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C. Korstanje, R. Sprenkels, H. N. Doods, J. G. Hugtenburg, E. Boddeke, H. D. Batink, M. J. Thoolen and P. A. Van Zwieten, “Characterization of Flufylline, Fluprofylline, Ritanserin, Butanserin and R 56413 With Respect to in-Vivo Alpha1-,Alpha2- and 5-HT2-Receptor Antagonism and in-Vitro Affinity for Alpha1-, Alpha2- and 5-HT2-Receptors: Comparison With Ketanserin,” Journal of Pharmacy and Pharmacology, Vol. 38, No. 5, 1986, pp. 374-379. doi:10.1111/j.2042-7158.1986.tb04590.x

has been cited by the following article:

• TITLE: 5-HT2A Receptor Activation Normalizes Exaggerated Fear Behavior in p-Chlorophenylalanine (PCPA)-Treated Rats

  AUTHORS: Cathryn R. Hughes, Lee Tran, N. Bradley Keele

  KEYWORDS: Fear Conditioning; Startle Reflex; 5-HT2; DOI; Ketanserin; SB 206553

  JOURNAL NAME: Journal of Behavioral and Brain Science, Vol.2 No.4, November 30, 2012

  ABSTRACT: Deficits in serotonin (5-hydroxytryptamine, 5-HT) neurotransmission are implicated in abnormal emotional behaviors such as aggression, anxiety, and depression. However, the specific 5-HT receptor mechanisms involved are not well understood. The role of 5-HT2 receptors in fear potentiated startle, (FPS) was examined in rats chronically treated with pchlorophenylalanine (PCPA) to reduce brain 5-HT. PCPA-treated rats show an enhanced magnitude of FPS. Systemic administration of the 5-HT2 receptor agonist (±)-2,5-Dimethoxy-4-iodoamphetamine hydrochloride (DOI) reduced FPS in both PCPA-treated and saline (SAL)-treated control animals, normalizing the exaggerated fear response in PCPA-treated rats. In both SAL- and PCPA-treated animals, the DOI-induced reduction of learned fear was reversed by the 5-HT2 antagonist ketanserin, but not by the 5-HT2B/2C antagonist SB 206553. Together, these findings suggest 5-HT2A receptors are critical regulators of learned fear, and that 5-HT2A receptors may be an important pharmacological target to normalize exaggerated learned fear resulting from chronic 5-HT-ergic disruption.