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Departments of 1Surgery and 2Pediatrics, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9160
Submitted 23 September 2002 ; accepted in final form 18 February 2003
Early fluid resuscitation, antimicrobials, early excision, and grafting
have improved survival in the early postburn period; however, a significant
incidence of pneumonia-related sepsis occurs after burn injury, often
progressing to multiple organ failure. Recent studies have suggested that this
initial injury (burn injury) primes the subject, producing an exaggerated
response to a second insult, such as pneumonia-related sepsis. We developed an
experimental animal model that included a third-degree burn over 40% of the
total body surface area, followed by sepsis (intratracheal administration of
Streptococcus pneumoniae, 4 x 106 colony-forming
unit), which was produced either 48 or 72 h after burn injury in adult male
rats. Hearts harvested after either burn alone, sepsis alone, or burn plus
sepsis were used to assess either contractile function (Langendorff) or
cardiomyocyte secretion of tumor necrosis factor-
, interleukin
(IL)-1
, IL-6, and IL-10 (ELISA). Experimental groups included the
following: 1) sham (sham burn and no sepsis); 2) burn injury
alone studied either 24, 48, or 72 h postburn; 3) pneumonia-related
sepsis in the absence of burn injury; and 4) pneumonia-induced sepsis
studied either 48 or 72 h after an initial burn injury. Burn injury alone (24
h) or sepsis alone produced myocardial contractile defects and increases in
pro- and anti-inflammatory cytokine secretion by cardiomyocytes. Sepsis that
occurred 48 h postburn exacerbated the cardiac contractile defects seen with
either burn alone or sepsis alone. Sepsis that occurred 72 h postburn produced
contractile defects resembling those seen in either burn alone or sepsis
alone. In conclusion, our data suggest that burn injury primes the subject
such that a second insult early in the postburn period produces significantly
greater cardiac abnormalities than those seen with either burn alone or sepsis
alone.
rats; contraction and relaxation; cardiomyocytes; collagenase digestion; cardiomyocyte secretion; inflammatory cytokines; tumor necrosis factor-
; interleukins
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