Fluoxetine HCl

Short Summary : Serotonin reuptake inhibitor,selective

Category : Neuroscience|5-HT Receptor

Purity : 0.9991

CAS Number : 56296-78-7

Formula : C17H18F3NO.HCl

Molecular Weight : 345.79

SMILE : CNCCC(C1=CC=CC=C1)OC2=CC=C(C=C2)C(F)(F)F.Cl

Solubility : >17.3mg/mL in DMSO

Storage : Store at -20°C

Description : Fluoxetine is a specific presynaptic serotonin-reuptake inhibitor (SSRI) at the neuronal membrane, used in the treatment of depression.The serotonin receptor, also known as 5-HT receptor, is a member of G protein-coupled receptorfound in the central and peripheral nervous systems. The serotonin receptors, activated by the natural ligand serotonin,have been involved in a variety of biological and neurological processes such as aggression, anxiety, cognition, learning, memory, mood[1].In vitro:In Xenopusoocytes expressing either cloned 5HT2C receptors or 5HT receptors, micromolar concentrations of fluoxetine (Prozac) inhibited the membrane currents elicited by serotonin (5-hydroxytryptamine; 5HT). For responses elicited by 1 M 5-HT, the IC50 of fluoxetine was about 20 M. Fluoxetine also inhibited the binding of [3H]5HT to 5HT2C receptors expressed in HeLa cells and the binding of [3H]5HT to 5HT receptors in rat cortex membranes, with Ki of 65C97 nM and 56 M, respectively[2]. Administration of fluoxetine blocked the downregulation of cell proliferation of hippocampal cells resulting from inescapable shock (IS), which resulted in a state of behavioral despair[3]. Fluoxetine increased the number of newborn cells in the dentate gyrus of the hippocampus of adult rat. Fluoxetine also increased the number of proliferating cells in the prelimbic cortex[4]. Fluoxetine accelerated the maturation of immature neurons. Fluoxetine enhanced neurogenesis-dependent long-term potentiation (LTP) in the dentate gyrus [5]. Fluoxetine, but not other selective serotonin uptake inhibitors such as citalopram, fluvoxamine, paroxetine and sertraline, increased norepinephrine and dopamine extracellular levels in prefrontal cortex. Fluoxetine produced robust and sustained increases in extracellular concentrations of norepinephrine and dopamine after acute systemic administration [6]. In vivo: Fluoxetine reversed the deficit in escape latency observed in animals exposed to inescapable shock in adult male SpragueCDawley rats [3].The combination of olanzapine and fluoxetine produced robust, sustained increases of extracellular levels of dopamine ([DA](ex)) and norepinephrine ([NE](ex)) up to 361 28% and 272 16% of the baseline, respectively[7]. Fluoxetine (5 and 10 mg/kg) reduced cocaine infusions (0.2 mg/kg), and cocaine infusions returned to baseline levels within 48 hr after fluoxetine treatments were terminated [8]. In sham-operated or adrenalectomized/castrated (ADX/CX) male rats, administration of fluoxetine dose-dependently (2.9-58 mumol/kg i.p.) increased the brain content of the neurosteroid 3 alpha-hydroxy-5 alpha-pregnan-20-one (allopregnanolone, 3 alpha, 5 alpha-TH PROG)[9]. Clinical trials: In a 5-wk double-blind, parallel study with 40 depressed 23C69 yr olds, fluoxetine(20C80 mg/day) provided effective antidepressant activity, with fewer and less side effects[10].References:[1]. Hoyer D, Clarke DE, Fozard JR, Hartig PR, Martin GR, Mylecharane EJ, Saxena PR, Humphrey PP (1994).”International Union of Pharmacology classification of receptors for 5-hydroxytryptamine (Serotonin)”.Pharmacol. Rev.46(2): 157C203.[2]. Ni Y G, Miledi R. Blockage of 5HT2C serotonin receptors by fluoxetine (Prozac)[J]. Proceedings of the National Academy of Sciences, 1997, 94(5): 2036-2040.[3]. Malberg J E, Duman R S. Cell proliferation in adult hippocampus is decreased by inescapable stress: reversal by fluoxetine treatment[J]. Neuropsychopharmacology, 2003, 28(9): 1562-1571.[4]. Kodama M, Fujioka T, Duman R S. Chronic olanzapine or fluoxetine administration increases cell proliferation in hippocampus and prefrontal cortex of adult rat[J]. Biological psychiatry, 2004, 56(8): 570-580.[5]. Wang J W, David D J, Monckton J E, et al. Chronic fluoxetine stimulates maturation and synaptic plasticity of adult-born hippocampal granule cells[J]. The Journal of neuroscience, 2008, 28(6): 1374-1384.[6]. Bymaster F P, Zhang W, Carter P A, et al. Fluoxetine, but not other selective serotonin uptake inhibitors, increases norepinephrine and dopamine extracellular levels in prefrontal cortex[J]. Psychopharmacology, 2002, 160(4): 353-361.[7]. Zhang W, Perry K W, Wong D T, et al. Synergistic effects of olanzapine and other antipsychotic agents in combination with fluoxetine on norepinephrine and dopamine release in rat prefrontal cortex[J]. Neuropsychopharmacology, 2000, 23(3): 250-262.[8]. Carroll M E, Lac S T, Asencio M, et al. Fluoxetine reduces intravenous cocaine self-administration in rats[J]. Pharmacology Biochemistry and Behavior, 1990, 35(1): 237-244.[9]. (Uzunov D P, Cooper T B, Costa E, et al. Fluoxetine-elicited changes in brain neurosteroid content measured by negative ion mass fragmentography[J]. Proceedings of the National Academy of Sciences, 1996, 93(22): 12599-12604.[10]. Bremner J D. Fluoxetine in depressed patients: a comparison with imipramine[J]. Journal of Clinical Psychiatry, 1984.

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