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Reduced albumin extravasation in experimental rat skin and muscle burn injury by D-myo-inositol-1,2,6-trisphosphate treatment.

Tarnow, Peter, 1963 (author)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för plastikkirurgi,Institute of Surgical Sciences, Department of Plastic Surgery
Jönsson, Anders, 1959 (author)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för ortopedi,Institute of Surgical Sciences, Department of Orthopaedics
Nellgård, Per, 1956 (author)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för anestesiologi och intensivvård,Institute of Surgical Sciences, Department of Anaesthesiology and Intensive Care
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Cassuto, Jean (author)
Gothenburg University,Göteborgs universitet,Institutionen för de kirurgiska disciplinerna, Avdelningen för anestesiologi och intensivvård,Institute of Surgical Sciences, Department of Anaesthesiology and Intensive Care
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 (creator_code:org_t)
1996
1996
English.
In: The Journal of burn care & rehabilitation. - 0273-8481. ; 17:3, s. 207-12
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • This study investigated the effects of the anti-inflammatory agent D-myo-inositol-1,2,6-trisphosphate (IP3) on burn edema. Two sets of experiments were performed. In the first set, a full-thickness burn injury was induced in the abdominal skin of anesthetized rats. Postburn intravenous treatment was given with IP3, indomethacin or saline solution. Extravasation of Evans blue albumin in the burned tissue was quantified by a spectrophotometric technique. Results showed significant inhibition of albumin extravasation by IP3 in three of five different doses compared to saline-treated animals. In the second set of experiments, a deep full-thickness burn through the abdominal skin and rectus muscle was induced. The therapeutic window of IP3 could be more well-defined. Resulted showed a significant reduction of albumin extravasation in the skin at all four dose levels and in the abdominal muscle at three of four doses. Indomethacin had no significant effect on postburn edema formation. The mechanisms responsible for the inhibition of albumin leakage by IP3 could be secondary to reduced formation of edema-promoting inflammatory mediators by the agent, resulting in improved vascular patency.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Anestesi och intensivvård (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Anesthesiology and Intensive Care (hsv//eng)

Keyword

Albumins
metabolism
Analysis of Variance
Animals
Anti-Inflammatory Agents
Non-Steroidal
administration & dosage
therapeutic use
Burns
drug therapy
metabolism
pathology
Confidence Intervals
Disease Models
Animal
Dose-Response Relationship
Drug
Edema
drug therapy
etiology
pathology
Evans Blue
diagnostic use
Extravasation of Diagnostic and Therapeutic Materials
Indomethacin
administration & dosage
therapeutic use
Inositol Phosphates
administration & dosage
therapeutic use
Muscles
drug effects
metabolism
pathology
Rats
Rats
Sprague-Dawley
Skin
drug effects
metabolism
pathology
Sodium Chloride
administration & dosage
therapeutic use

Publication and Content Type

ref (subject category)
art (subject category)

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