Distribution of serotonin 5-HT 1A -binding sites in the brainstem and the hypothalamus, and their roles in 5-HT-induced sleep and ingestive behaviors in rock pigeons ( Columba livia )
“…Likewise, alterations have been reported in the pattern of expression for the HTR1A and HTR2A genes in mental illnesses related to mood and response to stress [51, 52], panic attacks, [53], bipolar disorder, anxiety, and depression, among others [54–56], but not in behaviors such as suicide [49]. Reports of expression of the 5-HT1A receptor in the hippocampus, cortex, and hypothalamic regions correspond to the expression reported in this study [16, 55]. Other sources that provide data on serotonin genes are postmortem studies that report increases in genes such as HTR2A in patients with conditions such as depression and schizophrenia [54, 57, 58].…”
Section: Serotonin (5-ht)supporting
confidence: 81%
“…They have helped refine anatomical [4, 9, 11, 14, 15], taxonomical [9, 16, 17], and statistical methods [18], which allow us to partly identify the relationship between structures and functions upon examining expression patterns [4, 14, 15, 19] and compare expression levels in different states [20] and anatomical correlations and phenotypes between different species [5, 14, 15, 18, 19]. …”
Section: Genetic Atlasesmentioning
confidence: 99%
“…Serotonin or 5-hydroxytryptamine (5-HT) was chosen as the focus of this study for various reasons: first, because many behavioral disorders and the drugs used to treat them have been linked to serotonergic mechanisms [27, 38–40]; second, 5-HT projections and receptors have been described in multiple sites [14–16, 27], facilitating the search for the expression of related genes. Given that a broad area of research in psychobiology and behavioral neuroscience is the use of animal models, it is of interest to compare the distribution of serotonin-related gene expression, as this may help confirm the validity of interspecies models, in this case mouse-human [17, 41].…”
Section: Serotonin (5-ht)mentioning
confidence: 99%
“…Changes in its synthesis, bioavailability, and expression of receptors and other molecules related to its functioning have been associated with changes in behavior [12, 17, 27]. Many clinical conditions have been linked to altered serotonergic functions, including eating disorders, anxiety, issues with endocrine and circadian rhythm regulation, perception problems, compulsive behavior, pain, schizophrenia, sexual dysfunction, sleep disorders, and depression [12, 16, 27, 42, 43]. …”
Brain atlases are tools based on comprehensive studies used to locate biological characteristics (structures, connections, proteins, and gene expression) in different regions of the brain. These atlases have been disseminated to the point where tools have been created to store, manage, and share the information they contain. This study used the data published by the Allen Mouse Brain Atlas (2004) for mice (C57BL/6J) and Allen Human Brain Atlas (2010) for humans (6 donors) to compare the expression of serotonin-related genes. Genes of interest were searched for manually in each case (in situ hybridization for mice and microarrays for humans), normalized expression data (z-scores) were extracted, and the results were graphed. Despite the differences in methodology, quantification, and subjects used in the process, a high degree of similarity was found between expression data. Here we compare expression in a way that allows the use of translational research methods to infer and validate knowledge. This type of study allows part of the relationship between structures and functions to be identified, by examining expression patterns and comparing levels of expression in different states, anatomical correlations, and phenotypes between different species. The study concludes by discussing the importance of knowing, managing, and disseminating comprehensive, open-access studies in neuroscience.
“…Likewise, alterations have been reported in the pattern of expression for the HTR1A and HTR2A genes in mental illnesses related to mood and response to stress [51, 52], panic attacks, [53], bipolar disorder, anxiety, and depression, among others [54–56], but not in behaviors such as suicide [49]. Reports of expression of the 5-HT1A receptor in the hippocampus, cortex, and hypothalamic regions correspond to the expression reported in this study [16, 55]. Other sources that provide data on serotonin genes are postmortem studies that report increases in genes such as HTR2A in patients with conditions such as depression and schizophrenia [54, 57, 58].…”
Section: Serotonin (5-ht)supporting
confidence: 81%
“…They have helped refine anatomical [4, 9, 11, 14, 15], taxonomical [9, 16, 17], and statistical methods [18], which allow us to partly identify the relationship between structures and functions upon examining expression patterns [4, 14, 15, 19] and compare expression levels in different states [20] and anatomical correlations and phenotypes between different species [5, 14, 15, 18, 19]. …”
Section: Genetic Atlasesmentioning
confidence: 99%
“…Serotonin or 5-hydroxytryptamine (5-HT) was chosen as the focus of this study for various reasons: first, because many behavioral disorders and the drugs used to treat them have been linked to serotonergic mechanisms [27, 38–40]; second, 5-HT projections and receptors have been described in multiple sites [14–16, 27], facilitating the search for the expression of related genes. Given that a broad area of research in psychobiology and behavioral neuroscience is the use of animal models, it is of interest to compare the distribution of serotonin-related gene expression, as this may help confirm the validity of interspecies models, in this case mouse-human [17, 41].…”
Section: Serotonin (5-ht)mentioning
confidence: 99%
“…Changes in its synthesis, bioavailability, and expression of receptors and other molecules related to its functioning have been associated with changes in behavior [12, 17, 27]. Many clinical conditions have been linked to altered serotonergic functions, including eating disorders, anxiety, issues with endocrine and circadian rhythm regulation, perception problems, compulsive behavior, pain, schizophrenia, sexual dysfunction, sleep disorders, and depression [12, 16, 27, 42, 43]. …”
Brain atlases are tools based on comprehensive studies used to locate biological characteristics (structures, connections, proteins, and gene expression) in different regions of the brain. These atlases have been disseminated to the point where tools have been created to store, manage, and share the information they contain. This study used the data published by the Allen Mouse Brain Atlas (2004) for mice (C57BL/6J) and Allen Human Brain Atlas (2010) for humans (6 donors) to compare the expression of serotonin-related genes. Genes of interest were searched for manually in each case (in situ hybridization for mice and microarrays for humans), normalized expression data (z-scores) were extracted, and the results were graphed. Despite the differences in methodology, quantification, and subjects used in the process, a high degree of similarity was found between expression data. Here we compare expression in a way that allows the use of translational research methods to infer and validate knowledge. This type of study allows part of the relationship between structures and functions to be identified, by examining expression patterns and comparing levels of expression in different states, anatomical correlations, and phenotypes between different species. The study concludes by discussing the importance of knowing, managing, and disseminating comprehensive, open-access studies in neuroscience.
“…Aside from 5-HT3, which is a ligand-gated ion channel that belongs to the nicotinic acetylcholine receptor superfamily7, the 5-HT receptors belong to the superfamily of G protein coupled receptors (GPCRs)89. Orthologous G protein-coupled 5-HT receptors have been identified and functionally characterised in deuterostomes including humans10, mammals11, birds12 and fishes13, and in protostomes including nematodes14, crustaceans15 and insects1617. Furthermore, these G protein-coupled 5-HT receptors are mainly classified in three groups: (1) 5-HT1 and 5-HT5 receptors that couple preferentially to Gi proteins and inhibit cAMP synthesis, (2) 5-HT2 receptors that activate Gq proteins, which mediate the hydrolysis of inositol phosphates and cause a subsequent increase in cytosolic Ca 2+ , and (3) 5-HT4, 5-HT6, and 5-HT7 receptors that couple to Gs proteins and promote cAMP formation1819.…”
Serotonin (5-HT) is an important neurotransmitter and neuromodulator that controls a variety of sensory and motor functions through 5-HT receptors (5-HTRs). The 5-HT4R subfamily is linked to Gs proteins, which activate adenylyl cyclases (ACs), and is involved in many responses in peripheral organs. In this study, the 5-HT4R from Apostichopus japonicus (Aj5-HT4R) was identified and characterised. The cloned full-length Aj5-HT4R cDNA is 1,544 bp long and contains an open reading frame 1,011 bp in length encoding 336 amino acid proteins. Bioinformatics analysis of the Aj5-HT4R protein indicated this receptor was a member of class A G protein coupled receptor (GPCR) family. Further experiments using Aj5-HT4R-transfected HEK293 cells demonstrated that treatment with 5-HT triggered a significant increase in intracellular cAMP level in a dose-dependent manner and induced a rapid internalisation of Aj5-HT4R fused with enhanced green fluorescent protein (Aj5-HT4R-EGFP) from the cell surface into the cytoplasm. In addition, the transcriptional profiles of Aj5-HT4R in aestivating A. japonicas and phosphofructokinase (AjPFK) in 5-HT administrated A. japonicus have been analysed by real-time PCR assays. Results have led to a basic understanding of Aj5-HT4R in A. japonicus, and provide a foundation for further exploration of the cell signaling and regulatory functions of this receptor.
Due to the prevalence of depression in women, female rats may be a better models for antidepressant research than males. In male rats, fluoxetine inhibited the serotonin (5‐hydroxytryptamine, 5‐HT) transporter (SERT) which is reducing the immobility time in the repeated forced swimming test (rFST). The performance of female rats in this test is unknown. In this study, responses of male and female rats in the rFST under chronic treatment with fluoxetine and the function of SERT in their brains were examined. Wistar rats received oral fluoxetine (females: 0, 1, 2.5, or 5 mg kg‐1 day‐1; males: 0 or 2.5 mg kg‐1 day‐1; in sucrose 10%, 1.5 ml/rat) 1 hr before the test daily for 12 days over the course of the rFST. rFST consisted of a 15 min pretest followed by 5 min sessions of swimming at 1 (test), 7 (retest 1), and 14 (retest 2) days later. SERT functioning was assessed by ex vivo assays of the frontal cortex and hippocampus of rats. Fluoxetine reduced immobility time of males in the rFST while it failed to do so in females. In vitro treatment with fluoxetine inhibited the uptake of 5‐HT of both sexes similarly, while in vivo chronic administration of fluoxetine failed to do so. In summary, rats responded to the chronic treatment with fluoxetine in a sexually dimorphic fashion during the rFST despite the functioning of SERT in their brains remaining equally unchanged. Hence, our data suggest that sexually dimorphic responses to fluoxetine in rFST may be unrelated to the function of SERT in rat brains.
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