Protective effect of the aqueous extract from the root of Platycodon grandiflorum on cholestasis-induced hepatic injury in mice

被引:24
作者
Kim, Tae-Won [1 ]
Lee, Hong-Ki [1 ]
Song, In-Bae [1 ]
Kim, Myoung-Seok [1 ]
Hwang, Youn-Hwan [1 ]
Lim, Jong-Hwan [2 ]
Park, Sang-Jin [2 ]
Lee, Sang-Wook [2 ]
Kim, Jong-Woo [2 ]
Yun, Hyo-In [1 ]
机构
[1] Chungnam Natl Univ, Coll Vet Med, Taejon 305764, South Korea
[2] B&C Biopharm, Adv Inst Convergence Technol, Suwon, Gyonggi Do, South Korea
关键词
Bile duct ligation; cholestasis; hepatotoxicity; platycodin D; Platycodon grandilflorum; standardized aqueous extract; DUCT LIGATION; LIVER-DAMAGE; BILE-SALTS; APOPTOSIS; RAT; MOUSE;
D O I
10.3109/13880209.2012.680973
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Context: The root of Platycodon grandiflorum (Jacq.) A. DC. (Campanulaceae) has been widely studied for its hepatoprotective effects against various hepatotoxicants. Objective: The present study evaluated the protective effect of the standardized aqueous extract of P. grandiflorum (BC703) on cholestasis-induced hepatic injury in mice. Materials and methods: BC703 is a standardized aqueous extract of P. grandiflorum in reference to platycodin D (at least 0.8%). The mice were allocated into five groups as follows: Sham-operated, bile duct ligation (BDL) alone, and BDL with BC703 (1, 5, and 10 mg/kg BW) treated group. BC703 was given for 3 consecutive days before BDL operation. The animals were sacrificed by CO2 anesthesia post-24 h of BDL operations. Results and discussion: Serum alanine aminotransferase and serum aspartate aminotransferase increased to 395.2 +/- 90.0 and 266.0 +/- 45.6 Unit/L in the BDL alone group and decreased with BC703 in a dose-dependent manner. Especially the 10 mg/kg of BC703-treated mice showed a 77% decrease of serum alanine aminotransferase and 56% of aspartate aminotransferase as compared with BDL alone. Decreased antioxidant enzyme levels in BDL alone group were elevated in BC703-treated groups ranging from 7 to 29% for glutathione and from 13 to 25% for superoxide dismutase. BC703 treatment also attenuated malondialdehyde (from 3 to 32%) and nitric oxide levels (from 32 to 50%) as compared with BDL alone. Histopathological studies further confirmed the hepatoprotective effect of BC703 in BDL-induced cholestesis. Conclusion: BC703 could attenuate liver injury by BDL in mice, and test results indicate that BC703 might be useful in cholestatic liver injury.
引用
收藏
页码:1473 / 1478
页数:6
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