Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/14988
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dc.contributor.authorWu, Qi-
dc.contributor.authorZhao, Wanlong-
dc.contributor.authorChen, Gangling-
dc.contributor.authorSu, Xue-
dc.contributor.authorLi, Rong-
dc.date.accessioned2022-12-13T09:39:25Z-
dc.date.available2022-12-13T09:39:25Z-
dc.date.issued2019-01-04-
dc.identifier.citationWu, Q., Zhao, W., Chen, G., Su, X., & Li, R. (2019). Relevant effects of Taohong Siwu decoction on isolated rat aortic ring dependent on endothelium nitric oxide-cGMP pathway. Pakistan Journal of Pharmaceutical Sciences, 36(1SI), 261-269.en_US
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/14988-
dc.description.abstractUsing rat thoracic aortic rings to test the relaxing effects of the 95% ethanol extract and aqueous extract of Taohong Siwu decoction (THSW) on endothelium intact or endothelium removed aortic rings. Results showed that the 95% ethanol extract (0.1, 1, 10, 100, 1000 mg·L-1 ) and aqueous extract (0.1, 1, 10, 100, 1000 mg·L-1 ) of THSW were able to relax the intact endothelium aortic rings pre-contracted by 10-6 mol·L-1 PE. 10-4 mol·L-1 L-NAME and 10-5 mol·L-1 methylene blue both were able to inhibit the relaxation other than indomethacin. For the endothelium removed aortic rings, potassium channel blocker 3×10-3mol·L-1 tetraethylammonium chloride and 10-5 mol·L-1 glibenclamide had no effect on the relaxation effects caused by the 95% ethanol extract and aqueous extract of THSW. It could be concluded that the 95% ethanol extract and aqueous extract of THSW relax blood vessel by endothelium-dependent wayen_US
dc.language.isoenen_US
dc.publisherKarachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachien_US
dc.subjectTaohong Siwuen_US
dc.subjectthoracic aortaen_US
dc.subjectraten_US
dc.subjectaortic ringen_US
dc.subjectrelaxationen_US
dc.titleRelevant effects of Taohong Siwu decoction on isolated rat aortic ring dependent on endothelium nitric oxide-cGMP pathwayen_US
dc.typeArticleen_US
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