Catecholamine/Serotonin Interactions
Open accessAbstract
This chapter brings together the work of several leading laboratories, each an outstanding example of integrative approaches to complex diseases of the central nervous system. Cognitive dysfunction and negative symptoms associated with schizophrenia are believed to result from hypofunction of the mesocortical dopaminergic projections to prefrontal cortex (PFC). Noradrenergic targets for the augmentation of dopaminergic function in PFC show promise to improve cognitive deficits as well as negative symptoms. Serotonergic targets for the modulation of mesocortical dopaminergic neurotransmission include 5-HT2A and 5-HT1A receptors. The hallmark of Parkinson's disease is the destruction of nigrostriatal dopaminergic neurons. l-DOPA, a metabolic precursor of dopamine, is the standard of treatment. However, the ectopic release of dopamine (DA) from serotonin neurons and the clearance of extracellular DA by the norepinephrine transporter in areas enriched with noradrenergic terminals contribute to extracellular DA produced by l-DOPA and offer opportunities to improve l-DOPA therapy. The high-affinity transporters for monoamines are the primary targets for antidepressant drugs. However, many patients experience suboptimal therapeutic benefit or fail to respond to treatment. Organic cation transporters and plasma membrane monoamine transporter serve an important function in regulating monoamine neurotransmission and hold potential utility as targets for the development of therapeutic drugs. Improved therapeutic approaches will arise from not only understanding how monoamines influence one another within the central nervous system as an integrated whole but also addressing the pathophysiology of specific core symptoms or distinct syndromal dimensions (cognitive impairment, motor slowing, and negative affect) regardless of disease classification, for example, psychotic, affective, and neurodegenerative.
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During embryonic development there is convergence of the various neurotransmitter signaling pathways and they influence each other's development and functioning.
“There is, furthermore, ample evidence now that during embryonic development there is convergence of the various neurotransmitter signaling pathways and influence each other’s development and functioning [153, 227–231].”
From Development of prefrontal cortex (2022) · cites this paper as [230]
The Introduction (page unavailable) describes overlapping innervation and functional interactions among dopamine, norepinephrine, and serotonin systems, supporting the claim that these pathways interact in brain function. It does not establish that they converge during embryonic development or influence one another’s development; searches for embryonic and developmental interactions found no such passage. (LLM, conf=0.86)
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- Authors
- Hensler, J. G., Artigas, F., Bortolozzi, A., Daws, L. C., De Deurwaerdère, P., Milan, L., Navailles, S., & Koek, W.
- Affiliations
- The University of Texas at San Antonio Health Science Center (US)
- Consejo Superior de Investigaciones Científicas (ES)
- Centre National de la Recherche Scientifique (FR)
- Corresponding author
- Hensler, Julie G.
- Venue
- Advances in Pharmacology
- Publisher
- Elsevier
- Published
- 2013
- Volume
- 68
- Pages
- 167-197
- ISSN
- 1054-3589 (ISSN-L)
- PMC
- PMC3902978
- OpenAlex
- W1822757692
- Cited by
- 73
- References
- 53
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 4 · 2023: 5 · 2022: 8 · 2021: 4 · 2020: 8 · 2019: 4 · 2018: 11 · 2017: 6 · 2016: 9 · 2015: 7 · 2014: 3
- FWCI
- 10.47
- Type
- book chapter
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Advances in pharmacology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion)
- Funders
- Generalitat de Catalunya
- Centro de Investigación Biomédica en Red de Salud Mental
- Instituto de Salud Carlos III
- National Institute of Mental Health (R01MH064489, R01MH093320)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
- Keywords
- catecholamines, serotonin, schizophrenia, cognitive impairment, negative symptoms, prefrontal cortex, 5-HT2A receptor, 5-HT1A receptor, Parkinson's disease, nigrostriatal dopaminergic neurons, L-DOPA, norepinephrine transporter, extracellular dopamine, antidepressant targets, organic cation transporters, plasma membrane monoamine transporter, monoamine neurotransmission
- MeSH terms
- Animals, Antidepressive Agents, Brain, Depression, Dopamine, Humans, Parkinson Disease, Schizophrenia, Serotonin
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