Calcium antagonists improve cardiac mechanical performance after thermal trauma

Citation
Jw. Horton et al., Calcium antagonists improve cardiac mechanical performance after thermal trauma, J SURG RES, 87(1), 1999, pp. 39-50
Citations number
47
Categorie Soggetti
Surgery,"Medical Research Diagnosis & Treatment
Journal title
JOURNAL OF SURGICAL RESEARCH
ISSN journal
00224804 → ACNP
Volume
87
Issue
1
Year of publication
1999
Pages
39 - 50
Database
ISI
SICI code
0022-4804(199911)87:1<39:CAICMP>2.0.ZU;2-G
Abstract
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.