Kinetics of decreased LPS-stimulated cytokine release by macrophages exposed to CO2

被引:85
作者
West, MA [1 ]
Baker, J [1 ]
Bellingham, J [1 ]
机构
[1] MINNEAPOLIS MED RES FDN INC,LAB SURG CELLULAR BIOL & METAB,MINNEAPOLIS,MN
关键词
D O I
10.1006/jsre.1996.0259
中图分类号
R61 [外科手术学];
学科分类号
摘要
The mechanisms responsible for the lack of inflammation after laparoscopic surgery remain unknown. Peritoneal macrophages (MO) incubated in carbon dioxide (CO2), but not air or helium (He), had significant, reversible inhibition of lipopolysaccharide (LPS)-stimulated tumor necrosis factor (TNF) and interleukin-1 (IL-1) release, In these experiments the kinetics of these CO2-induced alterations in cytokine secretion were examined. Murine peritoneal MO were stimulated with LPS for 4 hr and incubated in different test gases (95% air/5% CO2, 80% CO2/20% O-2, 80% He/20% O-2) for intervals between 0.25 and 4 hr. Time between gas incubation and LPS stimulation was varied to determine the persistence of CO2 inhibition. Parallel MO groups received LPS stimulation 24 hr later. Supernatant TNF and IL-1 were measured by bioassay and polymerase chain reaction was used to examine cytokine mRNA. Significant reversible inhibition of TNF and IL-1 was seen with CO2, but not He or air. Inhibition of IL-1 occurred 15 min after CO2 exposure, was associated with decreased IL-1 mRNA, and was rapidly lost following incubation in the control atmosphere. TNF inhibition was seen despite normal levels of TNF message, required more than 30 min of CO2 exposure, and persisted after CO2 removal, CO2 produced profound, reversible, inhibition of LPS-stimulated cytokine release by peritoneal MO. The transient inability to secrete inflammatory cytokines after CO2 exposure may explain the lack of systemic inflammation after laparoscopic surgery with CO2. (C) 1996 Academic Press, Inc.
引用
收藏
页码:269 / 274
页数:6
相关论文
共 25 条
  • [1] AGGARWAL BB, 1985, METHOD ENZYMOL, V116, P441
  • [2] LAPAROSCOPIC VERSUS OPEN INGUINAL HERNIORRHAPHY - PRELIMINARY-RESULTS OF A RANDOMIZED CONTROLLED TRIAL
    BARKUN, JS
    WEXLER, MJ
    HINCHEY, EJ
    THIBEAULT, D
    MEAKINS, JL
    [J]. SURGERY, 1995, 118 (04) : 703 - 710
  • [3] Carozzi S, 1994, ASAIO J, V40, P20
  • [4] CHO JM, 1994, SURG ENDOSC-ULTRAS, V8, P1380
  • [5] SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION
    CHOMCZYNSKI, P
    SACCHI, N
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) : 156 - 159
  • [6] COLLET D, 1995, SURG ENDOSC-ULTRAS, V9, P1059
  • [7] TUMOR-NECROSIS-FACTOR (CACHECTIN) IS AN ENDOGENOUS PYROGEN AND INDUCES PRODUCTION OF INTERLEUKIN-1
    DINARELLO, CA
    CANNON, JG
    WOLFF, SM
    BERNHEIM, HA
    BEUTLER, B
    CERAMI, A
    FIGARI, IS
    PALLADINO, MA
    OCONNOR, JV
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 163 (06) : 1433 - 1450
  • [8] INTERLEUKIN-1
    DINARELLO, CA
    [J]. REVIEWS OF INFECTIOUS DISEASES, 1984, 6 (01): : 51 - 95
  • [9] GLASER F, 1995, ANN SURG, V221, P372
  • [10] ENDOTOXIN-RESPONSIVE SEQUENCES CONTROL CACHECTIN TUMOR NECROSIS FACTOR BIOSYNTHESIS AT THE TRANSLATIONAL LEVEL
    HAN, J
    BROWN, T
    BEUTLER, B
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 171 (02) : 465 - 475