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Phagocytic reticuloendothelial function after hemorrhage and resuscitation: modulation by different fluids
E A van Rijen1, J J Ward, R A Little
1North Western Injury Research Centre, University of Manchester, United Kingdom.
Shock (Augusta, Ga.)
|September 26, 1997
Summary
Resuscitating hemorrhagic shock mice with Haemaccel increased reticuloendothelial system (RES) phagocytic activity, unlike shed blood or hydroxyethyl starch. This suggests Haemaccel alters RES function post-hemorrhage.
Area of Science:
- Immunology
- Hematology
- Pharmacology
Background:
- Colloid resuscitation fluids are vital for cardiovascular restoration in hemorrhagic shock.
- The impact of these fluids on the reticuloendothelial system (RES) activity remains unclear.
- RES function is crucial for immune response and infection susceptibility post-resuscitation.
Purpose of the Study:
- To investigate the effects of hydroxyethyl starch, Haemaccel, and fresh autologous blood on RES function following hemorrhage.
- To assess the phagocytic activity and organ uptake of RES after resuscitation with different colloid fluids.
Main Methods:
- BALB/C mice underwent 40% hemorrhage, followed by resuscitation with shed blood, hydroxyethyl starch, or Haemaccel.
- Whole-body phagocytic activity was measured by clearance rate (K) of 51Cr-labeled sheep red blood cells at various time points.
- Hepatic, splenic, and lung uptake of red blood cells were analyzed to evaluate RES organ function.
Main Results:
- Shed blood resuscitation showed no significant change in phagocytic activity (K).
- Haemaccel resuscitation led to a significant increase in K at 48 hours post-hemorrhage.
- Haemaccel increased hepatic uptake and decreased splenic uptake, effects partially mitigated by co-administration with autologous red blood cells.
Conclusions:
- Haemaccel significantly alters RES phagocytic activity and organ uptake following hemorrhagic shock.
- Hydroxyethyl starch and autologous blood did not exhibit the same RES-modulating effects as Haemaccel.
- These findings highlight the differential impact of colloid resuscitation fluids on immune function post-hemorrhage.