ライフサイエンスコーパス: nucleus accumbens

1 (ventromedial prefrontal cortex (vmPFC) and nucleus accumbens).

2 of KOR regulation of dopamine release in the nucleus accumbens.

3 sembled from activity across the VTA and the nucleus accumbens.

4 modulation of cocaine potency at DATs in the nucleus accumbens.

5 le of glutamatergic hippocampal outputs onto nucleus accumbens.

6 panied by enhanced dopamine signaling in the nucleus accumbens.

7 of reward processing within the caudate and nucleus accumbens.

8 ced DARPP-32 phosphorylation at Thr75 in the nucleus accumbens.

9 by stimulation of oxytocin terminals in the nucleus accumbens.

10 D(1)-expressing medium spiny neurons in the nucleus accumbens.

11 ons projecting to lateral or medial shell of nucleus accumbens.

12 facilitating D(1)-mediated excitation in the nucleus accumbens.

13 and interact with distinct subregions of the nucleus accumbens.

14 or, mid- and posterior), caudate nucleus and nucleus accumbens.

15 ritical mediator of cocaine responses in the nucleus accumbens.

16 al area (VTA), with no apparent input to the nucleus accumbens.

17 ng the anterior limb of the internal capsule/nucleus accumbens.

18 ion in RGS12-null mice are restricted to the nucleus accumbens.

19 eptive opioid peptide (NOP) receptors in the nucleus accumbens.

20 m 2.42 in the globus pallidus to 8.48 in the nucleus accumbens.

21 nal measurements of dopamine dynamics in the nucleus accumbens.

22 This effect is prominent within the nucleus accumbens, a brain region associated with mood r

23 D(1) receptors on astrocytes located in the nucleus accumbens, a key structure of the brain's reward

24 entral to this view is the engagement of the nucleus accumbens-a brain region that processes reward e

25 biting D1 medium spiny neurons (MSNs) in the nucleus accumbens-a population that has been linked to r

26 rs (D2R) in the dorsal striatum (DS) and the nucleus accumbens (Acb) jointly but differentially contr

27 We identified a cell type in the nucleus accumbens activated downstream of long-range exc

28 t fMRI experiment, we show that learning and nucleus accumbens activation in a simple unidimensional

29 owed a positive correlation with caudate and nucleus accumbens activity during placebo, which was abs

30 , lithium administration reduced caudate and nucleus accumbens activity during reward outcome.

31 f evidence for co-use differences related to nucleus accumbens activity during reward processing.

32 risk for developing chronic pain and altered nucleus accumbens activity is a signature of the state o

33 etic variation related to the volumes of the nucleus accumbens, amygdala, brainstem, caudate nucleus,

34 coded RPEs and did so more robustly than the nucleus accumbens, an input to the VP.

35 with AN displayed blunted reactivity in the nucleus accumbens and amygdala.

36 as negatively correlated with gaze duration (nucleus accumbens and anterior insular cortex), while tw

37 d functional connectivity locally within the nucleus accumbens and basal forebrain, and reversed the

38 reases in functional connectivity within the nucleus accumbens and basal forebrain.

39 ggest that the connectivity patterns for the nucleus accumbens and cortico-striatal motor circuits (p

40 g structural spine plasticity changes in the nucleus accumbens and depressive-like behavior.

41 drug-evoked transcriptional changes in both nucleus accumbens and dorsal striatum, dramatically incr

42 genome-wide transcriptional profiling in the nucleus accumbens and dorsal striatum.

43 eable binding potential, particularly in the nucleus accumbens and globus pallidus, where the change

44 oscopy ((1)H-MRS) at ultra-high-field in the nucleus accumbens and inquired whether levels of glutama

45 vivo dopamine and glutamate microdialysis in nucleus accumbens and medial prefrontal cortex, and ex v

46 lcholine receptor subunit mRNA levels in the nucleus accumbens and medial prefrontal cortex.

47 pocampus) and reward systems (orbital gyrus, nucleus accumbens and putamen) in driving pre-training d

48 te functional connectivity between bilateral nucleus accumbens and rostral anterior cingulate cortex

49 , connectivity changes were observed between nucleus accumbens and rostral anterior cingulate cortex

50 The reduced metabolism in nucleus accumbens and the disrupted thalamo-accumbens co

51 yporeactivity of striatal (caudate, putamen, nucleus accumbens) and cortical (insula, anterior cingul

52 adulthood on the function of the mesolimbic (nucleus accumbens) and nigrostriatal (dorsal striatum) d

53 lia regions, including the caudate, putamen, nucleus accumbens, and globus pallidus.

54 ires activation of oxytocin receptors in the nucleus accumbens, and is recapitulated by stimulation o

55 several brain regions (ventral hippocampus, nucleus accumbens, and medial prefrontal cortex) of susc

56 NA-sequencing in the ventral tegmental area, nucleus accumbens, and prefrontal cortex of male and fem

57 limbic structures involving the hippocampus, nucleus accumbens, and prefrontal cortex.

58 changes, attenuated dopamine release in the nucleus accumbens, and reduced cocaine-seeking behavior.

59 mo in most areas except for the hippocampus, nucleus accumbens, and thalamus.

60 apid upregulation of Gadd45b mRNA in the rat nucleus accumbens, and that knockout or site-specific CR

61 =51), globus pallidus internus (GPi) (n=47), nucleus accumbens/anterior limb of the internal capsule

62 These results point to Cdk5 in the nucleus accumbens as a critical contributor to depressiv

63 eural pathway tracing analyses implicate the nucleus accumbens as a putative downstream target of vHP

64 plasticity and suggest this mechanism in the nucleus accumbens as a target for ethanol modulation of

65 ions from the anterior insular cortex to the nucleus accumbens as modulating highly compulsive-like f

66 n left rostral medial frontal gyrus and left nucleus accumbens as well as right frontal pole and left

67 ons on cocaine potency at distal DATs in the nucleus accumbens as well as the behavioral economics of

68 e gyrus, hippocampus, prefrontal cortex, and nucleus accumbens) as well as chromatin accessibility in

69 5 main reward-aversion brain centers (i.e., nucleus accumbens, bed nucleus of the stria terminalis,

70 netic activation of the basolateral amygdala-nucleus accumbens (BLA-NAc) glutamatergic circuit reduce

71 electively elevated dopamine overflow in the nucleus accumbens, but not prefrontal cortex, without in

72 ally on neuromodulatory signaling within the nucleus accumbens, but the neuronal dynamics underlying

73 itatory synapses, which are generated in the nucleus accumbens by cocaine self-administration, and su

74 nding does not elicit differences in overall nucleus accumbens Ca(2+) activity.

75 the ventromedial prefrontal cortex (vmPFC), nucleus accumbens, caudate nucleus, and putamen.

76 ntly higher in SAD patients in the amygdala, nucleus accumbens, caudate, putamen, and posterior ventr

77 cute back pain patients showed altered local nucleus accumbens connectivity between putative shell an

78 (IC), which is anatomically connected to the nucleus accumbens core (NAc).

79 In two experiments, we induced nucleus accumbens core (NAcc) dysfunction in rats receiv

80 rature has highlighted the importance of the nucleus accumbens core (NAcC) in behavioral tasks depend

81 Here, we examined a possible role for the nucleus accumbens core (NAcc) in the acquisition and exp

82 action to perform.SIGNIFICANCE STATEMENT The nucleus accumbens core (NAcC) is essential to process in

83 ts, we investigated the DNA methylome of the nucleus accumbens core (NAcc) of rhesus macaques after c

84 tween the basolateral amygdala (BLA) and the nucleus accumbens core (NAcC).

85 The nucleus accumbens core (NAcore) contains two predominate

86 tion (t-SP) at glutamatergic synapses in the nucleus accumbens core (NAcore).

87 of the prelimbic cortex that project to the nucleus accumbens core (PrL->NAcC).

88 s is regulated by synaptic plasticity in the nucleus accumbens core and involves distinct plasticity

89 nfusions of D2R and D1R antagonists into the nucleus accumbens core and shell (NAcC; NAcS), the anter

90 for differences in dopamine signaling in the nucleus accumbens core at baseline, in response to a sin

91 While PL projections to nucleus accumbens core have been shown to be involved in

92 of cocaine to inhibit dopamine uptake in the nucleus accumbens core using fast scan cyclic voltammetr

93 ease in mouse dorsolateral striatum, but not nucleus accumbens core, is governed by GAT-1 and GAT-3.

94 ingulate, prelimbic, and infralimbic cortex; nucleus accumbens core, medial shell, and lateral shell;

95 These regions, comprising the nucleus accumbens core, shell, and caudate-putamen, are

96 nhibitory synaptic transmission in the mouse nucleus accumbens core.

97 projecting neurons to each region except the nucleus accumbens core.

98 rior cingulate cortices, caudate nucleus and nucleus accumbens (corrected P = 0.043).

99 ter, rats were tested for their locomotor or nucleus accumbens dopamine (NAcc DA) response to ampheta

100 Nucleus accumbens dopamine 1 receptor medium spiny neuro

101 re body temperature and selectively enhanced nucleus accumbens dopamine release, consistent with acti

102 ein restriction during adolescence decreased nucleus accumbens dopamine release.

103 load and tyrosine hydroxylase levels in the nucleus accumbens, dorsal putamen and caudate using immu

104 ion in the bilateral ventral caudate and the nucleus accumbens during reward receipt relative to loss

105 shRNA-mediated knockdown of Lmo4 in the nucleus accumbens enhanced alcohol consumption, whereas

106 ometry revealed that dopamine release in the nucleus accumbens evoked by reward-predictive cues is ac

107 nucleus; GPi, globus pallidus internus; NAc, nucleus accumbens) evoked a sufficiently distinctive blo

108 While nucleus accumbens excitatory synaptic plasticity is well

109 explore changes in lipid composition of the nucleus accumbens from mice subjected to two lipid diets

110 dopamine D3 receptors protein levels in the nucleus accumbens, frontal cortex and putamen were deter

111 or hypothesis posits neuronal inhibitions in nucleus accumbens generate intense motivation.

112 aptations, suggesting a complete recovery of nucleus accumbens glutamatergic synaptic plasticity when

113 rojections from the prefrontal cortex to the nucleus accumbens has been argued to underlie motivation

114 d reward signals in areas which included the nucleus accumbens in 475 participants.

115 alterations in medial prefrontal cortex and nucleus accumbens in human MDD and the 3 mouse chronic s

116 Substantial evidence implicates the nucleus accumbens in motivated performance, but very lit

117 umental task and (2) dopamine release in the nucleus accumbens in response to electrical stimulation

118 iated with hyporeactivity exclusively in the nucleus accumbens in response to the anticipation of a r

119 The nucleus accumbens is a critical integration center for r

120 These results may be relevant to roles of nucleus accumbens mechanisms in pathological motivations

121 nto D1 medium spiny neurons (D1-MSNs) in the nucleus accumbens medial shell (NAcmSh), and with latera

122 dulate behavior, with a specific emphasis on nucleus accumbens medial shell and stress responsivity.

123 ferent reward-related regions, including the nucleus accumbens, medial prefrontal cortex, and orbitof

124 matter volumes, most prominent in thalamus, nucleus accumbens, medial temporal, medial prefrontal/fr

125 synaptic potentiation (t-SP) induced in the nucleus accumbens mediates cued cocaine seeking in rat m

126 Subtypes of nucleus accumbens medium spiny neurons (MSNs) promote di

127 ect was seen specifically on the inputs from nucleus accumbens medium spiny neurons expressing either

128 afferents from the ventral tegmental area to nucleus accumbens (mesolimbic circuit) and frontal corte

129 ergic signaling in the reward circuit is the nucleus accumbens, more specifically, the dopamine D1 re

130 ransporter GLT-1 and glutamate efflux in the nucleus accumbens (NA) core during the reinstatement of

131 In the nucleus accumbens (NAc) activation of oxytocin receptors

132 In rodents, nucleus accumbens (NAc) afferents from the ventral hippo

133 of changes in the proteomic landscape in the nucleus accumbens (NAc) and medial prefrontal cortex (mP

134 or through effects on dopamine output in the nucleus accumbens (NAc) and on neurotransmission in the

135 metry, to record haemodynamic signals in the nucleus accumbens (NAc) and orbitofrontal cortex (OFC),

136 nscriptional and morphological events in the nucleus accumbens (NAc) and other brain reward regions c

137 eptor beta (IGF-1Rbeta) were assessed in the nucleus accumbens (NAc) and ventral tegmental area (VTA)

138 from the ventral tegmental area (VTA) to the nucleus accumbens (NAc) are critical in regulating cue-m

139 xpressing medium spiny neurons (MSNs) of the nucleus accumbens (NAc) are fundamental to neuropsychiat

140 oking in human postmortem brain, focusing on nucleus accumbens (NAc) as a key brain region in develop

141 te AMPA antagonist (DNQX) in medial shell of nucleus accumbens (NAc) can cause either intense appetit

142 rowth response 3) is oppositely regulated in nucleus accumbens (NAc) cell subtypes 24 hours following

143 The nucleus accumbens (NAc) controls multiple facets of impu

144 pression was increased in D1+ neurons in the nucleus accumbens (NAc) core and dorsolateral (DLS) stri

145 TA neurons with divergent projections to the nucleus accumbens (NAc) core and shell.

146 eports indicate enhancing activity of either nucleus accumbens (NAc) core MSN subtype augments reward

147 The ventromedial striatum, including the nucleus accumbens (NAc) core, is typically associated wi

148 ated behavior is known to be mediated by the nucleus accumbens (NAc) core.

149 STATEMENT Glutamatergic transmission in the nucleus accumbens (NAc) critically contributes to goal-d

150 Here we studied the role of nucleus accumbens (NAc) dopamine receptor (Drd)1- and Dr

151 Complex circuit interactions within the nucleus accumbens (NAc) facilitate goal-directed behavio

152 ulnerable individuals remains ambiguous, the nucleus accumbens (NAc) has been shown to play a central

153 Cholinergic interneurons (ChIs) in the nucleus accumbens (NAc) have been implicated in drug add

154 IGNIFICANCE STATEMENT Given the roles of the nucleus accumbens (NAc) in integrating cortical and allo

155 thin the vmPFC with different outputs to the nucleus accumbens (NAc) in male and female rats.

156 y assessed the role of stress systems in the nucleus accumbens (NAc) in promoting sex differences in

157 Here we studied the role of the nucleus accumbens (NAc) in this model.

158 Outputs from the nucleus accumbens (NAc) include projections to the ventr

159 ogical conditions.SIGNIFICANCE STATEMENT The nucleus accumbens (NAc) is a key part of the striatal li

160 The nucleus accumbens (NAc) is a mesocorticolimbic structure

161 The nucleus accumbens (NAc) is a reward processing hub sensi

162 ithin the reward circuitry, within which the nucleus accumbens (NAc) is anatomically positioned as an

163 nvestigated whether GSK3beta activity in the nucleus accumbens (NAc) is associated with depression-li

164 jection from ventral tegmental area (VTA) to nucleus accumbens (NAc) is critical for motivation to wo

165 The nucleus accumbens (NAc) is essential for cued approach b

166 The nucleus accumbens (NAc) is part of a brain reward circui

167 In particular, the nucleus accumbens (NAc) medial shell has repeatedly demo

168 CP-AMPARs in the nucleus accumbens (NAc) mediate cue-triggered motivation

169 xpression in the prefrontal cortex (PFC) and nucleus accumbens (NAc) of mice exposed to multimodal ch

170 ed nicotine on rapid dopamine signals in the nucleus accumbens (NAc) of rats.

171 inals in the ventral tegmental area (VTA) or nucleus accumbens (NAc) of the mesolimbic DA system.

172 e discrete projections from the vHipp to the nucleus accumbens (NAc) or prefrontal cortex (mPFC).

173 Within this circuit, two distinct nucleus accumbens (NAc) output neuron types, dopamine D1

174 ngs indicate the insular cortex (IC) and the nucleus accumbens (NAc) play important roles in social b

175 hippocampus (vHPC) neurons projecting to the nucleus accumbens (NAc) regulates mood-related behaviora

176 ectivity (FC) of reward neurocircuitry using nucleus accumbens (NAc) seed regions of interest, and th

177 We then quantified DA release in the nucleus accumbens (NAc) shell after treatment with d-Amp

178 ntal area (VTA), central amygdala (CeA), and nucleus accumbens (NAc) shell had no such effect.

179 ines observed in medium spiny neurons of the nucleus accumbens (NAc) shell of alcohol-dependent rats

180 The nucleus accumbens (NAc) shell, which integrates the aver

181 corded activity in DA terminals in different nucleus accumbens (NAc) subnuclei during an aversive and

182 aving ultimately depends on strengthening of nucleus accumbens (NAc) synapses through an accumulation

183 ection from dorsal CA1 (dCA1) hippocampus to nucleus accumbens (NAc) that enables the behavioral mani

184 s firing of CINs in both dorsal striatum and nucleus accumbens (NAc) through activation of CRF type 1

185 ests that medium spiny neurons (MSNs) in the nucleus accumbens (NAc) undergo structural plasticity; h

186 Energy metabolic changes in the nucleus accumbens (NAc) were recently related to hierarc

187 , ventromedial prefrontal cortex (vmPFC) and nucleus accumbens (NAc)).

188 s dopamine receptor D1 (DRD1) agonist in the nucleus accumbens (NAc), a brain area involved in mediat

189 The nucleus accumbens (NAc), a central component of the midb

190 mics in medium spiny neurons (MSNs) from the nucleus accumbens (NAc), a hub of the brain's motivation

191 xamined the expression of the lncRNA Gas5 in nucleus accumbens (NAc), a key brain reward region, of a

192 t in freely behaving mice, astrocytes in the nucleus accumbens (NAc), a key reward center in the brai

193 ed in the mammalian forebrain, including the nucleus accumbens (NAc), a major neural substrate of mot

194 ission at medium spiny neurons (MSNs) in the nucleus accumbens (NAc), a region critical for reward pr

195 s reward behaviors through its action in the nucleus accumbens (NAc), but the impact of NPY on the hu

196 The nucleus accumbens (NAc), considered the hub of reward ci

197 medial prefrontal cortex (mPFC), but not to nucleus accumbens (NAc), contributed to the antidepressi

198 In the nucleus accumbens (NAc), structural and physiological pl

199 CRH(+) fibers are found in nucleus accumbens (NAc), where CRH modulates reward/moti

200 ute or chronic cocaine exposure in the mouse nucleus accumbens (NAc)-a key reward region of brain.

201 CA) neurons form functional connections with nucleus accumbens (NAc)-projecting neurons of the poster

202 and decreases AMPAR-mediated currents in the nucleus accumbens (NAc).

203 of DA release from their distal terminals in nucleus accumbens (NAc).

204 -week morphine and cocaine abstinence in the nucleus accumbens (NAc).

205 ically in medium spiny neurons (MSNs) of the nucleus Accumbens (nAc).

206 1), lateral OFC (BA47), head of caudate, and nucleus accumbens (NAc).

207 receptors (DORs), are highly enriched in the nucleus accumbens (NAc).

208 dritic spine signaling and morphology in the nucleus accumbens (NAc).

209 Gadd45b downstream of BDNF signaling in the nucleus accumbens (NAc).

210 iatal and mesolimbic networks, including the nucleus accumbens (NAc).

211 he central nucleus of the amygdala (CeA) and nucleus accumbens (NAc).

212 uit interactions between the hippocampus and nucleus accumbens (NAc).

213 latable food (HPF), which is mediated by the nucleus accumbens (NAc).

214 Finally, patch recordings in nucleus accumbens (NAcc) medium spiny neurons (MSNs) rev

215 nforcement of non-drug rewards by increasing nucleus accumbens (NAcc) reactivity to anticipatory cues

216 er problems on adolescent depression through nucleus accumbens (NAcc) volume alteration, but not thro

217 ility in functional connectivity between the nucleus accumbens (NAcc), a key structure of the reward

218 e amygdala, anterior cingulate cortex (ACC), nucleus accumbens (NAcc), and orbitofrontal cortex (OFC)

219 and avoidance responses [bilateral amygdala, nucleus accumbens (NAcc), and ventromedial prefrontal co

220 ith volumes of the hippocampus, thalamus and nucleus accumbens (NAcc)-three subcortical regions selec

221 PAR/GluR composition both in the PFC and the nucleus accumbens (NAcc).

222 ral regions (i.e., increased activity in the nucleus accumbens [NAcc] and medial prefrontal cortex [M

223 s of reward-related brain regions (e.g., the nucleus accumbens [NAcc]) and unhealthy eating behaviors

224 logical restructuring of dendritic spines of nucleus accumbens neurons is thought to be one of the ce

225 ncement of total spine number in a subset of nucleus accumbens neurons that prevents stress-related e

226 ow this catalytic activity communicates with nucleus accumbens neurons to induce t-SP and cocaine see

227 such as the ventral tegmental area (VTA) or nucleus accumbens neurons, but less is known about cocai

228 erotonin efflux in the prefrontal cortex and nucleus accumbens of conscious rats were assessed using

229 Microinjections in nucleus accumbens of glutamate antagonist, DNQX, which m

230 activity in spiny projection neurons in the nucleus accumbens of mice during learning.

231 ase in amperometric glutamate sensing in the nucleus accumbens of mouse brain tissue.

232 ally label activated neural ensembles in the nucleus accumbens of the mouse brain during brief stimul

233 d in depression-medial prefrontal cortex and nucleus accumbens-of humans with MDD and of 3 chronic st

234 ined the effect of ZIP administration in the nucleus accumbens on reinstatement (RI) of cocaine seeki

235 examined the effect of ZIP infused into the nucleus accumbens on the reinstatement (RI) of cocaine s

236 cortex reflected this interaction, while the nucleus accumbens only reflected uncertainty.

237 The latest research demonstrates that in the nucleus accumbens, opioid-induced excitatory synaptic pl

238 ow this family regulates activity within the nucleus accumbens or behavioral responses to drugs of ab

239 ior limb of the internal capsule (ALIC), the nucleus accumbens or the subthalamic nucleus (STN).

240 , putamen, globus pallidus, hippocampus, and nucleus accumbens) other than amygdala volume.

241 involved in the pair-bonding process in the nucleus accumbens, our work illustrates the vast extent

242 against acute oxycodone-induced decreases in nucleus accumbens oxygen levels.

243 ntal cortices, and between orbitofrontal and nucleus accumbens, predict individual differences in sen

244 f Fos-immunoreactive (Fos-ir) neurons in the nucleus accumbens predicted the frequency of the feeding

245 We found that activity in the nucleus accumbens promotes cheating, particularly for in

246 In the nucleus accumbens, protein restriction in adults increas

247 , we find that PVT neurons projecting to the nucleus accumbens (PVT-NAc) develop inhibitory responses

248 als in regions associated with reward (i.e., nucleus accumbens, r = 0.24), memory (i.e., hippocampus,

249 neural activation in reward-related regions (nucleus accumbens, r = 0.29; caudate nucleus, r = 0.27)

250 he anterior limb of the internal capsule and nucleus accumbens region (ALIC-NAcc) on OCD symptoms, ex

251 Glutamatergic synapses in the nucleus accumbens regulate the motivation to relapse to

252 ncluding bed nucleus of stria terminalis and nucleus accumbens) remains investigational.

253 ng and altered glutamate connectivity in the nucleus accumbens represent the neuroanatomical basis fo

254 Is neuronal inhibition in nucleus accumbens required for such pharmacologically-in

255 Analysis of the power spectral density of nucleus accumbens resting-state activity in the subacute

256 as positively associated with HOMA-IR in the nucleus accumbens, right and left insula, and right cing

257 Ablation of OFC neurons projecting to the nucleus accumbens selectively disrupted performance foll

258 e that the RMTg-ventral tegmental area (VTA)-nucleus accumbens shell (Acb) circuit plays a role in th

259 l prefrontal cortex (mPFC) projecting to the nucleus accumbens shell (AcbSh) in female Sprague Dawley

260 cal, sensory, and limbic information, to the nucleus accumbens shell (an area known to be important f

261 rojection from the infralimbic cortex to the nucleus accumbens shell (IL-NAc) is thought to inhibit c

262 ontrol over subcortical regions, such as the nucleus accumbens shell (NAcS) and basolateral amygdala,

263 ry in male Long-Evans rats to test if phasic nucleus accumbens shell (NACs) dopamine dynamics are ass

264 LDT test and higher MSN excitability in the nucleus accumbens shell (NAcS).

265 Pharmacological manipulations of the nucleus accumbens shell (NAcSh) have repeatedly been dem

266 Compromised signaling between the mPFC and nucleus accumbens shell (NAcSh) is thought to underlie t

267 e found that cocaine-induced hypoactivity of nucleus accumbens shell (NAcSh) medium spiny neurons (MS

268 RNAi-mediated knockdown of G9a expression in nucleus accumbens shell (NAcSh) of male rats reduces bot

269 ntral tegmental area (VTA) projection to the nucleus accumbens shell (NAcSh) regulates NAcSh-mediated

270 glutamatergic projections from the IL to the nucleus accumbens shell (NAcSh) suppresses the aversive

271 r-silent glutamatergic synapses in the adult nucleus accumbens shell (NAcSh).

272 asing extracellular DA concentrations in the nucleus accumbens shell (NAS) efficaciously and more pot

273 infralimbic cortex and its projection to the nucleus accumbens shell in suppressing learned negative

274 hat optical activation of the infralimbic to nucleus accumbens shell pathway attenuates learned avers

275 ts indicate an important role for the PVT to nucleus accumbens shell projections in the augmentation

276 RNA-seq of the nucleus accumbens shell revealed hundreds of differentia

277 mRNA reductions in the cingulate cortex and nucleus accumbens shell, regardless of MIA timing; (2) S

278 ral (Caudato-Putamen, DLS) and ventromedial (Nucleus Accumbens Shell, VS) striatal subregions was exa

279 e incentive value and dopamine levels in the nucleus accumbens shell.

280 eptor-expressing medium spiny neurons in the nucleus accumbens shell.

281 Nucleus accumbens-specific RhoA inhibition is capable of

282 ated within DS synapses, but enhanced in the nucleus accumbens, suggesting a dichotomous role of BDNF

283 Subcortical volumes (pallidum, nucleus accumbens, thalamus) were also different among g

284 ation of a discrete number of neurons in the nucleus accumbens that are causally linked to reward-rel

285 oved after dopamine receptor blockade in the nucleus accumbens; the D1R antagonist, SCH23390, in the

286 Neural responses in the nucleus accumbens to anticipated reward and non-loss out

287 late pathways between the OFC, amygdala, and nucleus accumbens to reveal their separable contribution

288 This led to a highly sexually biased nucleus accumbens transcriptome at 3 weeks related to pr

289 reoptic area, hypothalamus, rostral pallium, nucleus accumbens, ventral pallidum, and bed nucleus of

290 Our results provide evidence that lower nucleus accumbens volume confers risk for developing chr

291 or developing chronic pain exhibit a smaller nucleus accumbens volume, which persists in the chronic

292 ions were found for analyses of thalamus and nucleus accumbens volumes.

293 t in CUD compared to controls, metabolism in nucleus accumbens was lower for the placebo and MPH meas

294 Myelin protein content in the nucleus accumbens was reduced in all mice exposed to str

295 ifically, prediction-error activation in the nucleus accumbens was similar across age groups, and num

296 weeks, and transcriptomic regulations in the nucleus accumbens were measured by RNA sequencing.

297 associated with anticipatory activity in the nucleus accumbens, whereas perceptual bias tracked categ

298 atients exhibited higher SERT binding in the nucleus accumbens while DAT availability in the amygdala

299 ciated with more focal hyporeactivity in the nucleus accumbens, while depression severity during earl

300 n may underlie augmented connectivity of the nucleus accumbens with fear/anxiety regions, disrupting