7 research outputs found
The Control of Feather Pecking by Serotonin
Feather-pecking behavior in laying hens (Gallus gallus) may be considered a behavioral pathology, comparable to human psychopathological disorders. Scientific knowledge on the causation of such disorders strongly suggests involvement of the serotonergic (5-hydroxytryptamine; 5-HT) system in feather pecking. Previously, chicks from a high-feather-pecking (HFP) line were found to display lower 5-HT turnover levels than chicks from a low-feather-pecking (LFP) line (in response to acute stress). The present study investigated whether low 5-HT neurotransmission modulates feather pecking. First, S-15535, a somatodendritic 5-HT1A autoreceptor agonist, was demonstrated to be an excellent tool for reducing 5-HT turnover in the forebrain of LFP and HFP chicks. Second, the most effective dose of S-15535 (4.0 mg/kg body weight) significantly increased severe feather-pecking behavior. The results confirmed the postulation that the performance of feather pecking is triggered by low 5-HT neurotransmission.
The development of feather pecking behaviour and targeting of pecking in chicks from a high and low feather pecking line of laying hens
Large individual differences between adult laying hens in their propensity for feather pecking are known to exist. However, not much research has been carried out into the individual differences concerning the development of feather pecking behaviour. The purpose of this study was to investigate whether contrasting levels of feather pecking, observed among adult birds from two lines of laying hens, already occur at an early age. Furthermore, an important question to be discussed was whether different behavioural systems may be related to the occurrence of feather pecking. Therefore, this study consisted of studying and comparing the behaviour of White Leghorn laying hens from a high (HFP) and low feather pecking line (LFP) during the first 8 weeks of life. Chicks were reared in litter-floor pens and were kept in groups of five animals per line (12 groups per line).HFP chicks showed significantly higher levels of gentle feather pecking (gentle FP) than LFP chicks at the age of 14 and 28 days. Furthermore, HFP chicks spent significantly more time preening than LFP chicks on days 14, 28 and 41. Duration of foraging behaviour and feeding behaviour was significantly higher in the LFP line compared to the HFP line on days 41 and 56 and days 28, 41 and 56, respectively. HFP chicks showed a significant negative correlation between gentle FP and preening on days 3 (r=-0.49) and 41 (r=-0.86). In the LFP line duration of feeding correlated negatively with gentle FP on day 3 (r=-0.63). A principal component analysis (PCA) revealed that in the HFP line, gentle FP and preening exhibited high and opposite loadings on the same component at all ages, whereas feeding consistently loaded on the other component. This outcome contrasted with that of the LFP line. In this line feeding predominantly loaded on the same principal component as gentle FP, with loadings opposite to those of gentle FP, whereas preening showed the same loadings as gentle FP, on days 3 and 41.In conclusion, differences in feather pecking behaviour between HFP and LFP chicks can already be observed at a very early age during development. Furthermore, our results indicate that HFP and LFP chicks differ in the way pecking behaviour is targeted. This difference could be related to the existence of a difference in underlying motivational system controlling the development of feather pecking between the two lines
Chicks from a high and low feather pecking line of laying hens differ in apomorphine sensitivity
Proactive rodents show a larger behavioral response to apomorphine (APO) than reactive copers, suggesting a more sensitive DA system in proactive individuals. Previously, chicks from a high feather pecking (HFP) and low feather pecking line (LFP) have been suggested to display a proactive and reactive coping strategy, respectively. Therefore, at approximately 4 weeks of age, the behavior of 48 LFP and 48 HFP chicks in response to an APO injection was studied using an open field. Another objective of the present study was to determine whether behavioral variation (in an open field) between HFP and LFP birds, after APO injection, is also reflected by variation of D1 and D2 receptor densities in the brain. Receptor binding capacities were assessed by measuring specific binding of tritiated D1 and D2 receptor ligands in different regions of the brain of control HFP and LFP chicks.
In the present study, it is shown that indeed HFP chicks display a more enhanced behavioral response to acute APO treatment (0.5 mg/kg BW) than LFP birds in an open field. This difference was not reflected by variation of D1 and D2 receptor densities in the brain between both lines.