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Popova; Nina K. Popova Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia Search for other works by this author on: This Site PubMed Google Scholar Tamara G. Amstislavskaya Tamara G. Amstislavskaya Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia Search for other works by this author on: This Site PubMed Google Scholar Neuroendocrinology (2002) 76 (1): 28–34. https://i646f69o6f7267z.oszar.com/10.1159/000063681 Article history Published Online: July 01 2002 Content Tools * Views Icon Views * Article contents * Share Icon Share * Facebook * Twitter * LinkedIn * Email * Tools Icon Tools * Get Permissions * Cite Icon Cite * Search Site Citation Nina K. Popova, Tamara G. Amstislavskaya; 5-HT2A and 5-HT2C Serotonin Receptors Differentially Modulate Mouse Sexual Arousal and the Hypothalamo-Pituitary-Testicular Response to the Presence of a Female. Neuroendocrinology 1 July 2002; 76 (1): 28–34. https://i646f69o6f7267z.oszar.com/10.1159/000063681 Download citation file: * Ris (Zotero) * Reference Manager * EasyBib * Bookends * Mendeley * Papers * EndNote * RefWorks * BibTex toolbar search Search Dropdown Menu toolbar search search input Search input auto suggest filter your search All ContentAll JournalsNeuroendocrinology Search Advanced Search ABSTRACT The role of 5-HT2A and 5-HT2C subtypes of serotonergic receptors in the control of sexual behavior and plasma testosterone regulation was studied in male CBA mice exposed to a sexually receptive female separated by a transparent partition. Introduction of the receptive female induced sexual motivation and arousal in males, as evidenced by a prolonged time spent at the partition, unsuccessful attempts to step across it and a significant increase in plasma testosterone levels. Administration of 5-HT2A receptor antagonists ketanserin (1.0 and 2.0 mg/kg i.p.) or cyproheptadine (1.0 and 2.0 mg/kg i.p.) diminished the behavioral components and prevented the hormonal components of male sexual arousal. Administration of the selective 5-HT2C antagonist RS 102221 (1.0 and 2.0 mg/kg) considerably increased the time spent by males at the partition (p < 0.001) and, at the dose of 2.0 mg/kg, increased plasma testosterone levels (p < 0.01). Administration of ritanserin – a nonselective 5-HT2A/2C antagonist and, to a smaller degree, 5-HT2B antagonist – at doses of 0.1 and 0.5 mg/kg did not significantly influence male behavior and the activating effect of the presence of a female on the hypothalamo-pituitary-testicular system, although it increased resting testosterone levels (p < 0.05). The present findings suggest that 5-HT2A/5-HT2C receptors may be involved in the neural control of male sexual motivation and arousal, presumably by exerting reciprocal facilitative (5-HT2A) or suppressive (5-HT2C) influences. Keywords: Sexual arousal, Serotonin receptors, Gonadal steroids, Serotonin antagonists REFERENCES 1. Naumenko EV, Shishkina GT: Role of serotonin in feedback control of hypothalamic-pituitary-testicular complex in male rats. Neuroendocrinology 1978;26:359–366. 2. Armario A, Marti O, Gavalda A, Lopez-Calderon A: Evidence for the involvement of serotonin in acute stress-induced release of luteinizing hormone in the male rat. Brain Res Bull 1993;31:29–31. 3. Popova NK, Naumenko EV, Kolpakov VG: Serotonin and Behavior (in Russian). Novosibirsk, Nauka, 1978. 4. Olivier B, van Oorschot R, Waldinger MD: Serotonin, serotonergic receptors, selective serotonin reuptake inhibitors and sexual behaviour. Int Clin Psychopharmacol 1998;13(suppl 6):S9–S14. 5. 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Griebel G: 5-Hydroxytryptamine-interacting drugs in animal models of anxiety disorders: More than 30 years of research. Pharmacol Ther 1995;65:319–395. 23. Bonhaus DW, Weinhardt KK, Taylor M, DeSouza A, McNeeley PM, Szczepanski K, Fontana DJ, Trinh J, Rocha CL, Dawson MW, Flippin LA, Eglen RM: RS-102221: A novel high affinity and selective 5HT2C receptor antagonist. Neuropharmacology 1997;36:621–629. 24. Baxter G, Kennett G, Blaney F, Blackburn T: 5-HT2 receptor subtypes: A family re-united? Trends Pharmacol Sci 1995;16:105–110. 25. Amstislavsky SY, Amstislavskaya TG, Eroschenko VP: Methoxychlor given in the periimplantation period blocks sexual arousal in male mice. Reprod Toxicol 1999;13:405–411. 26. Novikov SN: Pheromones and Reproduction in Mammals: Physiological Aspects (in Russian). Leningrad, Nauka, 1988. 27. Morozov VI, Tchaikowsky VS, Pryatkin SA, Rogozkin VA, Savchenko ON, Shaliapina VG, Zorina AD, Lushchitskaya IM, Saltykova IA, Mishin VI, Timofeeva LA, Stepanov GS: Radioimmunoassay of steroids. Scientific and practical aspects. Physiologichesky J 1988;8:1049–1072. 28. Leysen JE, Niemegeers CJE, van Nueten JM, Laduron PM: [3H]Ketanserin (R 41 468), a selective 3H-ligand for serotonin2 receptor binding sites. Binding properties, brain distribution, and functional role. Mol Pharmacol 1982;21:301–314. 29. Leysen JE: Use of 5-HT receptor agonists and antagonists for the characterization of their respective receptor sites. Neuromethods 1989;12:299–350. 30. Meyerson BJ: Drugs and sexual motivation in the female rat; in Sandler M, Gessa G (eds): Sexual Behavior: Pharmacology and Biochemistry. New York, Raven, 1975, pp 21–32. 31. Maruniak JA, Bronson FH: Gonadotropic responses of male mice to female urine. Endocrinology 1976;99:963–969. 32. Pazos A, Cortes R, Palacios J: Quantitative autoradiographic mapping of serotonin receptors in the rat brain. 2. Serotonin-2 receptors. Brain Res 1985;346:231–249. 33. Zifa E, Fillion G: 5-Hydroxytryptamine receptors. Pharmacol Rev 1992;44:401–458. © 2002 S. Karger AG, Basel 2002 Copyright / Drug Dosage / Disclaimer Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher. Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. 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