Treatment with recombinant bactericidal/permeability-increasing protein to prevent endotoxin-induced mortality in bile duct-ligated rats

被引:22
作者
Kimmings, AN
van Deventer, SJH
Obertop, H
Gouma, DJ
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Surg, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Ctr Hemostasis Thrombosis Atherosclerosis & Infla, NL-1105 AZ Amsterdam, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Lab Expt Internal Med, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1016/S1072-7515(99)00164-7
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background: Operation in patients with obstructive jaundice is associated with substantial morbidity because of increased susceptibility to endotoxin (lipopolysaccharide) and the inflammatory cascade. Different interventions to reduce endotoxemia and cytokine induction, and resulting complications, have been studied. Bactericidal/permeability-increasing protein (BPI) is a naturally occurring endotoxin-binding protein produced in neutrophils. It binds endotoxin, neutralizing the activity and inhibiting cytokine production by mononuclear cells. In experimental endotoxemia in animals and in healthy human volunteers, BPI has shown a protective effect; The aim of this study was to determine whether BPI could protect against increased endotoxin sensitivity in rats with obstructive jaundice and reduce endotoxin-induced mortality. Study Design: Male Wistar rats were used. Intraperitoneal Escherichia coli 2 mg/kg was given 1 week after sham operation or bile duct ligation (BDL). Three groups were studied: sham, BDL with placebo, and BDL with 5 mg/kg recombinant BPI21. Results: BDL rats were jaundiced (mean bilirubin 186 mu mol/L; no difference between BDL rats without or with BPI). Bilirubin remained less than 1 mu mol/L in sham-operated rats (p = 0.002). Endotoxin levels were 3.4 pg/mL in sham controls and 3.1 pg/mL in BDL rats before administration of-lipopolysaccharide (p=NS) Two hours after administration, levels were 615.4 ng/mL in placebo BDL rats and 10 times less in BPI-treated BDL rats, at 60.2 ng/mL (p = 0.03). The same trend was found at 6 hours. At 24 hours, mortality was 1 of 6 in sham-operated rats (15%) versus 8 of 11 in untreated BDL rats (75%). BPI intervention reduced the death rate to 1 of 12 BDL rats (8%) (p = 0.003). Conclusions: Intraperitoneal recombinant BPI21 in rats having BDL reduced endotoxin-induced mortality from 75% to 8%, a death rate comparable to that in nonjaundiced rats. BPI could be an interesting perioperative treatment in clinical obstructive jaundice. (J Am Coil Surg 1999;189:374-379. (C) 1999 by the American College of Surgeons).
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页码:374 / 379
页数:6
相关论文
共 25 条
[1]   HIDDEN ENDOTOXIN IN PLASMA OF PATIENTS WITH ALCOHOLIC LIVER-DISEASE [J].
BODE, C ;
FUKUI, H ;
BODE, JC .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 1993, 5 (04) :257-262
[2]  
BOERMEESTER MA, 1995, AM J PATHOL, V147, P1428
[3]   PRESENCE OF BACTERICIDAL PERMEABILITY-INCREASING PROTEIN IN DISEASE - DETECTION BY ELISA [J].
DENTENER, MA ;
FRANCOT, GJM ;
SMIT, FT ;
FROON, AHM ;
PENNINGS, HJ ;
WOUTERS, EFM ;
BUURMAN, WA .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (03) :739-743
[4]   ROLE OF TUMOR NECROSIS FACTOR IN THE ENHANCED SENSITIVITY OF MICE TO ENDOTOXIN AFTER EXPOSURE TO LEAD [J].
DENTENER, MA ;
GREVE, JW ;
MAESSEN, JG ;
BUURMAN, WA .
IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY, 1989, 11 (2-3) :321-334
[5]  
DIAMOND T, 1990, SURGERY, V108, P370
[6]  
Diamond T, 1991, HPB Surg, V4, P81, DOI 10.1155/1991/48672
[7]   THE ROLE OF BILE AND BILE-ACIDS IN BACTERIAL TRANSLOCATION IN OBSTRUCTIVE-JAUNDICE IN RATS [J].
DING, JW ;
ANDERSSON, R ;
SOLTESZ, V ;
WILLEN, R ;
BENGMARK, S .
EUROPEAN SURGICAL RESEARCH, 1993, 25 (01) :11-19
[8]   LIPOPOLYSACCHARIDE TOXICITY-REGULATING PROTEINS IN BACTEREMIA [J].
FROON, AHM ;
DENTENER, MA ;
GREVE, JWM ;
RAMSAY, G ;
BUURMAN, WA .
JOURNAL OF INFECTIOUS DISEASES, 1995, 171 (05) :1250-1257
[9]  
GOUMA DJ, 1987, ARCH SURG-CHICAGO, V122, P731
[10]   PREVENTION OF POSTOPERATIVE COMPLICATIONS IN JAUNDICED RATS - INTERNAL BILIARY DRAINAGE VERSUS ORAL LACTULOSE [J].
GREVE, JW ;
MAESSEN, JG ;
TIEBOSCH, T ;
BUURMAN, WA ;
GOUMA, DJ .
ANNALS OF SURGERY, 1990, 212 (02) :221-227