Draper & Whitehead (1944) showed that dogs maintained in apnoea with large doses of thiopentone could survive for periods of half an hour or longer when exposed to 100% oxygen through a patent airway at atmospheric pressure. The critical factor limiting the duration of this condition, termed 'diffusion respiration', was a severe respiratory acidosis secondary to progressive elevation of alveolar carbon dioxide tension (Draper, Whitehead & Spencer, 1947).-Provided that alveolar and tissue nitrogen are at least partially eliminated beforehand, such states of oxygenated apnoea provide an opportunity to study the effects of progressive rises in arterial C02 tension, with a minimum of interference from anoxia, and without respiratory stimulation (Holmdahl, 1956). In this study direct measurement has been made of plasma adrenaline and noradrenaline concentrations during diffusion respiration in dogs maintained in apnoea by means of a continuous infusion of succinyl choline.
METHODSSeven dogs (7-16 kg) were lightly anaesthetized with intravenous thiopentone. The trachea was intubated with a No. 9 Magill cuffed portex tube, this being connected through a T-piece to an expiratory valve and a 51. rubber bag, which was kept partly filled by a flow of 100% oxygen. The femoral artery on one side was cannulated after infiltration of the groin with 5-10 ml. of 1 % lignocaine solution; arterial blood pressure was measured continuously by means of a Statham strain gauge (Model p 23-A), Sanborn amplifier and recorder; a three-way tap allowed withdrawal of blood samples as required. Heparin 10,000 u. was injected intravenously.The dogs were allowed to breathe 100 % oxygen for 20-30 min, after which spontaneous respiration was abolished by means of a continuous intravenous infusion, containing 200 mg succinyl choline chloride in each 100 ml. of 0.9% (w/v) sodium chloride solution, which was given at a very slow rate throughout each study. Before the start of diffusion respiration the dogs were ventilated manually for 10 min with 100% oxygen, using high gas flows to obtain good oxygenation with adequate elimination of nitrogen and carbon dioxide. The first arterial blood sample for assay was withdrawn during this period of ventilation. Manual respiration was then stopped and the endotracheal tube left attached to the gas bag which was kept partly filled with 100% oxygen. The expiratory valve was loose to ensure that no positive pressure was applied to the airway.