Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/74762
PIRA download icon_1.1View/Download Full Text
DC FieldValueLanguage
dc.contributorDepartment of Health Technology and Informatics-
dc.creatorGao, L-
dc.creatorSiu, PM-
dc.creatorChan, SW-
dc.creatorLai, CWK-
dc.date.accessioned2018-03-29T09:33:48Z-
dc.date.available2018-03-29T09:33:48Z-
dc.identifier.issn1942-0900en_US
dc.identifier.urihttp://hdl.handle.net/10397/74762-
dc.language.isoenen_US
dc.publisherHindawi Limiteden_US
dc.rightsCopyright © 2017 Lei Gao et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsThe following article: Lei Gao, Parco M. Siu, Shun-wan Chan, and Christopher W. K. Lai, “Cardiovascular Protective Effects of Salvianic Acid A on db/db Mice with Elevated Homocysteine Level,” Oxidative Medicine and Cellular Longevity, vol. 2017, Article ID 9506925, 10 pages, 2017 is available at https://doi.org/10.1155/2017/9506925.en_US
dc.titleCardiovascular protective effects of salvianic acid a on db/db mice with elevated homocysteine levelen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume2017en_US
dc.identifier.doi10.1155/2017/9506925en_US
dcterms.abstractThe onsets of left ventricular hypertrophy (LVH) and endothelial dysfunction (ED) in diabetics, especially in those with elevated homocysteine (Hcy), precede the development of cardiovascular (CV) events. Salvianic acid A (SAA) is a renowned Traditional Chinese Medicine (TCM) that has been applied in the treatment of cardiovascular disease for many decades. In this study, we aimed (1) to investigate the CV protective effects of SAA on ameliorating LVH and ED in db/db mice with elevated blood Hcy level and (2) to decipher whether the observed CV protective effects of SAA are associated with Hcy metabolism by modulating the methylation potential and redox status in the liver of the db/db mice with elevated blood Hcy level. Our results found that the administration of SAA could significantly slow down the build-up of left ventricular mass and ameliorate ED. Immunological assay analysis on the mouse liver tissue also indicated that SAA treatment on db/db mice with elevated Hcy was associated with reduced methylation potential but improved redox status. In conclusion, we revealed that SAA has the potential to protect against the hyperglycemia- and hyperhomocysteinemia-induced oxidative stress on diabetic mice via modulation in Hcy metabolism.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOxidative medicine and cellular longevity, 2017, v. 2017, 9506925-
dcterms.isPartOfOxidative medicine and cellular longevity-
dcterms.issued2017-
dc.identifier.scopus2-s2.0-85030757533-
dc.identifier.eissn1942-0994en_US
dc.identifier.artn9506925en_US
dc.identifier.rosgroupid2017000201-
dc.description.ros2017-2018 > Academic research: refereed > Publication in refereed journal-
dc.description.validate201811_a bcmaen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
Appears in Collections:Journal/Magazine Article
Files in This Item:
File Description SizeFormat 
Gao_Cardiovascular_protective_effects.pdf1.92 MBAdobe PDFView/Open
Open Access Information
Status open access
File Version Version of Record
Access
View full-text via PolyU eLinks SFX Query
Show simple item record

Page views

109
Last Week
2
Last month
Citations as of Apr 21, 2024

Downloads

99
Citations as of Apr 21, 2024

SCOPUSTM   
Citations

7
Last Week
0
Last month
Citations as of Apr 19, 2024

WEB OF SCIENCETM
Citations

5
Last Week
0
Last month
Citations as of Apr 25, 2024

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.