نمایش مختصر رکورد

dc.contributor.authoryazdi, Hamidrezaen_US
dc.contributor.authorSeifi, Akhtaren_US
dc.contributor.authorChangizi, Shimaen_US
dc.contributor.authorKhori, Vahiden_US
dc.contributor.authorHossini, Fatemehen_US
dc.contributor.authorDavarian, Alien_US
dc.contributor.authorJand, Yahyaen_US
dc.contributor.authorEnayati, Ayeshehen_US
dc.contributor.authorMazandarani, Masumehen_US
dc.contributor.authorNanvabashi, Fatemeen_US
dc.date.accessioned1399-07-09T12:38:58Zfa_IR
dc.date.accessioned2020-09-30T12:38:58Z
dc.date.available1399-07-09T12:38:58Zfa_IR
dc.date.available2020-09-30T12:38:58Z
dc.date.issued2017-06-01en_US
dc.date.issued1396-03-11fa_IR
dc.date.submitted2016-07-15en_US
dc.date.submitted1395-04-25fa_IR
dc.identifier.citationyazdi, Hamidreza, Seifi, Akhtar, Changizi, Shima, Khori, Vahid, Hossini, Fatemeh, Davarian, Ali, Jand, Yahya, Enayati, Ayesheh, Mazandarani, Masumeh, Nanvabashi, Fateme. (2017). Hydro-alcoholic extract of Matricaria recutita exhibited dual anti-spasmodic effect via modulation of Ca2+ channels, NO and PKA2-kinase pathway in rabbit jejunum. Avicenna Journal of Phytomedicine, 7(4), 334-344. doi: 10.22038/ajp.2017.8607en_US
dc.identifier.issn2228-7930
dc.identifier.issn2228-7949
dc.identifier.urihttps://dx.doi.org/10.22038/ajp.2017.8607
dc.identifier.urihttp://ajp.mums.ac.ir/article_8607.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/425678
dc.description.abstractObjective: Several studies have shown the antispasmodic activity of Matricariarecutita without detailing the underlying mechanism(s). The present study was designed to determine whether the antispasmodic mechanisms of M. recutita extract mediated via histaminergic/cholinergic receptors, Ca<sup>2+</sup>channels, activation of PKA<sub>2 </sub>and NO release in isolated rabbit jejunum.<br /> Methods and Materials: The concentration- dependent (3 × 10<sup>-3</sup>–1.3 × 10<sup>-2</sup> mg/ml) antispasmodic effect of the hydro-alcoholic extract of M. recutita flowers was studied in isolated rabbit jejunum. The isolated jejunum preparations were divided into seven groups, including the pharmacological probes that modulate cholinergic, histaminergic, and nitrergic receptors, as well as PKA<sub>2</sub>. <br /> Results: M. recutita inhibited spontaneous smooth muscle contractility of the jejunum in a concentration-dependent manner (3 × 10<sup>-3</sup>–1.3 × 10<sup>-2 </sup>mg/ml) and reduced both K<sup>+</sup>- and Ca<sup>2+</sup>-induced contractions, which is similar to the effect of verapamil. The antispasmodic effect of M. recutita wasinhibited by H89 (a PKA<sub>2 </sub>inhibitor). The myorelaxant effect of M. recutita increased in the presence of ACh/His and H89. <br /> Conclusion: M. recutita evoked antispasmodic and spasmolytic effects mediated through different signaling pathways. Our results have shown this dual inhibitory effect is mediated by blocking Ca<sup>2+</sup> channels, activating His and ACh receptors, releasing NO, and activating PKA<sub>2</sub>.en_US
dc.format.extent790
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofAvicenna Journal of Phytomedicineen_US
dc.relation.isversionofhttps://dx.doi.org/10.22038/ajp.2017.8607
dc.subjectMatricariaen_US
dc.subjectCholinergic Agentsen_US
dc.subjectHistamine Agentsen_US
dc.subjectJejunumen_US
dc.subjectRabbiten_US
dc.subjectNitric oxideen_US
dc.subjectPharmacologyen_US
dc.titleHydro-alcoholic extract of Matricaria recutita exhibited dual anti-spasmodic effect via modulation of Ca2+ channels, NO and PKA2-kinase pathway in rabbit jejunumen_US
dc.typeTexten_US
dc.typeOriginal Research Articleen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iran.en_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.contributor.departmentDepartment of Botany, Islamic Azad University, Gorgan, Iranen_US
dc.contributor.departmentIschemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iranen_US
dc.citation.volume7
dc.citation.issue4
dc.citation.spage334
dc.citation.epage344


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