Abstract
Serum concentrations of corticosterone were increased following activation of 5-HT1A receptors with 8-OH-DPAT or activation of 5-HT2 receptors with MK-212 or DOI. The repeated administration of a 5-HT1A agonist, 5-MeODMT, selectively diminished the corticosterone response to 8-OH-DPAT, whereas the repeated administration of a 5-HT2 agonist, DOI, selectively diminished the corticosterone response to MK-212. Serum concentrations of PRL were increased following the administration of a 5-HT2 agonist (viz., DOI) but not 5-HT1A agonists (viz., 8-OH-DPAT, ipsapirone, gepirone). It is concluded that corticosterone secretion can be enhanced through the activation of either 5-HT1A or 5-HT2 receptors. The role of subtypes, other than 5-HT2, in the stimulation of PRL secretion is less clear.
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Gudelsky, G.A., Nash, J.F., Koenig, J.I., Meltzer, H.Y. (1990). Serotonin Agonist Induced Corticosterone and Prolactin Secretion: Role of 5-HT2 and 5-HT1A Receptors. In: Paoletti, R., Vanhoutte, P.M., Brunello, N., Maggi, F.M. (eds) Serotonin. Springer, Dordrecht. https://doi.org/10.1007/978-94-009-1912-9_76
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DOI: https://doi.org/10.1007/978-94-009-1912-9_76
Publisher Name: Springer, Dordrecht
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