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Can albumin administration relieve lung injury in trauma/hemorrhagic shock?

AbstractAIM:
To study the effect of albumin administration on lung injury in trauma/hemorrhagic shock (T/HS).
METHODS:
Sixty experimental animals were randomly divided into three groups: rats undergoing laparotomy without shock (T/SS); rats with T/HS and resuscitation with blood plus twice the volume of shed blood as Ringer's lactate (RL), and rats with T/HS and resuscitation with blood plus additional 3 mL of 50 g/L human albumin. Expression of polymorphonuclear neutrophil (PMN) CD11b/CD18, intercellular adhesion molecule-1 (ICAM-1) of jugular vein blood and the severity of lung injuries [determined mainly by measuring activity of lung tissue myeloperoxidase (MPO) and lung injury score (LIS)] were measured after a 3-h recovery period.
RESULTS:
All three groups showed a significant difference in the expressions of CD11b/CD18, ICAM-1, and severity of lung injury. The expressions of CD11b/CD18 in T/SS group, T/HS + RL group, T/HS + albumin group were 17.76% +/- 2.11%, 31.25% +/- 3.48%, 20.36% +/- 3.21%, respectively (F = 6.25, P < 0.05). The expressions of ICAM-1 (U/mL) in T/SS group, T/HS + RL group, T/HS + albumin group were 258.76 +/- 98.23, 356.23 +/- 65.6, 301.01 +/- 63.21, respectively (F = 5.86, P < 0.05). The expressions of MPO (U/g) in T/SS group, T/HS + RL group, T/HS + albumin group were 2.53 +/- 0.11, 4.63 +/- 1.31, 4.26 +/- 1.12, respectively (F = 6.26, P < 0.05). Moreover, LIS in T/HS + RL group, T/HS + albumin group was 2.62 +/- 0.23, 1.25 +/- 0.24, respectively. The expressions of CD11b/CD18, ICAM-1 and MPO in T/HS + RL group were significantly increased compared to T/SS group (P = 0.025, P = 0.036, P = 0.028, respectively). However, administration of 3 mL of 50 g/L albumin significantly down-regulated the expressions of CD11b/CD18, ICAM-1 and lung injury index (MPO and LIS) when compared with the T/HS + RL rats (P = 0.035, P = 0.046, P = 0.038, P = 0.012, respectively).
CONCLUSION:
The infusion of albumin during resuscitation period can protect lung from injury and decrease the expressions of CD11b/CD18, ICAM-1 in T/HS rats.
AuthorsZuo-Bing Chen, Zi-Wei Wang, Chen-Yan Ding, Jian-Hua Yan, Yuan Gao, Yun Zhang, Lin-Mei Ni, Yong-Qing Zhou
JournalWorld journal of gastroenterology (World J Gastroenterol) Vol. 12 Issue 42 Pg. 6884-8 (Nov 14 2006) ISSN: 1007-9327 [Print] United States
PMID17106942 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Albumins
  • CD11b Antigen
  • CD18 Antigens
  • Intercellular Adhesion Molecule-1
  • Peroxidase
Topics
  • Albumins (pharmacology, therapeutic use)
  • Animals
  • CD11b Antigen (genetics, metabolism)
  • CD18 Antigens (genetics, metabolism)
  • Gene Expression Regulation (drug effects)
  • Gene Expression Regulation, Enzymologic (drug effects)
  • Intercellular Adhesion Molecule-1 (genetics, metabolism)
  • Lung (enzymology, pathology)
  • Lung Injury
  • Neutrophils (drug effects, metabolism)
  • Peroxidase (genetics, metabolism)
  • Rats
  • Rats, Sprague-Dawley
  • Respiratory Distress Syndrome (drug therapy, etiology, prevention & control)
  • Shock, Hemorrhagic (complications)
  • Wounds and Injuries (complications)

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