The serotonergic system and anxiety.

Abstract:

:The wide use of serotonin reuptake inhibitors and serotonin receptor agonists in anxiety disorders has suggested a key role for the modulatory neurotransmitter in anxiety. However, serotonin's specific role is still uncertain. This article reviews the literature concerning how and where serotonergic agents modulate anxiety. Varying and sometimes conflicting data from human and animal studies argue for both anxiolytic and anxiogenic roles for serotonin, depending on the specific disorder, structure, or behavioral task studied. However, recent data from molecular genetic studies in the mouse point toward two important roles for the serotonin 1A receptor. In development, serotonin acts through this receptor to promote development of the circuitry necessary for normal anxiety-like behaviors. In adulthood, serotonin reuptake inhibitors act through the same receptor to stimulate neurogenesis and reduce anxiety-like behaviors. These studies highlight that the complex serotonin system likely plays various roles in the regulation of anxiety both during development and in adulthood.

journal_name

Neuromolecular Med

journal_title

Neuromolecular medicine

authors

Gordon JA,Hen R

doi

10.1385/NMM:5:1:027

keywords:

subject

Has Abstract

pub_date

2004-01-01 00:00:00

pages

27-40

issue

1

eissn

1535-1084

issn

1559-1174

pii

NMM:5:1:027

journal_volume

5

pub_type

杂志文章,评审
  • Autoimmune modulation of astrocyte-mediated homeostasis.

    abstract::Astrocytes are principal mediators of homeostasis in the central nervous system (CNS). They supply neurons and oligodendrocytes with substrates for energy metabolism and clear the extracellular space of excess neurotransmitters. In neuroinflammation, astrocytes have classically been regarded as unimportant since their...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1385/nmm:9:1:1

    authors: Korn T,Rao M,Magnus T

    更新日期:2007-01-01 00:00:00

  • Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease.

    abstract::The gene encoding alpha-T-catenin, CTNNA3, is positioned within a region on chromosome 10, showing strong evidence of linkage to Alzheimer's disease (AD), and is therefore a good positional candidate gene for this disorder. We have demonstrated that alpha-T-catenin is expressed in human brain, and like other alpha-cat...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:5:2:133

    authors: Busby V,Goossens S,Nowotny P,Hamilton G,Smemo S,Harold D,Turic D,Jehu L,Myers A,Womick M,Woo D,Compton D,Doil LM,Tacey KM,Lau KF,Al-Saraj S,Killick R,Pickering-Brown S,Moore P,Hollingworth P,Archer N,Foy C,Wal

    更新日期:2004-01-01 00:00:00

  • Clinacanthus nutans Extracts Modulate Epigenetic Link to Cytosolic Phospholipase A2 Expression in SH-SY5Y Cells and Primary Cortical Neurons.

    abstract::Clinacanthus nutans Lindau (C. nutans), commonly known as Sabah Snake Grass in southeast Asia, is widely used in folk medicine due to its analgesic, antiviral, and anti-inflammatory properties. Our recent study provided evidence for the regulation of cytosolic phospholipase A2 (cPLA2) mRNA expression by epigenetic fac...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-016-8404-z

    authors: Tan CS,Ho CF,Heng SS,Wu JS,Tan BK,Ng YK,Sun GY,Lin TN,Ong WY

    更新日期:2016-09-01 00:00:00

  • The molecular basis of familial dysautonomia: overview, new discoveries and implications for directed therapies.

    abstract::Familial dysautonomia (FD) is a sensory and autonomic neuropathy that affects the development and survival of sensory, sympathetic, and some parasympathetic neurons. It is autosomally inherited and occurs almost exclusively among individuals of Ashkenazi Jewish descent. The pathological and clinical manifestations of ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-007-8019-5

    authors: Rubin BY,Anderson SL

    更新日期:2008-01-01 00:00:00

  • Epileptic seizures in AD patients.

    abstract::Epileptic seizures have long been recognised as a complication of the clinical syndrome of Alzheimer's disease, particularly in advanced disease, but have hitherto been viewed essentially as epiphenomena of the neurodegenerative process. Progress with animal models of Alzheimer's disease has suggested that this view m...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-009-8076-z

    authors: Larner AJ

    更新日期:2010-03-01 00:00:00

  • Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.

    abstract::Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurodegenerative disorder characterized by progressive cerebellar ataxia and epilepsy. The disease is caused by a pentanucleotide ATTCT expansion in intron 9 of the ATXN10 gene on chromosome 22q13.3. SCA10 has shown a geographical distribution throughout...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-017-8464-8

    authors: Bampi GB,Bisso-Machado R,Hünemeier T,Gheno TC,Furtado GV,Veliz-Otani D,Cornejo-Olivas M,Mazzeti P,Bortolini MC,Jardim LB,Saraiva-Pereira ML,Rede Neurogenetica.

    更新日期:2017-12-01 00:00:00

  • Reduction of AP180 and CALM produces defects in synaptic vesicle size and density.

    abstract::Clathrin assembly proteins AP180 and CALM regulate the assembly of clathrin-coated vesicles (CCVs), which mediate diverse intracellular trafficking processes, including synaptic vesicle (SV) recycling at the synapse. Although studies using several invertebrate model systems have indicated a role for AP180 in SV recycl...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-012-8194-x

    authors: Petralia RS,Wang YX,Indig FE,Bushlin I,Wu F,Mattson MP,Yao PJ

    更新日期:2013-03-01 00:00:00

  • Scutellarin Exerts Anti-Inflammatory Effects in Activated Microglia/Brain Macrophage in Cerebral Ischemia and in Activated BV-2 Microglia Through Regulation of MAPKs Signaling Pathway.

    abstract:BACKGROUND:Scutellarin, an herbal compound, can effectively suppress the inflammatory response in activated microglia/brain macrophage(AM/BM) in experimentally induced cerebral ischemia; however, the underlying mechanism for this has not been fully clarified. We sought to elucidate if scutellarin would exert its anti-i...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-019-08582-2

    authors: Chen HL,Jia WJ,Li HE,Han H,Li F,Zhang XL,Li JJ,Yuan Y,Wu CY

    更新日期:2020-06-01 00:00:00

  • Preclinical and Clinical Evidence for the Involvement of Sphingosine 1-Phosphate Signaling in the Pathophysiology of Vascular Cognitive Impairment.

    abstract::Sphingosine 1-phosphates (S1Ps) are bioactive lipids that mediate a diverse range of effects through the activation of cognate receptors, S1P1-S1P5. Scrutiny of S1P-regulated pathways over the past three decades has identified important and occasionally counteracting functions in the brain and cerebrovascular system. ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-020-08632-0

    authors: Chua XY,Ho LTY,Xiang P,Chew WS,Lam BWS,Chen CP,Ong WY,Lai MKP,Herr DR

    更新日期:2020-11-12 00:00:00

  • Mitochondrial UCP4 mediates an adaptive shift in energy metabolism and increases the resistance of neurons to metabolic and oxidative stress.

    abstract::The high-metabolic demand of neurons and their reliance on glucose as an energy source places them at risk for dysfunction and death under conditions of metabolic and oxidative stress. Uncoupling proteins (UCPs) are mitochondrial inner membrane proteins implicated in the regulation of mitochondrial membrane potential ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:8:3:389

    authors: Liu D,Chan SL,de Souza-Pinto NC,Slevin JR,Wersto RP,Zhan M,Mustafa K,de Cabo R,Mattson MP

    更新日期:2006-01-01 00:00:00

  • Does Concurrent Use of Some Botanicals Interfere with Treatment of Tuberculosis?

    abstract::Millions of individuals with active TB do not receive recommended treatments, and instead may use botanicals, or use botanicals concurrently with established treatments. Many botanicals protect against oxidative stress, but this can interfere with redox-dependent activation of isoniazid and other prodrugs used for pro...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-016-8402-1

    authors: Folk WR,Smith A,Song H,Chuang D,Cheng J,Gu Z,Sun G

    更新日期:2016-09-01 00:00:00

  • The mammalian RNA-binding protein Staufen2 links nuclear and cytoplasmic RNA processing pathways in neurons.

    abstract::Members of the Staufen family of RNA-binding proteins are highly conserved cytoplasmic RNA transporters associated with RNA granules. staufen2 is specifically expressed in neurons where the delivery of RNA to dendrites is thought to have a role in plasticity. We found that Staufen2 interacts with the nuclear pore prot...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:6:2-3:127

    authors: Monshausen M,Gehring NH,Kosik KS

    更新日期:2004-01-01 00:00:00

  • Correction to: Mild TBI Results in a Long-Term Decrease in Circulating Phospholipids in a Mouse Model of Injury.

    abstract::The original version of this article unfortunately contained a mistake. Gary S. Laco should not be listed as an author in the author group. ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,已发布勘误

    doi:10.1007/s12017-020-08593-4

    authors: Emmerich T,Abdullah L,Ojo J,Mouzon B,Nguyen T,Crynen G,Evans JE,Reed J,Mullan M,Crawford F

    更新日期:2020-06-01 00:00:00

  • Aberrant miRNAs Regulate the Biological Hallmarks of Glioblastoma.

    abstract::GBM is the highest incidence in primary intracranial malignancy, and it remains poor prognosis even though the patient is gave standard treatment. Despite decades of intense research, the complex biology of GBM remains elusive. In view of eight hallmarks of cancer which were proposed in 2011, studies related to the ei...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-018-8507-9

    authors: Yu W,Liang S,Zhang C

    更新日期:2018-12-01 00:00:00

  • Alzheimer's disease and neuronal network activity.

    abstract::The amyloid beta-peptide theory of Alzheimer's Disease has helped to advance our understanding of the disease tremendously. A new area of research focuses on the changes in neuronal network activity that take place and may contribute to the clinical and pathological picture of Alzheimer's Disease. An apparent symptom ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-009-8100-3

    authors: Gleichmann M,Mattson MP

    更新日期:2010-03-01 00:00:00

  • The neuroprotective factor Wlds does not attenuate mutant SOD1-mediated motor neuron disease.

    abstract::Selective degeneration and death of motor neurons in SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS) is accompanied by axonal disorganization and reduced slow axonal transport in the three most frequently used mouse models of mutant SOD1-mediated ALS. To test whether suppression of axonal degeneration (freque...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:5:3:193

    authors: Vande Velde C,Garcia ML,Yin X,Trapp BD,Cleveland DW

    更新日期:2004-01-01 00:00:00

  • Association Between NOS1 Gene Polymorphisms and Schizophrenia in Asian and Caucasian Populations: A Meta-Analysis.

    abstract::Schizophrenia is a complex psychiatric disorder characterized by memory impairments with delusions and hallucinations. Several investigations have focused on determining the association between NOS1 (nitric oxide synthase-1) polymorphisms and risk of schizophrenia (SZ). However, the association of rs2682826, rs3782206...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,meta分析

    doi:10.1007/s12017-017-8460-z

    authors: Ahmed SSSJ,Akram Husain RS,Suresh Kumar,Ramakrishnan V

    更新日期:2017-09-01 00:00:00

  • Neuroprotective Effect of Hydrogen Sulfide in Hyperhomocysteinemia Is Mediated Through Antioxidant Action Involving Nrf2.

    abstract::Homocysteine (Hcy) is a sulfur-containing amino acid derived from methionine metabolism. Elevated plasma Hcy levels (> 15 µM) result in a condition called hyperhomocysteinemia (HHcy), which is an independent risk factor in the development of various neurodegenerative disorders. Reactive oxygen species (ROS) produced b...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-018-8505-y

    authors: Kumar M,Sandhir R

    更新日期:2018-12-01 00:00:00

  • Cerebrospinal Fluid C-Reactive Protein in Parkinson's Disease: Associations with Motor and Non-motor Symptoms.

    abstract::Parkinson' disease (PD) is characterized by motor symptoms including bradykinesia, resting tremor, postural instability, and rigidity and non-motor symptoms such as cognitive impairment, sleep disorder, and depression. Neuroinflammation has been recently implicated in pathophysiology of both motor and non-motor sympto...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-018-8499-5

    authors: Sanjari Moghaddam H,Valitabar Z,Ashraf-Ganjouei A,Mojtahed Zadeh M,Ghazi Sherbaf F,Aarabi MH

    更新日期:2018-09-01 00:00:00

  • Role of protein aggregation in mitochondrial dysfunction and neurodegeneration in Alzheimer's and Parkinson's diseases.

    abstract::Abnormal interactions and misfolding of synaptic proteins in the nervous system are being extensively explored as important pathogenic events resulting in neurodegeneration in various neurological disorders. These include Alzheimer's disease (AD), Parkinson's disease (PD), and dementia with Lewy bodies (DLB). In AD, m...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1385/NMM:4:1-2:21

    authors: Hashimoto M,Rockenstein E,Crews L,Masliah E

    更新日期:2003-01-01 00:00:00

  • MiR-5787 Attenuates Macrophages-Mediated Inflammation by Targeting TLR4/NF-κB in Ischemic Cerebral Infarction.

    abstract::Accumulating studies have suggested the important role of microRNA (miRNA) in ischemic cerebral infarction. However, little is known of the modifying effect of miR-5787, a newly found miRNA, in ischemic cerebral infarction. We aim to elucidate the effect and underlying molecular mechanism of miR-5787 in the pathogenes...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-020-08628-w

    authors: Bao Z,Zhang S,Li X

    更新日期:2020-11-09 00:00:00

  • Scutellarin as a Potential Therapeutic Agent for Microglia-Mediated Neuroinflammation in Cerebral Ischemia.

    abstract::The cerebral ischemia is one of the most common diseases in the central nervous system that causes progressive disability or even death. In this connection, the inflammatory response mediated by the activated microglia is believed to play a central role in this pathogenesis. In the event of brain injury, activated mic...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-016-8394-x

    authors: Yuan Y,Fang M,Wu CY,Ling EA

    更新日期:2016-09-01 00:00:00

  • LncRNA LINC00689 Promotes the Tumorigenesis of Glioma via Mediation of miR-526b-3p/IGF2BP1 Axis.

    abstract::Glioma ranks first among the aggressive brain tumors all over the world. LncRNA LINC00689 has been confirmed to play key roles in the progression of cancers, and LINC00689 was upregulated in glioma. However, the biological function of LINC00689 in glioma is unclear. qRT-PCR was applied to detect the expressions of LIN...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-020-08635-x

    authors: Zhan WL,Gao N,Tu GL,Tang H,Gao L,Xia Y

    更新日期:2021-01-03 00:00:00

  • Novel mutations in cyclin-dependent kinase-like 5 (CDKL5) gene in Indian cases of Rett syndrome.

    abstract::Rett syndrome is a severe neurodevelopmental disorder, almost exclusively affecting females and characterized by a wide spectrum of clinical manifestations. Both the classic and atypical forms of Rett syndrome are primarily due to mutations in the methyl-CpG-binding protein 2 (MECP2) gene. Mutations in the X-linked cy...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-012-8212-z

    authors: Das DK,Mehta B,Menon SR,Raha S,Udani V

    更新日期:2013-03-01 00:00:00

  • Attenuation of reserpine-induced pain/depression dyad by gentiopicroside through downregulation of GluN2B receptors in the amygdala of mice.

    abstract::Epidemiological studies demonstrate that pain frequently occurs comorbid with depression. Gentiopicroside (Gent) is a secoiridoid compound isolated from Gentiana lutea that exhibits analgesic properties and inhibits the expression of GluN2B-containing N-methyl-D-aspartate (NMDA) receptors in the anterior cingulate cor...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-013-8280-8

    authors: Liu SB,Zhao R,Li XS,Guo HJ,Tian Z,Zhang N,Gao GD,Zhao MG

    更新日期:2014-06-01 00:00:00

  • Therapeutic strategies for the inherited neuropathies.

    abstract::More than 30 genetic causes have been identified for the inherited neuropathies collectively referred to as Charcot-Marie-Tooth (CMT) disease. Previous therapies for CMT were limited to traditional approaches such as rehabilitation medicine, ambulation aids, and pain management. Identification of the genes causing CMT...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/nmm:8:1-2:255

    authors: Shy ME

    更新日期:2006-01-01 00:00:00

  • Synaptogenesis: Modulation by Availability of Membrane Phospholipid Precursors.

    abstract::Phospholipids are the main constituents of brain membranes. Formation of new membranes requires that uridine, the omega-3 polyunsaturated fatty acids such as docosahexaenoic acid (DHA), and choline, the three circulating precursors of major phospholipids, interact via the Kennedy pathway. Supplementation of laboratory...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-016-8414-x

    authors: Cansev M

    更新日期:2016-09-01 00:00:00

  • The cell biology of alpha-synuclein: a sticky problem?

    abstract::Parkinson's disease (PD) is the most common neurodegenerative motor disorder, marked by chronic progressive loss of neurons in the substantia nigra, thereby damaging purposeful control of movement. For decades, it was believed that PD was caused solely by environmental causes. However, the discovery of genetic factors...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1385/NMM:1:2:95

    authors: Cole NB,Murphy DD

    更新日期:2002-01-01 00:00:00

  • Perturbed autonomic nervous system function in metabolic syndrome.

    abstract::The metabolic syndrome is characterized by the clustering of various common metabolic abnormalities in an individual and it is associated with increased risk for the development of type 2 diabetes and cardiovascular diseases. Its prevalence in the general population is approximately 25%. Central fat accumulation and i...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-008-8022-5

    authors: Tentolouris N,Argyrakopoulou G,Katsilambros N

    更新日期:2008-01-01 00:00:00

  • Overexpression of Human Mutant PANK2 Proteins Affects Development and Motor Behavior of Zebrafish Embryos.

    abstract::Pantothenate Kinase-Associated Neurodegeneration (PKAN) is a genetic and early-onset neurodegenerative disorder characterized by iron accumulation in the basal ganglia. It is due to mutations in Pantothenate Kinase 2 (PANK2), an enzyme that catalyzes the phosphorylation of vitamin B5, first and essential step in coenz...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-018-8508-8

    authors: Khatri D,Zizioli D,Trivedi A,Borsani G,Monti E,Finazzi D

    更新日期:2019-06-01 00:00:00