1. The present study examined the effects of the addition of 100 mg/kg L-carnitine to the basal starter (containing 17.8 mg/kg L-carnitine) and finisher (containing 22.9 mg/kg L-carnitine) diets on performance, organ weights and plasma hormone and metabolite concentrations of male and female broiler chickens. The broiler chickens were reared either in a room with a normal temperature (NT) program or with a low temperature (LT) program (rapid decrease from 28 degrees C to 20 degrees C at 14 d of age). 2. Broiler chickens reared under the LT schedule consumed more food and attained a greater body weight at 42 d of age than their counterparts reared under NT schedule, without any difference in food efficiency or abdominal fat content. Dietary L-carnitine supplementation had no significant effects on any of these production parameters, except for a reduction in the abdominal fat content of female NT chickens. However, the LT schedule and dietary L-carnitine supplementation greatly increased absolute and proportional heart weights. The elevated heart weights were not due to right ventricle hypertrophy. 3. Both the LT program and L-carnitine supplementation increased circulating plasma triiodothyronine concentrations. There were also some transient effects of both experimental variables on plasma growth hormone, glucose and triglyceride concentrations. 4. L-carnitine did not improve broiler performance. However, this result does not mean that L-carnitine supplementation cannot have beneficial effects in other circumstances. In view of the elevated proportional heart weights, it can also be argued that L-carnitine is a potential agent for reducing the incidence of metabolic diseases in broiler chickens.

The purpose of this study was to validate dual-energy x-ray absorptiometry (DXA) for measuring the body composition of chickens in vivo. Four trials were conducted with broiler chickens using a DXA instrument (Lunar, DPX-L) and small animal total body scan software (version 4.7a). In the first 2 trials, the effects of scan mode (high resolution or detail slow), scanning position (ventral or dorsal), and the use of attenuating materials (AM) (2-mm polyvinyl chloride or 4-mm polystyrene) on the precision and values of the DXA parameters body mass, lean tissue mass, fat tissue mass and percentage, bone mineral content (BMC), and bone mineral density (BMD) were evaluated. The precision was highest for body mass and lean tissue mass, followed by BMC and BMD, and was lowest for fat tissue mass and percentage. The precision of the measurements was not influenced by scan mode, position, or type of AM. In contrast, the values for all DXA parameters except body mass were significantly influenced by the scan mode but not by the position. The high resolution mode gave significantly higher estimates of fat mass and BMC but significantly lower measures of lean tissue mass and BMD compared with the detail slow mode. A significant difference between AM was only observed for the DXA estimates of fat tissue mass and fat percentage. In trial 3, the accuracy of the DXA measurements was tested by comparison with chemical body composition analysis. Linear regression equations between the respective DXA and chemical parameters were established. High correlations (r > 0.9; P < 0.0001) were obtained for all parameters, except for fat percentage (r = 0.593; P < 0.05). The purpose of the validation trial was to compare the predicted body composition based on the DXA measurements with established equations and the chemical body composition. There was extremely good agreement for body mass, lean tissue mass, and fat tissue mass and percentage, but not for ash weight. It is concluded that, after proper methodological standardization and application of specifically determined regression equations, DXA can be used for estimating the body composition of chickens in vivo. However, the regression equations are strictly limited to one particular instrument, software version, and applied methodology.

The objective of this study was to investigate the effect of dietary macronutrient ratio on energy, protein, and lipid metabolism and on the involvement of diet-induced thermogenesis in feed intake regulation of broiler chickens. Male broilers were reared from 1 to 7 wk on isoenergetic diets with substitutions between fat and protein and similar carbohydrate content [low protein (LP): 126 vs. 242 g of protein/kg; low fat (LF): 43 vs. 106 g of fat/kg]. Every week from 21 d onward, 3 chickens per group were placed in open-circuit respiratory cells to measure energy and protein metabolism in fasting, short-term refeeding (5 h) and ad libitum conditions. As LP chickens had a significantly lower BW from 2 wk onward, all parameters were expressed per kilograms of metabolic BW. Feed intake, gross energy intake, and apparent metabolizable energy intake were significantly higher in LP than LF birds. The excessive energy relative to protein intake resulted in significantly increased heat production and energy retention as fat. The latter effect and a significantly increased respiratory quotient indicated higher de novo lipogenesis in the LP chickens. Furthermore, the efficiency of protein retention was significantly better in LP broilers. Neither diet-induced thermogenesis nor feed intake during a 5-h refeeding period was affected by diet composition. Our results indicate that isoenergetic substitution of fat for protein has a strong effect on growth and on energy and protein balance in broilers. The theory linking diet-induced thermogenesis to feed intake could not be corroborated or countered, and further research is warranted.

In order to evaluate the effect of insoluble and soluble fibre on the levels of post-prandial glycaemia, six healthy dogs were fed three different diets: a low-fibre control diet, a high-fibre diet (HF; mainly insoluble fibre) and the control diet with 10% iso-malto-oligosaccharides (IMO) added. The diets were fed for 2 days before the blood collections were started on the third day. Serial blood samples were taken 20, 60, 90, 150, 180, 240 and 360 min after feeding and one sample was taken just before the feeding after a fasting period of at least 20 h. There were no problems concerning the faecal consistency. The post-prandial glycaemia curve was significantly lower in the HF and IMO group in comparison with the control group. At 20 and 60 min the glucose concentration was significantly lower in the HF and IMO groups. At 90 and 150 min only the IMO group had a significantly lower glucose concentration. At 360 min there was a trend for a lower glucose concentration in the IMO group. The results show that both the HF and the IMO diets had a beneficial effect on post-prandial hyperglycaemia. Substitution of IMO may have the same or a slightly better effect, but this has to be confirmed in diabetic dogs and the effect may depend on the composition of the basal diet.

Research has shown that broiler chickens reared on a low-protein diet have a more efficient protein digestion. However, information on the fate of absorbed amino acids in relation to the dietary crude protein level in poultry is sparse. Therefore, this study aimed at developing a methodology for a 1-(13)C(1)-leucine breath test combined with indirect calorimetry, and to apply this technique using broiler diets known to induce differences in protein retention. From 14 days of age onwards, broiler chickens were reared on one of two isocaloric diets with substitutions between fat and protein [low-protein (LP) vs. high-protein (HP) diet: 130.4 vs. 269 g protein/kg; and 101.8 vs. 27.9 g fat/kg]. Every 4 or 5 days, three chickens per diet were placed in the respiratory cells for 48 h. The broilers were intubated with 40 mg 1-(13)C(1)-leucine/kg body weight, followed by breath sampling for 4 h at 15-min intervals and mass spectrometric analysis of the (13)C:(12)C ratio in the samples. The CO(2) level in the respiratory cell air was monitored and excreta samples were collected. The methodology to study l[1-(13)C(1)]leucine decarboxyation in chickens using a breath test combined with indirect calorimetry was accomplished. Results of the nitrogen balance test indicated that the LP broilers had an improved dietary protein retention compared with the HP animals. Moreover, LP chickens decarboxylated a significantly lower percentage of l[1-(13)C(1)]leucine, demonstrating several 'protein- or amino acid-sparing' mechanisms in animals reared on a diet with lower protein level, both at the digestive and at the postabsorptive level.