Please use this identifier to cite or link to this item: https://doi.org/10.1186/1749-8546-7-6
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dc.titleMetabolomic profiles of myocardial ischemia under treatment with salvianolic acid B
dc.contributor.authorLu, Y
dc.contributor.authorZheng, Y
dc.contributor.authorLiu, X
dc.contributor.authorLiang, X
dc.contributor.authorNgai, S
dc.contributor.authorLi, T
dc.contributor.authorZhang, W
dc.date.accessioned2020-10-20T08:07:41Z
dc.date.available2020-10-20T08:07:41Z
dc.date.issued2012
dc.identifier.citationLu, Y, Zheng, Y, Liu, X, Liang, X, Ngai, S, Li, T, Zhang, W (2012). Metabolomic profiles of myocardial ischemia under treatment with salvianolic acid B. Chinese Medicine 7 : 6. ScholarBank@NUS Repository. https://doi.org/10.1186/1749-8546-7-6
dc.identifier.issn1749-8546
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/178152
dc.description.abstractBackground: Radix Salvia miltiorrhiza (Danshen) has been used as a principal herb in treating cardiovascular diseases in Chinese medicine. Salvianolic acid B (SA-B), a water-soluble active component of Danshen, was found to have anti-myocardial ischemia (anti-MI) effect. This study aims to investigate mechanisms of SA-B on MI.Methods: Five conventional Western medicines (isosorbide dinitrate, verapamil, propranolol, captopril and trimethazine) with different mechanisms for treating cardiovascular diseases were selected as positive references to compare with SA-B in changing of the metabolomic profiles in MI rats under treatment. Potential mechanisms of SA-B were further investigated in H9C2 cell line.Results: The metabolomic profiles between SA-B- and propranolol-treated MI rats were similar, since there was a big overlap between the two groups in the PLS-DA score plot. Finally, it was demonstrated that SA-B exhibited a protective effect on MI mainly by decreasing the concentration of cyclic adenosine monophosphate (cAMP) and Ca2+and inhibiting protein kinase A (PKA).Conclusion: SA-B and propanolol exhibited similar metabolomic profiles, indicating that the two drugs might have a similar mechanism. © 2012 Lu et al; licensee BioMed Central Ltd.
dc.publisherBMC
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectcalcium ion
dc.subjectcaptopril
dc.subjectcyclic AMP
dc.subjectcyclic AMP dependent protein kinase
dc.subjectisosorbide dinitrate
dc.subjectpropranolol
dc.subjectsalvianolic acid B
dc.subjectverapamil
dc.subjectanimal cell
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectarticle
dc.subjectcardiovascular disease
dc.subjectcell line
dc.subjectcontrolled study
dc.subjectheart muscle ischemia
dc.subjectmale
dc.subjectmetabolomics
dc.subjectnonhuman
dc.subjectrat
dc.subjectSalvia miltiorrhiza
dc.typeArticle
dc.contributor.departmentSAW SWEE HOCK SCHOOL OF PUBLIC HEALTH
dc.description.doi10.1186/1749-8546-7-6
dc.description.sourcetitleChinese Medicine
dc.description.volume7
dc.description.page6
dc.published.statepublished
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