In many animal experiments the use of a non-inhaled anaesthetic drug is required. In non-recovery experiments urethane and chloral hydrate are commonly used anaesthetics, whereas in recovery experiments ketamine/xylazine, pentobarbital, and tribromoethanol are preferred. The duration and the depth of anaesthesia induced by these injectable anaesthetic drugs in small laboratory animals are known (Wixson et al. 1987, Field et al. 1993. But in most experiments additional substances given to the animal might in uence the time and/or depth of anaesthesia. For example,
SummaryWe analysed the effect of intraperitoneal insuf ated ozonized oxygen on the anaesthetic strength generated by tribromoethanol, ketamine/xylazine, chloral hydrate, pentobarbital, and urethane in male Wistar rats. High dosages of anaesthetic drugs normally used for deep surgical anaesthesia were injected. The ozonized oxygen gas mixture was given ve times daily on ve consecutive days at 0.8 mg ozone/kg body weight before anaesthesia. The re exes were measured 15, 30, 60, 90, 120, 180, and 240 min after injection of the anaesthetic drug. The sleeping time and the loss and regain of six different re exes on noxious and non-aversive stimuli were recorded during the 4 h of observation. O 3 /O 2 -pneumoperitoneum (O 3 /O 2 -PP) reduced the sleeping time induced by tribromoethanol and ketamine/xylazine and increased it for chloral hydrate and pentobarbital. In accordance to the changes in the duration of anaesthesia, the O 3 /O 2 -PP induced signi cant changes in the loss of different re exes. Additionally, the modulatory effect of the anaesthetic drugs on splenic cytokine mRNA expression was further in uenced by O 3 /O 2 -PP. Thus, the in uence of an oxidative stressor on anaesthetic potency and on the resting immune system has to be taken into account for experimental designs in which surgical anaesthesia is necessary for small laboratory animals.