1. We investigated the effects of 1-(3-tert-butyl-2-hydroxy-5-methoxyphenyl
)-3-(3-pyridylmethyl)urea hydrochloride (T-0162), a novel low-molecular wei
ght free radical scavenger, on the generation of superoxide anions and hydr
oxyl radicals in vitro and in vivo and on myocardial infarct (MI) size in a
n in vivo model of MI in rabbits.
2. It was found that T-0162 scavenged both superoxide anions and hydroxyl r
adicals in a concentration-dependent manner in vitro.
3. In an in vivo rabbit model with 30 min coronary occlusion and 30 min rep
erfusion, T-0162 scavenged hydroxyl radicals generated in the myocardium du
ring reperfusion.
4. Anaesthetized open-chest Japanese white male rabbits were subjected to 3
0 min coronary occlusion and 48 h reperfusion. The control group (n = 10) w
as infused with 10% lecithin solution for 220 min from 10 min before occlus
ion to 180 min after reperfusion. The pretreatment group (n = 10) was infus
ed with T-0162 dissolved in 10% lecithin solution for 220 min from 10 min b
efore occlusion to 180 min after reperfusion at a rate of 400 mu g/kg per m
in. The post-treatment group (n = 10) was injected with an i.v. bolus of 10
mg/kg T-0162 and was then infused with 400 mu g/kg per min T-0162 for 190
min from 10 min before reperfusion to 180 min after reperfusion. After 48 h
reperfusion, infarct size was measured histologically and expressed as a p
ercentage of area at risk (AAR).
5. There was no significant difference in haemodynamic parameters among the
three groups throughout the experimental period. The per cent infarct size
of the AAR in the T-0162 groups (24.8 +/- 4.3 and 30.5 +/- 3.9% for pre- a
nd posttreatment groups, respectively) was significantly reduced compared w
ith control (44.7 +/- 4.1%: P < 0.05). There was no significant difference
in the AAR among the three groups.
6. In conclusion, T-0162 reduces MI size through the inhibition of reperfus
ion injury.