41 research outputs found
Stress-Induced Reinstatement of Drug Seeking: 20 Years of Progress
- Author
- A Cippitelli
- A Cippitelli
- A Cippitelli
- A Ettenberg
- A Ettenberg
- A Plaza-Zabala
- A Sekino
- A Van't Veer
- AC Hansson
- AD Le
- AD Le
- AD Le
- AD Le
- AD Le
- AD Le
- AD Le
- AD Le
- AD Le
- AE Higley
- AM Chirila
- AM Polter
- AM Thierry
- AN Carey
- Anh D LĂȘ
- AS Kreibich
- AY Deutch
- B Boutrel
- B Lee
- B Ribeiro Do Couto
- B Setlow
- B Wang
- B Wang
- B Wang
- B Wang
- B Wang
- BB Land
- BH Westerink
- BL Lewis
- BM Cox
- BR Lee
- C Cifani
- C Li
- CD Schmoutz
- CJ Sanchez
- CJ Sanchez
- CK Nielsen
- CL Pickens
- CP Ford
- CP O'Brien
- CR Gerfen
- D Economidou
- D Epstein
- D Funk
- D Funk
- D Highfield
- D Highfield
- D Highfield
- D Liu
- D Rodaros
- D Rotllant
- David A Baker
- DC Glass
- DEJ Redmond
- DH Epstein
- DJ Calu
- DJ Calu
- DM Buffalari
- DM Buffalari
- DM Buffalari
- Douglas Funk
- DR Gehlert
- DR Staub
- DS Zahm
- DT George
- DW Schulz
- DW Self
- E Krupitsky
- EA Stone
- EB Margolis
- EJ Khantzian
- EN Graf
- EN Graf
- EP Zorrilla
- EP Zorrilla
- F Chaouloff
- F Cohen
- F Georges
- F Leri
- F Sedki
- F Weiss
- FC Cruz
- FJ White
- G Aston-Jones
- G de Guglielmo
- G Zislis
- GF Koob
- GP Chrousos
- GR Valdez
- H Selye
- H Yamada
- HC Fox
- HC Fox
- J Jenkins
- J Stewart
- J Wang
- JA Deutch
- JA Gray
- JA Simms
- JC Umhau
- JD Bremner
- JD Bremner
- JD Shepard
- JE LeDoux
- JE Morley
- JJ Anker
- JJ Anker
- JK Richards
- JK Seamans
- JL McGaugh
- JM Blacktop
- JM Bossert
- JM Bossert
- JM Bossert
- JM Fritschy
- JN Cleck
- John R Mantsch
- JP McLaughlin
- JP Schroeder
- JR Glowa
- JR Mantsch
- JR Mantsch
- JR Mantsch
- JR Mantsch
- JR McReynolds
- JR Schank
- JR Schank
- JR Schank
- JV Aldrich
- JV Aldrich
- K McFarland
- K Van Pett
- KJ Jackson
- KL Conrad
- KL Shelton
- L Lu
- L Lu
- L Lu
- L Lu
- L Zhou
- LA Briand
- LE Kwako
- LG Kirby
- LK Vaughn
- M Davis
- M Davis
- M Heilig
- M Sakanaka
- MA Ungless
- MB Bannon
- MD Cassell
- ME Bouton
- ME Bouton
- ME Carroll
- MEP Seligman
- MF Dallman
- MK Greenwald
- ML Jobes
- ML Price
- MM Moran-Santa Maria
- MM Moran-Santa Maria
- MR Bruchas
- MR Bruchas
- MT Stefanik
- MW Feltenstein
- MW Feltenstein
- MW Hale
- N Capriles
- N Omelchenko
- N Sidhpura
- NA Chen
- NM Graziane
- O Vranjkovic
- O Vranjkovic
- P Enrico
- PE Sawchenko
- PJ Fletcher
- PM Beardsley
- PM Beardsley
- PS Regier
- PV Piazza
- PW Kalivas
- PW Kalivas
- PW Kalivas
- PW Marinelli
- R Ciccocioppo
- R Haynes
- R Kvetnansky
- R Martin-Fardon
- R Mongeau
- R Sinha
- R Sinha
- R Sinha
- R Sinha
- R Sinha
- R Sinha
- R Sinha
- R Sinha
- R Takahata
- RC Pierce
- RC Twining
- RD Weiss
- RE See
- RE See
- RJ Smith
- RM Gold
- RP Vertes
- RP Vertes
- RP Waters
- RY Moore
- S Cabib
- S Cohen
- S Erb
- S Erb
- S Erb
- S Erb
- S Erb
- S Erb
- S Erb
- S Fanous
- S Geisler
- S Grimwood
- S Shiffman
- S Stopponi
- S Stopponi
- S Stopponi
- S Tobin
- S Tobin
- SA Flavin
- SE Back
- SF Maier
- SF Maier
- SG Nair
- SG Nair
- SG Nair
- SH Ahmed
- SH Ahmed
- SL Grella
- SM Antelman
- SO Eans
- SR Bornstein
- SR Sesack
- SV Mahler
- SV Mahler
- T Holdstock
- T Maric
- TL Bale
- TR Kosten
- U Shalev
- U Shalev
- U Shalev
- U Shalev
- U Shalev
- U Shalev
- UE Ghitza
- V Deroche
- VA Redila
- WA Hunt
- WB Cannon
- WM Meil
- X Liu
- X Liu
- X Wang
- Y Buczek
- Y Figueroa-Guzman
- Y Nawata
- Y Shaham
- Y Shaham
- Y Shaham
- Y Shaham
- Y Shaham
- Y Shaham
- Y Shaham
- Y Silberman
- Y Zhao
- Yavin Shaham
- YW Chen
- YY Ma
- YY Ma
- Z Sarnyai
- ZJ Brown
- ZJ Brown
- ZX Xi
- Publication venue
- e-Publications@Marquette
- Publication date
- 24/06/2015
- Field of study
In human addicts, drug relapse and craving are often provoked by stress. Since 1995, this clinical scenario has been studied using a rat model of stress-induced reinstatement of drug seeking. Here, we first discuss the generality of stress-induced reinstatement to different drugs of abuse, different stressors, and different behavioral procedures. We also discuss neuropharmacological mechanisms, and brain areas and circuits controlling stress-induced reinstatement of drug seeking. We conclude by discussing results from translational human laboratory studies and clinical trials that were inspired by results from rat studies on stress-induced reinstatement. Our main conclusions are (1) The phenomenon of stress-induced reinstatement, first shown with an intermittent footshock stressor in rats trained to self-administer heroin, generalizes to other abused drugs, including cocaine, methamphetamine, nicotine, and alcohol, and is also observed in the conditioned place preference model in rats and mice. This phenomenon, however, is stressor specific and not all stressors induce reinstatement of drug seeking. (2) Neuropharmacological studies indicate the involvement of corticotropin-releasing factor (CRF), noradrenaline, dopamine, glutamate, kappa/dynorphin, and several other peptide and neurotransmitter systems in stress-induced reinstatement. Neuropharmacology and circuitry studies indicate the involvement of CRF and noradrenaline transmission in bed nucleus of stria terminalis and central amygdala, and dopamine, CRF, kappa/dynorphin, and glutamate transmission in other components of the mesocorticolimbic dopamine system (ventral tegmental area, medial prefrontal cortex, orbitofrontal cortex, and nucleus accumbens). (3) Translational human laboratory studies and a recent clinical trial study show the efficacy of alpha-2 adrenoceptor agonists in decreasing stress-induced drug craving and stress-induced initial heroin lapse
Acute Pain and a Motivational Pathway in Adult Rats: Influence of Early Life Pain Experience
- Author
- A Ennaceur
- A Plaza-Zabala
- A Taddio
- A Taddio
- AD Craig
- AJ Lawrence
- AT Bhutta
- B Seymour
- BM Schmelzle-Lubiecki
- C Hermann
- C Shimada
- C Torsney
- C Torsney
- CC Johnston
- CJ LaBuda
- CR Pryce
- CS Hall
- D Borsook
- D Georgescu
- D Liu
- DGM Ririe
- DJ Scott
- DJ Scott
- DR Britton
- DR Loyd
- E Jennings
- F Wehmer
- FA Champagne
- FA Champagne
- FA Champagne
- G Aston-Jones
- G Paxinos
- GC Harris
- GC Harris
- GJ Hathway
- GJ Hathway
- H Van Praag
- I Chahoud
- I Tracey
- J De Lima
- J Hohmeister
- JD Talbot
- JK Cheng
- JK Zubieta
- JL La Prairie
- JL La Prairie
- JL La Prairie
- JL Thompson
- JWB Peters
- K Hargreaves
- K Ren
- K Ren
- KC Jen
- KJS Anand
- KJS Anand
- L Becerra
- Louis S. Premkumar
- Lucie A. Low
- M Hummel
- M Millecamps
- M Papp
- MA Ruda
- Maria Fitzgerald
- ML Reynolds
- MN Baliki
- MS Lidow
- NM Vittoz
- NM Vittoz
- P Ferre
- R Carbajal
- R Slater
- R Winsky-Sommerer
- RA Shephard
- RA Shephard
- RM Chemelli
- RN Hughes
- RN Walsh
- RVE Grunau
- S Beggs
- S Beggs
- S Bingham
- S Johnson
- S Johnson
- S Johnson
- S Kajiyama
- SC Dulawa
- SHP Simons
- SL Borgland
- SL Borgland
- SL Borgland
- SL Borgland
- SM Walker
- SM Walker
- SM Walker
- SR Bodnoff
- T Boucher
- T Sakurai
- T Yamamoto
- TJ Brennan
- TM Korotkova
- TW Robbins
- Y Zhou
- Publication venue
- Public Library of Science
- Publication date
- 28/03/2012
- Field of study
The importance of neonatal experience upon behaviour in later life is increasingly recognised. The overlap between pain and reward pathways led us to hypothesise that neonatal pain experience influences reward-related pathways and behaviours in adulthood
Convergent functional genomics of anxiety disorders: translational identification of genes, biomarkers, pathways and mechanisms
- Author
- A Bilkei-Gorzo
- A Niculescu
- A Plaza-Zabala
- A Shekhar
- AB Amstadter
- AB Niculescu
- AB Niculescu III
- AB Niculescu III
- AC Magalhaes
- AH Zohar
- AJ de Mooij-van Malsen
- AJ Fyer
- AJ Grottick
- AM Karssen
- B Bertsch
- B Brocke
- B Kaabi
- BM Neale
- BR Lawford
- C Hohoff
- CA Ogden
- CH Duman
- CL McGrath
- CR Cloninger
- DS Charney
- E Eren-Kocak
- E Maron
- E Maron
- EB Binder
- EI Charych
- G Xing
- G Zai
- G Zai
- GE Miller
- GL Hanna
- H Le-Niculescu
- H Le-Niculescu
- H Le-Niculescu
- H Le-Niculescu
- H Le-Niculescu
- H Le-Niculescu
- H Le-Niculescu
- H Wang
- HC Lee
- HS Bracha
- I Hovatta
- I Skre
- J Deckert
- J Donner
- J Gelernter
- J Gelernter
- J Gelernter
- J Huang
- J Quackenbush
- J Samuels
- J Zieker
- JA Oler
- JC Wang
- JD Buxbaum
- JL Kennedy
- JP Lepine
- JW Smoller
- JW Smoller
- JW Smoller
- JW Smoller
- K Morita
- K Mozhui
- KC Koenen
- KK Nicodemus
- KY Liang
- M Elovainio
- M Gratacos
- M Luciano
- M Michail
- M Orsetti
- MM Weissman
- MW Logue
- MW Nash
- N Hlavacova
- N Omata
- N Sarrazin
- P Frisch
- PD Arnold
- PF Buckley
- PH Lysaker
- PJ Rogers
- PN Dannon
- Q Chen
- R Cheng
- RA Kroes
- RA Philibert
- RA Shih
- RA Vasa
- RC Kessler
- RC Kessler
- RH Segman
- RM Youngs
- RR Crowe
- S Buervenich
- S Li
- S Uchida
- S Zhang
- SC Dilsaver
- SC Pandey
- SD Patel
- SJ Mathew
- SM Kurian
- SP Hamilton
- SP Hamilton
- SP Hamilton
- SW Cole
- T Kawai
- T Ohmori
- T Sherrin
- T Sherrin
- T Sipila
- TC Neylan
- TE Thorgeirsson
- TF Ejchel-Cohen
- TM Reyes
- V Krishnan
- VB Risbrough
- VB Risbrough
- VG Hosing
- VL Willour
- Y Joo
- YA Su
- YY Shugart
- ZA Rodd
- Publication venue
- Nature Publishing Group
- Publication date
- 01/05/2011
- Field of study
Anxiety disorders are prevalent and disabling yet understudied from a genetic standpoint, compared with other major psychiatric disorders such as bipolar disorder and schizophrenia. The fact that they are more common, diverse and perceived as embedded in normal life may explain this relative oversight. In addition, as for other psychiatric disorders, there are technical challenges related to the identification and validation of candidate genes and peripheral biomarkers. Human studies, particularly genetic ones, are susceptible to the issue of being underpowered, because of genetic heterogeneity, the effect of variable environmental exposure on gene expression, and difficulty of accrual of large, well phenotyped cohorts. Animal model gene expression studies, in a genetically homogeneous and experimentally tractable setting, can avoid artifacts and provide sensitivity of detection. Subsequent translational integration of the animal model datasets with human genetic and gene expression datasets can ensure cross-validatory power and specificity for illness. We have used a pharmacogenomic mouse model (involving treatments with an anxiogenic drugâyohimbine, and an anti-anxiety drugâdiazepam) as a discovery engine for identification of anxiety candidate genes as well as potential blood biomarkers. Gene expression changes in key brain regions for anxiety (prefrontal cortex, amygdala and hippocampus) and blood were analyzed using a convergent functional genomics (CFG) approach, which integrates our new data with published human and animal model data, as a translational strategy of cross-matching and prioritizing findings. Our work identifies top candidate genes (such as FOS, GABBR1, NR4A2, DRD1, ADORA2A, QKI, RGS2, PTGDS, HSPA1B, DYNLL2, CCKBR and DBP), brainâblood biomarkers (such as FOS, QKI and HSPA1B), pathways (such as cAMP signaling) and mechanisms for anxiety disordersânotably signal transduction and reactivity to environment, with a prominent role for the hippocampus. Overall, this work complements our previous similar work (on bipolar mood disorders and schizophrenia) conducted over the last decade. It concludes our programmatic first pass mapping of the genomic landscape of the triad of major psychiatric disorder domains using CFG, and permitted us to uncover the significant genetic overlap between anxiety and these other major psychiatric disorders, notably the under-appreciated overlap with schizophrenia. PDE10A, TAC1 and other genes uncovered by our work provide a molecular basis for the frequently observed clinical co-morbidity and interdependence between anxiety and other major psychiatric disorders, and suggest schizo-anxiety as a possible new nosological domain
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
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- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
- Abdoli A.
- Abel S.
- Abeliovich H.
- Abildgaard M. H.
- Abudu Y. P.
- Acevedo-Arozena A.
- Adamopoulos I. E.
- Adeli K.
- Adolph T. E.
- Adornetto A.
- Aflaki E.
- Agam G.
- Agarwal A.
- Aggarwal B. B.
- Agnello M.
- Agostinis P.
- Agrewala J. N.
- Agrotis A.
- Aguilar P. V.
- Ahmad S. T.
- Ahmed Z. M.
- Ahumada-Castro U.
- Aits S.
- Aizawa S.
- Akkoc Y.
- Akoumianaki T.
- Akpinar H. A.
- Al-Abd A. M.
- Al-Akra L.
- Al-Gharaibeh A.
- Alaoui-Jamali M. A.
- Alberti S.
- Alcocer-Gomez E.
- Alessandri C.
- Ali M.
- Alim Al-Bari M. A.
- Aliwaini S.
- Alizadeh J.
- Almacellas E.
- Almasan A.
- Alonso A.
- Alonso G. D.
- Altan-Bonnet N.
- Altieri D. C.
- Alvarez E. M. C.
- Alves da Costa C.
- Alves S.
- Alzaharna M. M.
- Amadio M.
- Amantini C.
- Amaral C.
- Ambrosio S.
- Amer A. O.
- Ammanathan V.
- An Z.
- Andersen S. U.
- Andrabi S. A.
- Andrade-Silva M.
- Andres A. M.
- Angelini S.
- Ann D.
- Anozie U. C.
- Ansari M. Y.
- Antas P.
- Antebi A.
- Anton Z.
- Anwar T.
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- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
- Author
- Abdel-Aziz AK
- Abdelfatah S
- Abdellatif M
- Abdoli A
- Abel S
- Abeliovich H
- Abildgaard MH
- Abudu YP
- Acevedo-Arozena A
- Adamopoulos IE
- Adeli K
- Adolph TE
- Adornetto A
- Aflaki E
- Agam G
- Agarwal A
- Aggarwal BB
- Agnello M
- Agostinis P
- Agrewala JN
- Agrotis A
- Aguilar PV
- Ahmad ST
- Ahmed ZM
- Ahumada-Castro U
- Aits S
- Aizawa S
- Akkoc Y
- Akoumianaki T
- Akpinar HA
- Al-Abd AM
- Al-Akra L
- Al-Gharaibeh A
- Alaoui-Jamali MA
- Alberti S
- Alcocer-GĂłmez E
- Alessandri C
- Ali M
- Alim Al-Bari MA
- Aliwaini S
- Alizadeh J
- Almacellas E
- Almasan A
- Alonso A
- Alonso GD
- Altan-Bonnet N
- Altieri DC
- Alves da Costa C
- Alves S
- Alzaharna MM
- Amadio M
- Amantini C
- Amaral C
- Ambrosio S
- Amer AO
- Ammanathan V
- An Z
- Andersen SU
- Andrabi SA
- Andrade-Silva M
- Andres AM
- Angelini S
- Ann D
- Anozie UC
- Ansari MY
- Antas P
- Antebi A
- AntĂłn Z
- Anwar T
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- Apostolova N
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- Arasaki K
- Araya J
- AraĂșjo WL
- Arden C
- Arguelles S
- Arias E
- Arikkath J
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- Ariosa AR
- Armstrong-James D
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- Aroca A
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- Arsov I
- Artero R
- Arévalo M-A
- Asaro DML
- Aschner M
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- Ashur-Fabian O
- Atanasov AG
- Au AK
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- Zorzano A
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- Ălvarez ĂMC
- Ăvalos Y
- Ănal G
- ĂstĂŒn S
- ÄoliÄ M
- ÄokiÄ J
- Ćœerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
An investigation of interactions between hypocretin/orexin signaling and glutamate receptor surface expression in the rat nucleus accumbens under basal conditions and after cocaine exposure
- Author
- Ahmed
- Ainhoa Plaza-Zabala
- Argilli
- Aston-Jones
- Aston-Jones
- Baldo
- Bonci
- Borgland
- Borgland
- Boutrel
- Cluderay
- Conrad
- de Lecea
- Fernando Berrendero
- Ferrario
- Gozzi
- Hervieu
- Jacobs
- James
- Jessica A. Loweth
- Li
- Loweth
- LĂŒscher
- Mahler
- Mahler
- Mameli
- Marcus
- Marina E. Wolf
- Mike Milovanovic
- Mu
- Nair
- Paxinos
- Peyron
- Pickens
- Plaza-Zabala
- Plaza-Zabala
- Rafael Maldonado
- Richardson
- Sakurai
- Shin
- Smith
- Smith
- Sutcliffe
- Trivedi
- Ungless
- Vanderschuren
- Wang
- Wolf
- Xuan Li
- Zhang
- Zhou
- Zhou
- Publication venue
- 'Elsevier BV'
- Publication date
- 01/01/2013
- Field of study
Hypocretin peptides are critical for the effects of cocaine on excitatory synaptic strength in the ventral tegmental area (VTA). However, little is known about their role in cocaine-induced synaptic plasticity in the nucleus accumbens (NAc). First, we tested whether hypocretin-1 by itself could acutely modulate glutamate receptor surface expression in the NAc, given that hypocretin-1 in the VTA reproduces cocaine's effects on glutamate transmission. We found no effect of hypocretin-1 infusion on AMPA or NMDA receptor surface expression in the NAc, measured by biotinylation, either 30 min or 3h after the infusion. Second, we were interested in whether changes in hypocretin receptor-2 (Hcrtr-2) expression contribute to cocaine-induced plasticity in the NAc. As a first step towards addressing this question, Hcrtr-2 surface expression was compared in the NAc after withdrawal from extended-access self-administration of saline (control) versus cocaine. We found that surface Hcrtr-2 levels remain unchanged following 14, 25 or 48 days of withdrawal from cocaine, a time period in which high conductance GluA2-lacking AMPA receptors progressively emerge in the NAc. Overall, our results fail to support a role for hypocretins in acute modulation of glutamate receptor levels in the NAc or a role for altered Hcrtr-2 expression in withdrawal-dependent synaptic adaptations in the NAc following cocaine self-administration
An investigation of interactions between hypocretin/orexin signaling and glutamate receptor surface expression in the rat nucleus accumbens under basal conditions and after cocaine exposure
- Author
- Publication venue
- Elsevier
- Publication date
- Field of study
Hypocretin peptides are critical for the effects of cocaine on excitatory synaptic strength in the ventral tegmental area (VTA). However, little is known about their role in cocaine-induced synaptic plasticity in the nucleus accumbens (NAc). First, we tested whether hypocretin-1 by itself could acutely modulate glutamate receptor surface expression in the NAc, given that hypocretin-1 in the VTA reproduces cocaine's effects on glutamate transmission. We found no effect of hypocretin-1 infusion on AMPA or NMDA receptor surface expression in the NAc, measured by biotinylation, either 30 min or 3h after the infusion. Second, we were interested in whether changes in hypocretin receptor-2 (Hcrtr-2) expression contribute to cocaine-induced plasticity in the NAc. As a first step towards addressing this question, Hcrtr-2 surface expression was compared in the NAc after withdrawal from extended-access self-administration of saline (control) versus cocaine. We found that surface Hcrtr-2 levels remain unchanged following 14, 25 or 48 days of withdrawal from cocaine, a time period in which high conductance GluA2-lacking AMPA receptors progressively emerge in the NAc. Overall, our results fail to support a role for hypocretins in acute modulation of glutamate receptor levels in the NAc or a role for altered Hcrtr-2 expression in withdrawal-dependent synaptic adaptations in the NAc following cocaine self-administration
MICROGLIA BRAINIZATION: THE SHIFT FROM INITIAL COLONIZATION TO ADULT-LIKE DYNAMICS, MORPHOLOGY AND FUNCTION IN THE POSTNATAL HIPPOCAMPUS AND CEREBELLUM
- Author
- Publication venue
- Elsevier
- Publication date
- 01/10/2023
- Field of study