Activation of somatodendritic 5-HT(1A) autoreceptors reduces the acquisition and expression of cued fear in the rat fear-potentiated startle test

RATIONALE: Fear conditioning is an important factor in the etiology of anxiety disorders. Previous studies have demonstrated a role for serotonin (5-HT)(1A) receptors in fear conditioning. However, the relative contribution of somatodendritic 5-HT(1A) autoreceptors and post-synaptic 5-HT(1A) heteror...

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Detalles Bibliográficos
Autores principales: Zhao, Yulong, Bijlsma, Elisabeth Y., ter Heegde, Freija, Verdouw, Monika P., Garssen, J., Newman-Tancredi, Adrian, Groenink, Lucianne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591185/
https://www.ncbi.nlm.nih.gov/pubmed/30539269
http://dx.doi.org/10.1007/s00213-018-5124-0
Descripción
Sumario:RATIONALE: Fear conditioning is an important factor in the etiology of anxiety disorders. Previous studies have demonstrated a role for serotonin (5-HT)(1A) receptors in fear conditioning. However, the relative contribution of somatodendritic 5-HT(1A) autoreceptors and post-synaptic 5-HT(1A) heteroreceptors in fear conditioning is still unclear. OBJECTIVE: To determine the role of pre- and post-synaptic 5-HT(1A) receptors in the acquisition and expression of cued and contextual conditioned fear. METHODS: We studied the acute effects of four 5-HT(1A) receptor ligands in the fear-potentiated startle test. Male Wistar rats were injected with the 5-HT(1A) receptors biased agonists F13714 (0–0.16 mg/kg, IP), which preferentially activates somatodendritic 5-HT(1A) autoreceptors, or F15599 (0–0.16 mg/kg, IP), which preferentially activates cortical post-synaptic 5-HT(1A) heteroreceptors, with the prototypical 5-HT(1A) receptor agonist R(+)8-OH-DPAT (0–0.3 mg/kg, SC) or the 5-HT(1A) receptor antagonist WAY100,635 (0–1.0 mg/kg, SC). RESULTS: F13714 (0.16 mg/kg) and R(+)-8-OH-DPAT (0.03 mg/kg) injected before training reduced cued fear acquisition. Pre-treatment with F15599 or WAY100,635 had no effect on fear learning. In the fear-potentiated startle test, F13714 (0.04–0.16 mg/kg) and R(+)-8-OH-DPAT (0.1–0.3 mg/kg) reduced the expression of cued and contextual fear, whereas F15599 had no effect. WAY100,635 (0.03–1.0 mg/kg) reduced the overall startle response. CONCLUSIONS: The current findings indicate that activation of somatodendritic 5-HT(1A) autoreceptors reduces cued fear learning, whereas 5-HT(1A) receptors seem not involved in contextual fear learning. Moreover, activation of somatodendritic 5-HT(1A) autoreceptors may reduce cued and contextual fear expression, whereas we found no evidence for the involvement of cortical 5-HT(1A) heteroreceptors in the expression of conditioned fear.

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