Document Type
Journal Article
Department/Unit
School of Chinese Medicine
Language
English
Abstract
Ethnopharmacological relevance
As folk medicines used in China since 1950s, Dioscorea nipponicaMakino (DN), D. panthaica Prain et Burkill (DP), and D. zingiberensis C.H. Wright (DZ) are regarded as having more or less the same traditional therapeutic actions, such as activating blood, relieving pain, and dispersing swelling. It is noteworthy that, of the 49 species of the genus Dioscorea distributed in China, based on such traditional efficacies, only these three have been further developed as effective single-herb medicines for treating cardiovascular diseases by the modern pharmaceutical industry. In our previous study, it was found that the chemical compositions of DN and DP were similar, and both were distinct from that of DZ. Hence, whether their different chemical profiles support their anti-IHD (ischemic heart disease) activity in common still needs to be answered. So far it is still unknown whether the efficacies of these three herbs act via similar mechanism and whether they possess comparable therapeutic efficacy for experimental myocardial ischemia (MI).
Aim of the study
The present study aimed to further investigate the underlying mechanisms with respect to antioxidative stress activity by which these Dioscorea spp. attenuate MI, and to compare the therapeutic effect of total saponins from these three species on myocardial antioxidant levels and myocardial histology.
Material and methods
The serum levels of creatine kinase (CK), lactate dehydrogenase (LDH), aspartate aminotransferase (AST), total superoxide dismutases (SOD), catalase (CAT), glutathione peroxidase (GPx), the total antioxidant capacity (T-AOC), and malondialdehyde (MDA), as well as myocardial histology, were compared among rat groups administered with total saponins (TS) of DN, DP or DZ (abbreviated as DNTS, DPTS and DZTS, respectively). The rats experienced myocardial ischemia induced by isoprenaline (ISO) injection; the test solutions (DNTS, DPTS, DZTS) were administered either after the ISO injection, or both before and after.
Results
Compared with the model group (ISO injection only), TS groups exhibited significantly reduced activities of CK, LDH and AST, lowered level of MDA, and increased activities of SOD, CAT, GPx and T-AOC; heart tissues from TS groups revealed less severe histological damage. The cardioprotective efficacy of these three Dioscorea TS for rat MI was closely comparable based on the above observations.
Conclusion
The findings of the present study provide evidence that the anti-MI effect of DNTS, DPTS and DZTS can be attributed to the increase of myocardial antioxidant levels and decrease of lipid peroxidation formation, and the closely comparable results observed from these three Dioscorea saponins thereby explains the similarity in their clinical efficacy as anti-MI drugs.
Keywords
Dioscorea nipponica, D. Panthaica, D. Zingiberensis, Total saponins, Myocardial ischemia, Antioxidative activity
Publication Date
12-4-2015
Source Publication Title
Journal of Ethnopharmacology
Volume
175
Start Page
451
End Page
455
Publisher
Elsevier
Peer Reviewed
1
Copyright
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.
Funder
The work described in this paper was supported by the Faculty Research Grant of Hong Kong Baptist University (FRG2/13-14/031 and FRG1/12-13/035) and the Natural Science Foundation of Guangdong Province (2014A030313766). The authors would like to thank Mr. Alan Ho (Senior Technical Instructor, Teaching Division, School of Chinese Medicine, Hong Kong Baptist University) for technical support with the UPLC-QTOF-MS experiments.
DOI
10.1016/j.jep.2015.10.004
Link to Publisher's Edition
ISSN (print)
03788741
ISSN (electronic)
18727573
Recommended Citation
Tang, Yi-Na, Xi-Cheng He, Min Ye, Hao Huang, Hong-Li Chen, Wan-Ling Peng, Zhong-Zhen Zhao, Tao Yi, and Hu-Biao Chen. "Cardioprotective effect of total saponins from three medicinal species of Dioscorea against isoprenaline-induced myocardial ischemia." Journal of Ethnopharmacology 175 (2015): 451-455.