Rn. Upton et al., The cerebral and systemic kinetics of thiopentone and propofol in halothane anaesthetized sheep, ANAESTH I C, 29(2), 2001, pp. 117-123
The cerebral and systemic kinetics of intravenous thiopentone (250 mg over
2 minutes, n = 5) and propofol (100 mg over 2 minutes, n = 6) were determin
ed in sheep anaesthetized with halothane (2.0%) and mechanically ventilated
to an end-expired carbon dioxide tension of 40 mmHg. The sheep were previo
usly instrumented with arterial and sagittal sinus (effluent from the brain
) blood sampling catheters. Systemic kinetics were inferred from the time-c
ourse of the arterial blood concentrations, and cerebral kinetics from the
time-course of the arterio-sagittal sinus concentration difference across t
he brain. Under halothane anaesthesia, the peak arterial concentrations of
each drug occurred at the end of the two-minute infusion, and was 42.3 mg/l
and 12.3 mg/l for thiopentone and propofol, respectively. Propofol had a s
ignificantly larger systemic clearance (3.19 l/min) than thiopentone (0.99
l/min). The brain concentrations of propofol equilibrated more slowly with
the arterial concentrations than those of thiopentone. The extraction ratio
across the brain neat the end of the infusions (1.5 min) were 0.85 and 0.4
6 respectively. These data were also compared to analogous previously publi
shed data for initially conscious sheep. The systemic kinetics of thiopento
ne were little affected by halothane anaesthesia. For propofol, halothane a
naesthesia was associated with a statistically significant reduction in cle
arance (50% of awake), a slower initial half-life (247% of awake), and the
emergence of a second slower half-life in some sheep. The cerebral kinetics
of both drugs were subtly altered by halothane anaesthesia.