The influence of polymorphonuclear leukocytes on altered pulmonary epithelial permeability during ozone exposure

Toxicology ◽  
1998 ◽  
Vol 127 (1-3) ◽  
pp. 17-28 ◽  
Author(s):  
Paul G Reinhart ◽  
David J.P Bassett ◽  
Deepak K Bhalla
CHEST Journal ◽  
1998 ◽  
Vol 113 (2) ◽  
pp. 459-466 ◽  
Author(s):  
Ulf Ludwigs ◽  
Anders Philip

1986 ◽  
Vol 61 (3) ◽  
pp. 971-981 ◽  
Author(s):  
I. H. Ahmed ◽  
E. el-Khatib ◽  
J. W. Logus ◽  
G. C. Man ◽  
J. Jacques ◽  
...  

A radioaerosol scanning technique measuring regional clearance of sodium pertechnetate (99mTcO-4) and 99mTc-labeled diethylenetriaminepentaacetate (99mTc-DTPA) was used to assess changes in canine pulmonary epithelial permeability following lung irradiation. Doses of 2,000 cGy (11 dogs), 1,000 cGy (2 dogs), and 500 cGy (2 dogs) were given in one fraction to either the entire right hemithorax (500 cGy) or the right lower lung (1,000 and 2,000 cGy). Radioaerosol scans, chest roentgenograms, and computerized tomograms (CT) were obtained before and serially after irradiation. A dose of 2,000 cGy resulted in a decrease in regional pulmonary epithelial permeability to both 99mTcO4- and 99mTc-DTPA; both showed significant decreases from the 2nd wk postirradiation onward. In comparison, CT and chest roentgenogram did not become abnormal until 7.1 +/- 2.8 (SD) and 8.2 +/- 2.6 wk, respectively. Doses of 1,000 and 500 cGy produced reversible decreases in 99mTcO4- clearance. Lung morphology showed definite changes of radiation pneumonitis after 2,000 and 1,000 cGy but not after 500 cGy at approximately 9, 17, and 12 wk postirradiation, respectively. These results suggest that dose-dependent changes in pulmonary physiology may precede obvious structural alterations in radiation lung injury.


Thorax ◽  
1982 ◽  
Vol 37 (3) ◽  
pp. 169-174 ◽  
Author(s):  
J G Jones ◽  
B D Minty ◽  
J M Beeley ◽  
D Royston ◽  
J Crow ◽  
...  

1985 ◽  
Vol 1 (1) ◽  
pp. 52-57 ◽  
Author(s):  
Arlene A. Hutchison ◽  
Kenneth J. McNicol ◽  
Gerald M. Loughlin

Thorax ◽  
1985 ◽  
Vol 40 (10) ◽  
pp. 734-740 ◽  
Author(s):  
A R Gellert ◽  
C A Lewis ◽  
J A Langford ◽  
S E Tolfree ◽  
R M Rudd

1993 ◽  
Vol 265 (1) ◽  
pp. L33-L37
Author(s):  
M. Takahashi ◽  
S. R. Kleeberger ◽  
T. L. Croxton

The effects of ozone on tracheal electrical potential were investigated in inbred strains of mice that are differentially susceptible to ozone-induced inflammation. In male mice (9–13 wk), a tracheostomy was made under pentobarbital anesthesia for spontaneous breathing and tracheal potential was measured in the cephalad portion of the bisected trachea using Hanks' salt/agar-capped KCl bridges connected to a pair of calomel half cells. The mean tracheal potentials of five different strains of mice (C3H/HeJ, DBA/2J, C57BL/6J, BALB/cJ, and 129/J) were approximately 10 mV (lumen negative) with no significant interstrain difference. Amiloride reduced mouse tracheal potentials by approximately 70% in both C3H/HeJ and C57BL/6J mice, indicating that sodium absorption is the predominant ion transport across this tissue. Relative to air-exposed controls, acute ozone exposure (2 ppm for 3 h) significantly attenuated tracheal potential of inflammation-susceptible C57BL/6J mice by approximately 50% at 6 h and 40% at 24 h postexposure but had no effect immediately after exposure. The mean tracheal potential of C3H/HeJ mice was not changed by ozone. The differential effect of acute ozone exposure on tracheal potential in C57BL/6J and C3H/HeJ mice is consistent with differential susceptibility to ozone-induced increases in epithelial permeability in these strains.


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