Abstract | BACKGROUND & AIMS:
Acetaminophen ( APAP) is widely used as an antipyretic agent which is safe at therapeutic doses. However, overdose of APAP induces fatal and non-fatal hepatic necroses. The chemical reactive metabolites of APAP initiate toxicity and inflammatory response within the liver and lead to acute liver failure. However, the mechanism underlying APAP-induced liver injury is unknown. Thioredoxin-1 (TRX-1) is an important redox regulator, which plays roles in resisting oxidative stress, regulating inflammation and inhibiting apoptosis. Panaxatriol saponin (PTS) is one of the biologically active fractions of Panax notoginseng which is a traditional Chinese medicine. The aim of this study was to investigate the mechanism on PTS protecting liver from APAP hepatotoxicity. METHODS: Mice were divided into three groups, control group, APAP group and APAP combined with PTS group. Alanine aminotransferase (ALT) and tumour necrosis factor-alpha (TNF-α) were detected by ELISA. TRX-1 and pro-caspase-12 were examined by Western blotting. RESULTS: Our results showed PTS inhibited the levels of ALT and TNF-α by APAP. Pretreatment with PTS ameliorated liver injury induced by APAP. The decrease in TRX-1 expression was restored by PTS, as well as decreased pro-caspase-12 expression was inhibited by PTS. These data suggest that PTS has roles in suppressing the hepatotoxicity by APAP. CONCLUSION:
Panaxatriol saponin ameliorated liver injury by APAP through restoring the expression TRX-1 and inhibiting pro-caspase-12 decrease.
|
Authors | Shengdong Wang, Xiao Wang, Fucheng Luo, Xiaodan Tang, Kui Li, Xiaomei Hu, Jie Bai |
Journal | Liver international : official journal of the International Association for the Study of the Liver
(Liver Int)
Vol. 34
Issue 7
Pg. 1068-73
(Aug 2014)
ISSN: 1478-3231 [Electronic] United States |
PMID | 24119161
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Copyright | © 2013 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd. |
Chemical References |
- Ginsenosides
- Tumor Necrosis Factor-alpha
- Txn1 protein, mouse
- Acetaminophen
- Thioredoxins
- panaxatriol
- Alanine Transaminase
- Caspase 12
|
Topics |
- Acetaminophen
(adverse effects)
- Alanine Transaminase
(blood)
- Analysis of Variance
- Animals
- Blotting, Western
- Caspase 12
(metabolism)
- Chemical and Drug Induced Liver Injury
(drug therapy)
- Enzyme-Linked Immunosorbent Assay
- Ginsenosides
(pharmacology, therapeutic use)
- Mice
- Thioredoxins
(metabolism)
- Tumor Necrosis Factor-alpha
(blood)
|