Effects of duloxetine, a new serotonin and norepinephrine uptake inhibitor, on extracellular monoamine levels in rat frontal cortex.
Abstract
The effects of duloxetine (LY248686), a new inhibitor of serotonin (5-hydroxytryptamine; 5-HT) and norepinephrine (NE) uptake on extracellular levels of NE, 5-HT and dopamine (DA), were studied in the rat frontal cortex and nucleus accumbens, using in vivo microdialysis. The oral administration of duloxetine (3.125-12.5 mg/kg) produced a dose-dependent increase in the output of both NE and 5-HT from the frontal cortex, this increase being maintained throughout the 4-hr observation period. Chronic administration of duloxetine (6.25 mg/kg, p.o.) for 14 days failed to alter basal NE and 5-HT levels in the frontal cortex, but augmented the duloxetine-induced increase in output of NE and 5-HT. Amitriptyline and maprotiline, administered p.o. at doses of 6.25 to 25 mg/kg, increased NE output, but the effect was weaker than that of duloxetine, and neither amitriptyline nor maprotiline changed 5-HT output from the frontal cortex. Duloxetine, amitriptyline, and maprotiline brought about increases in DA levels in the rat frontal cortex, the increase in DA levels induced by duloxetine being approximately two or three times more potent than that induced by amitriptyline and maprotiline. In the nucleus accumbens, duloxetine also produced a dose-dependent increase in DA output more potent than that produced by amitriptyline and maprotiline. These results show that duloxetine causes a potent and sustained increase in the output of both NE and 5-HT in the rat frontal cortex, related to its inhibition of NE and 5-HT uptake; these results also show that duloxetine increases DA output in the frontal cortex.
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Duloxetine has been shown to increase extracellular 5-HT, norepinephrine, and dopamine in rat frontal cortex.
“has been shown to increase extracellular 5-HT, norepinephrine, and dopamine in rat frontal cortex [31]”
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“…chronic treatment of antidepressants causes an increase in basal extracellular 5-HT levels, in 5-HT release after antidepressant challenge in vivo, or in electrically evoked 5-HT release from slices (Bel and Artigas, 1993; Blier and Bouchard, 1994; Kihara and Ikeda, 1994; Kreiss and Lucki, 1995).”
BackgroundEffect of acute treatment with YM992 on extracellular serotonin levels in the rat frontal cortex
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“In vivo and in vitro studies indicate that duloxetine inhibits the presynaptic neuronal reuptake of the neurotransmitters serotonin and norepinephrine, leading to their greater availability at the neuronal junctions and potentiating their action in the central nervous system [15, 16].”
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“1 Acute duloxetine treatment In rat microdialysis studies, acute duloxetine increases 5-HT, NA and DA levels in the cerebral cortex [13-17], 5-HT and NA levels in the hippocampus [11,18] and DA levels in nucleus accumbens [15] in a dose-dependent manner.”
BackgroundEngleman, E. A., Perry, K. W., Mayle, D. A., et al. (1995) · Neuropsychopharmacology · doi:10.1038/sj.npp.1380263 · Cited by 12 · see citing works
Role of Axonal and Somatodendritic Monoamine Transporters in Action of Uptake Blockers
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Peters, M. M. M. S., Park, C. H. J., Turner, A., Guérin, A., & Kim, J. H. (2023) · Addiction Neuroscience · doi:10.1016/j.addicn.2023.100064 · Cited by 9 · see citing works
Dual serotonin and noradrenaline reuptake inhibitors: Focus on their differences
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“Although amitriptyline can also facilitate ascending a2-adrenergic transmission to forebrain structures involved in cognitive processing [35], the strong anti-muscarinic (i.”
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Effect of a combination of duloxetine with hydroxyzine on experimental models of anxiety in mice
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“Similarly, the duloxetine treatment-induced increase in brain monoamine profile [Table 3] is in agreement with previous reports.[19,20] The 5-HT and NE reuptake action of the duloxetine help in treating anxiety associated neurobiological dysfunctions of the serotonergic and noradrenergic system.”
ResultDing, H., Wang, Y., Gao, Y., Ye, F., Yao, K., Cao, L., Liu, Z., Wang, G., & Zhang, J. (2024) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2024.116950 · Cited by 6 · see citing works
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“Kihara and Ikeda (Kihara & Ikeda, 1995) also showed using microdialysis that duloxetine administration in rats results in balanced increases in 5-HT and NE even at the lowest doses (without having to “push” the dose).”
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Future Strategies for the Treatment of Depression
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- Authors
- Kihara, T., & Ikeda, M.
- Affiliations
- Shionogi (Japan) (JP)
- Venue
- The Journal of Pharmacology and Experimental Therapeutics
- Publisher
- Elsevier BV
- Published
- 1995-01
- Volume
- 272
- Issue
- 1
- Pages
- 177-183
- ISSN
- 0022-3565 (ISSN-L)
- OpenAlex
- W1846318813
- Cited by
- 123
- References
- 0
- Citations by year
- 2025: 1 · 2024: 1 · 2023: 4 · 2022: 3 · 2021: 4 · 2020: 2 · 2019: 3 · 2018: 6 · 2017: 3 · 2016: 2 · 2015: 4 · 2014: 5 · 2013: 7 · 2012: 3
- FWCI
- 2.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Pharmacology and Experimental Therapeutics (publishedVersion)
- PubMed (publishedVersion)
- PubMed
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- duloxetine, serotonin-norepinephrine reuptake inhibitors, serotonin, norepinephrine, dopamine, frontal cortex, nucleus accumbens, amitriptyline, maprotiline, chronic drug administration, antidepressant effects
- MeSH terms
- Duloxetine Hydrochloride, Amitriptyline, Animals, Biological Transport, Cerebral Cortex, Dopamine, Male, Maprotiline, Norepinephrine, Nucleus Accumbens, Serotonin, Thiophenes, Rats, Wistar, Rats
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