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Thoracic peridural block in experimental endotoxin shock
G Richardt1, U Börner, W Reinhardt
1Department of Internal Medicine, University of Giessen, Federal Republic of Germany.
Summary
Thoracic peridural block (PDB) in rabbits prevented metabolic changes and reduced blood pressure during endotoxin shock. However, this sympathetic blockade did not significantly decrease mortality rates.
Area of Science:
- Anesthesiology
- Critical Care Medicine
- Physiology
Background:
- Endotoxin shock triggers significant metabolic and hemodynamic disturbances.
- Sympathetic nervous system activation plays a crucial role in the pathophysiology of endotoxin shock.
- Understanding interventions that modulate these responses is vital for improving patient outcomes.
Purpose of the Study:
- To investigate the effects of thoracic peridural block (PDB) on metabolic and hemodynamic changes during endotoxin shock in rabbits.
- To assess the impact of PDB on sympathetic response, glucose metabolism, and circulatory parameters.
- To determine if PDB influences mortality in this animal model of shock.
Main Methods:
- Rabbits subjected to endotoxin shock received intermittent bupivacaine via a thoracic peridural catheter for sympathetic blockade.
- Metabolic markers (plasma glucose, lactate, glycerol) and hemodynamic parameters (mean arterial pressure, cardiac output) were monitored.
- Glucose clearance was assessed using plasma half-life measurements after intravenous glucose injection.
- Mortality rates were recorded at 24 hours.
Main Results:
- PDB prevented the endotoxin-induced increase in plasma glucose, lactate, and free glycerol.
- Animals with PDB exhibited accelerated glucose clearance.
- PDB led to reduced mean arterial pressure and total peripheral resistance, indicating peripheral vasodilatation.
- PDB did not significantly alter right ventricular pressure, cardiac output, O2 consumption, or 24-hour mortality.
Conclusions:
- Thoracic PDB effectively blocks the sympathetic response in endotoxin shock.
- PDB alters metabolic disturbances by inhibiting glycogenolytic and lipolytic responses.
- Despite metabolic improvements, PDB did not significantly reduce mortality in this rabbit model of endotoxin shock.