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The Safety Evaluation of Salvianolic Acid B and Ginsenoside Rg1 Combination on Mice.

Authors :
Qun Zhao
Min Yang
Yanping Deng
Haitao Yu
Linlin Wang
Fukang Teng
Kenka Cho
Hongmei Ma
Peng Wu
Xue Li
Wanying Wu
Xuan Liu
Feng Xu
Baohong Jiang
De-An Guo
Source :
International Journal of Molecular Sciences; 2015, Vol. 16 Issue 12, p29345-29356, 13p, 2 Color Photographs, 1 Diagram, 6 Charts, 3 Graphs
Publication Year :
2015

Abstract

Our previous study indicated that the combination of salvianolic acid B (SalB) and ginsenoside Rg1 (Rg1), the main components of Salvia miltiorrhizae and Panax notoginseng, improves myocardium structure and ventricular function in rats with ischemia/reperfusion injury. The present study aimed to determine the safety of the combined SalB and Rg1 (SalB-Rg1) in mice. The safety of SalB-Rg1 was evaluated through acute toxicity and repeated-dose toxicity. In the acute toxicity study, the up and down procedure was carried out firstly, and then, the Bliss method was applied. In the toxicity study for seven-day repeated treatment of SalB-Rg1, forty Kunming mice were randomly divided into four groups. The intravenous median lethal dose (LD<subscript>50</subscript>) of the SalB-Rg1 combination was 1747 mg/kg using the Bliss method. For both the acute toxicity study and the seven-day repeated toxicity study, SalB-Rg1 did not induce significant abnormality on brain, heart, kidney, liver and lung structure at any dose based on H&E stain. There were no significant changes related to the SalB-Rg1 toxicity detected on biochemical parameters for two kinds of toxicity studies. The LD<subscript>50</subscript> in mice was 1747 mg/kg, which was more than one hundred times higher than the effective dose. Both studies of acute toxicity and seven-day repeated dose toxicity indicated the safety of the SalB-Rg1 combination. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16616596
Volume :
16
Issue :
12
Database :
Complementary Index
Journal :
International Journal of Molecular Sciences
Publication Type :
Academic Journal
Accession number :
111988335
Full Text :
https://doi.org/10.3390/ijms161226176