Nitric oxide is not involved in lipopolysaccharide and cytokine mixture-induced cellular injuries in primary cultured hepatocytes

被引:7
作者
Liang, JF
Akaike, T
Kim, SC
机构
[1] TOKYO INST TECHNOL,DEPT BIOMOL ENGN,YOKOHAMA,KANAGAWA 227,JAPAN
[2] KOREA ADV INST SCI & TECHNOL,DEPT SCI BIOL,TAEJON 305701,SOUTH KOREA
关键词
D O I
10.1006/bbrc.1997.7700
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nitric oxide (NO) from artificial NO donors induces cell death through complete inhibition of mitochondrial respiration of hepatocytes. Treatment of hepatocytes with lipopolysaccharide (LPS) and cytokine mixture (interferon gamma and tumor necrosis factor alpha) not only results in NO production but also causes cellular respiration suppression and cell death in hepatocytes. N-G-monomethyl-L-arginine, a specific inhibitor of nitric oxide synthase, inhibits hepatocyte NO synthesis but cannot prevent hepatocytes from LPS and cytokine mixture-induced cellular injuries. Similarly, some metabolic intermediates capable of inhibiting hepatocyte NO synthesis cannot block LPS and cytokine mixture-mediated cellular injuries in hepatocytes. These results imply that lipopolysaccharide and cytokine mixture-induced cellular injuries and NO syntheses are parallel events, NO is not involved in LPS and cytokine mixture-induced cell damage. (C) 1997 Academic Press.
引用
收藏
页码:664 / 668
页数:5
相关论文
共 24 条
[11]   INHIBITION OF NITRIC-OXIDE SYNTHESIS DURING ENDOTOXEMIA PROMOTES INTRAHEPATIC THROMBOSIS AND AN OXYGEN RADICAL-MEDIATED HEPATIC-INJURY [J].
HARBRECHT, BG ;
BILLIAR, TR ;
STADLER, J ;
DEMETRIS, AJ ;
OCHOA, J ;
CURRAN, RD ;
SIMMONS, RL .
JOURNAL OF LEUKOCYTE BIOLOGY, 1992, 52 (04) :390-394
[12]   NITRIC-OXIDE SYNTHESIS SERVES TO REDUCE HEPATIC DAMAGE DURING ACUTE MURINE ENDOTOXEMIA [J].
HARBRECHT, BG ;
BILLIAR, TR ;
STADLER, J ;
DEMETRIS, AJ ;
OCHOA, JB ;
CURRAN, RD ;
SIMMONS, RL .
CRITICAL CARE MEDICINE, 1992, 20 (11) :1568-1574
[13]   INDUCTION OF HEPATIC ITO CELL NITRIC-OXIDE PRODUCTION AFTER ACUTE ENDOTOXEMIA [J].
HELYAR, L ;
BUNDSCHUH, DS ;
LASKIN, JD ;
LASKIN, DL .
HEPATOLOGY, 1994, 20 (06) :1509-1515
[14]   DIFFERENTIAL INDUCTION OF BRAIN, LUNG AND LIVER NITRIC-OXIDE SYNTHASE BY ENDOTOXIN IN THE RAT [J].
KNOWLES, RG ;
MERRETT, M ;
SALTER, M ;
MONCADA, S .
BIOCHEMICAL JOURNAL, 1990, 270 (03) :833-836
[15]   Nitric oxide-associated regulation of hepatocyte glutathione synthesis is a guanylyl cyclase-independent event [J].
Kuo, PC ;
Abe, KY .
SURGERY, 1996, 120 (02) :309-314
[16]   Interleukin-1-induced nitric oxide production modulates glutathione synthesis in cultured rat hepatocytes [J].
Kuo, PC ;
Abe, KY ;
Schroeder, RA .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 271 (03) :C851-C862
[17]   Role of metabolic intermediates in lipopolysaccharide/cytokine-mediated production of nitric oxide in isolated mouse hepatocytes [J].
Liang, JF ;
Akaike, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 236 (02) :379-382
[18]  
MOLINA VL, 1992, J BIOL CHEM, V267, P24929
[19]  
MORITA M, 1995, HEPATOLOGY, V21, P1585, DOI 10.1016/0270-9139(95)90463-8
[20]   TUMOR-NECROSIS-FACTOR-ALPHA DIFFERENTIALLY MODULATES THE CELLULAR-RESPONSE OF RAT HEPATOCYTES IN PERIPORTAL-EQUIVALENT AND PERICENTRAL-EQUIVALENT CULTURES [J].
OHNO, K ;
MAIER, P .
EUROPEAN JOURNAL OF PHARMACOLOGY-ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY SECTION, 1995, 292 (3-4) :205-214