Assessment of lung inflammation in a mouse model of smoke inhalation and burn injury: Strain-specific differences

Toxicology Mechanisms and Methods

Volumn 18, Issue 7, 2008, Pages 551-559

  Jacob, Sam ^a   Deyo, Donald J ^a   Cox, Robert A ^a   Traber, Daniel L ^a   Hawkins, Hal K ^a  

^a SHRINERS HOSPITALS FOR CHILDREN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BUPRENORPHINE; EVANS BLUE; KETAMINE; MYELOPEROXIDASE; SODIUM CHLORIDE; XYLAZINE;

ACUTE LUNG INJURY; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APNEA; ARTICLE; BAGG ALBINO MOUSE; BODY SURFACE; C57BL 6 MOUSE; CONTROLLED STUDY; DISEASE MODEL; ENDOTRACHEAL INTUBATION; ENZYME IMMUNOASSAY; LUNG BURN; LUNG PERFUSION; LUNG WEIGHT; MALE; MOUSE; NONHUMAN; PNEUMONIA; PRIORITY JOURNAL; STRAIN DIFFERENCE;

ANIMALIA; GOSSYPIUM HIRSUTUM; MURINAE; MUS; OVIS;

EID: 51649100828     PISSN: 15376516     EISSN: 15376524     Source Type: Journal    
DOI: 10.1080/15376510802251993     Document Type: Article

References (35)

1. Atochina, E. N., Beers, M. F., Tomer, Y., Scanlon, S. T., Russo, S. J., Panettieri, R. A., , and Haczku, A. 2003. Attenuated allergic airway hyperresponsiveness in C57BL/6 mice is associated with enhanced surfactant protein (SP)-D production following allergic sensitization. Respir. Res. 4:15.
2. Barrow, R. E. 1990. Chemical structure of phospholipids in the lungs and airways of sheep. Respir. Physiol. 79:1-8.
3. Barrow, R. E., Morris, S. E., Linares, H. A., and Herndon DN. 1991. Tracheal venous blood and lymph collection: a model to study airway injury in sheep. J. Appl. Physiol. 70:1645-1649.
4. Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:248-254.
5. Cox, R. A., Burke, A. S., and Soejima, K. 2003. Airway obstruction in sheep with burn and smoke inhalation injuries. Am. J. Respir. Cell Mol. Biol. 29:295-302.
6. Cox, R. A., Mlcak, R. P., and Chinkes, D. L. 2008. Upper airway mucus deposition in lung tissue of burn trauma victims. Shock 29:356-361.
7. Cox, R. A., Burke, A. S., Traber, D. L., Herndon, D. N., and Hawkins, H. K. 2007. Production of pro-inflammatory polypeptides by airway mucous glands and its potential significance. Pulm. Pharmacol. Ther. 20:172-177.
8. Dodd-o, J. M., Hristopoulos, M. L., Welsh-Servinsky, L. E., Tankersley, C. G., and Pearse D. B. 2006. Strain-specific differences in sensitivity to ischemia-reperfusion lung injury in mice. J. Appl. Physiol. 100:1590-1595.
9. Dost, F. N. 1991. Acute toxicology of components of vegetation smoke. Rev. Environ. Contam. Toxicol. 119:1-46.
10. Enkhbaatar, P., and Traber, D. L. 2004. Pathophysiology of acute lung injury in combined burn and smoke inhalation injury. Clin. Sci. (Lond). 107:137-143.
11. Gur, I., Or, R., Segel, M. J., Shriki, M., Izbicki, G., and Breuer, R. 2000. Lymphokines in bleomycin-induced lung injury in bleomycin-sensitive C57BL/6 and -resistant BALB/c mice. Exp. Lung Res. 26:521-534.
12. Hoyt, D. G., and Lazo, J. S. 1992. Murine strain differences in acute lung injury and activation of poly(ADP-ribose) polymerase by in vitro exposure of lung slices to bleomycin. Am. J. Respir. Cell Mol. Biol. 7:645-651.
13. Kolb, M., Bonniaud, P., Galt, T., Sime, P. J., Kelly, M. M., Margetts, P. J., and Gauldie, J. 2002. Differences in the fibrogenic response after transfer of active transforming growth factor-beta1 gene to lungs of "fibrosis-prone" and "fibrosis-resistant" mouse strains. Am. J. Respir. Cell Mol. Biol. 27:141-150.
14. LaLonde, C., Nayak, U., Hennigan, J., and Demling, R. 1996. Antioxidants prevent the cellular deficit produced in response to burn injury. J. Burn Care Rehabil. 17:379-383.
15. Lee, H. M., Greeley, G. H., Herndon, D. N., Sinha, M., Luxon, B. A., and Englander, E. W. 2005. A rat model of smoke inhalation injury: influence of combustion smoke on gene expression in the brain. Toxicol. Appl. Pharmacol. 208:255-265.
16. Linares, H. A. 1981. A report of 115 consecutive autopsies in burned children: 1966-80. Burns 8:263-270.
17. Ma, B., Blackburn, M. R., Lee, C. G., Homer, R. J., Liu, W., Flavell, R. A., Boyden, L., Lifton, R. P., Sun, C. X., Young, H. W., and Elias, J. A. 2006. Adenosine metabolism and murine strain-specific IL-4-induced inflammation, emphysema, and fibrosis. J. Clin. Invest. 116:1274-1283.
18. Mizutani, A., Enkhbaatar, P., Esechie, A., Traber, L. D., Cox, R. A., Hawkins, H. K., Deyo,,D. J., Murakami, K., Noguchi, T., and Traber, D. L. 2008. Pulmonary changes in a mousemodel of combined burn and smoke inhalation-induced injury. J. Appl. Physiol. 105:678-684.
19. Mogil, J. S., Smith, S. B., O'Reilly, M. K., and Plourde, G. 2005. Influence of nociception and stress-induced antinociception on genetic variation in isoflurane anesthetic potency among mouse strains. Anesthesiology 103:751-758.
20. Ozaki, M., Ozaki, K., Watanabe, T., Uwagawa, S., Okuno, Y., and Shirai, T. 2005. Susceptibilities of p53 knockout and rasH2 transgenic mice to urethane-induced lung carcinogenesis are inherited from their original strains. Toxicol. Pathol. 33:267-271.
21. Peng, X., Hassoun, P. M., Sammani, S., McVerry, B. J., Burne, M. J, Rabb, H., Pearse, D., Tuder, R. M., and Garcia, J. G. 2004. Protective effects of sphingosine 1-phosphate in murine endotoxin-induced inflammatory lung injury. Am. J. Respir. Crit. Care Med. 169:1245-1251.
22. Preston, J. A., Beagley, K. W., Gibson, P. G., and Hansbro, P. M. 2004. Genetic background affects susceptibility in nonfatal pneumococcal bronchopneumonia. Eur. Respir. J. 23:224-231.
23. Prows, D. R., Daly, M. J., Shertzer, H. G., and Leikauf, G. D. 1999. Ozone-induced acute lung injury: genetic analysis of F(2) mice generated from A/J and C57BL/6J strains. Am. J. Physiol. 277:L372-L380.
24. Rowland, R. R., Yamaguchi, K. T., Santibanez, A. S., Kodama, K. T., Ness, V. T., and Grubbs D. E. 1986. Smoke inhalation model for lung permeability studies. J. Trauma 26:153-156.
25. Sakurai, H., Johnigan, R., Kikuchi, Y., Harada, M., Traber, L. D., and Traber, D. L. 1998. Effect of reduced bronchial circulation on lung fluid flux after smoke inhalation in sheep. J. Appl. Physiol. 84:980-986.
26. Shirani, K. Z., Moylan, J. A., and Pruitt, B. A., 1987. The influence of inhalation injury and pneumonia on burn mortality. Ann. Surg. 205(1):82-87.
27. Stone, R. A., Tisher, C. C., Hawkins, H. K., and Robinson, R. R. 1973. Juxtaglomerular hyperplasia and hyperreninemia in progressive systemic sclerosis complicated by acute renal failure. Am. J. Med. 56:119-123.
28. Takeda, K., Haczku, A., Lee, J. J., Irvin, C. G., and Gelfand, E. W. 2001. Strain dependence of airway hyperresponsiveness reflects differences in eosinophil localization in the lung. Am. J. Physiol. Lung Cell Mol. Physiol. 281:L394-L402.
29. Tankersley, C. G., Fitzgerald, R. S., and Kleeberger, S. R. 1994. Differential control of ventilation among inbred strains of mice. Am. J. Physiol. Regul. Int. Comp. Physiol. 267:R1371-R1377.
30. Toliver-Kinsky, T. E., Varma, T. K., Lin, C. Y., Herndon, D. N., and Sherwood, E. R. 2002. Interferon-gamma production is suppressed in thermally injured mice: decreased production of regulatory cytokines and corresponding receptors. Shock 18:322-330.
31. Traber, D. L., and Herndon, D. N.Pathophysiology of smoke inhalation. In: Respiratory Injury, Ed. Haponik, E. F., and Munster, A. M. New York: McGraw-Hill, 1990, pp. 61-71.
32. Tsuno, K., Prato, P., and Kolobow, T. 1990. Acute lung injury from mechanical ventilation at moderately high airway pressures. J. Appl. Physiol. 69:956-961.
33. Wang, I. F., Patel, M., Razavi, H. M., Weicker, S., Joseph, M. G., McCormack, D. G., and Mehta, S. 2002. Role of inducible nitric oxide synthase in pulmonary microvascular protein leak in murine sepsis. Am. J. Respir. Crit. Care Med. 165:1634-1639.
34. Weissmann, N., Akkayagil, E., Quanz, K., Schermuly, R. T., Ghofrani, H. A., Fink, L., Hanze, J., Rose, F., Seeger, W., and Grimminger, F. 2004. Basic features of hypoxic pulmonary vasoconstriction inmice. Respir. Physiol. Neurobiol. 139:191-202.
35. Zhao, M., Fernandez, L. G., Doctor, A., Sharma, A. K., Zarbock, A., Tribble, C. G., Kron, I. L., and Laubach, E. 2006. Alveolar macrophage activation is a key initiation signal for acute lung ischemia-reperfusion injury. Am. J. Physiol. Lung Cell Mol. Physiol. 291:L1018-L1026.