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Study on the mechanism of PPAR-γ dependent immunological idiosyncrasy liver injury induced by Polygonum multiflorum
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Lan-zhi HE1, 2, Ping YIN1, 3, Ya-kun MENG1, 3, Zhen-fang ZHANG1, Hui-min LIU1, He-rong CUI1, Hao-tian NI1, Jia-bo WANG1, *, Xiao-he XIAO4, *, Zhao-fang BAI1, *
Acta Pharmaceutica Sinica | 2017, 52(7) : 1027 - 1032
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Acta Pharmaceutica Sinica | 2017, 52(7): 1027-1032
SPECIAL REPORTS Herb-Induced Liver Injury and Safe Usage
Study on the mechanism of PPAR-γ dependent immunological idiosyncrasy liver injury induced by Polygonum multiflorum
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Lan-zhi HE1, 2, Ping YIN1, 3, Ya-kun MENG1, 3, Zhen-fang ZHANG1, Hui-min LIU1, He-rong CUI1, Hao-tian NI1, Jia-bo WANG1, *, Xiao-he XIAO4, *, Zhao-fang BAI1, *
Affiliations
  • 1. China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China
  • 2. School of Pharmacy, Hunan University of Traditional Chinese Medicine, Changsha 410208, China
  • 3. School of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China
  • 4. Integrative Medical Center for Liver Diseases, 302 Military Hospital, Beijing 100039, China
Published: 2017-07-12 doi: 10.16438/j.0513-4870.2016-0774
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To investigate the effects of peroxisome proliferator-activated receptor gamma(PPAR-γ)on the liver injury of Polygonum multiflorum, we established a model of immunological idiosyncrasy liver injury induced by lipopolysaccharide. The 70 Sprague-Dawley(SD)rats were randomly divided into control group, LPS group(2.8 mg·kg-1), PM group(crude drug, 2.16 g·kg-1), PPAR-γ agonist group(pioglitazone, 0.5 mg·kg-1), PM+LPS group(crude drug 2.16 g·kg-1, 2.8 mg·kg-1), PPAR-γ agonist+LPS group(0.5 mg·kg-1, 2.8 mg·kg-1)and PM+LPS+PPAR-γ agonist group(crude drug, 2.16 g·kg-1, 2.8 mg·kg-1, 0.5 mg·kg-1). The rats were orally given PM, once a day for consecutive 2 days. The control rats were given the same amount of distilled water. Liver injury was induced by intravenous injection of LPS. Sodium pentobarbital was injected intraperitoneally for anesthesia, and liver samples were collected together with blood. The plasma levels of alanine transaminase(ALT), aspartate aminotransferase(AST), tumor necrosis factor-α(TNF-α), interleukin-1β(IL-1β), interleukin-6(IL-6) and interferon-γ(IFN-γ)were measured. Pathological changes and hepatocellular apoptosis were examined by liver biopsy, and immunohistochemical observation of liver tissue expression of PPAR-γ and NF-κB p65. A negative correlation was observed between the expression of PPAR-γ in hepatic tissue and liver injury of Polygonum multiflorum. PPAR-γ agonist significantly reduced the PM-induced idiosyncratic liver injury in rats according to serum ALT and AST(P < 0.05), reduced liver pathological injury and hepatocyte apoptosis, decreased serum TNF-α and other inflammatory cytokines(P < 0.05), liver tissue PPAR-γ expression, and inhibited expression of NF-κB p65(P < 0.05). The results suggest that the occurrence of immunological idiosyncrasy liver injury of PM is related to inhibition of the PPAR-γ pathway and elevation of inflammatory factors. PPAR-γ agonist can reverse the idiosyncratic liver injury induced by PM, and provide a reference for elucidating mechanism of idiosyncratic liver injury induced by Polygonum multiflorum.

Polygonum multiflorum  /  idiosyncratic hepatotoxicity  /  PPAR-γ agonist  /  NF-κB p65
Lan-zhi HE, Ping YIN, Ya-kun MENG, Zhen-fang ZHANG, Hui-min LIU, He-rong CUI, Hao-tian NI, Jia-bo WANG, Xiao-he XIAO, Zhao-fang BAI. Study on the mechanism of PPAR-γ dependent immunological idiosyncrasy liver injury induced by Polygonum multiflorum[J]. Acta Pharmaceutica Sinica, 2017 , 52 (7) : 1027 -1032 . DOI: 10.16438/j.0513-4870.2016-0774
Year 2017 volume 52 Issue 7
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doi: 10.16438/j.0513-4870.2016-0774
  • Receive Date:2017-04-08
  • Online Date:2026-01-14
  • Published:2017-07-12
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History
  • Received:2017-04-08
  • Revised:2017-04-28
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Affiliations
    1. China Military Institute of Chinese Medicine, 302 Military Hospital, Beijing 100039, China
    2. School of Pharmacy, Hunan University of Traditional Chinese Medicine, Changsha 410208, China
    3. School of Pharmacy, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China
    4. Integrative Medical Center for Liver Diseases, 302 Military Hospital, Beijing 100039, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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