Hepatoprotective Effect of Pinoresinol on Carbon Tetrachloride-Induced Hepatic Damage in Mice
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- Kim Hyo-Yeon
- School of Pharmacy, Sungkyunkwan University, Korea
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- Kim Joon-Ki
- School of Pharmacy, Sungkyunkwan University, Korea
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- Choi Jun-Ho
- School of Pharmacy, Sungkyunkwan University, Korea
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- Jung Joo-Yeon
- School of Pharmacy, Sungkyunkwan University, Korea
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- Oh Woo-Yong
- School of Pharmacy, Sungkyunkwan University, Korea
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- Kim Dong Chun
- College of Pharmacy, Yeungnam University, Korea
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- Lee Hee Sang
- College of Pharmacy, Yeungnam University, Korea
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- Kim Yeong Shik
- College of Pharmacy, Seoul National University, Korea
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- Kang Sam Sik
- College of Pharmacy, Seoul National University, Korea
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- Lee Seung-Ho
- College of Pharmacy, Yeungnam University, Korea
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- Lee Sun-Mee
- School of Pharmacy, Sungkyunkwan University, Korea
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説明
Forsythiae Fructus is known to have diuretic, anti-bacterial, and anti-inflammatory activities. This study examined the hepatoprotective effects of pinoresinol, a lignan isolated from Forsythiae Fructus, against carbon tetrachloride (CCl4)–induced liver injury. Mice were treated intraperitoneally with vehicle or pinoresinol (25, 50, 100, and 200 mg/kg) 30 min before and 2 h after CCl4 (20 μl/kg) injection. In the vehicle-treated CCl4 group, serum aminotransferase activities were significantly increased 24 h after CCl4 injection, and these increases were attenuated by pinoresinol at all doses. Hepatic glutathione contents were significantly decreased and lipid peroxidation was increased after CCl4 treatment. These changes were attenuated by 50 and 100 mg/kg of pinoresinol. The levels of protein and mRNA expression of inflammatory mediators, including tumor necrosis factor-α, inducible nitric oxide synthase, and cyclooxygenase-2, were significantly increased after CCl4 injection; and these increases were attenuated by pinoresinol. Nuclear translocation of nuclear factor-κB (NF-κB) and phosphorylation of c-Jun, one of the components of activating protein 1 (AP-1), were inhibited by pinoresinol. Our results suggest that pinoresinol ameliorates CCl4-induced acute liver injury, and this protection is likely due to anti-oxidative activity and down-regulation of inflammatory mediators through inhibition of NF-κB and AP-1.
収録刊行物
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- Journal of Pharmacological Sciences
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Journal of Pharmacological Sciences 112 (1), 105-112, 2010
公益社団法人 日本薬理学会
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詳細情報 詳細情報について
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- CRID
- 1390282680155075456
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- NII論文ID
- 10027908791
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- NII書誌ID
- AA11806667
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- ISSN
- 13478648
- 13478613
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- NDL書誌ID
- 10524890
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
- Crossref
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- 抄録ライセンスフラグ
- 使用不可