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Interactions of selective serotonin reuptake inhibitors with the serotonin 5-HT2C receptor

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Abstract

Interactions of the selective serotonin reuptake inhibitors (SSRIs) citalopram, fluoxetine and its main metabolite norfluoxetine, and the tricyclic anti-depressant (TCA) imipramine with the rat serotonin 5-HT2C receptor in a clonal cell line and in the rat choroid plexus were investigated by radioligand binding and phosphoinositide (PI) hydrolysis assays. For comparison, the affinities of a variety of other antidepressants of different chemical classes for the cloned rat 5-HT2C and 5-HT2A receptors were also determined by radioligand binding assays. Fluoxetine displayed relatively high affinity for the 5-HT2C receptor in the choroid plexus, with a Ki value for inhibition of [3H]mesulergine binding of 55.4 nM. The Ki values for imipramine, norfluoxetine and citalopram were 136 nM, 203 nM, and 298 nM, respectively. Similar rank order of potency was detected in PI hydrolysis assays, which showed that these drugs are antagonists at the 5-HT2C receptor without exhibiting inverse agonist activity. [3H]Ketanserin (5-HT2A) binding assays revealed that the SSRIs fluoxetine, norfluoxetine and citalopram show 10- to 23-fold selectivity for the 5-HT2C receptor in vitro, whereas the TCA imipramine does not. Many other TCAs also had high to intermediate affinity for both 5-HT2A and 5-HT2C receptors. The present data provide evidence that fluoxetine, norfluoxetine and citalopram, along with many other antidepressant compounds, interact directly with the 5-HT2C receptor.

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References

  • Abramowski D, Staufenbiel M (1995) Identification of the 5-hydroxytryptamine2C receptor as a 60-kDaN-glycosylated protein in choroid plexus and hippocampus. J Neurochem 65:782–790

    Google Scholar 

  • Appel NM, Mitchell WM, Garlick RK, Glennon RA, Teitler M, De Souza EB (1990) Autoradiographic characterization of (±)-1-(2,5-dimethoxy-4-[125I]iodophenyl)-2-aminopropane ([125I]DOI) binding to 5-HT2 and 5-HT1C receptors in the rat brain. J Pharmacol Exp Ther 255:843–857

    Google Scholar 

  • Beasley CM, Masica DN, Potvin JH (1992) Fluoxetine: a review of receptor and functional effects and their clinical implications. Psychopharmacology 107:1–10

    Google Scholar 

  • Benfield P, Heel RC, Lewis SP (1986) Fluoxetine — a review of its pharmacodynamic and pharmacokinetic properties, and therapeutic efficacy in depressive illness. Drugs 32:481–508

    Google Scholar 

  • Caccia S, Fracasso C, Garattini S, Guiso G, Darati S (1992) Effects of short- and long-term administration of fluoxetine on the monoamine content in rat brain. Neuropharmacology 31:343–347

    Google Scholar 

  • Canton H, Verrièle L, Colpaert FC (1990) Binding of typical and atypical antipsychotics to 5-HT1C and 5-HT2C sites: clozapine potently interacts with 5-HT1C sites. Eur J Pharmacol 191:93–96

    Google Scholar 

  • Cheetham SC, Viggers JA, Slater NA, Heal DJ, Buckett WR (1993) [3H]Paroxetine binding in rat frontal cortex strongly correlates with [3H]5-HT uptake: effect of administration of various antidepressant treatments. Neuropharmacology 32[8]:737–743

    Google Scholar 

  • Conn PJ, Sanders-Bush E (1986) Agonist-induced phosphoinositide hydrolysis in choroid plexus. J Neurochem 47:1754–1760

    Google Scholar 

  • Fabre LF, Crismon ML (1985) Efficacy of fluoxetine in outpatients with major depression. Curr Ther Res 37[1]:115–123

    Google Scholar 

  • Fuller RW, Snoddy HD, Perry KW, Bymaster FP, Wong DT (1978) Importance of duration of drug action in the antagonism ofp-chloroamphetamine depletion of brain serotonin — comparison of fluoxetine and chlorimipramine. Biochem Pharmacol 27:193–198

    Google Scholar 

  • Gerione RA, Codina J, Benovic JL, Lefkowitz RJ, Birnbaumer L, Caron MG (1984) The mammalian beta 2-adrenergic receptor: reconstitution of functional interactions between pure receptor and pure stimulatory nucleotide binding protein of the adenylate cyclase system. Biochemistry 23:4519–4525

    Google Scholar 

  • Han C, Minneman KP (1991) Interaction of subtype-selective antagonists with α1-adrenergic receptor binding sites in rat tissues. Mol Pharmacol 40:531–538

    Google Scholar 

  • Harker EL, Westphal RS, Schmidt D, Sanders-Bush E (1994) Constitutively active 5-hydroxytryptamine 2C (5-HT2C) receptors reveal novel inverse agonist activity of receptor ligands. J Biol Chem 269:11687–11690

    Google Scholar 

  • Havlik S, Peroutka SJ (1992) Differential radioligand binding properties of [3H]5-hydroxytryptamine and [3H]mesulergine in a clonal 5-hydroxytryptamine2C cell line. Brain Res 584:191–196

    Google Scholar 

  • Hietala J, Salonen I, Lappalainen J, Syvälahti E (1990) Ethanol administration does not alter dopamine D1 and D2 receptor characteristics in rat brain. Neurosci Lett 108:289

    Google Scholar 

  • Hietala J, Koulu M, Kuoppamäki M, Lappalainen J, Syvälahti E (1992) Chronic clozapine treatment down-regulates serotonin 5-HT-1c receptors in rat brain. Prog Neuropsychopharmacol Biol Psychiatry 16:727–732

    Google Scholar 

  • Hoffman BJ, Mezey E (1989) Distribution of serotonin 5-HT1C receptor mRNA in adult rat brain. FEBS Lett 247[2]:453–462

    Google Scholar 

  • Jenck F, Moreau J-L, Mutel V, Martin JR, Haefely WE (1993) Evidence for a role of 5-HT1C receptors in the antiserotonergic properties of some antidepressant drugs. Eur J Pharmacol 231:223–229

    Google Scholar 

  • Karson CN, Newton JEO, Livingston R, Jolly JB, Cooper TB, Sprigg J, Komoroski RA (1993) Human brain fluoxetine concentrations. J Neuropsychiatr Clin Neurosci 5:322–329

    Google Scholar 

  • Kuoppamäki M, Syvälahti E, Hietala J (1993) Clozapine andN-desmethylclozapine are potent 5-HT1C receptor antagonists. Eur J Pharmacol [Mol Pharmacol Sect] 245:179–182

    Google Scholar 

  • Kuoppamäki M, Pälvimäki E-P, Syvälahti E, Hietala J (1994) 5-HT1C receptor-mediated phosphoinositide hydrolysis in the rat choroid plexus after chronic treatment with clozapine. Eur J Pharmacol 255:91–97

    Google Scholar 

  • Kuoppamäki M, Pälvimäki E-P, Hietala J, Syvälahti E (1995) Differential regulation of rat 5-HT2A and 5-HT2C receptors after chronic treatment with clozapine, chlorpromazine and three putative atypical antipsychotic drugs. Neuropsychopharmacology 13:139–151

    Google Scholar 

  • Laakso A, Pälvimäki E-P, Kuoppamäki M, Suvälahti E, Hietala J (1996) Chronic citalopram and fluoxetine treatments up-regulate 5-HT2C receptors in the rat choroid plexus. Neuropsychopharmacology (in press)

  • Leonhardt S, Gorospe E, Hoffman BJ, Teitler M (1992) Molecular pharmacological differences in the interaction of serotonin with 5-hydroxytryptamine1C and 5-hydroxytryptamine2 receptors. Mol Pharmacol 42:328–335

    Google Scholar 

  • Leysen JE, Niemegeers CJE, Van Nueten JM, Laduron PM (1982) [3H]Ketanserin (R 41 468), a selective3H-ligand for serotonin2 receptor binding sites; binding properties, brain distribution and functional role. Mol Pharmacol 21:301

    Google Scholar 

  • Mann CD, Bich Vu T, Hrdina PD (1995) Protein kinase C in rat brain cortex and hippocampus: effect of repeated administration of fluoxetine and desipramine. Brit J Pharmacol 115:595–600

    Google Scholar 

  • Milligan G, Bond RA, Lee M (1995) Inverse agonism: pharmacological curiosity or potential therapeutic strategy? Trneds Pharmacol Sci 16:10–13

    Google Scholar 

  • Molineaux SM, Jessell TM, Axel R, Julius D (1989) 5-HT1C receptor is a prominent serotonin receptor subtype in the central nervous system. Proc Natl Acad Sci USA 86[17]:6793–6797

    Google Scholar 

  • Morin D, Zini R, Urien S, Tillement JP (1989) Pharmacological profile of binedaline, a new antidepressant drug. J Pharmacol Exp Ther 249[1]:288–296

    Google Scholar 

  • Pazos A, Palacios JM (1985) Quantitative autoradiographic mapping of serotonin receptors in the rat brain. I. Serotonin-1 receptors. Brain Res 346:205–230

    Google Scholar 

  • Pompeiano M, Palacios JM, Mengod G (1994) Distribution of the serotonin 5-HT2 receptor family mRNAs: comparison between 5-HT2A and 5-HT2C receptors. Brain Res Mol Brain Res 23[1–2]:163–178

    Google Scholar 

  • Richelson E, Pfenning M (1984) Blockade by antidepressants and related compounds of biogenic amine uptake into rat brain synaptosomes: most antidepressants selectively block norepinephrine uptake. Eur J Pharmacol 104:277–286

    Google Scholar 

  • Rickels K, Amsterdam JD, Avallone MF (1986) Fluoxetine in major depression: a controlled study. Curr Ther Res 39[4]:559–563

    Google Scholar 

  • Roth BL, Hamblin MW, Ciaranello RD (1991) Mianserin decreases 5-HT2 radioligand binding without altering 5-HT2 receptor mRNA levels. Eur J Pharmacol 207:169–172

    Google Scholar 

  • Roth BL, Ciaranello RD, Meltzer HY (1992) Binding of typical and atypical antipsychotic agents to transiently expressed 5-HT1C receptors. J Pharmacol Exp Ther 260:1361–1366

    Google Scholar 

  • Sanders-Bush E, Breeding M (1988) Putative selective 5-HT-2 antagonists block 5-HT-1c receptors in the choroid plexus. J Pharmacol Exp Ther 247:169–173

    Google Scholar 

  • Sanders-Bush E, Breeding M (1990) Serotonin1c receptor reserve in choroid plexus masks receptor subsensitivity. J Pharmacol Exp Ther 252[3]:984–988

    Google Scholar 

  • Sommi RW, Crismon ML, Bowden CL (1987) Fluoxetine: a serotonin-specific, second-generation antidepressant. Pharmacotherapy 7[1]:001–015

    Google Scholar 

  • Torok-Both GA, Baker GB, Coutts RT, McKenna KF, Aspeslet LJ (1992) Simultaneous determination of fluoxetine and norfluoxetine enantiomers in biological samples by gas chromatography with electron-capture detection. J Chromatogr 579:99–106

    Google Scholar 

  • Westphal RS, Sanders-Bush E (1994) Reciprocal binding properties of 5-hydroxytryptamine type 2C receptor agonists and inverse agonists. Mol Pharmacol 46:937–942

    Google Scholar 

  • Wong DT, Threlkeld PG, Robertson DW (1991) Affinities of fluoxetine, its enantiomers, and other inhibitors of serotonin uptake for subtypes of serotonin receptors. Neuropsychopharmacology 5[1]:43–47

    Google Scholar 

  • Wood MD, Glen A, Blackburn TP, Lee JA, Sutiphong JA, Kumar C, Carey J, Robinson J (1993) (-)-Fluoxetine has high affinity for the cloned rat and human 5-HT1C receptor and the human 5-HT2 receptor. Br J Pharmacol 110 [Proceedings Supplement]: 102P

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Pälvimäki, E.P., Majasuo, H., Laakso, A. et al. Interactions of selective serotonin reuptake inhibitors with the serotonin 5-HT2C receptor. Psychopharmacology 126, 234–240 (1996). https://doi.org/10.1007/BF02246453

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  • DOI: https://doi.org/10.1007/BF02246453

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