographic analysis of DECd-b suggests the cordiaquinones presence with double conjugated bounds such as menaquinone.
Results suggest that DECd-b induces relaxation mainly by cAMP increase and Ca2+ channel blockade. The chromatographic profiles and UV spectrum of DECd-b and HECd-l suggest the presence of molecules with structure of meroterpenoid naphthoquinones. This work report scientific evidence of C. dodecandra medicinal specie, which contributes to the pharmacological and phytochemical background of C. dodecandra providing an added value to the traditional use of this specie.
[Display omitted]</description><subject>Animals</subject><subject>Calcium channel blockade</subject><subject>Calcium Channel Blockers - pharmacology</subject><subject>cAMP</subject><subject>Chromatographic fingerprint</subject><subject>Cordia</subject><subject>Cordia dodecandra</subject><subject>Cyclic AMP - metabolism</subject><subject>In Vitro Techniques</subject><subject>Male</subject><subject>Muscle Relaxation - drug effects</subject><subject>Muscle, Smooth - drug effects</subject><subject>Muscle, Smooth - physiology</subject><subject>Parasympatholytics - pharmacology</subject><subject>Plant Bark</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Leaves</subject><subject>Rats, Wistar</subject><subject>Relaxant activity</subject><subject>Smooth muscle</subject><subject>Trachea - drug effects</subject><subject>Trachea - physiology</subject><subject>Trachea relaxation</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE2P0zAQhi0EYsvCD-CCfOSS4InT2BGnqnxKi-AAZ2synmpdkrjYyS7596TqwpHTaEbP-0rzCPESVAkKmjfH8sinslJg171UoB-JDVhTFWZr9GOxUdrYwpoarsSznI9KKQO1eiqutNJ1Ba3eiPtdSPe4yDzEON3KYc7Us0zc428cJ4k0hbswLTIe5D4mH1D66Jlw9AnlrpTv9qUcMIz9IrtF0u7LNxlGSoyZ5QpJwp7CPEi6xXHkXnZ9pJ_o-bl4csA-84uHeS1-fHj_ff-puPn68fN-d1OQNu1U1I1vjbcH8BZa1Rm03Kr1YKFBgq5pD1ZXWAFsoaqNIWgAGS1R3WwNdEpfi9eX3lOKv2bOkxtCJu57HDnO2VVQaQNNXW9XFC4opZhz4oM7pTBgWhwod_btjm717c6-z6fV95p59VA_dwP7f4m_glfg7QXg9cm7wMllCjwS-5CYJudj-E_9H63lj6I</recordid><startdate>20190130</startdate><enddate>20190130</enddate><creator>Sánchez-Recillas, Amanda</creator><creator>Rivero-Medina, Laura</creator><creator>Ortiz-Andrade, Rolffy</creator><creator>Araujo-León, Jesus Alfredo</creator><creator>Flores-Guido, J. Salvador</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>20190130</creationdate><title>Airway smooth muscle relaxant activity of Cordia dodecandra A. DC. mainly by cAMP increase and calcium channel blockade</title><author>Sánchez-Recillas, Amanda ; Rivero-Medina, Laura ; Ortiz-Andrade, Rolffy ; Araujo-León, Jesus Alfredo ; Flores-Guido, J. Salvador</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-46d97d8f1d8190b7a8e907d8816ac1b69f832a211512477c161aea8cc46571b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Calcium channel blockade</topic><topic>Calcium Channel Blockers - pharmacology</topic><topic>cAMP</topic><topic>Chromatographic fingerprint</topic><topic>Cordia</topic><topic>Cordia dodecandra</topic><topic>Cyclic AMP - metabolism</topic><topic>In Vitro Techniques</topic><topic>Male</topic><topic>Muscle Relaxation - drug effects</topic><topic>Muscle, Smooth - drug effects</topic><topic>Muscle, Smooth - physiology</topic><topic>Parasympatholytics - pharmacology</topic><topic>Plant Bark</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Leaves</topic><topic>Rats, Wistar</topic><topic>Relaxant activity</topic><topic>Smooth muscle</topic><topic>Trachea - drug effects</topic><topic>Trachea - physiology</topic><topic>Trachea relaxation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sánchez-Recillas, Amanda</creatorcontrib><creatorcontrib>Rivero-Medina, Laura</creatorcontrib><creatorcontrib>Ortiz-Andrade, Rolffy</creatorcontrib><creatorcontrib>Araujo-León, Jesus Alfredo</creatorcontrib><creatorcontrib>Flores-Guido, J. 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DC. mainly by cAMP increase and calcium channel blockade</atitle><jtitle>Journal of ethnopharmacology</jtitle><addtitle>J Ethnopharmacol</addtitle><date>2019-01-30</date><risdate>2019</risdate><volume>229</volume><spage>280</spage><epage>287</epage><pages>280-287</pages><issn>0378-8741</issn><eissn>1872-7573</eissn><abstract>The fight against chronic respiratory diseases needs the exploration of new active compounds with properties that contribute to diminish the symptoms or resolve the disease alongside current therapy.
Eight extracts obtained from the bark and leaves of a Mayan medicinal plant used to treat asthma, Cordia dodecandra A. DC., were investigated for their relaxant effect on rat isolated tracheal rings pre-contracted with carbachol [1 µM]. The underlying functional mode of action of the most effective extract was assessed and the chromatographic fingerprints of more active extracts were analyzed.
The dichloromethane bark extract (DECd-b) was the most effective and potent (Emax= 87.57 ± 1.32 %; EC50 = 392.7 ± 5.18 µg/mL). DECd-b relaxant effect was maximized in presence of isoproterenol (β-adrenergic agonist, [10 µM]) and theophylline (phosphodiesterase unspecific inhibitor, [10 µM]). DECd-b also showed efficient relaxation of KCl [80 mM]-induced contraction and inhibition of CaCl2-induced contraction. Pre-incubation with propranolol (non-selective β-adrenergic antagonist, [10 µM]), SQ22536 (adenylyl cyclase inhibitor; [100 µM]), ODQ (guanylyl cyclase inhibitor; [10 µM]), l-NAME (nitric oxide synthase inhibitor; [10 µM]), indomethacin (a cyclooxygenase unspecific inhibitor; [10 µM]), glibenclamide (ATP-sensitive potassium channel blocker; [10 µM]) and 2-aminopyridine (voltage-gated potassium channel blocker [100 µM]) did not modify the DECd-b relaxant-effect curve. The chromatographic analysis of DECd-b suggests the cordiaquinones presence with double conjugated bounds such as menaquinone.
Results suggest that DECd-b induces relaxation mainly by cAMP increase and Ca2+ channel blockade. The chromatographic profiles and UV spectrum of DECd-b and HECd-l suggest the presence of molecules with structure of meroterpenoid naphthoquinones. This work report scientific evidence of C. dodecandra medicinal specie, which contributes to the pharmacological and phytochemical background of C. dodecandra providing an added value to the traditional use of this specie.
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subjects | Animals Calcium channel blockade Calcium Channel Blockers - pharmacology cAMP Chromatographic fingerprint Cordia Cordia dodecandra Cyclic AMP - metabolism In Vitro Techniques Male Muscle Relaxation - drug effects Muscle, Smooth - drug effects Muscle, Smooth - physiology Parasympatholytics - pharmacology Plant Bark Plant Extracts - pharmacology Plant Leaves Rats, Wistar Relaxant activity Smooth muscle Trachea - drug effects Trachea - physiology Trachea relaxation |
title | Airway smooth muscle relaxant activity of Cordia dodecandra A. DC. mainly by cAMP increase and calcium channel blockade |
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