Modification of 3′-AMP forming enzyme activity by a potent immunosuppressant, ISP-I/myriocin, in liver of mice treated with carbon tetrachloride

被引:2
作者
Fujimori, H [1 ]
Fujita, T [1 ]
Pan-Hou, H [1 ]
机构
[1] Setsunan Univ, Fac Pharmaceut Sci, Osaka 5730101, Japan
关键词
adenosine 3 '-monophosphate forming enzyme; ISP-I/myriocin; carbon tetrachloride; adenosine 3 '-monophosphate; mouse liver;
D O I
10.1248/jhs.47.314
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The effect of ISP-I/myriocin on adenosine 3'-monophosphate (3'-AMP) forming enzyme activity in carbon tetrachloride (CCl4)-induced hepatitis was examined, The 3'-AMP forming enzyme activity in mouse liver was enhanced by the treatment of CCl4. The increase in the activity in cytosol mag result from the leakage of the enzyme from mitochondria via the damage of mitochondrial membrane induced by CCl4. Pretreatment of mice with ISP-I/myriocin for 24 hr, significantly inhibited both the CCl4-induced activities of serum alanine aminotransferase and the 3'-AMP forming enzyme in the supernatant of liver homogenate prepared immediately after the organ excision, These results suggest that the inhibitory effects of ISP-I/myriocin may be due to inhibition of lipid peroxidation of intracellular membranes caused by CCl4, in turn inhibiting the leakage of the 3'-AMP forming enzyme from mitochondria to cytosol, Our results demonstrated for the first time that ISP-I/myriocin has a protective effect on the CCl4-induced hepatotoxicity.
引用
收藏
页码:314 / 317
页数:4
相关论文
共 10 条
[1]  
BUSHFIELD M, 1990, MOL PHARMACOL, V38, P848
[2]  
Fujimori H, 1998, BIOL PHARM BULL, V21, P624
[3]  
Fujimori H, 1998, BIOL PHARM BULL, V21, P1348
[4]  
FUJIMORI H, 1991, CHEM EXPRESS, V6, P715
[5]   FUNGAL METABOLITES .11. A POTENT IMMUNOSUPPRESSIVE ACTIVITY FOUND IN ISARIA-SINCLAIRII METABOLITE [J].
FUJITA, T ;
INOUE, K ;
YAMAMOTO, S ;
IKUMOTO, T ;
SASAKI, S ;
TOYAMA, R ;
CHIBA, K ;
HOSHINO, Y ;
OKUMOTO, T .
JOURNAL OF ANTIBIOTICS, 1994, 47 (02) :208-215
[6]  
JOHNSON RA, 1989, MOL PHARMACOL, V35, P681
[7]   REGULATION OF KETOGENESIS AND THE RENAISSANCE OF CARNITINE PALMITOYLTRANSFERASE [J].
MCGARRY, JD ;
WOELTJE, KF ;
KUWAJIMA, M ;
FOSTER, DW .
DIABETES-METABOLISM REVIEWS, 1989, 5 (03) :271-284
[8]   SERINE PALMITOYLTRANSFERASE IS THE PRIMARY TARGET OF A SPHINGOSINE-LIKE IMMUNOSUPPRESSANT, ISP-1/MYRIOCIN [J].
MIYAKE, Y ;
KOZUTSUMI, Y ;
NAKAMURA, S ;
FUJITA, T ;
KAWASAKI, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 211 (02) :396-403
[9]   Dual roles of sphingolipids in signaling of the escape from and onset of apoptosis in a mouse cytotoxic T-cell line, CTLL-2 [J].
Nakamura, S ;
Kozutsumi, Y ;
Sun, YD ;
Miyake, Y ;
Fujita, T ;
Kawasaki, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (03) :1255-1257
[10]   THE ROLE OF LIPID-PEROXIDATION IN LIVER-DAMAGE [J].
POLI, G ;
ALBANO, E ;
DIANZANI, MU .
CHEMISTRY AND PHYSICS OF LIPIDS, 1987, 45 (2-4) :117-142