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Molecules. 2016 Apr 1;21(4):443. doi: 10.3390/molecules21040443.

Silymarin Prevents Restraint Stress-Induced Acute Liver Injury by Ameliorating Oxidative Stress and Reducing Inflammatory Response.

Author information

1
College of Pharmacy, Pusan National University, Busan 609-735, Korea. hyunie9808@naver.com.
2
The K-herb Research Center, Korea Institute of Oriental Medicine, Daejeon 305-811, Korea. dalsoh@gmail.com.
3
College of Pharmacy, Pusan National University, Busan 609-735, Korea. pooh7282@naver.com.
4
Division for Research Center, Dongnam Institute of Radiological and Medical Science, Busan 619-953, Korea. tgson@hanmail.net.
5
College of Pharmacy, Chungbuk National University, Cheongju 361-763, Korea. julycosmos@gmail.com.
6
College of Pharmacy, Pusan National University, Busan 609-735, Korea. youngjung@pusan.ac.kr.

Abstract

Silymarin is a flavonoid extracted from the milk thistle Silybum marianum. It has been reported to prevent liver injuries induced by various chemicals or toxins. Our recent study suggested that silymarin induces hepatic synthesis of glutathione by increasing cysteine availability, which may consequently contribute to increased antioxidant capacity of the liver. In the present study, we investigated the effects of silymarin on acute liver injury induced by restraint stress. Silymarin (100 mg/kg) was orally administered to BALB/c mice every 12 h (3 times in total). After the last dose, mice were subjected to restraint stress for 6 h, and serum levels of aspartate and alanine aminotransferases, and hepatic levels of lipid peroxidation were determined. Hepatic levels of sulfur-containing metabolites such as methionine, S-adenosylmethionine, cysteine, and glutathione were also measured. The level of pro-inflammatory mediators in both liver and serum was determined. To study the mechanism of the effects of silymarin, we assessed Jun N-terminal kinase (JNK) activation and apoptotic signaling. Restraint stress induced severe oxidative stress and increased mRNA levels of pro-inflammatory mediators; both effects of restraint stress were significantly inhibited by silymarin. Moreover, administration of silymarin significantly prevented acute liver injury induced by restraint stress by blocking JNK activation and subsequently apoptotic signaling. In conclusion, these results suggest that the inhibition of restraint stress-induced liver injury by silymarin is due at least in part to its anti-oxidant activity and its ability to suppress the inflammatory response.

KEYWORDS:

acute liver injury; inflammation; oxidative stress; restraint stress; silymarin

PMID:
27043523
PMCID:
PMC6274117
DOI:
10.3390/molecules21040443
[Indexed for MEDLINE]
Free PMC Article

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