Effects of nicarbazin on the blood glucose and liver glycogen statuses of male broilers.

Nicarbazin (NCZ), an effective anticoccidial widely used by the global broiler industry, is known to produce some side effects in broilers. Recent field observations have suggested that NCZ could be associated with spiking mortality syndrome, a disease of uncertain etiology that is most commonly characterized by hypoglycemia. In turn, 2 trials were conducted to investigate the effects of NCZ on the blood glucose levels and liver glycogen content of Ross × Ross 708 male broilers. In 6 of 12 pens beginning at 1 d of age, NCZ was added to basal broiler diets at a rate of 125 mg/kg, and the other 6 pens were control pens in which birds received salinomycin instead of NCZ, at a rate of 66 mg/kg. Feed and water were provided ad libitum, feed was closely monitored in all pens to avoid shortages, no coccidial challenge was imposed, and room temperature never exceeded 29.4°C. At the end of the second trial, a photoperiod increase from 8L:16D to 24L:0D was imposed in an effort to induce stress due to feed engorgement. In response to NCZ in trial 1, 0 to 28 d feed conversion and relative liver weights on d 21 and 28 were higher, whereas 0 to 28 d cumulative BW gain was lower. In response to NCZ in trial 2, 0 to 13 d feed conversion was higher, whereas 0 to 13 d cumulative BW gain was lower. The added NCZ increased blood glucose on d 13 in trial 2, but did not affect at any time the liver constituents analyzed in both trials. In conclusion, the uninterrupted feeding of NCZ at 125 mg/kg in the starter and grower diets of male Ross × Ross 708 broilers increased feed conversion and reduced BW gain, but despite an increase in relative liver weight on d 21 and 28 posthatch, liver glucose and glycogen concentrations were not affected.

Physiological relationships of the early posthatch performance of broilers to their embryo and eggshell characteristics.

Relationships between physiological parameters of early posthatch chicks with their corresponding egg and embryo parameters were examined in progeny of young broiler breeders. Four hundred and 80 broiler hatching eggs that were obtained from a 29-wk-old Ross 308 breeder flock were incubated on 8 replicate tray levels of an incubator until hatch. Between 10.5 and 18.5 d of incubation, internal (T(emb)) and external (T(ext)) egg temperatures were recorded twice daily using temperature transponders. Beginning at 18.5 d, the eggs were individually monitored for hatch every 12 h. Average T(emb), T(ext), and average daily incubational egg weight loss (EWL) for the 10.5- to 18.5-d incubation period were used to calculate eggshell water vapor conductance (G(H2O)), specific G(H2O) (g(H2O); G(H2O) adjusted to 100 g of set egg weight basis), and a G(H2O) constant (K(H2O)) for each egg. Chicks were grown out for 10 d in pens of a single battery brooder. In each pen, on d 3 posthatch, carcasses, yolk sac, liver, and pipping muscle samples were collected from at least 2 chicks that hatched from eggs implanted with transponders for determination of their relative weights and moisture concentrations. Livers and pipping muscles were also analyzed for glucose, glycogen, fat, and protein concentrations. Yolk sac weight as a percentage of chick BW (YW) and its moisture concentration (YSM) were positively correlated with T(emb). Egg g(H2O) was positively correlated with chick carcass moisture concentration and its relative weight as a percentage of set egg weight, but it was negatively correlated with YW. The positive functional relationship between T(emb) and incubation length may be mediated via their common positive relationships to YSM. A negative correlation was observed between percentage EWL and relative BW on d 0 and 0.5 posthatch for chicks hatched from unimplanted eggs. The results suggest that a higher g(H2O) results in an increased metabolism of the broiler embryo, which subsequently increases growth and yolk sac absorption in broiler chicks through 3 d posthatch.

Determination of embryonic temperature profiles and eggshell water vapor conductance constants in incubating Ross x Ross 708 broiler hatching eggs using temperature transponders.

The comprehensive profiles of the internal and external temperatures of embryonated Ross × Ross 708 broiler hatching eggs during incubation were determined using temperature transponders, and eggshell water vapor conductance (G(H2O)), specific G(H2O) (g(H2O); G(H2O) adjusted to a 100 g set egg weight basis), and G(H2O) constants (K(H2O)) were calculated. On each of 8 replicate tray levels of an incubator, 2 nonembryonated and 4 embryonated eggs were each implanted with a transponder on d 10.5 of incubation for the determination of internal (air cell) temperatures of nonembryonated (T(nem)) and embryonated (T(emb)) eggs, respectively. In addition, 2 water-filled vials, each containing a transponder, were used on each tray level for the determination of the external microenvironment temperatures (T(ext)) of the embryonated and nonembryonated eggs. Between 10.5 and 18 d of incubation, incubator data logger temperatures were determined every 5 min; and incubator dry bulb temperature, T(ext), T(nem), T(emb), and the difference between T(emb) and T(nem) (T) were determined every 12 h. Over the days of incubation, regression coefficients for T(emb) and T were positive, whereas the regression coefficient for T(nem) was negative. There was a significant day of incubation × type of temperature measurement (T(ext), T(nem), and T(emb)) interaction for temperature. Between 13 and 18 d of incubation, mean values of T(emb) readings that were recorded every 12 h were consistently higher than those of T(ext) and T(nem), indicating the importance of air cell transponder implantation for the efficient estimation of broiler embryo temperature. Furthermore, mean values of the percentage of daily incubational egg weight loss, G(H2O), g(H2O), and K(H2O) of the embryonated eggs were 0.54 ± 0.019%, 14.4 ± 0.56 mg of H2O/d per Torr, 25.0 ± 0.96 mg of H2O/d per Torr per 100 g, and 5.20 ± 0.205, respectively. The results suggest that transponders may be implanted in the air cells of broiler hatching eggs to detect incubational variations in T(emb) and to subsequently calculate G(H2O), g(H2O), and K(H2O).

Effects of in ovo injection of carbohydrates on somatic characteristics and liver nutrient profiles of broiler embryos and hatchlings.

Effects of the in ovo injection of commercial diluent supplemented with dextrin or with dextrin in combination with various other carbohydrates on the somatic characteristics and liver nutrient profiles of Ross × Ross 708 broiler embryos and chicks were investigated. Results include information concerning the gluconeogenic energy status of the liver before and after hatch. Eggs containing live embryos were injected in the amnion on d 18 of incubation using an automated multiple-egg injector for the delivery of the following carbohydrates dissolved in 0.4 mL of commercial diluent: 1) 6.25% glucose and 18.75% dextrin; 2) 6.25% sucrose and 18.75% dextrin; 3) 6.25% maltose and 18.75% dextrin; and 4) 25% dextrin. Also, a noninjected control and a 0.4-mL diluent-injected control were included. Body weight relative to set egg weight on d 19 of incubation (E19) was increased by the injection of all carbohydrate solutions, and on the day of hatch was increased by the injection of diluent, sucrose and dextrin, and maltose and dextrin solutions. Hatchability of the fertilized eggs, residual yolk sac weight, and liver weight were not affected by any injection treatment; however, as compared with the 0.4 mL diluent-injected group, all of the supplementary carbohydrates, except for the glucose and dextrin combination group, increased liver glycogen and glucose concentrations on E19. Furthermore, all carbohydrates, except for the 25% dextrin treatment, decreased liver fat concentration on E19. From E19 to the day of hatch, liver glycogen concentrations dropped dramatically from an average of 3.2 to 0.6%. Despite treatment differences observed on E19 for liver glycogen, glucose, and fat concentrations, these differences were lost by the day of hatch. Nevertheless, liver glycogen and glucose concentrations were positively correlated on the day of hatch. In conclusion, the in ovo injection of various supplemental carbohydrates dissolved in 0.4 mL of commercial diluent altered the liver nutrient profile of Ross × Ross 708 broiler embryos before hatch. However, the subsequent pattern of energy utilization during the hatching process modified these effects.

Effects of in ovo injection of carbohydrates on embryonic metabolism, hatchability, and subsequent somatic characteristics of broiler hatchlings.

The effects of the in ovo injection of different carbohydrate solutions on the internal egg temperature (IT), hatchability, and time of hatch of embryonated Ross × Ross 708 broiler hatching eggs were determined. In addition, the BW, liver weight, yolk sac weight (YSW), and yolk-free BW (YFBW) of the embryos on d 19.5 of incubation and of the chicks on day of hatch were determined. Eggs containing live embryos were injected in the amnion on d 18.5 of incubation using an automated multiple-egg injector. Solution injections delivered 1.2 mL of physiological saline (0.85%) alone or with a supplemental carbohydrate. The following supplemental carbohydrates were separately dissolved in saline at a concentration of 0.3 g/mL: glucose, fructose, sucrose, maltose, and dextrin. Temperature transponders were implanted in the air cells of embryonated and nonembryonated eggs after in ovo injection for the detection of IT at 6, 14, and 22 h after injection. The IT of embryonated eggs was significantly greater than that of nonembryonated eggs at all 3 times after the treatment period. Eggs that were injected with saline with or without supplemental carbohydrates experienced a reduction in IT when compared with control eggs whose shells were perforated without solution delivery, and the decrease in IT was associated with a delay in hatch time. Liver weight was negatively related to YSW and positively related to YFBW, and YSW was negatively related to YFBW. Although the saline and carbohydrate solution injections increased chick BW compared with noninjected controls, chick YFBW was decreased in the maltose- and sucrose-injected groups. In conclusion, the injection of 1.2 mL of saline with or without supplemental carbohydrates lowered embryonic metabolism, as reflected by a lower IT and a delay in time of hatch. However, effects of the different carbohydrate solutions on yolk absorption and tissue deposition in yolk-free embryos varied. These results suggest that lower volumes for solutions containing maltose, sucrose, or fructose should be considered for in ovo injection.

Use of implantable temperature transponders for the determination of air cell temperature, eggshell water vapor conductance, and their functional relationships in embryonated broiler hatching eggs.

Broiler hatching eggs obtained from a 29-wk-old Ross 308 breeder flock were weighed and set on 8 tray levels (60 eggs/level) of a single incubator. On d 10.5 of incubation, the eggs were weighed, and temperature transponders were implanted in the air cells of 4 randomly selected embryonated eggs per tray level for determination of internal egg temperature (IT). Two water-filled vials per tray level containing transponders were also placed within 5 cm of the implanted eggs for determination of external egg temperature (ET). Between 10.5 and 18.5 d of incubation, ET and IT were recorded every 12 h. Egg weights and embryo survival were determined on 10.5 and 18.5 d of incubation and were used for the calculation of average daily incubational weight loss of embryonated eggs (EWL) and average daily percentage of EWL. Approximately 75% (24 out of 32) of the embryos in the implanted eggs survived through d 18.5 of incubation. Mean ET and IT were used to calculate the water vapor pressure gradient across the eggshell, which was subsequently used with EWL to calculate eggshell water vapor conductance (G(H2O)) and specific G(H2O) (g(H2O); G(H2O) adjusted to a 100-g set egg weight basis). Mean percentage of EWL, ET, IT, G(H2O), and g(H2O) for the 10.5- to 18.5-d incubation period were 0.546 ± 0.02%, 37.1 ± 0.03°C, 37.8 ± 0.09°C, 13.9 ± 0.47 mg of H(2)O/d per Torr, and 24.5 ± 0.75 mg of H(2)O/d per Torr per 100 g, respectively. It was concluded that temperature transponders may be successfully implanted in the air cells of broiler hatching eggs to determine ET, IT, G(H2O), and g(H2O) in Ross × Ross 308 broiler hatching eggs. Nevertheless, increased embryo survivability by further improving the implantation procedure may increase the practicality of temperature transponder use in commercial settings.

Physiological responses of broiler embryos to in ovo implantation of temperature transponders.

Previous techniques that have been used to monitor broiler embryonic temperature and metabolism during incubation either have been invasive to the embryo or have not directly determined internal egg temperature. Therefore, the current investigation was conducted to determine the earliest day of incubation on which temperature transponder implantation in the egg air cell could be performed with minimal invasiveness to broiler embryogenesis. Eggs from young broiler breeder hens (Ross 308; 27 wk of age) were weighed and set on 3 tray levels (approximately 120 eggs per tray level) of a single incubator. Randomly, on each tray level and on each day between d 10 and 14 of incubation, 4 embryonated eggs were assigned to an invasive control (IC) treatment (shell perforation only) and 4 other embryonated eggs were assigned to a transponder implantation (TI) treatment (shell perforation, followed by transponder implantation in the air cell). Four embryonated eggs per tray were also assigned to a noninvasive control treatment on d 10 of incubation. Percentage of embryo survivability through d 18 of incubation, and percentages of mean daily incubational egg weight loss between d 18 and each respective day of implantation were calculated. Furthermore, various internal organ and tissue parameters were examined on d 18 of incubation. Embryo survivability was reduced because of transponder implantation on d 10 and 11 of incubation; however, embryo survivability was not different between eggs in the noninvasive control and IC treatments and the eggs that received the TI treatment on d 12, 13, and 14 of incubation. In comparison with eggs in the IC treatment, those in the TI treatment had a higher percentage of embryo weight. Conversely, yolk sac moisture was significantly higher in IC-treated eggs than in TI-treated eggs. It was concluded that temperature transponders may be inserted into the air cells of broiler hatching eggs between d 12 and 14 of incubation without adversely affecting eggshell porosity or embryogenesis and without causing physiological stress to growing broiler embryos.

Effects of in ovo injection of L-carnitine on hatchability and subsequent broiler performance and slaughter yield.

Effects of in ovo injection of L-carnitine on the hatchability, grow-out performance, and slaughter yield of Ross x Ross 308 broilers from a young breeder flock were determined through 48 d of age. Fertilized eggs 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. Hatchability and hatch rate of fertilized eggs were assessed. Furthermore, subsequent mortality, BW gain, feed intake per bird, and feed conversion were determined through 46 d posthatch. On d 47, live body, carcass, and abdominal fat pad weights, along with the weights of all major commercial cuts including the thigh, drumstick, wings, and breast muscles, were determined. Individual doses of supplemental L-carnitine had no significant effect on the hatchability or rate of hatch of fertilized eggs; however, significant trends were noted for increased hatchability and length of egg incubation in conjunction with increases in L-carnitine dose. Nevertheless, there were no significant treatment effects on any of the grow-out performance or slaughter yield parameters investigated. In conclusion, although increasing the levels of L-carnitine added to commercial vaccine diluent between 0.5 and 8.0 mg/100 microL for commercial in ovo injection did not significantly influence subsequent broiler grow-out performance or slaughter yield, L-carnitine dosages above those used in this study have the potential for significantly increasing incubation length and hatchability of broiler hatching eggs.

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 liver's 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 embryo's preparation for hatch.

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.

Adaptation of beef cattle to high-concentrate diets: performance and ruminal metabolism.

The diet adaptation period is widely considered a critical period of time in which nutritional management practices can promote or impair subsequent performance and health. Performance studies indicate that adapting feedlot cattle with incremental increases in dietary concentrate, from approximately 55 to 90% of diet DM, in 14 d or less, while allowing ad libitum access to the diet, generally results in reduced performance during adaptation or over the entire feeding period. However, the number of cattle involved in these studies does not allow insight into the frequencies of metabolic disorders associated with the management practices tested. Adapting cattle by restricting the quantity of higher-concentrate diets offered shows promise for improving production efficiency, but further development is needed for application in commercial feedlots. Evidence suggests considerable diversity in the ability of animals to cope with ingested cereal grain, and indicates that diet adaptation procedures should affect the frequency of health-impaired or low-performing cattle in a pen. Individuals that seem to effectively regulate voluntary feed intake during adaptation generally display a steady increase in DMI as dietary concentrate is increased. These data also highlight a seemingly counterproductive, repeating cycle of overconsumption, followed by a pronounced reduction in ruminal pH, by cattle that appear to cope less favorably with grain adaptation. At least a portion of this diversity may relate to the maintenance of protozoal populations. Increases in amylolytic bacteria seemed to follow the increment of additional concentrate. Protozoa were most numerous when the diet contained approximately 60% concentrate, and lactate-utilizing bacteria increased more markedly when the diet contained more than approximately 70% concentrate. Available in vivo data suggest that the number of lactate-utilizing bacteria may reach a plateau for a given diet composition after 2 to 7 d, but thorough assessments of the time course of events using modern techniques are lacking. Further research is needed to characterize how the quantity and frequency of increases in cereal grain consumption, reflective of industry practices, impact microbial dynamics, and to identify the biological features that allow certain animals to adapt more readily to high-concentrate diets.