Study on potential hepatotoxicity of main monomers of Polygonum multiflorum based on liver micro-tissue.
10.19540/j.cnki.cjcmm.20200322.401
- Author:
Qi WANG
1
;
Qian-Hui ZHANG
2
;
Hai-Ruo WEN
1
;
Hao-Xiang GUO
2
;
Le-Shuai ZHANG
2
;
Shuang-Cheng MA
1
Author Information
1. National Institutes for Food and Drug Control Beijing 100050, China.
2. State Key Laboratory of Radiation Medicine and Protection, School of Radiation Medicine and Protection, Suzhou University Suzhou 215123, China.
- Publication Type:Journal Article
- Keywords:
Polygonum multiflorum;
anthraquinone;
hepatotoxicity;
liver micro-tissue;
rat primary hepatocytes
- MeSH:
Animals;
Chemical and Drug Induced Liver Injury;
Emodin;
Fallopia multiflora;
Glucosides;
Plant Extracts;
Polygonum;
Rats
- From:
China Journal of Chinese Materia Medica
2020;45(12):2954-2959
- CountryChina
- Language:Chinese
-
Abstract:
In this study, we aimed to establish a rat liver micro-tissue evaluation system to evaluate the hepatotoxicity of the main monomers in Polygonum multiflorum. Rat primary hepatocytes were isolated and purified by two-step in situ perfusion method to prepare hepatic parenchymal cells. The ultra-low adsorption plate and the inverted model were used to establish an in vitro hepatotoxicity evaluation system. After the system was established, the main monomer components(monanthone with emodin type, rhein, emodin, emodin-8-O-β-D-glucopyranoside, physcion) of P. multiflorum were selected for in vitro hepatotoxicity evaluation. This study showed that the primary cells of the liver can form liver micro-tissues in the low adsorption plate method and the mold perfusion method, with good liver structure and function, which can be used to evaluate the hepatotoxicity of the drug to be tested after long-term administration. The five monomers to be tested in P. multiflorum can significantly affect the proliferation of primary liver micro-tissues in rats in a dose-and time-dependent manner. The hepatotoxic effects were as follows: monanthone with emodin type > rhein > emodin > emodin-8-O-β-D-glucopyranoside > physcion. The results suggested that the emodin-type monoterpene and rhein might be the potential hepatotoxic components, while the metabolites of emodin-8-O-β-D-glucoside and emodin methyl ether showed more toxic risks. The rat primary hepatocyte micro-tissue model system established in this experiment could be used to achieve long-term drug administration in vitro, which was consistent with the clinical features of liver injury caused by long-term use of P. multiflorum. The experimental results provided important information and reference on the clinical application and toxic component of P. multiflorum.
