R. W. Keirs

Effects of in ovo injection of l-carnitine on subsequent broiler chick tissue nutrient profiles

Effects of in ovo injection of L-carnitine on BW and the moisture and nutrient biochemical concentrations of various organs and muscles of Ross x Ross 308 broiler chicks, hatched from eggs laid by a 28-wk-old breeder flock, were determined through 48 d posthatch. Eggs containing live embryos were injected in the amnion with L-carnitine (0.5, 2.0, or 8.0 mg dissolved in 100 microL of a commercial diluent) on d 18 of incubation using an automated egg injector. Three control groups (noninjected and injected with or without diluent) were also included. On d 0, 3, 10, 28, and 48 posthatch, bird BW and the proportional weights and moisture concentrations of various organs and muscles were determined. Glycogen, glucose, protein, and fat concentrations were also determined in certain tissue samples. Bird BW; proportional liver weight; breast, thigh, and gastrocnemius muscle moisture; liver glycogen, glucose, and protein concentrations; and breast and thigh muscle fat and protein concentrations changed with posthatch bird age. Liver glucose on d 0 and pipping muscle moisture on d 3 posthatch were significantly affected by treatment. In comparison to eggs injected with commercial diluent with no added L-carnitine, liver glucose was reduced by the injection of diluent containing either 0.5 or 8.0 mg of L-carnitine, and pipping muscle moisture was increased by the injection of commercial diluent containing either 0.5 or 2.0 mg of L-carnitine. The modified concentrations of the 2 parameters in response to these treatments were not different from those in noninjected control eggs. In conclusion, L-carnitine added to commercial vaccine diluent at levels between 0.5 and 8.0 mg/100 microL for the commercial injection of broiler hatching eggs may decrease liver glucose and increase pipping muscle moisture concentrations of chicks on d 0 and 3 posthatch, respectively, so that their levels are commensurate with noninjected controls.

Pipping muscle and liver metabolic profile changes and relationships in broiler embryos on days 15 and 19 of incubation

The relative proportions and relationships of pipping muscle and liver nutrients in broiler embryos on d 15 and 19 of incubation were determined. Ninety hatching eggs obtained from a 30-wk-old broiler breeder flock were incubated on 3 replicate tray levels (30 eggs per tray) for 19 d. On 15 and 19 d of incubation, 10 live embryos per tray level were necropsied to collect pipping muscle and liver samples. As the broiler embryo developed between d 15 and 19 of incubation, the glycogen and protein concentrations of the pipping muscle increased, whereas those of the liver decreased, and the fat concentration of the pipping muscle decreased, whereas that of the liver increased. Across d 15 and 19, pipping muscle glycogen was negatively correlated with liver fat, whereas on d 15, pipping muscle glucose was negatively correlated with liver fat, and pipping muscle glycogen was negatively correlated with liver glucose and glycogen. Pipping muscle fat was negatively correlated with liver glucose on d 15 but positively correlated with liver glycogen on d 19. In conclusion, in preparation for hatch between d 15 and 19 of incubation, weights of the liver and pipping muscle of broiler embryos increased relative to their BW. This occurred in association with the accumulation of glucose, glycogen, and protein and with the loss of fat in the pipping muscle. The carbohydrate stores in the pipping muscle were supported by the active metabolism of the liver before 19 d of incubation, which included the transfer of glucose and fatty acids to the pipping muscle via the circulation. Despite the livers active supply of these nutrient subunits for assimilation and oxidation by the pipping muscle, there was an overall accumulation of hepatic fat between d 15 and 19 of incubation. These data suggest that the integrated changes in the energy profiles of pipping muscle and liver between 15 and 19 d of embryogenesis are integral to the broiler embryos preparation for hatch.