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Relationship: 3475
Title
Increased, extracellular serotonin leads to Increased, stimulation of brain serotonin 5-HT1a, 5-HT2c receptors
Upstream event
Downstream event
Key Event Relationship Overview
AOPs Referencing Relationship
| AOP Name | Adjacency | Weight of Evidence | Quantitative Understanding | Point of Contact | Author Status | OECD Status |
|---|---|---|---|---|---|---|
| Inhibition, 5-hydroxytryptamine transporter (5-HTT; SERT) leads to Inhibition, Feeding | adjacent | High | Not Specified | John Frisch (send email) | Under development: Not open for comment. Do not cite |
Taxonomic Applicability
| Term | Scientific Term | Evidence | Link |
|---|---|---|---|
| fish | fish | High | NCBI |
Sex Applicability
| Sex | Evidence |
|---|---|
| Unspecific | High |
Life Stage Applicability
| Term | Evidence |
|---|---|
| All life stages | Moderate |
Key Event Relationship Description
Serotonin (5-HT) is a neurotransmitter with multiple classes of cellular receptors that regulates a variety of organism functions (for review see Barnes et al. 2021). Increased extracellular serotonin leads to increased stimulation of brain 5-HT1a, 5-HT2c receptors.
Evidence Collection Strategy
This Key Event Relationship was developed as part of an Environmental Protection Agency effort to represent putative AOPs from peer-reviewed literature which were heretofore unrepresented in the AOP-Wiki. McDonald (2017) focused on using an Adverse Outcome Pathway framework to examine inhibition of 5-hydroxytryptamine transporters in fish by selective serotonin reuptake inhibitor (SSRI) toxicants, to review known roles of serotonin receptors to explore mechanisms of action, and to determine toxicity endpoints. McDonald (2017) used the Read-Across Hypothesis, which postulates that pharmaceuticals will cause comparable effects in different taxa if the pathways and targets are evolutionarily and functionally conserved (Rand-Weaver et al. 2013), to link effects of serotonin pathways in fish and mammals.
Cited empirical studies are focused on increased extracellular serotonin levels and resulting increased stimulation of brain 5-HT1a, 5-HT2c receptors in fish, in support of development of AOP 568 for McDonald (2017) content.
Authors of KER 3475 did a further evaluation of published peer-reviewed literature to provide additional evidence in support of the key event relationship.
Evidence Supporting this KER
Biological Plausibility
Stimulation of brain 5-HT1a, 5-HT2c receptors by serotonin (5-HT) is often measured indirectly by use of antagonist compounds to block activation of receptors (methysergide for 5-HT1/5-HT2 in Ortega et al. 2013, 8-OH-DPAT for 5-HT1a in Perez-Maceira et al. 2014 and Perez-Maceria et al. 2016; MK212 for 5-HT2c in Perez-Maceira et al. 2014 and Perez-Maceria et al. 2016; WAY 161503 for 5-HT2c in Perez-Maceria et al. 2016). Often the relationship between increased levels of serotonin and increased simulation of serotonin receptors is assumed and focus placed on downstream effects of activation of serotonin pathways and/or behavior effects, with more extensive study in laboratory mammals than fish (see Ramsteijn et al. 2020 for review of mammal studies). Empirical mammal studies show additional support for the mechanism of stimulation of brain 5-HT1a, 5-HT2c receptors by serotonin because of the evolutionarily and functionally conserved pathways modulated by the neurotransmitter serotonin.
Empirical Evidence
Uncertainties and Inconsistencies
Known modulating factors
Quantitative Understanding of the Linkage
Response-response Relationship
Time-scale
Known Feedforward/Feedback loops influencing this KER
Domain of Applicability
Life Stage: Applies to all life stages with developed brain and central nervous systems.
Sex: Applies to both males and females.
Taxonomic: Studied in fish, with similarities expected in laboratory mammals and humans due to evolutionary and functional conservation of serotonin-induced pathways.
References
Barnes, N.M., Ahern, G.P., Becamel, C., Bockaert, J., Camilleri, M., Chaumont-Dubel, S., Claeysen, S., Cunningham, K.A., Fone, K.C., Gershon, M., Di Giovanni, G., Goodfellow, N.M., Halberstadt, A.L., Hartley, R.M., Hassaine, G., Herrick-Davis, K., Hovius, R., Lacivita, E., Lambe, E..K, Leopoldo, M., Levy, F.O., Lummis, S.C.R, Marin, P., Maroteaux, L., McCreary, A.C., Nelson, D.L., Neumaier, J.F., Newman-Tancredi, A., Nury, H., Roberts, A., Roth, B.L., Roumier, A., Sanger, G.J., Teitler, M., Sharp, T., Villalon, C.M., Vogel, H., Watts, S.W., and Hoyer, D. 2021. International Union of Basic and Clinical Pharmacology. CX. Classification of Receptors for 5-hydroxytryptamine; Pharmacology and Function. Pharmacological Reviews 73(1): 310-520.
McDonald, M.D. 2017. An AOP analysis of selective serotonin reuptake inhibitors (SSRIs) for fish. Comparative Biochemistry and Physiology, Part C-Toxicology and Pharmacology 197: 19–31.
Ortega, V.A., Lovejoy, D.A., and Bernier, N.J. 2013. Appetite-suppressing effects and interactions of centrally administered corticotropin-releasing factor, urotensin I and serotonin in rainbow trout (Oncorhynchus mykiss). Frontiers in Neuroscience 7: 196.
Perez-Maceira, J.J., Mancebo, M.J., and Aldegunde, M. 2014. The involvement of 5-HT-like receptors in the regulation of food intake in rainbow trout (Oncorhynchus mykiss). Comparative Biochemistry and Physiology, Part C-Toxicology and Pharmacology 161: 1–6.
Perez-Maceira, J.J., Otero-Rodino, C., Mancebo, M.J., Soengas, J.L., and Aldegunde, M. 2016. Food intake inhibition in rainbow trout induced by activation of serotonin 5‑HT2C receptors is associated with increases in POMC, CART and CRF mRNA abundance in hypothalamus. Comparative Biochemistry and Physiology, Part B-Biochemical Systems and Environmental Physiology 186(3): 313-321.
Ramsteijn A.S., Van de Wijer, L., Rando, J., van Luijk, J., Homberg, J.R., and Olivier, J.D.A. 2020. Perinatal selective serotonin reuptake inhibitor exposure and behavioral outcomes: A systematic review and meta-analyses of animal studies. Neuroscience and Biobehavior Reviews 114: 53–69.
NOTE: Italics indicate edits from John Frisch January 2025.