Rearing cage type and dietary limestone particle size: II, effects on egg production, eggshell, and bone quality in Lohmann selected Leghorn-Lite hens.

We investigated effects of rearing cage type and dietary limestone particle size (LPS) on egg production, egg weight, eggshell, and bone quality in laying hens. The pullets were reared in conventional (CON; 20 chicks/cage, 270 cm2/chick) or furnished (FUR; 30 chicks/cage; 636 cm2/chick) cages and fed 3 LPS (fine, <0.595 mm; medium, 0.595 to <1.68 mm; and 1:1 mixture of F and M wt/wt) to 16 wk of age (woa). Pullets were transitioned to laying furnished cages and retained rearing treatment combination identities (n = 5, 20 hens/cage). Hens had free access to common commercial layer diet and water through to 40 woa. Eggs were recorded daily for calculation of hen day egg production (HDEP). Subsamples of eggs laid on the first day of 24, 28, 32, 36, and 40 woa were used for eggshell quality analyses. Two hens per cage were sacrificed on the last day of 24 and 40 woa for femur and tibia quality assessments. There was no interaction (P > 0.05) between rearing cage type and dietary LPS on response variables. At 19 and 20 woa, HDEP was higher (P < 0.01) for FUR than CON reared hens but was similar (P > 0.05) afterward. At 40 woa, FUR reared hens had higher (P < 0.05) body weight (BW), egg weight (EW), eggshell thickness, and eggshell weight and tended (P < 0.10) to have higher femur and tibia mineral density (BMD) and mineral content (BMC) than CON reared hens. Rearing dietary LPS had no effect (P > 0.05) on HDEP, BW, EW, and eggshell quality. Although, rearing dietary LPS did not affect (P > 0.05) femur and tibia BMD and BMC; at 24 woa, hens reared on medium LPS tended to have higher femur BMD (0.17 vs. 0.14 g/cm2; P = 0.079) and BMC (0.99 vs.0.78 g; P = 0.088) than hens reared on fine LPS. In conclusion, hens reared in furnished cages had better eggshell quality but had marginal effects on femur and tibia quality, whereas rearing dietary LPS had no effects on eggshell and bone attributes in hens.

Differential housing and novelty response: Protection and risk from locomotor sensitization.

High novelty seeking increases the risk for drug experimentation and locomotor sensitization. Locomotor sensitization to psychostimulants is thought to reflect neurological adaptations that promote the transition to compulsive drug taking. Rats reared in enrichment (EC) show less locomotor sensitization when compared to rats reared in isolation (IC) or standard conditions (SC). The current research study was designed to test if novelty response contributed locomotor sensitization and more importantly, if the different housing environments could change the novelty response to protect against the development of locomotor sensitization in both adolescence and adulthood. Experiment 1: rats were tested for their response to novelty using the inescapable novelty test (IEN) and pseudorandomly assigned to enriched (EC), isolated (IC), or standard (SC) housing conditions for 30days. After housing, they were tested with IEN. Rats were then administered amphetamine (0.5mg/kg) or saline and locomotor activity was measured followed by a sensitization test 14days later. Experiment 2: rats were tested in the IEN test early adulthood and given five administrations of amphetamine (0.3mg/kg) or saline and then either stayed in or switched housing environments for 30days. Rats were then re-tested in the IEN test in late adulthood and administered five more injections of their respective treatments and tested for locomotor sensitization. Results indicate that IC and SC increased the response to novelty. EC housing decreased locomotor response to amphetamine and saline, and SC housing increased the locomotor response to amphetamine. Mediation results indicated that the late adult novelty response fully mediates the locomotor response to amphetamine and saline, while the early adulthood novelty response did not. CONCLUSIONS: Differential housing changes novelty and amphetamine locomotor response. Novelty response is altered into adulthood and provides evidence that enrichment can be used to reduce drug vulnerability.