This study investigated the relationship between oxygen radicals and e
xsanguination-induced bronchoconstriction using antioxidant in guinea
pigs. To accomplish this, two phases of studies were carried out. In p
hase I, 34 guinea pigs weighing 342 +/- 11 g were divided into five gr
oups: control (n = 7); acute dimethylthiourea (DMTU, n = 7); chronic D
MTU (n = 8); superoxide dismutase (SOD, n = 6); and catalase (n = 6).
Animals in the control group were not treated. DMTU, SOD, and catalase
were employed for the scavenging of hydroxyl radical, superoxide anio
n, and hydrogen peroxide, respectively. Ten additional guinea pigs wei
ghing 293 +/- 6 g were divided into two groups in phase 2: sham (n = 6
) and chronic apocynin (n = 4). Animals in the sham group received inj
ections of the vehicle, whereas apocynin was used to suppress the prod
uction of superoxide anion. All animals were anesthetized, sternotomiz
ed, and artificially ventilated. Before (baseline) as well as at fixed
intervals 5-30 minutes following the exsanguination, the maximal expi
ratory flow maneuver was performed and the dynamic compliance (Cdyn) w
as obtained. Decreases in the maximal expiratory flow at 50% baseline
vital capacity and Cdyn were used as indicators of bronchoconstriction
. Exsanguination in the control and sham groups caused a gradual incre
ase in airway constriction with time that was significantly ameliorate
d by chronic DMTU and chronic apocynin pretreatments but was not affec
ted by other acute treatments. These results indicate that chronic tre
atment with antioxidants ameliorates exsanguination-induced, tachykini
n-mediated airway constriction.