British Journal of Anaesthesia, 2001, Vol. 86, No. 1 127-130
© 2001 The Board of Management and Trustees of the British Journal of Anaesthesia
Effect of two anaesthetic regimens on airway nitric oxide production in horses
1Centre for Equine Studies, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk CB8 7UU, UK. 2Kansas State University, Manhattan, Kansas, USA. 3Centre for Small Animal Studies, Animal Health Trust, Lanwades Park, Kentford, Newmarket, Suffolk CB8 7UU, UK. 4Department of Veterinary Clinical Studies, R(D)SVS, Edinburgh, UK.*Corresponding author
There is evidence that halothane inhibits nitric oxide synthase in vitro, but the effect of intravenous anaesthetic agents is less clear. This study was undertaken to compare the rate of exhaled nitric oxide production (V²NO) in spontaneously breathing horses anaesthetized with halothane or an intravenous regimen. Seven adult horses were studied twice in random order. After premedication with romifidine 100 µg kg1, anaesthesia was induced with ketamine 2.2 mg kg1 and maintained with halothane in oxygen (HA) or by an intravenous infusion of ketamine, guaiphenesin and romifidine (IV). Inhaled and exhaled nitric oxide (NO) concentrations, respiratory minute ventilation (V²E), pulmonary artery pressure (PPA), fractional inspired oxygen concentration (FIO2), end-tidal carbon dioxide concentration (E'CO2), cardiac output (Q²) and partial pressures of oxygen and carbon dioxide in arterial blood (PaO2, PaCO2) were measured. Exhaled nitric oxide production rate was significantly lower (40 min, P<0.01; 60 min, P<0.02) during HA [40 min, 1.4 (SD 1.4) pmol l1 kg1 min1; 60 min, 0.7 (0.7) pmol l1 kg1 min1] than during IV [40 min, 9.3 (9.9) pmol l1 kg1 min1; 60 min, 12.5 (13.3) pmol l1 kg1 min1). Mean pulmonary artery pressure was significantly higher (40 min, P<0.01; 60 min, P<0.001) during HA [40 min, 5.9 (1.1) kPa; 60 min, 5.9 (0.9) kPa] compared with IV (40 min, 4.4 (0.4) kPa; 60 min, 4.4 (0.5) kPa]. NO is reduced in the exhalate of horses anaesthetized with halothane compared with an intravenous regimen. It is suggested that increased mean pulmonary artery pressure during halothane anaesthesia may be linked to the differences in NO production.
Br J Anaesth 2001; 86: 12730