Suppressive effects of Platycodon grandiflorum on the progress of carbon tetrachloride-induced hepatic fibrosis

被引:30
作者
Lee, KJ
Kim, JY
Jung, KS
Choi, CY
Chung, YC
Kim, DH
Jeong, HG
机构
[1] Chosun Univ, Dept Pharm, Kwangju 501759, South Korea
[2] Chosun Univ, Res Ctr Proteineous Mat, Kwangju 501759, South Korea
[3] Chinju Int Univ, Div Food Sci, Chinju, South Korea
[4] Daejeon Univ, Coll Oriental Med, Dept Pathol, Taejon, South Korea
关键词
Platycode Radix; carbon tetrachloride; hepatic fibrosis; hepatic stellate cells;
D O I
10.1007/BF02975888
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The suppressive effects of Platycodi Radix (Changkil: CK), the root of Platycodon grandiflorum A. DC (Campanulaceae), on the progress of acute carbon tetrachloride (CCl4)-induced hepatic fibrosis were investigated in the rat. CK significantly suppressed CCl4-induced hepatic necrosis and inflammation, as determined by the serum enzymatic activities of alanine and aspartate aminotransferase and serum tumor necrosis factor-a levels, in dose-dependent manners. In addition, the increased hepatic fibrosis after acute CCl4 treatment was suppressed by the administration of CK. CK also significantly prevented the elevation of hepatic alpha1 (I) procollagen (type I collagen) mRNA and alpha-smooth muscle actin (alpha-SMA) expressions in the liver of CCl4-intoxicated rats and also suppressed the induction of alpha-SMA and type I collagen in cultured hepatic stellate cells, in dose-dependent manners. These results suggest that the suppressive effects of CK against the progress of acute CCl4-induced hepatic fibrosis possibly involve mechanisms related to its ability to block both hepatic inflammation and the activation of hepatic stellate cells.
引用
收藏
页码:1238 / 1244
页数:7
相关论文
共 29 条
[1]  
Baroni GS, 1998, HEPATOLOGY, V27, P720
[2]   Lipopolysaccharide signal transduction, regulation of tumor necrosis factor biosynthesis, and signaling by tumor necrosis factor itself [J].
Beutler, B ;
Kruys, V .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1995, 25 :S1-S8
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   Expression of collagen α1(I) mRNA variants during tooth and bone formation in the rat [J].
Brandsten, C ;
Lundmark, C ;
Christersson, C ;
Hammarström, L ;
Wurtz, T .
JOURNAL OF DENTAL RESEARCH, 1999, 78 (01) :11-19
[5]  
BRATTIN W J, 1985, Journal of Free Radicals in Biology and Medicine, V1, P27, DOI 10.1016/0748-5514(85)90026-1
[6]   New aspects of hepatic fibrosis [J].
Brenner, DA ;
Waterboer, T ;
Choi, SK ;
Lindquist, JN ;
Stefanovic, B ;
Burchardt, E ;
Yamauchi, M ;
Gillan, A ;
Rippe, RA .
JOURNAL OF HEPATOLOGY, 2000, 32 :32-38
[7]   ACETALDEHYDE INCREASES PROCOLLAGEN TYPE-I AND FIBRONECTIN GENE-TRANSCRIPTION IN CULTURED RAT FAT-STORING CELLS THROUGH A PROTEIN-SYNTHESIS DEPENDENT MECHANISM [J].
CASINI, A ;
CUNNINGHAM, M ;
ROJKIND, M ;
LIEBER, CS .
HEPATOLOGY, 1991, 13 (04) :758-765
[8]   PREVENTION OF CARBON TETRACHLORIDE-INDUCED NECROSIS BY INHIBITORS OF DRUG-METABOLISM - FURTHER STUDIES ON THEIR MECHANISM OF ACTION [J].
CASTRO, JA ;
FERREYRA, EC ;
CASTRO, CRD ;
FENOS, OMD ;
SASAME, H ;
GILLETTE, JR .
BIOCHEMICAL PHARMACOLOGY, 1974, 23 (02) :295-&
[9]   Augmentation of macrophage functions by an aqueous extract isolated from Platycodon grandiflorum [J].
Choi, CY ;
Kim, JY ;
Kim, YS ;
Chung, YC ;
Hahm, KS ;
Jeong, HG .
CANCER LETTERS, 2001, 166 (01) :17-25
[10]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2