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      Serotonin Receptor Expression in Human Prefrontal Cortex: Balancing Excitation and Inhibition across Postnatal Development

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          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.

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          Most cited references93

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          Interneurons of the neocortical inhibitory system.

          Mammals adapt to a rapidly changing world because of the sophisticated cognitive functions that are supported by the neocortex. The neocortex, which forms almost 80% of the human brain, seems to have arisen from repeated duplication of a stereotypical microcircuit template with subtle specializations for different brain regions and species. The quest to unravel the blueprint of this template started more than a century ago and has revealed an immensely intricate design. The largest obstacle is the daunting variety of inhibitory interneurons that are found in the circuit. This review focuses on the organizing principles that govern the diversity of inhibitory interneurons and their circuits.
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            Serotonin1A receptor acts during development to establish normal anxiety-like behaviour in the adult.

            Serotonin is implicated in mood regulation, and drugs acting via the serotonergic system are effective in treating anxiety and depression. Specifically, agonists of the serotonin1A receptor have anxiolytic properties, and knockout mice lacking this receptor show increased anxiety-like behaviour. Here we use a tissue-specific, conditional rescue strategy to show that expression of the serotonin1A receptor primarily in the hippocampus and cortex, but not in the raphe nuclei, is sufficient to rescue the behavioural phenotype of the knockout mice. Furthermore, using the conditional nature of these transgenic mice, we suggest that receptor expression during the early postnatal period, but not in the adult, is necessary for this behavioural rescue. These findings show that postnatal developmental processes help to establish adult anxiety-like behaviour. In addition, the normal role of the serotonin1A receptor during development may be different from its function when this receptor is activated by therapeutic intervention in adulthood.
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              Expression of interneuron markers in the dorsolateral prefrontal cortex of the developing human and in schizophrenia.

              The onset of schizophrenia symptoms in late adolescence implies a neurodevelopmental trajectory for the disease. Indeed, the γ-aminobutyric acid (GABA) inhibitory system shows protracted development, and GABA-ergic deficits are widely replicated in postmortem schizophrenia studies. The authors examined expression of several interneuron markers across postnatal human development and in schizophrenia to assess whether protracted development of certain interneuron subpopulations may be associated with a particular vulnerability in schizophrenia. RNA was extracted postmortem from dorsolateral prefrontal cortex of individuals from age 6 weeks to 49 years (N=68) and from a cohort of normal comparison subjects and schizophrenia patients (N=74, 37 pairs). Expression levels of parvalbumin, cholecystokinin, somatostatin, neuropeptide Y, calretinin, calbindin, and vasoactive intestinal peptide were measured by quantitative reverse transcription-polymerase chain reaction. Changes in calretinin protein levels were examined by Western blot. Interneuron marker genes followed one of three general expression profiles: either increasing (parvalbumin, cholecystokinin) or decreasing (somatostatin, calretinin, neuropeptide Y) in expression over postnatal life, with the most dramatic changes seen in the first few years before reaching a plateau; or increasing to peak expression in the toddler years before decreasing (calbindin, vasoactive intestinal peptide). mRNA expression of all genes, with the exception of calbindin (which increased), showed a reduction (8%-31%) in schizophrenia. Somatostatin showed the most dramatic reduction (31%) in schizophrenia. It appears that a heterogeneous population of interneurons is implicated in schizophrenia. Further studies are needed to determine whether specific interneuron subpopulations are altered or whether common or distinct upstream pathways are responsible for interneuron deficits in schizophrenia.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2011
                29 July 2011
                02 August 2011
                : 6
                : 7
                : e22799
                Affiliations
                [1 ]Department of Physiology, University of Toronto, Toronto, Ontario, Canada
                [2 ]Department of Obstetrics and Gynaecology, University of Toronto, Toronto, Ontario, Canada
                [3 ]Schizophrenia Research Institute, Sydney, New South Wales, Australia
                [4 ]Schizophrenia Research Laboratory, Neuroscience Research Australia, Randwick, New South Wales, Australia
                [5 ]Faculty of Medicine, School of Psychiatry, University of New South Wales, Sydney, New South Wales, Australia
                [6 ]Stanley Medical Research Institute, Rockville, Maryland, United States of America
                Institut National de la Santé et de la Recherche Médicale, France
                Author notes

                Conceived and designed the experiments: EKL SGF CSW MJW. Performed the experiments: SGF MJW. Analyzed the data: SGF EKL CSW MJW. Contributed reagents/materials/analysis tools: CSW MJW. Wrote the paper: EKL SGF CSW MJW.

                Article
                PONE-D-11-04526
                10.1371/journal.pone.0022799
                3146513
                21829518
                942c9719-b066-48fc-8117-0a11559ebd59
                Lambe et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 3 March 2011
                : 5 July 2011
                Page count
                Pages: 10
                Categories
                Research Article
                Biology
                Biochemistry
                Neurochemistry
                Neurochemicals
                Serotonin
                Genetics
                Gene Expression
                Molecular Cell Biology
                Signal Transduction
                Membrane Receptor Signaling
                Neurotransmitter Receptor Signaling
                Neuroscience
                Neurochemistry
                Neurochemicals
                Serotonin
                Developmental Neuroscience
                Molecular Neuroscience
                Neurotransmitters
                Medicine
                Mental Health
                Psychiatry

                Uncategorized
                Uncategorized

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