D(3) and D(2) dopamine receptor agonists differentially modulate isolation-induced social-emotional reactivity in mice
| Autor: | John M. Petitto, Jean Louis Gariépy, Paul L. Gendreau, Mark H. Lewis, Andreana Petrova |
|---|---|
| Rok vydání: | 2000 |
| Předmět: |
Agonist
Male medicine.medical_specialty Tetrahydronaphthalenes medicine.drug_class Mice Inbred A Emotions Stimulation Social Environment Developmental psychology Behavioral Neuroscience chemistry.chemical_compound Mice Species Specificity Dopamine receptor D3 Dopamine Dopamine receptor D2 Internal medicine Oxazines medicine Animals Benzopyrans Neurotransmitter Receptor Social Behavior Receptors Dopamine D2 Receptors Dopamine D3 Aggression Mice Inbred C57BL Endocrinology chemistry Social Isolation Dopamine receptor Dopamine Agonists Psychology medicine.drug |
| Zdroj: | Behavioural brain research. 114(1-2) |
| ISSN: | 0166-4328 |
| Popis: | Following isolation housing, mice typically exhibit heightened emotional reactivity to mild social stimulation. Aggression, social avoidance and a variety of defensive behaviors that differ in terms of motor activation (e.g. freezing, escape) can be observed depending on strain. Previous studies suggested that D2-like dopamine (DA) receptors play an important, albeit strain specific, role in the mediation of particular forms of defensive behavior. D3 receptors are subtypes of D2-like receptors that are highly expressed in limbic areas of the brain and, therefore, they have been hypothesized to mediate emotional behavior. This study examined the effects of the putative D3 receptor agonists 7-OH-DPAT and PD128907 on social-emotional behavior in isolated C57BL:6J and A:J mice. These effects were compared with those of the selective D2 receptor agonist PNU91356A. All three DA agonists increased non-locomotor forms of defensive behavior (e.g. freezing, upright defensive posture). These effects were observed at low doses in C57BL:6J and at higher doses in A:J mice. Only the D3 receptor agonists were effective in increasing locomotor forms of defensive behavior (i.e. escape, jump) at higher doses. These effects were more pronounced in C57BL:6J mice than A:J mice. The increases in stationary and locomotor defensive behavior were accompanied by marked reduction in social investigation in both the strains. Aggressive behavior was also abolished in the aggressive C57BL:6J strain. These results support previous findings and suggest that DA agonists potentiate defensive behavior and:or social fearfulness. They also suggest that D3 and D2 DA receptors differentially modulate the expression of social-emotional reactivity and indicate the importance of strain in examining the effects of DA ligands on emotional behavior. © 2000 Elsevier Science B.V. All rights reserved. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full Text from ScienceDirect