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T Vilberg

Publications and source records attributed to T Vilberg.

3 recordsLinked to original sources

Opioid blockade and social comfort in chicks.

When young animals are separated from their normal social environment in groups they distress vocalize (DV) less than when isolated alone. Opioid blockade with naloxone (1 mg/kg peripherally, and 1 microgram centrally) increased crying more in group tested chicks than individually tested ones. The serotonin receptor blocking agent methysergide and the cholinergic blocking agent atropine sulfate produced similar effects. The testing of birds in mirrored environments also produced a reduction of DV's, and all three receptor blocking agents augmented DV's more in mirrored environments than in mirrorless ones. However, in studies evaluating changes in this comfort response by facilitation of opiate, serotonin (5 HT), and acetylcholine (ACh) activity (with morphine, quipazine and pilocarpine, respectively), only morphine was found to magnify the comforting effect of mirrors. The effects of naloxone on contact comfort, and the acquisition and expression of imprinting were further evaluated, and opioid blockade reduced all these measures of social comfort. It is concluded that endogenous opioid activity (and to a lesser extent, 5 HT and ACh) contribute to the comfort which animals derive from their social environment.

Animals↗

Endogenous opioids and social behavior.

Evidence for the hypothesis that brain-opioids mediate social affect and social attachments is summarized. Opiates and opioids are very effective in reducing social separation-induced distress vocalizations (DVs), in puppies, young guinea pigs and chicks, while opiate antagonists can increase DVs. In studies of specific social behaviors in rodents, morphine (at doses 1 mg/kg and below) decreases proximity maintenance time in socially housed animals, increased play, decreases maternal aggression but has no effect on pup retrieval. Naloxone reduces play and disrupts pup-retrieval, but has no consistent effect on proximity maintenance time of socially housed animals. In young rats tested in social learning situations, morphine delays and naloxone hasten extinction. These data are consistent with the proposition that brain opioids modulate social emotions and behaviors.

Aggression↗

Reduction of distress vocalization in chicks by opiate-like peptides.

All the opiate-like peptides we tested (Met-enkephalin, (D-Ala2)-Met-enkephalin-NH2, beta-endorphin, (D-Ala2)-beta-endorphin, (D-Ala2)-alpha-endorphin, (D-Ala2)-gamma-endorphin) were capable of reducing distress vocalizations (DV's) in socially-isolated chicks when injected into the vicinity of the fourth ventricle in doses as low as 100 picomoles. All of these substances were at least as potent as equimolar doses of morphine sulfate. In general, DV's were a more sensitive measure of opiate-like peptide effects than reductions in body temperature. In a more limited study using peripheral injections, it was determined that (D-Ala2)-Met-enkephalin at doses of 400 nanomoles/kg, like morphine sulfate, was more effective in reducing DV's, than an equimolar dose of beta-endorphin. beta-endorphin was not as effective via a peripheral route as it was via central administration.

Animals↗