Brain opioid receptor density reflects behavioral and heart rate responses in pigs.

Results from our previous research indicate that long-term tether-housed pigs with high and low levels of stereotypies show differences in the density of endogenous opioid receptors in the hippocampus and hypothalamus. It was not clear whether differences in opioid receptor density were induced by the chronic stress of tether housing or stereotypy performance, or were already present before the animals were tethered. The latter possibility was tested in the present experiment. We used a group of 18 nonstereotyping pigs that had no experience with tether housing and investigated whether the animals differed in the density of endogenous opioid receptors in the brain and, if so, whether these differences were related to the animals' reactions to acute challenges. The pigs were subjected to two tests: an open field test and a tethering test. Behavioral reactions as well as heart rate responses were measured. Opioid receptor densities were determined postmortem in the hippocampus and hypothalamus using a membrane binding assay with [(3)H]naloxone as a ligand. Animals differed widely in their responses to the two tests. In support of our hypothesis, we found a relationship between behavioral and heart rate responses and densities of naloxone binding sites in the hippocampus and hypothalamus. The data suggest that endogenous opioid systems in the brain contribute to differences in stress responding between individual pigs.

Opioid activity in behavioral and heart rate responses of tethered pigs to acute stress.

In a longitudinal experiment, effects of long-term tether housing on heart rate and behavioral responses to an acute stressor (a 15-min challenge with a nosesling) were investigated in pigs. The animals were challenged during loose housing and again after 10-11 weeks of tether housing. To detect possible changes in endogenous opioid systems modifying these responses, the pigs were pretreated with the opioid receptor antagonist naloxone (0.5 mg/kg body weight, iv). In response to the nosesling challenge, the animals showed pronounced resistance behavior and a sharp rise in heart rate. Following this initial phase of resistance, the heart rate dropped to prechallenge levels or below this line, and the pigs seemed to become sedated. Pretreatment with naloxone increased the heart rate response in animals that were long-term tether housed (n=12). No such effect was found in the control group (n=5) that was loose-housed during the entire experiment, indicating that the impact of endogenous opioid systems mitigating heart rate responses to acute stress had increased as a result of long-term tether housing. Changes in the effect of naloxone on the behavioral response were not found. Adaptive changes in opioid systems may prevent excessive physiological reactions to acute stress and, thus, may serve as a coping mechanism.