The effect of lymphatic blockage on the amount of endotoxin in portal circulation, nitric oxide synthesis, and the liver in dogs with peritonitis

被引:12
作者
Güler, O [1 ]
Ugras, S [1 ]
Aydin, M [1 ]
Dilek, FH [1 ]
Dilek, ON [1 ]
Karaayvaz, M [1 ]
机构
[1] Yuzuncu Yil Univ, Fac Med, Dept Gen Surg, Van, Turkey
来源
SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY | 1999年 / 29卷 / 08期
关键词
peritonitis; endotoxin; nitric oxide; hepatic damage;
D O I
10.1007/s005950050501
中图分类号
R61 [外科手术学];
学科分类号
摘要
This study was performed to investigate the effect of lymphatic blockage on the amount of endotoxin in portal venous blood, nitric oxide synthesis, the release of aspartate aminotransferase (AST) from the liver, hepatic damage, and survival in an experimental model of dogs with peritonitis, The dogs were divided into a control group (group 1), an unligated thoracic duct peritonitis group (group 2), and a ligated thoracic duct peritonitis group (group 3), Peritoneal fluid and blood from the portal vein and femoral artery were taken for peritoneal culture, endotoxin, and AST assay, respectively, and liver biopsies were performed to assess for hepatic damage and for nitric oxide assay, There was a higher bacteria count in the peritoneal fluid from group 3 than in that from group 2 (P < 0.0001), Bacteria grew in all of the blood cultures from the group 2 animals, but growth was seen only in blood cultures from four of the group 3 animals. The levels of endotoxin, nitrite, and AST levels in group 3 were significantly increased in comparison with those in group 2 (P < 0.0001), Extensive hepatocellular necrosis,vith hemorrhage was observed in the livers of the group 3 animals, and all of them died,within 48 h, The results of this study suggest that the blockage of lymph flow has a negative effect on liver and survival in dogs with peritonitis, and that hepatic damage is directly related to the amount of endotoxin to which the liver is exposed,
引用
收藏
页码:735 / 740
页数:6
相关论文
共 24 条
[1]  
BANKEY PE, 1993, PATHOPHYSIOLOGY SHOC, P948
[2]   INDUCIBLE CYTOSOLIC ENZYME-ACTIVITY FOR THE PRODUCTION OF NITROGEN-OXIDES FROM L-ARGININE IN HEPATOCYTES [J].
BILLIAR, TR ;
CURRAN, RD ;
STUEHR, DJ ;
STADLER, J ;
SIMMONS, RL ;
MURRAY, SA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 168 (03) :1034-1040
[3]  
BILLIAR TR, 1989, SURGERY, V106, P364
[4]   KUPFFER CELL - HEPATOCYTE COCULTURES RELEASE NITRIC-OXIDE IN RESPONSE TO BACTERIAL-ENDOTOXIN [J].
BILLIAR, TR ;
CURRAN, RD ;
FERRARI, FK ;
WILLIAMS, DL ;
SIMMONS, RL .
JOURNAL OF SURGICAL RESEARCH, 1990, 48 (04) :349-353
[5]  
CERRA FB, 1987, SURGERY, V101, P1
[6]   NITRIC-OXIDE AND NITRIC OXIDE-GENERATING COMPOUNDS INHIBIT HEPATOCYTE PROTEIN-SYNTHESIS [J].
CURRAN, RD ;
FERRARI, FK ;
KISPERT, PH ;
STADLER, J ;
STUEHR, DJ ;
SIMMONS, RL ;
BILLIAR, TR .
FASEB JOURNAL, 1991, 5 (07) :2085-2092
[7]   MULTIPLE CYTOKINES ARE REQUIRED TO INDUCE HEPATOCYTE NITRIC-OXIDE PRODUCTION AND INHIBIT TOTAL PROTEIN-SYNTHESIS [J].
CURRAN, RD ;
BILLIAR, TR ;
STUEHR, DJ ;
OCHOA, JB ;
HARBRECHT, BG ;
FLINT, SG ;
SIMMONS, RL .
ANNALS OF SURGERY, 1990, 212 (04) :462-471
[8]   IMMUNE LYSIS OF HEPATOCYTES IN CULTURE - ACCURATE DETECTION BY ASPARTATE-AMINOTRANSFERASE RELEASE MEASUREMENT [J].
FEUTREN, G ;
LACOUR, B ;
BACH, JF .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 75 (01) :85-94
[9]  
FRY DE, 1980, ARCH SURG-CHICAGO, V115, P136
[10]   NITRATE BIOSYNTHESIS IN MAN [J].
GREEN, LC ;
DELUZURIAGA, KR ;
WAGNER, DA ;
RAND, W ;
ISTFAN, N ;
YOUNG, VR ;
TANNENBAUM, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (12) :7764-7768