scholarly journals Study on the Rationality for Antiviral Activity of Flos Lonicerae Japonicae-Fructus Forsythiae Herb Couple Preparations Improved by Chito-Oligosaccharide via Integral Pharmacokinetics

Molecules ◽  
2017 ◽  
Vol 22 (4) ◽  
pp. 654 ◽  
Author(s):  
Wei Zhou ◽  
Ailing Yin ◽  
Jinjun Shan ◽  
Shouchuan Wang ◽  
Baochang Cai ◽  
...  
2016 ◽  
Vol 179 ◽  
pp. 280-290 ◽  
Author(s):  
Yoonjin Nam ◽  
Jong Mi Lee ◽  
Yiyi Wang ◽  
Hyun Su Ha ◽  
Uy Dong Sohn

2006 ◽  
Vol 20 (6-7) ◽  
pp. 634-641 ◽  
Author(s):  
Famei Li ◽  
Bo Yuan ◽  
Zhili Xiong ◽  
Xiumei Lu ◽  
Feng Qin ◽  
...  

2018 ◽  
Vol 10 (35) ◽  
pp. 4292-4300 ◽  
Author(s):  
Hai Jiang ◽  
Liu Yang ◽  
Xudong Xing ◽  
Meiling Yan ◽  
Bingyou Yang ◽  
...  

The chemical variation of 10 batches of Flos Lonicerae Japonicae from different geographical origins was investigated by quantitation of phenolic acids..


2018 ◽  
Vol 2018 ◽  
pp. 1-10 ◽  
Author(s):  
Yanfang Gao ◽  
Huanwen Tang ◽  
Liang Xiong ◽  
Lijun Zou ◽  
Wenjuan Dai ◽  
...  

Hydroquinone (HQ) is widely used in food stuffs and is an occupational and environmental pollutant. Although the hepatotoxicity of HQ has been demonstrated both in vitro and in vivo, the prevention of HQ-induced hepatotoxicity has yet to be elucidated. In this study, we focused on the intervention effect of aqueous extracts of Flos lonicerae Japonicae (FLJ) on HQ-induced cytotoxicity. We demonstrated that HQ reduced cell viability in a concentration-dependent manner by administering 160 μmol/L HQ for 12 h as the positive control of cytotoxicity. The aqueous FLJ extracts significantly increased cell viability and decreased LDH release, ALT, and AST in a concentration-dependent manner compared with the corresponding HQ-treated groups in hepatic L02 cells. This result indicated that aqueous FLJ extracts could protect the cytotoxicity induced by HQ. HQ increased intracellular MDA and LPO and decreased the activities of GSH, GSH-Px, and SOD in hepatic L02 cells. In addition, aqueous FLJ extracts significantly suppressed HQ-stimulated oxidative damage. Moreover, HQ promoted DNA double-strand breaks (DSBs) and the level of 8-hydroxy-2′-deoxyguanosine and apoptosis. However, aqueous FLJ extracts reversed HQ-induced DNA damage and apoptosis in a concentration-dependent manner. Overall, our results demonstrated that the toxicity of HQ was mediated by intracellular oxidative stress, which activated DNA damage and apoptosis. The findings also proved that aqueous FLJ extracts exerted protective effects against HQ-induced cytotoxicity in hepatic L02 cells.


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