Epidemiological studies have reported that elderly individuals have a highe
r risk of detrimental responses following exposure to elevated levels of am
bient particulate matter. To investigate this finding in a toxicological mo
del, aged Fisher rats were exposed for 3 days to concentrated urban air par
ticles (CAPs) from Boston. The hypothesis tested was that older animals wou
ld exhibit more severe pulmonary inflammation and hematological changes fol
lowing the CAPs exposure when compared to young normal animals. Aged Fisher
rats (> 77 mo) and juvenile Fisher rats (4-6 wk) were maintained in a viru
s-antigen free facility for 3 mo prior to exposure. Following this period,
aged and young rats were exposed to CAPs or sham-exposed to filtered air fo
r 5 h/day for 3 consecutive days (10 rats/group x 4 groups total = 40 rats)
. Daily integrated CAPs concentrations were 80, 170, and 50 mu g/m(3) on da
y 1, 2, and 3, respectively. None of the animals died throughout the durati
on of exposure. Twenty-Tour hours following the last day of exposure, blood
was collected by cardiac puncture, and bronchoalveolar lavage (BAL) was pe
rformed. Young rats had significantly higher total BAL cell counts compared
to old rats, as weil as a significant increase in BAL polymorphonuclear le
ukocytes (PMN) following CAPs exposure compared to sham. Old rats also exhi
bited a small, but significant increase in BAL PMN following exposure to CA
Ps compared to sham. There were no CAPs-related significant changes in aged
animals in total BAL cell counts, BAL lactate dehydrogenase, total white b
lood cell (WBC) counts, or the percent of WBC PMN, lymphocytes, and monocyt
es. When comparing aged versus young (CAPs- or filtered air-exposed) animal
s, advanced age was associated with significant decrements in the total BAL
cell counts, total WBC counts, percent or blood lymphocytes, and blood hem
oglobin, a significant increase in the percent of blood PMN was also observ
ed. The above results suggest: (1) Young fisher rats may represent a sensit
ive model for the examination of pulmonary inflammatory responses following
CAPs exposure, and (2) the lack of a pulmonary inflammatory response in th
e aged rats, despite the presence of a higher percentage of circulating neu
trophils, may reflect decreased sensitivity to inhaled particles.