Increase in serum 7S domain of type IV collagen and N-terminal propeptide of type III procollagen levels with normal serum transaminase levels after long-term oral administration of Tegaful-Uracil

2002 ◽  
Vol 24 (2) ◽  
pp. 184-191 ◽  
Author(s):  
T Suou
1994 ◽  
Vol 85 (12) ◽  
pp. 1263-1269 ◽  
Author(s):  
Kazuo Yudoh ◽  
Hisao Matsui ◽  
Masahiko Kanamori ◽  
Kazuo Ohmori ◽  
Haruo Tsuji ◽  
...  

1996 ◽  
Vol 31 (2) ◽  
pp. 242-248 ◽  
Author(s):  
Chisato Hirayama ◽  
Hiroshi Suzuki ◽  
Akira Takada ◽  
Kiyoshi Fujisawa ◽  
Kyuichi Tanikawa ◽  
...  

1988 ◽  
Vol 249 (3) ◽  
pp. 753-757 ◽  
Author(s):  
E R Savolainen ◽  
D Brocks ◽  
L Ala-Kokko ◽  
K I Kivirikko

Dimethylnitrosamine (DMN)-induced liver fibrosis was used as an experimental model to study the relationship between serum concentrations of the N-terminal propeptide of type III procollagen [S-Pro(III)-N-P] and the N-terminal (S-7S) and C-terminal (S-NC1) domains of type IV collagen and hepatic concentrations of type III and IV collagen mRNAs. Increases in S-Pro(III)-N-P, and especially in the two type IV collagen-related antigens, were found to be early events in the formation of DMN-induced hepatic fibrosis. The mean concentration of S-Pro(III)-N-P was 120% of the control mean on day 7 of DMN treatment, 230% on day 14 and 250% on day 21. The corresponding values for S-7S were 260, 950 and 1100% and, for S-NC1, 310, 820 and 1000%. All these changes were very similar to those found in the hepatic concentrations of the respective mRNAs. These data support a previous suggestion that an enhanced production of basement-membrane (type IV) collagen is an early event in the development of the DMN-induced hepatic fibrosis. The results also indicate that S-7S and S-NC1 are very sensitive indicators of changes in type IV collagen metabolism. Data obtained in gel-filtration experiments for these three serum antigens were consistent with the suggestion that all three antigens are mainly derived from the synthesis of the respective collagens.


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