1 This study was carried out to investigate novel cardioprotective effects
of urea and the underlying mechanisms. The cardiac functions under oxidativ
e stress were evaluated using Langendorff perfused isolated heart.
2 Isolated dogfish shark hearts tolerated the oxidative stress generated by
electrolysis (10 mA, min) of the perfusion solution (n=4), and also showed
normal cardiac functions during postischaemia reperfusion (n = 4). The hig
h concentration of urea (350 mM) in the heart perfusate was indispensable f
or maintaining the normal cardiac functions of the shark heart.
3 Urea at 3-300 mM (n=4 for each group) protected the isolated rat heart ag
ainst both electrolysis-induced heart damage and post-ischaemia reperfusion
-induced cardiac injury.
4 A concentration-dependent scavenging effect of urea (3-300 mM, n=4 for ea
ch group) against electrolysis-induced reactive oxygen species was also dem
onstrated ill vitro.
5 Urea derivatives as hydroxyurea, dimethylurea, and thiourea had antioxida
nt cardioprotective effect against the electrolysis-induced cardiac dysfunc
tion of rat heart, but were not as effective as urea in suppressing the pos
t-ischaemia reperfusion injury.
6 Our results suggest that urea and its derivatives are potential antioxida
nt cardioprotective agents against oxidative stress-induced myocardium dama
ge including the post-ischaemia reperfusion-induced injury.