Abstract
Serotonin and its receptors (HTRs) play critical roles in brain development and in the regulation of cognition, mood, and anxiety. HTRs are highly expressed in human prefrontal cortex and exert control over prefrontal excitability. The serotonin system is a key treatment target for several psychiatric disorders; however, the effectiveness of these drugs varies according to age. Despite strong evidence for developmental changes in prefrontal Htrs of rodents, the developmental regulation of HTR expression in human prefrontal cortex has not been examined. Using postmortem human prefrontal brain tissue from across postnatal life, we investigated the expression of key serotonin receptors with distinct inhibitory (HTR1A, HTR5A) and excitatory (HTR2A, HTR2C, HTR4, HTR6) effects on cortical neurons, including two receptors which appear to be expressed to a greater degree in inhibitory interneurons of cerebral cortex (HTR2C, HTR6). We found distinct developmental patterns of expression for each of these six HTRs, with profound changes in expression occurring early in postnatal development and also into adulthood. However, a collective look at these HTRs in terms of their likely neurophysiological effects and major cellular localization leads to a model that suggests developmental changes in expression of these individual HTRs may not perturb an overall balance between inhibitory and excitatory effects. Examining and understanding the healthy balance is critical to appreciate how abnormal expression of an individual HTR may create a window of vulnerability for the emergence of psychiatric illness.
Highlights
In the adult, modulation of the prefrontal cortex by the neuromodulator serotonin is critical for emotional regulation and resilience to stress [1,2,3,4]
We examine the developmental changes in the expression of these serotonin receptors in human prefrontal cortex from infancy to adulthood
Relationship with inhibitory interneuron marker mRNA Since HTR2C and HTR6 are thought to be more strongly expressed in cortical interneurons, we examined whether their expression was related to developmental changes in common interneuron markers, such as parvalbumin (PV), calbindin (CB), somatostatin (SST) and cholecystokinin (CCK)
Summary
Modulation of the prefrontal cortex by the neuromodulator serotonin is critical for emotional regulation and resilience to stress [1,2,3,4]. The prefrontal cortex is a late maturing brain region [5,6,7,8,9] with an extensive interrelationship with the serotonin system [10,11,12]. It is thought that these developmental changes in the functional and pharmacological effects of serotonin are due to changes in the expression of individual postsynaptic receptors [22,24]. Developmental changes in the expression of serotonin receptors (HTRs) would alter the functional effects of serotonin and serotonergic medicines, yet developmental changes in HTRs have not been systematically examined in human prefrontal cortex
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