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Review
. 2022 Aug 8;23(15):8814.
doi: 10.3390/ijms23158814.

The Implication of 5-HT Receptor Family Members in Aggression, Depression and Suicide: Similarity and Difference

Affiliations
Review

The Implication of 5-HT Receptor Family Members in Aggression, Depression and Suicide: Similarity and Difference

Nina K Popova et al. Int J Mol Sci. .

Abstract

Being different multifactorial forms of psychopathology, aggression, depression and suicidal behavior, which is considered to be violent aggression directed against the self, have principal neurobiological links: preclinical and clinical evidence associates depression, aggression and suicidal behavior with dysregulation in central serotonergic (5-HT) neurotransmission. The implication of different types of 5-HT receptors in the genetic and epigenetic mechanisms of aggression, depression and suicidality has been well recognized. In this review, we consider and compare the orchestra of 5-HT receptors involved in these severe psychopathologies. Specifically, it concentrates on the role of 5-HT1A, 5-HT1B, 5-HT2A, 5-HT2B, 5-HT2C, 5-HT3 and 5-HT7 receptors in the mechanisms underlying the predisposition to aggression, depression and suicidal behavior. The review provides converging lines of evidence that: (1) depression-related 5-HT receptors include those receptors with pro-depressive properties (5-HT2A, 5-HT3 and 5-HT7) as well as those providing an antidepressant effect (5-HT1A, 5-HT1B, 5-HT2C subtypes). (2) Aggression-related 5-HT receptors are identical to depression-related 5-HT receptors with the exception of 5-HT7 receptors. Activation of 5-HT1A, 5-HT1B, 5-HT2A, 5-HT2C receptors attenuate aggressiveness, whereas agonists of 5-HT3 intensify aggressive behavior.

Keywords: aggression; behavior; brain serotonin system; depression; serotonin receptors; suicide.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Hypothetical mechanism of 5-HT2B receptors implicated in the mechanisms of depression. Under physiological conditions, 5-HT2B receptors directly modulate serotonergic neurotransmission as well as astrocytic functions; under stressful conditions, the 5-HT2B receptors are downregulated which may lead to both serotonergic and astrocytic dysfunctions.
Figure 2
Figure 2
Schematic representation of mechanisms of 5-HT2A and 5-HT2C receptor involvement in the pathogenesis of depression. Under physiological conditions, postsynaptic 5-HT2A and 5-HT2C receptors regulate glutamate and/or GABA release; upon stress-induced serotonin depletion, 5-HT2A and 5-HT2C receptors are upregulated and sensitized. Sensitized 5-HT2A and 5-HT2C receptors indirectly inhibit serotonergic neurotransmission, aggravate serotonin deficit and provoke depressive-like behavior.
Figure 3
Figure 3
Hypothetical mechanism of the role of 5-HT1A/5-HT7 receptor heterodimerization in the mechanism of depression. Under physiological conditions, the amount of 5-HT1A/5-HT7 heterodimers in presynaptic neurons is higher than in postsynaptic neurons; under depression, the 5-HT1A/5-HT1A homo- and 5-HT1A/5-HT7 heterodimers ratio in presynaptic neurons shifts towards 5-HT1A/5-HT1A homodimers which decreases the amount of 5-HT in the synaptic cleft.

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