An acute reversible experimental model of pneumonia in pigs: time-related histological and clinical signs changes

被引:7
作者
Villarino, N. [1 ]
Garcia-Tapia, D. [2 ]
Lesman, S. [2 ]
Lucas, M. [2 ]
Robinson, J. [2 ]
Brown, S. A. [2 ]
Martin-Jimenez, T. [1 ]
机构
[1] Univ Tennessee, Coll Vet Med, Dept Biomed & Diagnost Sci, Knoxville, TN 37996 USA
[2] Pfizer Anim Hlth, Kalamazoo, MI USA
关键词
ACUTE LUNG INJURY; BACTERIAL-ENDOTOXIN; INFLAMMATORY RESPONSE; RESPIRATORY-DISEASE; VENTILATED PIGLETS; EXPRESSION; VIRUS;
D O I
10.1111/j.1365-2885.2012.01415.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The objective of this study was to evaluate the long-term survival rates, clinical response, and lung gross and microscopic changes in pigs treated intratracheally with lipopolysaccharide of Escherichia coli 0111:B4 (LPS-Ec). Healthy pigs were randomly allocated to three groups: (i) no-LPS-Ec (n=1), (ii) LPS-Ec-T1 (1mg/mL, 10mL/pig) (n=7), and (iii) LPS-Ec-T2 (0.5mg/mL, 10mL/pig) (n=6). Two pigs from each dose group were euthanized at 24 (n=3 for T1), 48 and 144h post-LPS-Ec challenge. LPS-Ec-treated animals showed macroscopic lesions in middle lobes of the lung. A reversible recruitment of macrophages and neutrophils was observed at 24, 48, and 144h post-LPS-Ec challenge. The highest cellular infiltration level was observed at 24h after challenge. The highest clinical scores were evident in both experimental dose levels within 3 and 5h after LPS-Ec administration. Administration of LPS-Ec, under the conditions evaluated, can be used to induce a reproducible model of acute pulmonary inflammation in pigs.
引用
收藏
页码:241 / 247
页数:7
相关论文
共 15 条
  • [1] Arbibe L, 1997, J IMMUNOL, V159, P391
  • [2] Pathophysiologic correlates of acute porcine pleuropneumonia
    Baarsch, MJ
    Foss, DL
    Murtaugh, MP
    [J]. AMERICAN JOURNAL OF VETERINARY RESEARCH, 2000, 61 (06) : 684 - 690
  • [3] BRIGHAM KL, 1986, AM REV RESPIR DIS, V133, P913
  • [4] Structural and functional analyses of bacterial lipopolysaccharides
    Caroff, M
    Karibian, D
    Cavaillon, JM
    Haeffner-Cavaillon, N
    [J]. MICROBES AND INFECTION, 2002, 4 (09) : 915 - 926
  • [5] Lung deposition and efficiency of nebulized amikacin during Escherichia coli pneumonia in ventilated piglets
    Goldstein, I
    Wallet, F
    Nicolas-Robin, A
    Ferrari, F
    Marquette, CH
    Rouby, JJ
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 166 (10) : 1375 - 1381
  • [6] Pathophysiological changes occurring during Escherichia coli endotoxin and Pasteurella multocida challenge in piglets:: relationship with cough and temperature and predicitive value for intensity of lesions
    Halloy, DJ
    Bouhet, S
    Oswald, IP
    Goret-Nicaise, M
    Kobisch, M
    Mainil, J
    Gustin, PG
    [J]. VETERINARY RESEARCH, 2004, 35 (03) : 309 - 324
  • [7] Innate immune recognition: mechanisms and pathways
    Medzhitov, R
    Janeway, C
    [J]. IMMUNOLOGICAL REVIEWS, 2000, 173 : 89 - 97
  • [8] Effects of oral administration of tilmicosin on pulmonary inflammation in piglets experimentally infected with Actinobacillus pleuropneumoniae
    Nerland, EM
    LeBlanc, JM
    Fedwick, JP
    Morck, DW
    Merrill, JK
    Dick, P
    Paradis, MA
    Buret, AG
    [J]. AMERICAN JOURNAL OF VETERINARY RESEARCH, 2005, 66 (01) : 100 - 107
  • [9] Expression of toll-like receptor 2 and 4 in lipopolysaccharide-induced lung injury in mouse
    Saito, T
    Yamamoto, T
    Kazawa, T
    Gejyo, H
    Naito, M
    [J]. CELL AND TISSUE RESEARCH, 2005, 321 (01) : 75 - 88
  • [10] Signaling through the A2B Adenosine Receptor Dampens Endotoxin-Induced Acute Lung Injury
    Schingnitz, Ulrich
    Hartmann, Katherine
    MacManus, Christopher F.
    Eckle, Tobias
    Zug, Stephanie
    Colgan, Sean P.
    Eltzschig, Holger K.
    [J]. JOURNAL OF IMMUNOLOGY, 2010, 184 (09) : 5271 - 5279