The cardioprotective effects of bisoprolol were studied in a rat model of s
evere heart failure induced by autoimmune myocarditis. Twenty-eight days af
ter immunization, Lewis rats were divided into four groups: 0.1 mg/kg/day b
isoprolol (Group 0.1), 1.0 mg/kg/day bisoprolol (Group 1) and 10 mg/kg/day
bisoprolol (Group 10), and vehicle (0.5% methylcellulose; Group V) (all gro
ups, n = 13). After oral administration for 1 month, heart weight, mean blo
od pressure, heart rate, central venous pressure, peak left ventricular pre
ssure, left ventricular end-diastolic pressure, +/- dP/dt, and area of fibr
osis were measured. Although bisoprolol reduced heart rate (399 +/- 11/min
in Group V, 382 +/- 10/min in Group 0.1, 348 +/- 8/min in Group 1 and 302 /- 9/min in Group 10) and increased survival (62% in Group V 69% in Group 0
.1, and 100% in Group 1 and Group 10) in a dose-dependent manner, this drug
did not change heart weight, the area of myocardial fibrosis or hemodynami
c parameters. These observations suggested that bisoprolol may improve surv
ival independently of its effect on left ventricular function by reducing s
udden death in patients with severe heart failure.