ライフサイエンスコーパス: nucleus accumbens

1 bic regions, including the ventral striatum (nucleus accumbens).

2 (but not with structural differences in the Nucleus Accumbens).

3 n thalamus), and limbic system (amygdala and nucleus accumbens).

4 trength at prefrontal cortex synapses in the nucleus accumbens.

5 ng the D1 dopamine receptor (D1-MSNs) in the nucleus accumbens.

6 e respective change of the RPE signal in the nucleus accumbens.

7 D1DR/PKA-dependent AMPA transmission in the nucleus accumbens.

8 inhibition of DA clearance in slices of the nucleus accumbens.

9 llial regions, particularly the striatum and nucleus accumbens.

10 gions of the CNS such as the hippocampus and nucleus accumbens.

11 e measuring phasic dopamine signaling in rat nucleus accumbens.

12 rter assays and in vivo microdialysis in rat nucleus accumbens.

13 ntration in the medial prefrontal cortex and nucleus accumbens.

14 d cocaine-induced release of dopamine in the nucleus accumbens.

15 g food picture evaluation in the caudate and nucleus accumbens.

16 ntials in direct-pathway MSNs (dMSNs) in the nucleus accumbens.

17 s cocaine-induced changes of dopamine in the nucleus accumbens.

18 rexcitability of medium spiny neurons of the nucleus accumbens.

19 al response to anticipation of reward in the nucleus accumbens.

20 mic oxytocin were mediated by actions in the nucleus accumbens.

21 age and was modulated by D1 availability in nucleus accumbens.

22 utamen and higher D1-receptor density in the nucleus accumbens.

23 e of the brain's reward regions, such as the nucleus accumbens.

24 and cocaine-enhanced extracellular DA in the nucleus accumbens.

25 effects depend on oxytocin signaling in the nucleus accumbens.

26 thylation at the Auts-Caln1 loop base in the nucleus accumbens.

27 in striatal projection neurons (SPNs) of the nucleus accumbens.

28 nal networks and their connectivity with the nucleus accumbens.

29 repressor of gene expression, acting in the nucleus accumbens, a brain reward region, is capable of

30 In the nucleus accumbens, a key region involved in reward proce

31 ward properties evoked activation within the nucleus accumbens, a subregion of the striatum.

32 We examined dopamine release in the nucleus accumbens across multiple time scales, using com

33 el-free analyses convergently indicated that nucleus accumbens activity can support aggregate forecas

34 re observed in striatum, olfactory tubercle, nucleus accumbens, amygdala, and neocortex, whereas in s

35 in reward processing, including the caudate, nucleus accumbens, amygdala, anterior insula, and orbito

36 seven bilateral subcortical structures: the nucleus accumbens, amygdala, caudate, hippocampus, palli

37 the volumes of eight subcortical structures (nucleus accumbens, amygdala, caudate, hippocampus, palli

38 th these conditions (i.e. prefrontal cortex, nucleus accumbens, amygdala, ventral tegmental area) is

39 rain sites on the mesolimbic reward pathway (nucleus accumbens; amygdala) that receive OT projections

40 Furthermore, medium spiny neurons in the nucleus accumbens, an area implicated in development of

41 cally in D2-type medium spiny neurons in the nucleus accumbens, an effect seen in male but not female

42 amine induced more expression changes in the nucleus accumbens and amygdala.

43 gene promoter regions, was evaluated in the nucleus accumbens and dorsal striatum of rats using west

44 s (MSNs), the main projection neurons in the nucleus accumbens and dorsal striatum, and their functio

45 so increased the expression of Zif268 in the nucleus accumbens and dorsolateral striatum of LgA rats.

46 vulnerability, we focused on the core of the nucleus accumbens and examined expression and epigenetic

47 s in excitability of medium spiny neurons in nucleus accumbens and gating the compositional plasticit

48 ture mechanistic studies of gene networks in nucleus accumbens and gene regulatory mechanisms across

49 thic care was preferentially associated with nucleus accumbens and medial orbitofrontal cortex activi

50 es positive emotionality potentially via the nucleus accumbens and miR-181.

51 similarities between the ventral striatum's nucleus accumbens and olfactory tubercle (OT) suggests t

52 , which is crucial for processing of affect; nucleus accumbens and orbitofrontal cortex of the reward

53 ed opposite effects on TrkB signaling in the nucleus accumbens and prefrontal cortex, tat-cyclotraxin

54 twork and increased connectivity between the nucleus accumbens and the cingulo-opercular network.

55 ated with decreased connectivity between the nucleus accumbens and the default mode network and incre

56 mate type 1 transporter observed in both the nucleus accumbens and the dorsolateral striatum.

57 striatal functional connectivity between the nucleus accumbens and the midcingulate cortex in respons

58 city at synapses between specific neurons in nucleus accumbens and ventral pallidum, and how these ch

59 The ventral striatum (nucleus accumbens) and its role in mood, reward, and mot

60 ium spiny neurons (D1-/D2-MSNs) comprise the nucleus accumbens, and activity in D1-MSNs promotes, whe

61 gression within the caudate, ventral caudate/nucleus accumbens, and anterior and posterior insula, 2)

62 er brain regions, including the hippocampus, nucleus accumbens, and anterior cingulate cortex, in ind

63 IT) targets, including contralateral cortex, nucleus accumbens, and basolateral amygdala.

64 on levels were increased in the amygdala and nucleus accumbens, and decreased in the hippocampus, but

65 xpression of Fgf2 in the dorsal hippocampus, nucleus accumbens, and dorsal striatum.

66 wo regions studied, orbitofrontal cortex and nucleus accumbens, are not sequentially dependent during

67 criptional and epigenetic alterations in the nucleus accumbens, are thought to contribute to this lif

68 findings identify a functional role for the nucleus accumbens as a critical brain region whereby CBD

69 bility to induce long-term depression in the nucleus accumbens, as well as increased potentiation at

70 zygous c.892C>T (p.Arg298Trp) variant in the nucleus accumbens associated 1 (NACC1) gene in seven aff

71 Nucleus accumbens-associated protein-1 (NAC1), a nuclear

72 l lateral core or caudal medial shell of the nucleus accumbens attenuated cocaine priming-induced rei

73 oding RNA RP1-269M15.3 in frontal cortex and nucleus accumbens basal ganglia, respectively, were sign

74 Subsequently, nucleus accumbens brain slices were prepared, and we tes

75 opamine neurotransmission in the core of the nucleus accumbens (but not the dorsolateral striatum).

76 d activation in brain reward regions such as nucleus accumbens, but could not address gene expression

77 e recruited a more excitable ensemble in the nucleus accumbens, but not orbitofrontal cortex, compare

78 y specific, in that activation of a vHipp to nucleus accumbens circuit did not do this.

79 s regulate reward, little is known about the nucleus accumbens circuitry underlying withdrawal.

80 In addition, nucleus accumbens core (NAc core) and cerebrospinal flui

81 Dopamine release in the nucleus accumbens core (NAc) is known to mediate the mot

82 porter 1 (GLT-1) and system xC- (Sxc) in the nucleus accumbens core (NAc).

83 napses on medium spiny neurons (MSNs) in the nucleus accumbens core (NAcore) and requires spillover o

84 ver from cortical terminals synapsing in the nucleus accumbens core (NAcore) to stimulate metabotropi

85 th response factor 1 immunoreactivity in the nucleus accumbens core and anteromedial BNST in female m

86 echanism for use-dependent inhibition in the nucleus accumbens core and dorsal striatum, is also mini

87 e strategy to knock down GLT-1 or xCT in the nucleus accumbens core and examined the behavioral and m

88 he excitability of neuronal ensembles in the nucleus accumbens core and shell (NAc(core) and NAc(shel

89 ral and dorsal medial prefrontal cortex, and nucleus accumbens core and shell.

90 prolonged mode of dopamine signaling in the nucleus accumbens core and that such signaling relates t

91 vior, as well as synaptic impairments in the nucleus accumbens core considered hallmarks of addiction

92 8,899 into the anteromedial BNST but not the nucleus accumbens core increased social approach and dec

93 rom the dorsomedial prefrontal cortex to the nucleus accumbens core makes it difficult to selectively

94 (t-SP) of cortical glutamatergic synapses on nucleus accumbens core medium spiny neurons, but it is u

95 itored dopamine concentration changes in the nucleus accumbens core of rats throughout acquisition an

96 immobilization stress, and 3 weeks later the nucleus accumbens core was examined for changes in gluta

97 ly, local administration of OSU6162 into the nucleus accumbens core, but not dorsolateral striatum, s

98 dings suggest that low D2 mRNA levels in the nucleus accumbens core, likely mediated via epigenetic m

99 sporter-inhibiting effects of cocaine in the nucleus accumbens core, which was normalized following a

100 n and exhibit reduced Crem expression in the nucleus accumbens core.

101 ytic subunit of Sxc)/Sxc upregulation in the nucleus accumbens core.

102 nset, long-lasting increase in extracellular nucleus accumbens DA, locomotion, and brain-stimulation

103 l (locus coeruleus) and preference/aversion (nucleus accumbens) demonstrate the unique capabilities o

104 We found in rats that nucleus accumbens dopamine following a reward-predicting

105 PDM increased nucleus accumbens dopamine levels and facilitated electr

106 lative activation of glutamatergic inputs to nucleus accumbens during cued reinstatement of cocaine s

107 ed genome-wide RNA expression in post-mortem nucleus accumbens from donors (N=26) with known loneline

108 We show that inputs to the nucleus accumbens from medial prefrontal cortex and amyg

109 regions studied (thalamus, caudate, putamen, nucleus accumbens, globus pallidus, and substantia nigra

110 Although the nucleus accumbens has an established role in representin

111 ), striatum (Hedge's g=0.57, P<0.05) and the nucleus accumbens (Hedge's g=1.30, P<0.05) compared to c

112 nonresponse in the prefrontal cortex (PFC), nucleus accumbens, hippocampus, and amygdala.

113 trics of the caudate, putamen, pallidum, and nucleus accumbens in 53 depressed patients (mean age: 44

114 classes of dopaminergic neurons in the mouse nucleus accumbens in a sensitized locomotor response to

115 subiculum and potentially its projections to nucleus accumbens in context-induced relapse after punis

116 e addition of the orbitofrontal cortices and nucleus accumbens in patients with semantic dementia.

117 naling across the rostral-caudal axis of the nucleus accumbens in the control of drug-induced negativ

118 , who explored the role of astrocytes in the nucleus accumbens in the neural mechanisms underlying co

119 hese results emphasize the centrality of the nucleus accumbens in the pathophysiology of reward defic

120 tion to acquire the skill, the volume of the nucleus accumbens increased.

121 in both medial prefrontal cortex (mPFC) and nucleus accumbens, increased anxiety-like behavior, and

122 orking model that synaptic plasticity in the nucleus accumbens is central to age-related changes in v

123 circuit from the medial prefrontal cortex to nucleus accumbens is dynamically modulated to enhance fe

124 thway from the prelimbic (PrL) cortex to the nucleus accumbens is implicated in reinstatement.

125 ymptoms motivate continued drug use, and the nucleus accumbens is important for orchestrating both pr

126 The SIIPS1 includes patterns of activity in nucleus accumbens, lateral prefrontal and parahippocampa

127 of the thalamus as a prominent input to the nucleus accumbens mediating the expression of opiate-wit

128 our current understanding about the role of nucleus accumbens MSN subtypes in stress-related depress

129 aimed to assess molecular differences in the nucleus accumbens (NAc) (a specific brain nucleus postul

130 hippocampus (male/female) and upregulated in nucleus accumbens (NAc) (male) in depressed human subjec

131 dorsal raphe nucleus (DRN) afferents to the nucleus accumbens (NAc) abolishes cocaine reward and pro

132 ls of the histone dimethyltransferase G9a in nucleus accumbens (NAc) after chronic cocaine administra

133 rp1), the mitochondrial fission mediator, in nucleus accumbens (NAc) after repeated cocaine exposure

134 day after the second extinction test and the nucleus accumbens (NAc) and dorsal striatum were collect

135 with the addiction cycle: the dopamine-dense nucleus accumbens (NAc) and norepinephrine-rich ventral

136 ned functional and structural changes in the nucleus accumbens (NAc) and prefrontal cortex (PFC) asso

137 la (BLA) sends excitatory projections to the nucleus accumbens (NAc) and regulates motivated behavior

138 as employed on tissue from subregions of the nucleus accumbens (NAc) and the amygdala to examine both

139 ated dopamine receptor (DRD)-1 and -2 in the nucleus accumbens (NAc) and with down-regulated Lepr in

140 atory glutamatergic neurotransmission in the nucleus accumbens (NAc) appear to drive this drug-induce

141 The medial prefrontal cortex (mPFC) and nucleus accumbens (NAc) are both integral components of

142 tic activation of cholinergic neurons in the nucleus accumbens (NAc) are inhibited by CB1 agonists an

143 ions in global DNA hydroxymethylation in the nucleus accumbens (NAc) because neuroplastic changes in

144 ) in medium spiny neurons (MSNs) of the core nucleus accumbens (NAc) by combining patch-clamp recordi

145 The nucleus accumbens (NAc) contains a hedonic hotspot in th

146 y measured real-time dopamine release in the nucleus accumbens (NAc) core or shell while rats receive

147 cocaine craving depends on strengthening of nucleus accumbens (NAc) core synapses through incorporat

148 ey brain reward regions, particularly in the nucleus accumbens (NAc) core.

149 Although dopamine in the nucleus accumbens (NAc) critically regulates motivation

150 napses on medium spiny neurons (MSNs) of the nucleus accumbens (NAc) drives behavioral adaptations in

151 from the ventral tegmental area (VTA) to the nucleus accumbens (NAc) fire in response to unpredicted

152 Transcriptional profiling of the nucleus accumbens (NAc) from handled rats following repe

153 The nucleus accumbens (NAc) gates motivated behaviors throug

154 sed in C57BL/6J mice to confirm the role for nucleus accumbens (NAC) glutamate/Homer2 expression in M

155 that the medial prefrontal cortex (mPFC)-to-nucleus accumbens (NAc) glutamatergic transmission is se

156 depression repeatedly showed stress-induced nucleus accumbens (NAc) hypertrophy.

157 lc6a15, a neutral amino acid transporter, in nucleus accumbens (NAc) in depression and stress suscept

158 nvestigated the role of AMPK activity in the nucleus accumbens (NAc) in relapse to cocaine seeking.

159 PV) expressing GABAergic interneurons of the nucleus accumbens (NAc) in the behavioral adaptations in

160 The nucleus accumbens (NAc) in the ventral striatum integrat

161 given growing evidence of Cdk5 expression in nucleus accumbens (NAc) influencing reward-related behav

162 The nucleus accumbens (NAc) integrates dopaminergic and glut

163 Excitatory synaptic transmission in the nucleus accumbens (NAc) is a key biological substrate un

164 We previously showed that DeltaFosB in the nucleus accumbens (NAc) is a key mediator of this cross-

165 The nucleus accumbens (NAc) is a primary brain reward region

166 KEY POINTS: The nucleus accumbens (nAc) is involved in addiction-related

167 Although the nucleus accumbens (NAc) is required for behavioral flexi

168 ed long-term potentiation (theta-LTP) in the nucleus accumbens (NAc) is significantly impaired in sli

169 The nucleus accumbens (NAc) mediates cue-triggered motivatio

170 ch plays a dynamic role in cocaine action in nucleus accumbens (NAc) medium spiny neuron (MSN) subtyp

171 ked to alterations of synaptic strength onto nucleus accumbens (NAc) medium spiny neurons (MSN).

172 Molecular and cellular adaptations in nucleus accumbens (NAc) medium spiny neurons (MSNs) unde

173 We examined adaptations in nucleus accumbens (NAc) neurons in mouse and rat periphe

174 uperficial mPFC projections to a subfield of nucleus accumbens (NAc) neurons naturally encodes the de

175 ing and spike timing-dependent plasticity in nucleus accumbens (NAc) neurons.

176 nd an increase in dendritic spine density on nucleus accumbens (NAc) neurons.

177 ptic protein expression are increased in the nucleus accumbens (NAc) of mice excessively consuming al

178 e task, we measured phasic DA release in the nucleus accumbens (NAc) of rats during presentation of c

179 response mediator protein-2 (CRMP-2), in the nucleus accumbens (NAc) of rodents.

180 dn5) and abnormal blood vessel morphology in nucleus accumbens (NAc) of stress-susceptible but not re

181 lar mechanisms of GLP-1R signaling on PVT-to-nucleus accumbens (NAc) projecting neurons.

182 ses within the basolateral amygdala (BLA) to nucleus accumbens (NAc) projection, and maturation of th

183 The nucleus accumbens (NAc) provides one of the most promine

184 nuclear histone deacetylase 5 (HDAC5) in the nucleus accumbens (NAc) reduced cocaine reward-context a

185 experiments, we euthanized rats and isolated nucleus accumbens (NAc) samples.

186 ctive excitatory glutamatergic inputs to the nucleus accumbens (NAc) shell and core, respectively.

187 y distinct downstream targets, including the nucleus accumbens (NAc) shell and core.

188 observed increased beta-gal staining in the nucleus accumbens (NAC) shell and dorsal raphe nucleus,

189 ptor-expressing neurons (D1+ neurons) in the nucleus accumbens (NAc) shell but not the core in mice,

190 nd depressive-like behavior through a common nucleus accumbens (NAc) shell calcium-permeable alpha-am

191 cue-activated orbitofrontal cortex (OFC) and nucleus accumbens (NAc) shell ensembles using wild-type

192 Here, we studied the role of projections to nucleus accumbens (NAc) shell from ventral subiculum (vS

193 neurons of a mouse and their projections to nucleus accumbens (NAc) shell play a necessary and suffi

194 Nucleus accumbens (NAc) shell shows unique dopamine (DA)

195 creased dopamine release and reuptake in the nucleus accumbens (NAc) shell, a major target region.

196 antagonist Ro25 was infused into IL-mPFC or nucleus accumbens (NAc) shell, another structure implica

197 ress regulates the expression of Fosb in the nucleus accumbens (NAc) to promote the cell-type-specifi

198 nent, increases dopamine (DA) release in the nucleus accumbens (NAc) via inhibition of local VTA GABA

199 c increases in dopamine concentration in the nucleus accumbens (NAc) while discrete aversive stimuli

200 subunits of AMPA glutamate receptors in the nucleus accumbens (NAc), a brain region critical for mod

201 sed whether impaired dopamine release in the nucleus accumbens (NAc), a brain region critical to goal

202 stone posttranslational modifications in the nucleus accumbens (NAc), a brain reward region.

203 spines on medium spiny neurons (MSNs) in the nucleus accumbens (NAc), a critical brain region for coc

204 In the nucleus accumbens (NAc), a key brain region regulating e

205 nxiety- and depression-like behaviors in the nucleus accumbens (NAc), a key brain reward region.

206 ssion in mice, increases SIRT1 levels in the nucleus accumbens (NAc), a key brain reward region.

207 ors, and examined Tet1 expression changes in nucleus accumbens (NAc), a key brain reward region.

208 ding RNA is also highly expressed within the nucleus accumbens (NAc), a pivotal brain region underlyi

209 ls exhibited preferential D2R changes in the nucleus accumbens (NAc), a striatal region that critical

210 have been implicated in social behavior: the nucleus accumbens (NAc), amygdala, and ventral tegmental

211 2) selective knockdown of Tlr4 mRNA in mouse nucleus accumbens (NAc), and (3) injection of the TLR4 a

212 mediated by the basolateral amygdala (BLA), nucleus accumbens (NAc), and medial prefrontal cortex (m

213 of reward-related brain regions, such as the nucleus accumbens (NAc), are linked to the pathophysiolo

214 , such as the basolateral amygdala (BLA) and nucleus accumbens (NAc), as important to valence encodin

215 xpression in brain reward regions, including nucleus accumbens (NAc), contribute to persistent functi

216 icity in the reward system, particularly the nucleus accumbens (NAc), drives drug-adaptive behavior.

217 f abuse, increases levels of dopamine in the nucleus accumbens (nAc), facilitating behavioural reinfo

218 ally specific changes in activity within the nucleus accumbens (NAc), which occur during anticipatory

219 to cocaine generates silent synapses in the nucleus accumbens (NAc), whose eventual unsilencing/matu

220 te a role for increased H3.3 dynamics in the nucleus accumbens (NAc)-a key limbic brain reward region

221 ipulated the serotonergic projections to the nucleus accumbens (NAc).

222 3-40 mug/kg) on oxygen and glucose levels in nucleus accumbens (NAc).

223 lterations in medium spiny neurons (MSNs) of nucleus accumbens (NAc).

224 eking by conveying upstream signals from the nucleus accumbens (NAc).

225 ally through remodeling neurocircuits in the nucleus accumbens (NAc).

226 to the core and shell subterritories of the nucleus accumbens (NAc).

227 s DA release in terminal regions such as the nucleus accumbens (NAc).

228 n of limbic system structures, including the nucleus accumbens (NAc).

229 ity to increase dopaminergic transmission in nucleus accumbens (NAc).

230 n cocaine-induced neuronal activation in the nucleus accumbens (NAc).

231 adaptations in key brain areas, such as the nucleus accumbens (NAc).

232 glutamate transporter 1 (EAAT2/GLT-1) in the nucleus accumbens (NAc).

233 es such as the basolateral amygdala (BLA) or nucleus accumbens (NAc).

234 ject to the ventral tegmental area (VTA) and nucleus accumbens (NAc); however, direct neuroanatomical

235 dy examined Slc6a15 in the ventral striatum [nucleus accumbens (NAc)] in depression.

236 Deep brain stimulation of the nucleus accumbens (NAc-DBS) is an emerging therapy for d

237 usion of varenicline (0.3 mul/side) into the nucleus accumbens (NAc; 0 or 3.5 mug), but not the ventr

238 PFC) and subcortical reward-related regions (nucleus accumbens, NAC) mediates the selection of approp

239 , we examined functional connectivity of the nucleus accumbens (NAcc) - a hub of the reward network -

240 ctional neuroimaging research indicates that nucleus accumbens (NAcc) and anterior insula (AIns) acti

241 Although activity in both the nucleus accumbens (NAcc) and medial prefrontal cortex pr

242 ammetry recordings of dopamine levels in the nucleus accumbens (NAcc) core and shell in rats working

243 subjective value-related activity within the nucleus accumbens (NAcc) during inter-temporal choice an

244 Abnormal reward-related responses in the nucleus accumbens (NAcc) have been reported for major de

245 g via the kappa-opioid receptor (KOR) in the nucleus accumbens (NAcc) powerfully mediates negative af

246 tronger responses to food commercials in the nucleus accumbens (NAcc) than children not at risk.

247 he contribution of neuronal ensembles in the nucleus accumbens (NAcc) to these behaviors.

248 arch, and in MDD more generally, include the nucleus accumbens (NAcc), lateral prefrontal cortex (LPF

249 eir infants and the connectivity between the nucleus accumbens (NAcc), the amygdala, and the medial p

250 ronal activity in the shell subregion of the nucleus accumbens (NASh).

251 he ortholog Kmt2b, in adult ventral striatum/nucleus accumbens neurons markedly increased anxiety sco

252 rphine reward by controlling the activity of nucleus accumbens neurons.

253 dback) and an alternate neurofeedback group (nucleus accumbens), none sustained activation in target

254 either altered extracellular dopamine in the nucleus accumbens nor maintained self-administration.

255 ssion was also upregulated postmortem in the nucleus accumbens of male human cocaine addicts.

256 ing of dopamine signaling in the core of the nucleus accumbens of rats to determine the relationship

257 hether this function is localized within the nucleus accumbens or distributed also within the OT.

258 according to their axonal projections to the nucleus accumbens or dorsal striatum in mice.

259 erior insula activity, but no differences in nucleus accumbens or orbitofrontal activation, compared

260 the medial orbitofrontal cortex (P=0.01) and nucleus accumbens (P=0.08).

261 e paraventricular nucleus of the thalamus to nucleus accumbens pathway is necessary and sufficient to

262 experience-induced neural adaptations in the nucleus accumbens, prefrontal cortex, and ventral tegmen

263 cordings reveal that spontaneous activity of nucleus accumbens-projecting VTA (VTA-NAc) neurons is se

264 (CP-AMPARs) to synapses in subregions of the nucleus accumbens promotes cocaine seeking.

265 d miR-181b in human brain and blood, greater nucleus accumbens reactivity to positive emotional stimu

266 ral to the processes described above) in the nucleus accumbens reduced wheel running.

267 While multiple inputs to the nucleus accumbens regulate reward, little is known about

268 nt of chromatin remodeling complexes, in the nucleus accumbens regulates reward-related behaviors in

269 GluA1-containing AMPARs in subregions of the nucleus accumbens reinstates cocaine seeking.

270 tor level within a key neural substrate, the nucleus accumbens, remains elusive.

271 ex formation with SMAD3 are increased in the nucleus accumbens, resulting in increased binding of BRG

272 nt component of this network is the anterior nucleus accumbens shell (aNAcSh), which sends GABAergic

273 d had elevated mRNA expression in the medial nucleus accumbens shell (NAcSh) and caudate nucleus in p

274 ated with prominent morphological changes in nucleus accumbens shell (NACsh) neurons, including incre

275 in U (NMU) is a neuropeptide enriched in the nucleus accumbens shell (NAcSh), a brain region associat

276 ADD to vmPFC and/or vmPFC projections to the nucleus accumbens shell allows the chemogenetic exploita

277 prefrontal cortex (vmPFC) projection to the nucleus accumbens shell is important for extinction of c

278 ubstantia nigra, entopeduncular nucleus, and nucleus accumbens shell measured using brain mapping ana

279 that blockade of PKA binding to AKAPs in the nucleus accumbens shell of Sprague-Dawley rats attenuate

280 of D1-like dopamine receptors (D1DRs) in the nucleus accumbens shell promoted cocaine seeking through

281 are formed only in neuronal ensembles of the nucleus accumbens shell that are related to associative

282 f nicotine to induce dopamine release in the nucleus accumbens shell, a brain area believed to underl

283 oject abundantly to cingulate cortex and the nucleus accumbens shell, and moderately to medial amygda

284 to vmPFC neurons that project to the medial nucleus accumbens shell, confirming that these neurons a

285 ed in stress-induced relapse, comprising the nucleus accumbens shell, the dorsal raphe nucleus and th

286 ion in dopamine concentration in the rostral nucleus accumbens shell.

287 in ventral subiculum neurons that project to nucleus accumbens shell.

288 levels produced by cocaine or heroin in the nucleus accumbens shell.

289 area and to increase dopamine levels in the nucleus accumbens shell.

290 nectivity in SPNs from the shell part of the nucleus accumbens, specifically.

291 gions (cortex, hippocampus, caudate-putamen, nucleus accumbens, thalamus, and hypothalamus) of BAC al

292 The nucleus accumbens (the pleasure and reward 'hub' in the

293 of cocaine to elevate dopamine levels in the nucleus accumbens, the ability of cocaine to establish a

294 y associated with reward responsivity in the nucleus accumbens, the default mode network, and the cin

295 trast, within the striatum, the shell of the nucleus accumbens, the hippocampal projection zone, and

296 axons continue to grow ectopically from the nucleus accumbens to the PFC and profoundly change PFC s

297 First, in cross-sectional analyses, right nucleus accumbens volume was inversely related to anhedo

298 y in particular brain regions, including the nucleus accumbens, where oxytocin receptor signaling fac

299 le to induce stable synaptic rewiring in the nucleus accumbens, which will likely influence responses

300 involve common brain regions afferent to the nucleus accumbens, within the mesolimbic pathway.