Stress and addiction: contribution of the corticotropin releasing factor (CRF) system in neuroplasticity.

Abstract:

:Corticotropin releasing factor (CRF) has been shown to induce various behavioral changes related to adaptation to stress. Dysregulation of the CRF system at any point can lead to a variety of psychiatric disorders, including substance use disorders (SUDs). CRF has been associated with stress-induced drug reinforcement. Extensive literature has identified CRF to play an important role in the molecular mechanisms that lead to an increase in susceptibility that precipitates relapse to SUDs. The CRF system has a heterogeneous role in SUDs. It enhances the acute effects of drugs of abuse and is also responsible for the potentiation of drug-induced neuroplasticity evoked during the withdrawal period. We present in this review the brain regions and circuitries where CRF is expressed and may participate in stress-induced drug abuse. Finally, we attempt to evaluate the role of modulating the CRF system as a possible therapeutic strategy for treating the dysregulation of emotional behaviors that result from the acute positive reinforcement of substances of abuse as well as the negative reinforcement produced by withdrawal.

journal_name

Front Mol Neurosci

authors

Haass-Koffler CL,Bartlett SE

doi

10.3389/fnmol.2012.00091

subject

Has Abstract

pub_date

2012-09-06 00:00:00

pages

91

issn

1662-5099

journal_volume

5

pub_type

杂志文章
  • Transient Receptor Potential Vanilloid 4 Inhibits γ-Aminobutyric Acid-Activated Current in Hippocampal Pyramidal Neurons.

    abstract::The balance between excitatory and inhibitory neurotransmitter systems is crucial for the modulation of neuronal excitability in the central nervous system (CNS). The activation of transient receptor potential vanilloid 4 (TRPV4) is reported to enhance the response of hippocampal glutamate receptors, but whether the i...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2016.00077

    authors: Hong Z,Tian Y,Qi M,Li Y,Du Y,Chen L,Liu W,Chen L

    更新日期:2016-08-26 00:00:00

  • Loss of DEK Expression Induces Alzheimer's Disease Phenotypes in Differentiated SH-SY5Y Cells.

    abstract::Alzheimer's disease (AD) is the most common cause of dementia and is characterized by the buildup of β-amyloid plaques and neurofibrillary Tau tangles. This leads to decreased synaptic efficacy, cell death, and, consequently, brain atrophy in patients. Behaviorally, this manifests as memory loss and confusion. Using a...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2020.594319

    authors: Greene AN,Parks LG,Solomon MB,Privette Vinnedge LM

    更新日期:2020-11-16 00:00:00

  • Functions of GSK-3 Signaling in Development of the Nervous System.

    abstract::Glycogen synthase kinase-3 (GSK-3) is central to multiple intracellular pathways including those activated by Wnt/β-catenin, Sonic Hedgehog, Notch, growth factor/RTK, and G protein-coupled receptor signals. All of these signals importantly contribute to neural development. Early attention on GSK-3 signaling in neural ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2011.00044

    authors: Kim WY,Snider WD

    更新日期:2011-11-17 00:00:00

  • Achaete-Scute Homolog 1 Expression Controls Cellular Differentiation of Neuroblastoma.

    abstract::Neuroblastoma, the major cause of infant cancer deaths, results from fast proliferation of undifferentiated neuroblasts. Treatment of high-risk neuroblastoma includes differentiation with retinoic acid (RA); however, the resistance of many of these tumors to RA-induced differentiation poses a considerable challenge. H...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2016.00156

    authors: Kasim M,Heß V,Scholz H,Persson PB,Fähling M

    更新日期:2016-12-21 00:00:00

  • Role of APP Interactions with Heterotrimeric G Proteins: Physiological Functions and Pathological Consequences.

    abstract::Following the discovery that the amyloid precursor protein (APP) is the source of β-amyloid peptides (Aβ) that accumulate in Alzheimer's disease (AD), structural analyses suggested that the holoprotein resembles a transmembrane receptor. Initial studies using reconstituted membranes demonstrated that APP can directly ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2017.00003

    authors: Copenhaver PF,Kögel D

    更新日期:2017-01-31 00:00:00

  • Combining Gene Transfer and Nonhuman Primates to Better Understand and Treat Parkinson's Disease.

    abstract::Parkinson's disease (PD) is a progressive CNS disorder that is primarily associated with impaired movement. PD develops over decades and is linked to the gradual loss of dopamine delivery to the striatum, via the loss of dopaminergic (DA) neurons in the substantia nigra pars compacta (SNpc). While the administration o...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2019.00010

    authors: Lasbleiz C,Mestre-Francés N,Devau G,Luquin MR,Tenenbaum L,Kremer EJ,Verdier JM

    更新日期:2019-02-11 00:00:00

  • Corrigendum: β2-Adrenergic Receptor-Mediated HIF-1α Upregulation Mediates Blood Brain Barrier Damage in Acute Cerebral Ischemia.

    abstract::[This corrects the article on p. 257 in vol. 10, PMID: 28855859.]. ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,已发布勘误

    doi:10.3389/fnmol.2017.00392

    authors: Sun Y,Chen X,Zhang X,Shen X,Wang M,Wang X,Liu WC,Liu CF,Liu J,Liu W,Jin X

    更新日期:2017-11-20 00:00:00

  • Intermittent Fasting Protects against Alzheimer's Disease Possible through Restoring Aquaporin-4 Polarity.

    abstract::The impairment of amyloid-β (Aβ) clearance in the brain plays a causative role in Alzheimer's disease (AD). Polarity distribution of aquaporin-4 (AQP4) is important to remove Aβ from brain. AQP4 polarity can be influenced by the ratio of two AQP4 isoforms M1 and M23 (AQP4-M1/M23), however, it is unknown whether the ra...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2017.00395

    authors: Zhang J,Zhan Z,Li X,Xing A,Jiang C,Chen Y,Shi W,An L

    更新日期:2017-11-29 00:00:00

  • Long Non-coding RNA TUG1 Sponges Mir-145a-5p to Regulate Microglial Polarization After Oxygen-Glucose Deprivation.

    abstract::Microglia plays a critical role in neuroinflammation after ischemic stroke by releasing diverse inflammatory cytokines. Long non-coding RNA taurine up-regulated gene 1 (lncRNA TUG1) is widely expressed in adult brain and has been reported to participate in multiple biological processes associated with nervous system d...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2019.00215

    authors: Wang H,Liao S,Li H,Chen Y,Yu J

    更新日期:2019-09-10 00:00:00

  • Re-innervation of the Denervated Dentate Gyrus by Sprouting Associational and Commissural Mossy Cell Axons in Organotypic Tissue Cultures of Entorhinal Cortex and Hippocampus.

    abstract::Collateral sprouting of surviving axons contributes to the synaptic reorganization after brain injury. To study this clinically relevant phenomenon, we used complex organotypic tissue cultures of mouse entorhinal cortex (EC) and hippocampus (H). Single EC-H cultures were generated to analyze associational sprouting, a...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2019.00270

    authors: Del Turco D,Paul MH,Beeg Moreno VJ,Hildebrandt-Einfeldt L,Deller T

    更新日期:2019-11-12 00:00:00

  • PTEN Inhibition Protects Against Experimental Intracerebral Hemorrhage-Induced Brain Injury Through PTEN/E2F1/β-Catenin Pathway.

    abstract::Intracerebral hemorrhage (ICH) is a subtype of stroke with highest mortality and morbidity. We have previously demonstrated that dipotassium bisperoxo (picolinato) oxovanadate (V), (bpV[pic]) inhibits phosphatase and tensin homolog (PTEN) and activates extracellular signal-regulated kinase (ERK)1/2. In this study, we ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2019.00281

    authors: Zhao D,Qin XP,Chen SF,Liao XY,Cheng J,Liu R,Lei Y,Zhang ZF,Wan Q

    更新日期:2019-12-05 00:00:00

  • Laminin and Integrin in LAMA2-Related Congenital Muscular Dystrophy: From Disease to Therapeutics.

    abstract::Laminin-α2-related congenital muscular dystrophy (LAMA2-CMD) is a devastating neuromuscular disease caused by mutations in the LAMA2 gene. These mutations result in the complete absence or truncated expression of the laminin-α2 chain. The α2-chain is a major component of the laminin-211 and laminin-221 isoforms, the p...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2020.00001

    authors: Barraza-Flores P,Bates CR,Oliveira-Santos A,Burkin DJ

    更新日期:2020-02-11 00:00:00

  • Localization of Retinal Ca2+/Calmodulin-Dependent Kinase II-β (CaMKII-β) at Bipolar Cell Gap Junctions and Cross-Reactivity of a Monoclonal Anti-CaMKII-β Antibody With Connexin36.

    abstract::Neuronal gap junctions formed by connexin36 (Cx36) and chemical synapses share striking similarities in terms of plasticity. Ca2+/calmodulin-dependent protein kinase II (CaMKII), an enzyme known to induce memory formation at chemical synapses, has recently been described to potentiate electrical coupling in the retina...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2019.00206

    authors: Tetenborg S,Yadav SC,Brüggen B,Zoidl GR,Hormuzdi SG,Monyer H,van Woerden GM,Janssen-Bienhold U,Dedek K

    更新日期:2019-08-28 00:00:00

  • Reducing Peripheral Inflammation with Infliximab Reduces Neuroinflammation and Improves Cognition in Rats with Hepatic Encephalopathy.

    abstract::Inflammation contributes to cognitive impairment in patients with hepatic encephalopathy (HE). However, the process by which peripheral inflammation results in cognitive impairment remains unclear. In animal models, neuroinflammation and altered neurotransmission mediate cognitive impairment. Taking into account these...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2016.00106

    authors: Dadsetan S,Balzano T,Forteza J,Cabrera-Pastor A,Taoro-Gonzalez L,Hernandez-Rabaza V,Gil-Perotín S,Cubas-Núñez L,García-Verdugo JM,Agusti A,Llansola M,Felipo V

    更新日期:2016-11-02 00:00:00

  • MotomiRs: miRNAs in Motor Neuron Function and Disease.

    abstract::MiRNAs are key regulators of the mammalian transcriptome that have been increasingly linked to degenerative diseases of the motor neurons. Although many of the miRNAs currently incriminated as participants in the pathogenesis of these diseases are also important to the normal development and function of motor neurons,...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2017.00127

    authors: Hawley ZCE,Campos-Melo D,Droppelmann CA,Strong MJ

    更新日期:2017-05-04 00:00:00

  • Cryptochrome Is a Regulator of Synaptic Plasticity in the Visual System of Drosophila melanogaster.

    abstract::Drosophila CRYPTOCHROME (CRY) is a blue light sensitive protein with a key role in circadian photoreception. A main feature of CRY is that light promotes an interaction with the circadian protein TIMELESS (TIM) resulting in their ubiquitination and degradation, a mechanism that contributes to the synchronization of th...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2017.00165

    authors: Damulewicz M,Mazzotta GM,Sartori E,Rosato E,Costa R,Pyza EM

    更新日期:2017-05-30 00:00:00

  • Bcl11 Transcription Factors Regulate Cortical Development and Function.

    abstract::Transcription factors regulate multiple processes during brain development and in the adult brain, from brain patterning to differentiation and maturation of highly specialized neurons as well as establishing and maintaining the functional neuronal connectivity. The members of the zinc-finger transcription factor fami...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2020.00051

    authors: Simon R,Wiegreffe C,Britsch S

    更新日期:2020-04-08 00:00:00

  • The Binding Properties and Physiological Functions of Recoverin.

    abstract::Recoverin (Rcv) is a low molecular-weight, neuronal calcium sensor (NCS) primarily located in photoreceptor outer segments of the vertebrate retina. Calcium ions (Ca2+)-bound Rcv has been proposed to inhibit G-protein-coupled receptor kinase (GRKs) in darkness. During the light response, the Ca2+-free Rcv releases GRK...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2018.00473

    authors: Zang J,Neuhauss SCF

    更新日期:2018-12-20 00:00:00

  • Exposure to Inorganic Mercury Causes Oxidative Stress, Cell Death, and Functional Deficits in the Motor Cortex.

    abstract::Mercury is a toxic metal that can be found in the environment in three different forms - elemental, organic and inorganic. Inorganic mercury has a lower liposolubility, which results in a lower organism absorption and reduced passage through the blood-brain barrier. For this reason, exposure models that use inorganic ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2018.00125

    authors: Teixeira FB,de Oliveira ACA,Leão LKR,Fagundes NCF,Fernandes RM,Fernandes LMP,da Silva MCF,Amado LL,Sagica FES,de Oliveira EHC,Crespo-Lopez ME,Maia CSF,Lima RR

    更新日期:2018-05-15 00:00:00

  • Metabotropic Glutamate Receptor 7: A New Therapeutic Target in Neurodevelopmental Disorders.

    abstract::Neurodevelopmental disorders (NDDs) are characterized by a wide range of symptoms including delayed speech, intellectual disability, motor dysfunction, social deficits, breathing problems, structural abnormalities, and epilepsy. Unfortunately, current treatment strategies are limited and innovative new approaches are ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2018.00387

    authors: Fisher NM,Seto M,Lindsley CW,Niswender CM

    更新日期:2018-10-23 00:00:00

  • Phorbol-Ester Mediated Suppression of hASH1 Synthesis: Multiple Ways to Keep the Level Down.

    abstract::Human achaete-scute homolog-1 (hASH1), encoded by the human ASCL1 gene, belongs to the family of basic helix-loop-helix transcription factors. hASH1 and its mammalian homolog Mash1 are expressed in the central and peripheral nervous system during development, and promote early neuronal differentiation. Furthermore, hA...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2011.00001

    authors: Benko E,Winkelmann A,Meier JC,Persson PB,Scholz H,Fähling M

    更新日期:2011-02-07 00:00:00

  • Fragile-X Syndrome Is Associated With NMDA Receptor Hypofunction and Reduced Dendritic Complexity in Mature Dentate Granule Cells.

    abstract::Fragile X syndrome (FXS) is the most common form of inherited intellectual disability. It is caused by the overexpansion of cytosine-guanine-guanine (CGG) trinucleotide in Fmr1 gene, resulting in complete loss of the fragile X mental retardation protein (FMRP). Previous studies using Fmr1 knockout (Fmr1 KO) mice have ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2018.00495

    authors: Yau SY,Bettio L,Chiu J,Chiu C,Christie BR

    更新日期:2019-01-17 00:00:00

  • Cloning and Phylogenetic Analysis of NMDA Receptor Subunits NR1, NR2A and NR2B in Xenopus laevis Tadpoles.

    abstract::N-methyl-d-aspartate receptors (NMDARs) play an important role in many aspects of nervous system function such as synaptic plasticity and neuronal development. NMDARs are heteromers consisting of an obligate NR1 and most commonly one or two kinds of NR2 subunits. While the receptors have been well characterized in som...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/neuro.02.004.2009

    authors: Ewald RC,Cline HT

    更新日期:2009-09-11 00:00:00

  • Early history of glycine receptor biology in Mammalian spinal cord circuits.

    abstract::In this review we provide an overview of key in vivo experiments undertaken in the cat spinal cord in the 1950s and 1960s, and point out their contributions to our present understanding of glycine receptor (GlyR) function. Importantly, some of these discoveries were made well before an inhibitory receptor, or its agon...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2010.00013

    authors: Callister RJ,Graham BA

    更新日期:2010-05-21 00:00:00

  • CSF Cholinergic Index, a New Biomeasure of Treatment Effect in Patients With Alzheimer's Disease.

    abstract::Alzheimer's disease (AD) is a progressive disease with early degeneration of the central cholinergic neurons. Currently, three of four AD drugs act by inhibiting the acetylcholine (ACh) degrading enzyme, acetylcholinesterase (AChE). Efficacy of these drugs depends on available amount of ACh, which is biosynthesized by...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2019.00239

    authors: Karami A,Eriksdotter M,Kadir A,Almkvist O,Nordberg A,Darreh-Shori T

    更新日期:2019-10-11 00:00:00

  • Transcriptional Reorganization of Drosophila Motor Neurons and Their Muscular Junctions toward a Neuroendocrine Phenotype by the bHLH Protein Dimmed.

    abstract::Neuroendocrine cells store and secrete bulk amounts of neuropeptides, and display morphological and molecular characteristics distinct from neurons signaling with classical neurotransmitters. In Drosophila the transcription factor Dimmed (Dimm), is a prime organizer of neuroendocrine capacity in a majority of the pept...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2017.00260

    authors: Luo J,Liu Y,Nässel DR

    更新日期:2017-08-14 00:00:00

  • Mecp2 Mediates Experience-Dependent Transcriptional Upregulation of Ryanodine Receptor Type-3.

    abstract::Mecp2 is a DNA methylation reader that plays a critical role in experience-dependent plasticity. Increasing evidence supports a role for epigenetic modifications in activity-induced gene expression. Hence, candidate genes related to such phenomena are of great interest. Ryanodine receptors are intracellular calcium ch...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章

    doi:10.3389/fnmol.2017.00188

    authors: Torres RF,Hidalgo C,Kerr B

    更新日期:2017-06-13 00:00:00

  • Regulation of intraocular pressure by soluble and membrane guanylate cyclases and their role in glaucoma.

    abstract::Glaucoma is a progressive optic neuropathy characterized by visual field defects that ultimately lead to irreversible blindness (Alward, 2000; Anderson et al., 2006). By the year 2020, an estimated 80 million people will have glaucoma, 11 million of which will be bilaterally blind. Primary open-angle glaucoma (POAG) i...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2014.00038

    authors: Buys ES,Potter LR,Pasquale LR,Ksander BR

    更新日期:2014-05-19 00:00:00

  • Subsynaptic Domains in Super-Resolution Microscopy: The Treachery of Images.

    abstract::The application of super-resolution optical microscopy to investigating synaptic structures has revealed a highly heterogeneous and variable intra-synaptic organization. Dense subsynaptic protein assemblies named subsynaptic domains or SSDs have been proposed as structural units that regulate the efficacy of neuronal ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2019.00161

    authors: Yang X,Specht CG

    更新日期:2019-07-02 00:00:00

  • Implications of DNA Methylation in Parkinson's Disease.

    abstract::It has been 200 years since Parkinson's disease (PD) was first described, yet many aspects of its etiopathogenesis remain unclear. PD is a progressive and complex neurodegenerative disorder caused by genetic and environmental factors including aging, nutrition, pesticides and exposure to heavy metals. DNA methylation ...

    journal_title:Frontiers in molecular neuroscience

    pub_type: 杂志文章,评审

    doi:10.3389/fnmol.2017.00225

    authors: Miranda-Morales E,Meier K,Sandoval-Carrillo A,Salas-Pacheco J,Vázquez-Cárdenas P,Arias-Carrión O

    更新日期:2017-07-18 00:00:00