Burn trauma initiates a pathophysiologic cascade, which includes cardiac dy
sfunction and intramyocyte calcium accumulation This study examined the hyp
othesis that therapeutic interventions which limit intracellular cardiac Ca
2+ accumulation after burn trauma will improve cardiac function. Guinea pig
s were anesthetized (methoxyflurane), burned over 43% of total body surface
area, and fluid resuscitated (FR) for 24 h. Burn guinea pigs were randomly
divided into three groups: Group 1, FR alone, Group 2, FR plus dantrolene
(10 mg/kg body wt, IV, 30 min, 8 and 22 h postburn), a drug which inhibits
the Ca2+ release channel (ryanodine receptor) of the cardiac sarcoplasmic r
eticulum, and Group 3, FR plus diltiazem (0.20-0.22 mg/kg given IV as a slo
w infusion over 6 h postburn), a drug which specifically blocks Ca2+ slow c
hannels; sham burn guinea pigs were given vehicle (Group 4), dantrolene (Gr
oup 5), or diltiazem (Group 6) as described above (respective controls). Ca
rdiac dysfunction was impaired in fluid-treated burns (Group 1) compared to
sham burns (Group 4) as indicated by reduced developed left ventricular pr
essure (LVP) (86 +/- 2 vs 52 + 3 mm Hg, P < 0.05), rate of LVP rise, (+dP/d
t max, 1379 +/- 64 vs 909 +/- 44 mm Hg/s, P < 0.05), and LVP fall (-dP/dt m
ax, 1184 +/- 31 vs 881 +/- 40 mm Hg/s, P < 0.05), and time to peak pressure
(110 +/- 2 vs 102 +/- 2 ms, P < 0.05). In addition, [Ca2+](i) rose in card
iomyocytes harvested from fluid-treated burns (Group 1, 307 +/- 29 nM) comp
ared to vehicle-treated controls (Group 4, 152 +/- 6 nM, P < 0.05). Neither
calcium antagonist altered ventricular function or [Ca2+](i) in sham burns
(Groups 5 and 6). In contrast, antagonists given after burn injury reduced
cardiomyocyte [Ca2+](i) (Group 2, dantrolene-treated burns: 196 +/- 8 nM,
and Group 3, diltiazem treated burns: 216 +/- 8 nM) and improved cardiac pe
rformance compared to that measured in burns given FR alone. Our data sugge
st that calcium antagonists given after burn trauma restored intracellular
Ca2+ homeostasis, decreased cardiac cell injury, and improved cardiac contr
actile function, (C) 1999 Academic Press.