Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward - Wikidata - awgldk - TriplyDB

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

http://www.wikidata.org/entity/Q27305210

about

Autism Spectrum Disorders and Drug Addiction: Common Pathways, Common Molecules, Distinct Disorders?Dynorphin Controls the Gain of an Amygdalar Anxiety Circuit A Trigger for Opioid Misuse: Chronic Pain and Stress Dysregulate the Mesolimbic Pathway and Kappa Opioid System Architectural Representation of Valence in the Limbic System.Stretchable multichannel antennas in soft wireless optoelectronic implants for optogenetics Neuroinflammation-a co-occurring phenomenon linking chronic pain and opioid dependence.Reduced Vglut2/Slc17a6 Gene Expression Levels throughout the Mouse Subthalamic Nucleus Cause Cell Loss and Structural Disorganization Followed by Increased Motor Activity and Decreased Sugar Consumption Nociceptin/Orphanin FQ Receptor Structure, Signaling, Ligands, Functions, and Interactions with Opioid Systems.Chemogenetic and Optogenetic Activation of Gαs Signaling in the Basolateral Amygdala Induces Acute and Social Anxiety-Like States Dopamine and opioid systems interact within the nucleus accumbens to maintain monogamous pair bonds Stress-Induced Reinstatement of Nicotine Preference Requires Dynorphin/Kappa Opioid Activity in the Basolateral Amygdala.A GABAergic Projection from the Centromedial Nuclei of the Amygdala to Ventromedial Prefrontal Cortex Modulates Reward Behavior.Nicotinic and opioid receptor regulation of striatal dopamine D2-receptor mediated transmission.Homeostasis Meets Motivation in the Battle to Control Food Intake.Allostatic Mechanisms of Opioid Tolerance Beyond Desensitization and Downregulation Molecular and Circuit-Dynamical Identification of Top-Down Neural Mechanisms for Restraint of Reward Seeking.Kappa Opioid Receptors Mediate Heterosynaptic Suppression of Hippocampal Inputs in the Rat Ventral Striatum.New Technologies for Elucidating Opioid Receptor Function.The long-term effects of stress and kappa opioid receptor activation on conditioned place aversion in male and female California mice.The dynamic interaction between pain and opioid misuse.Microfluidic neural probes: in vivo tools for advancing neuroscience.How contexts promote and prevent relapse to drug seeking.Emerging Role for Nucleus Accumbens Medium Spiny Neuron Subtypes in Depression.Role of the Dynorphin/Kappa Opioid Receptor System in the Motivational Effects of Ethanol.Cell-Type-Specific Epigenetic Editing at the Fosb Gene Controls Susceptibility to Social Defeat Stress."Quite a Profoundly Strange Experience": An Analysis of the Experiences of Salvia divinorum Users.Cocaine Experience Enhances Thalamo-Accumbens N-Methyl-D-Aspartate Receptor Function.Memories of Opiate Withdrawal Emotional States Correlate with Specific Gamma Oscillations in the Nucleus Accumbens.Locus coeruleus to basolateral amygdala noradrenergic projections promote anxiety-like behavior.Spotlight on pain: optogenetic approaches for interrogating somatosensory circuits.Pathway- and Cell-Specific Kappa-Opioid Receptor Modulation of Excitation-Inhibition Balance Differentially Gates D1 and D2 Accumbens Neuron Activity.Drive and Reinforcement Circuitry in the Brain: Origins, Neurotransmitters, and Projection Fields.Chronic ethanol exposure increases inhibition of optically targeted phasic dopamine release in the nucleus accumbens core and medial shell ex vivo.Optogenetic activation of amygdala projections to nucleus accumbens can arrest conditioned and unconditioned alcohol consummatory behavior.Dynorphin and κ-Opioid Receptor Dysregulation in the Dopaminergic Reward System of Human Alcoholics.Flexible Near-Field Wireless Optoelectronics as Subdermal Implants for Broad Applications in Optogenetics.Preparation and implementation of optofluidic neural probes for in vivo wireless pharmacology and optogenetics.Involvement of activated brain stress responsive systems in excessive and "relapse" alcohol drinking in rodent models: implications for therapeutics.Contemporary strategies for dissecting the neuronal basis of neurodevelopmental disorders.Ginsenoside Re protects methamphetamine-induced dopaminergic neurotoxicity in mice via upregulation of dynorphin-mediated κ-opioid receptor and downregulation of substance P-mediated neurokinin 1 receptor.

P2860

Q26768231-B819CDE2-EFC7-4FCB-A249-A4A0952F6A95 Q27319741-53F214E2-025A-48F6-B63F-6F326D93D8F3 Q28074686-E0260A8C-7B38-42C6-8A48-AF39C5AC7D7B Q30355371-26AD758B-7ADA-4AF5-A8A3-153D7543D6BA Q30832387-33009879-F2D9-433C-8469-3A73A1D2C33E Q33602197-B6196794-0889-4208-9AF6-B8724697CCDC Q36152395-34A8D385-9A8F-475D-A387-0B81102540FD Q36744366-41D8EC40-5BD2-49AB-B0A9-DE379A604D6F Q37006297-FB107F9D-6C18-40E8-8E62-AE914CD46491 Q37149935-F0677F62-BF0F-477E-992C-446814DC4EC7 Q37270938-263BA15A-7307-4B78-B597-19E141E61F7A Q37372041-D12E082E-BF20-40A8-8ADC-FD344DE7DC65 Q37439216-E2C3B39D-0099-432E-9D2E-0A1FF8B0CC8D Q37444966-DA61BEE0-6A02-4E35-B80E-5B3363D213C6 Q37590161-3683D57E-D77D-403A-891A-46B74B5EA2AD Q38371922-8FDCBB92-6986-432F-A5DC-41C341C252D4 Q38713108-CE05CFF3-981C-4034-A360-466EB1383701 Q38718788-2389E996-80EE-476E-8E03-1197C0E70EBA Q38720488-3CDF6FB3-D315-42D5-9E9D-255EC0AC9AAF Q38731968-90E278C9-787C-422A-B522-CD19B565F073 Q38738786-E20E445E-F929-405D-B745-44A10A37AE20 Q38950401-2E13BEEA-4838-41BE-8F08-C4D19C1E3887 Q39015823-A8EF4ADB-DB13-4FD1-9F14-E0D7C5CBFCD5 Q39251520-0DB2C64B-A0B7-4B4A-867D-5E61766BD5A6 Q39306654-72BCBAEC-9916-472E-9598-FFBB5222FD96 Q39769038-24E4FAF7-BAE6-4C65-9816-581A9105A492 Q40742869-B7FE9179-77FA-4695-9CAD-54C1ABEF8A4B Q40990836-106EB5BA-D3B7-4530-B2B9-88250BD7C2ED Q41329923-CE4BDA12-A91E-4F03-97F7-97984048E83C Q42669411-C01A150D-29D2-443F-9D6D-9B983279C96C Q44342408-F8F91F45-BF99-4EE7-BD66-56DF3A5A873D Q47315933-6C28A3DD-46A3-4E23-BED6-5E8E48B35B0A Q47319192-7AA5FF33-1921-40B6-BE31-97A1690AFFFF Q47328907-E27C0A06-4AE6-453C-8AD4-5A08E2D07AAA Q47550488-20DC20E2-9856-45A5-97E4-336EB8F31CE3 Q47992567-ADE454F6-3392-450A-AF73-4C848C4E04F4 Q48050521-B94A23B2-4ABF-4670-9778-1E7B13F1A490 Q52317998-44B88CEC-408C-4768-9BAB-833742ED7329 Q52351832-26C92361-2F86-482A-9859-A1FD0326984E Q53082241-95834A2A-07A4-4A90-8B3E-A3D5CF6BB1BD

P2860

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

http://www.wikidata.org/entity/Q27305210

description

2015 nî lūn-bûn

@nan

2015 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@ast

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@en

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@nl

type

label

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@ast

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@en

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@nl

prefLabel

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@ast

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@en

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@nl

P1433

Q27305210-B28EE8CA-5772-4190-B3ED-F388CE85D6B4

P1476

Q27305210-25270AAD-98B3-4138-B2AB-5E73E2AD8A87

P2093

Q27305210-0C2ABEBD-04A5-4AD4-82E9-A44A13D8F78F

Q27305210-2D60C99E-374D-4F2C-A998-C1F89B6B098C

Q27305210-523B57E2-0C6A-4800-820B-3B1ADA369EFA

Q27305210-5DD5CAC7-046B-41FF-9FB0-A52A1CE53443

Q27305210-68A78D57-24C7-4B7C-94E4-A4BDF53C4341

Q27305210-8EFD7124-33A4-47B8-9612-34704A6509FD

Q27305210-8F624EEF-809B-4D29-8774-DF72312EA850

Q27305210-9DDCEF4A-067C-402B-B259-077FE86B0FEF

Q27305210-A9E31957-24B2-4A22-8DBC-5FBEF36FB048

Q27305210-AAB3D922-088B-4C4E-B5D4-8C4FD88CBB70

P2860

Q27305210-09E8300A-0CE4-4977-B75C-72E6C122DA70

Q27305210-11AF16EB-2333-43EB-A868-11B18431DA9B

Q27305210-18B2998D-F76E-4435-AE2F-BF8574434ED6

Q27305210-18F4A325-AFDE-4248-8BFE-EFE7682B3349

Q27305210-193724A0-A4D5-4E30-B2D7-2A6FDEC2E67C

Q27305210-24BDE50E-775F-4E3A-A947-CACFA0968018

Q27305210-32629C88-2EC9-4B4A-82CA-207A5C24C8CB

Q27305210-3298023C-B261-4FCF-A543-433FD68F8924

Q27305210-34CBDFED-DF01-42E1-AD35-AA68ACEA06F2

Q27305210-39D906E4-D953-4307-8FA3-7A3617094B9F

P304

Q27305210-4EA20EF1-65C7-485B-B71F-F37ECA9475D9

P31

Q27305210-88764E2E-646F-492F-87DD-22649D0497C7

P3181

Q27305210-B886334F-F51D-4267-A6A3-EC7C1840D76D

P356

Q27305210-59E84972-E2A7-4F01-A94A-D56367788321

P407

Q27305210-8C54D20C-56D6-43E0-9B1D-654C141B865F

P433

Q27305210-22381D20-0FC3-4165-B136-2C4A282318E4

P478

Q27305210-C3D83E7D-F08A-4AC4-B83E-DBAED6A89C2D

P50

Q27305210-0D5C0DE7-BAED-4A96-B692-EFA38F700701

Q27305210-8455255F-A588-4F54-84B6-57CC89AEAA0F

Q27305210-D660E99E-47CA-473E-BBFB-061E4E58B3AB

P577

Q27305210-FEB891B4-2683-4338-B3D6-79F92B1941A4

P698

Q27305210-B27D472D-8CEE-4F9C-81C9-9D0ABD1A9DC6

P921

Q27305210-602F1199-9A0C-492E-BFE0-D1CA9CA1211A

Q27305210-eecf04ad-2e32-4a82-81d2-db1d5a6876f8

P932

Q27305210-765B1494-C288-434A-AC47-F8E63DAA3C05

P3181

P356

J.NEURON.2015.08.019

P1433

P1476

Distinct Subpopulations of Nucleus Accumbens Dynorphin Neurons Drive Aversion and Reward

@en

P2093

Bradford B Lowell

http://www.w3.org/2001/XMLSchema#string

Chang-O Pyo

http://www.w3.org/2001/XMLSchema#string

Gavin P Schmitz

http://www.w3.org/2001/XMLSchema#string

Gunchul Shin

http://www.w3.org/2001/XMLSchema#string

John A Rogers

http://www.w3.org/2001/XMLSchema#string

Jordan G McCall

http://www.w3.org/2001/XMLSchema#string

Julio M Bernardi

http://www.w3.org/2001/XMLSchema#string

Michael J Krashes

http://www.w3.org/2001/XMLSchema#string

Michael R Bruchas

http://www.w3.org/2001/XMLSchema#string

Nicole A Crowley

http://www.w3.org/2001/XMLSchema#string

P2860

Tuning arousal with optogenetic modulation of locus coeruleus neurons.

The dysphoric component of stress is encoded by activation of the dynorphin kappa-opioid system

Stress-induced p38 mitogen-activated protein kinase activation mediates kappa-opioid-dependent dysphoria.

CRH Engagement of the Locus Coeruleus Noradrenergic System Mediates Stress-Induced Anxiety.

Wireless Optofluidic Systems for Programmable In Vivo Pharmacology and Optogenetics

Psychotomimesis mediated by kappa opiate receptors

CRF1-R activation of the dynorphin/kappa opioid system in the mouse basolateral amygdala mediates anxiety-like behavior

Neural systems of reinforcement for drug addiction: from actions to habits to compulsion

A robust and high-throughput Cre reporting and characterization system for the whole mouse brain

Neurons containing hypocretin (orexin) project to multiple neuronal systems

P304

1063-77

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

2650196

http://www.w3.org/2001/XMLSchema#string

P356

10.1016/J.NEURON.2015.08.019

http://www.w3.org/2001/XMLSchema#string

P407

P433

5

http://www.w3.org/2001/XMLSchema#string

P478

87

http://www.w3.org/2001/XMLSchema#string

P50

Catherine A Marcinkiewcz

P577

2015-09-02T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26335648

http://www.w3.org/2001/XMLSchema#string

P921

nucleus accumbens

P932

4625385

http://www.w3.org/2001/XMLSchema#string