C Jacobs

Increased volume and neuronal number of the basolateral nuclear group of the amygdaloid body in aggressive dogs

Involvement of the basolateral nuclear group (BNG) in pathological canine aggression was assessed by stereological determination of the volume of the BNG and quantification of the numerical density and total number of BNG neurons in normally behaving and aggressive dogs. A bilateral BNG enlargement of 40% was observed in the aggressive group. This enlargement appeared to be caused by a significantly increased number of BNG neurons. Other alterations such as an increased vessel density, oedema and scar tissue were not observed in any of the examined BNGs. The potential role of neurotrophins and stress hormones in the increased number of BNG neurons is discussed.

Neurons expressing serotonin-1B receptor in the basolateral nuclear group of the amygdala in normally behaving and aggressive dogs.

The present study aimed to quantify neurons expressing the serotonin-1B receptor and evaluate numerical differences in normally behaving and pathologically aggressive dogs in order to assess whether the serotonin-1B receptor is involved in pathological canine aggression. Because previous studies have reported structural alterations in the basolateral nuclear group (BNG) of the amygdaloid body of aggressive dogs, this structure was selected as region of interest in the present study. Indirect immunohistochemistry was applied to visualise the serotonin-1B-receptor-positive neurons. Immunoreactivity was located predominantly within the neuronal cell bodies and adjacent neuronal processes. In the aggressive dogs the BNGs contained a significantly higher number of serotonin-1B-receptor-positive neurons compared to the normally behaving dogs. This number was strongly correlated with the total number of neurons per BNG, which was also significantly increased in aggressive dogs compared to normal dogs. The percentage of neurons expressing the serotonin-1B receptor did not differ significantly between both groups. No significant asymmetries were observed for the number and percentage of serotonin-1B-receptor-positive neurons. Potential relationships between the present findings and the etiology of aggressive behaviour, the neuroprotective role of the serotonin-1B receptor and receptor dysfunction are discussed.

Neurokinin-1 receptor in the basolateral nuclear group of the canine amygdala—Comparative study in normal and aggressive dogs

Substance P and its NK-1 receptor are involved in the modulation of aggressive behavior. Because of the role of the basolateral nuclear group (BNG) of the amygdala in canine aggression, neurokinin-1 receptor (NK-1) immunoreactivity in this brain region was assessed stereologically in 7 normally behaving and 6 pathologically aggressive dogs. The first aim of this study was to obtain information about the absolute number of neurons expressing the NK-1 receptor in the canine BNG because absolute numbers of neurons expressing the NK-1 receptor are not documented in literature. Additionally, an exploratory comparison was made between NK-1 expressing neurons in the BNGs of normally behaving and aggressive dogs. Results showed a very low amount (1-2%) of BNG neurons containing the NK-1 receptor in both groups. Aggressive dogs had significantly more NK-1-receptor-positive BNG neurons than normal dogs, but the numerical densities and fractions of receptor-positive neurons did not differ significantly between both groups. Combined with the fact that aggressive dogs have 27% more neurons in their BNGs than normal dogs, as reported in a previous study, these findings suggest a limited role for the NK-1-receptor-positive neurons within the BNG in the modulation of canine aggression. The present report of absolute numbers of neurons expressing the NK-1 receptor in the canine BNG could however be useful for further quantitative studies.