Hepatoprotective effects of oyster hydrolysate on lipopolysaccharide/D-galactosamine-induced acute liver injury in mice
- Authors
- Ryu, J.H.; Kim, E.-J.; Xie, C.; Nyiramana, M.M.; Siregar, A.S.; Park, S.-H.; Cho, S.B.; Song, D.H.; Kim, N.-G.; Choi, Y.J.; Kang, S.S.; Kang, D.
- Issue Date
- 2017
- Publisher
- Korean Society of Food Science and Nutrition
- Keywords
- Acute liver injury; Anti-inflammatory; Antioxidant; Apoptosis; Oyster hydrolysate
- Citation
- Journal of the Korean Society of Food Science and Nutrition, v.46, no.6, pp 659 - 670
- Pages
- 12
- Indexed
- SCOPUS
KCI
- Journal Title
- Journal of the Korean Society of Food Science and Nutrition
- Volume
- 46
- Number
- 6
- Start Page
- 659
- End Page
- 670
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/14932
- DOI
- 10.3746/jkfn.2017.46.6.659
- ISSN
- 1226-3311
2288-5978
- Abstract
- Oxidative stress and inflammation are key factors responsible for progression of liver injury. A variety of functions of oyster hydrolysate (OH) are affected by their antioxidant and anti-inflammatory activities. However, little is known regarding the effects of OH on a liver injury model. This study was performed to evaluate the effects of OH on acute liver injury induced by lipopolysaccharide/D-galactosamine (LPS/D-GalN) in mice. Experimental groups were divided into six groups as follows (each group, n=10): control (saline), LPS/D-GalN, LPS/D-GalN+OH (100 mg/kg), LPS/D-GalN+OH (200 mg/kg), LPS/D-GalN+OH (400 mg/kg), and LPS/D-GalN+silymarin (25 mg/kg, positive control). The experimental acute liver injury model was induced with LPS (1 μg/kg) and D-GalN (400 mg/kg). We first analyzed antioxidant and anti-inflammatory activities in OH. OH showed high DPPH and ABTS radical scavenging activities and reduced ROS generation in Chang cells in a dose-dependent manner. In addition, OH showed anti-inflammatory activities, such as inhibition of cyclooxygenase-2 and 5-lipooxygenase. Treatment with OH down-regulated tumor necrosis factor (TNF)-α, interleukin (IL)-6, and IL-1α expression levels in LPS-stimulated RAW264.7 cells. OH significantly reduced LPS/D-GalN-induced increases in the concentrations of alanine transaminase and aspartate aminotransferase in serum. In the LPS/D-GalN group, liver tissues exhibited apoptosis of hepatocytes with hemorrhages. These pathological alterations were ameliorated by OH treatment. Consistently, hepatic catalase activity was low in the LPS/D-GalN group compared to the control group, and catalase activity was significantly restored by OH treatment (P<0.05). Furthermore, OH markedly reduced the LPS/D-GalN-induced increase in TNF-α, IL-1β, and IL-6 levels in liver tissue. Taken together, these results show that OH has hepatoprotective effects on LPS/D-GalN-induced acute liver injury via inhibition of oxidative stress and inflammation, suggesting that OH could be used as a health functional food and potential therapeutic agent for acute liver injury. ? 2017, Korean Society of Food Science and Nutrition. All rights reserved.
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