Developing strategies for liver fibrosis treatment

被引:28
作者
Murphy, F [1 ]
Arthur, M [1 ]
Iredale, J [1 ]
机构
[1] Univ Southampton, Southampton Gen Hosp, Div Infect Inflammat & Repair, Liver Res Grp, Southampton SO16 6YD, Hants, England
关键词
antifibrotic therapy; hepatic stellate cell; liver fibrosis;
D O I
10.1517/13543784.11.11.1575
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Liver fibrosis represents a major worldwide healthcare burden. Current therapy is limited to removing the causal agent. This approach is successful in some diseases; particularly haemochromatosis and chronic viral hepatitis. However, for many patients treatment is not possible, while other patients present to medical attention at an advanced stage of fibrosis. There is therefore a great need for novel therapies for liver fibrosis. The hepatic stellate cell has been recognised to be responsible for most of the excess extracellular matrix observed in chronic liver fibrosis. The detailed understanding of hepatic stellate cell biology has allowed the rational design of novel antifibrotic therapies. This review describes for the general reader the novel emerging therapies for liver fibrosis.
引用
收藏
页码:1575 / 1585
页数:11
相关论文
共 112 条
[1]   Polyenylphosphatidylcholine prevents carbon tetrachloride-induced lipid peroxidation while it attenuates liver fibrosis [J].
Aleynik, SI ;
Leo, MA ;
Ma, XL ;
Aleynik, MK ;
Lieber, CS .
JOURNAL OF HEPATOLOGY, 1997, 27 (03) :554-561
[2]  
Baroni GS, 1996, HEPATOLOGY, V23, P1189
[3]   Angiotensin II induces contraction and proliferation of human hepatic stellate cells [J].
Bataller, R ;
Ginès, P ;
Nicolás, JM ;
Görbig, MN ;
Garcia-Ramallo, E ;
Gasull, X ;
Bosch, J ;
Arroyo, V ;
Rodés, J .
GASTROENTEROLOGY, 2000, 118 (06) :1149-1156
[4]   Successful targeting to rat hepatic stellate cells using albumin modified with cyclic peptides that recognize the collagen type VI receptor [J].
Beljaars, L ;
Molema, G ;
Schuppan, D ;
Geerts, A ;
De Bleser, PJ ;
Weert, B ;
Meijer, DKF ;
Poelstra, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (17) :12743-12751
[5]   Albumin modified with mannose 6-phosphate: A potential carrier for selective delivery of antifibrotic drugs to rat and human hepatic stellate cells [J].
Beljaars, L ;
Molema, G ;
Weert, B ;
Bonnema, H ;
Olinga, P ;
Groothuis, GMM ;
Meijer, DKF ;
Poelstra, K .
HEPATOLOGY, 1999, 29 (05) :1486-1493
[6]   Selective inhibition of hepatic collagen accumulation in experimental liver fibrosis in rats by a new prolyl 4-hydroxylase inhibitor [J].
Bickel, M ;
Baringhaus, KH ;
Gerl, M ;
Günzler, V ;
Kanta, J ;
Schmidts, L ;
Stapf, M ;
Tschank, G ;
Weidmann, K ;
Werner, U .
HEPATOLOGY, 1998, 28 (02) :404-411
[7]   Silymarin retards collagen accumulation in early and advanced biliary fibrosis secondary to complete bile duct obliteration in rats [J].
Boigk, G ;
Stroedter, L ;
Herbst, H ;
Waldschmidt, J ;
Riecken, EO ;
Schuppan, D .
HEPATOLOGY, 1997, 26 (03) :643-649
[8]   Inhibition of experimentally-induced liver cirrhosis in rats by a nonpeptidic mimetic of the extracellular matrix-associated Arg-Gly-Asp epitope [J].
Bruck, R ;
Hershkoviz, R ;
Lider, O ;
Aeed, H ;
Zaidel, L ;
Matas, Z ;
Barg, J ;
Haplern, Z .
JOURNAL OF HEPATOLOGY, 1996, 24 (06) :731-738
[9]   Analysis of Arg-Gly-Asp mimetics and soluble receptor of tumour necrosis factor as therapeutic modalities for concanavalin A induced hepatitis in mice [J].
Bruck, R ;
Shirin, H ;
Hershkoviz, R ;
Lider, O ;
Kenet, G ;
Aeed, H ;
Matas, Z ;
Zaidel, L ;
Halpern, Z .
GUT, 1997, 40 (01) :133-138
[10]  
CAMINO A, 2001, HEPATOLOGY, V34, pA936