Five experiments were carried out to extend knowledge of purine metabolism in the camel (Camelus dromedarius) and to establish a model to enable microbial protein outflow from the forestomachs to be estimated from the urinary excretion of purine derivatives (PD; i.e. xanthine, hypoxanthine, uric acid, allantoin). In experiment 1, four camels were fasted for five consecutive days to enable endogenous PD excretion in urine to be determined. Total PD excretion decreased during the fasting period to 267 (SE 41·5) mmol/kg body weight (W) 0·75 per d. Allantoin and xanthine þ hypoxanthine were consistently 86 and 6·1 % of total urinary PD during this period but uric acid increased from 3·6 % to 7·4 %. Xanthine oxidase activity in tissues (experiment 2) was (mmol/min per g fresh tissue) 0·038 in liver and 0·005 in gut mucosa but was not detected in plasma. In experiment 3, the duodenal supply of yeast containing exogenous purines produced a linear increase in urinary PD excretion rate with the slope indicating that 0·63 was excreted in urine. After taking account of endogenous PD excretion, the relationship can be used to predict purine outflow from the rumen. From the latter prediction, and also the purine:protein ratio in bacteria determined in experiment 5, we predicted the net microbial outflow from the rumen. In experiment 4, with increasing food intake, the rate of PD excretion in the urine increased linearly by about 11·1 mmol PD/kg digestible organic matter intake (DOMI), equivalent to 95 g microbial protein/kg DOMI.
Purine derivatives: Xanthine oxidase: Microbial protein: CamelsThe urinary excretion of purine derivatives (PD; i.e. allantoin, uric acid, hypoxanthine and xanthine) is proportional to the flow of purines into the small intestine. The relationship has been used as a predictor of microbial outflow from the rumen of sheep Balcells et al. 1992), cattle (Verbic et al. 1990;Orellana Boero et al. 2001), goats (Belenguer et al. 2002) and zebu cattle (Bos indicus; Pimpa et al. 2001). This technique has potential for use in other ruminant species of economic significance, provided prediction equations are defined to take account of differences in purine metabolism among species and even among breeds of the same species. For the camel (Camelus dromedarius) there is only limited information on purine metabolism (for example, Mura et al. 1986).The present study was designed to extend our understanding of purine metabolism in the camel and to establish a model for use in estimating net microbial protein outflow from the rumen of the camel. Five experiments were carried out. In experiment 1, endogenous urinary PD excretion was determined in fasting camels. In experiment 2, the activity in different tissues of xanthine oxidase (XO), a key enzyme of purine base (PB) metabolism, was determined. In experiment 3, a relationship was established between the duodenal infusion of exogenous purines and the excretion of PD in urine. In experiment 4 a relationship between food intake and the urinary excretion of PD was dete...