ライフサイエンスコーパス: accumbens

1 ons, including the ventral striatum (nucleus accumbens).

2 t with structural differences in the Nucleus Accumbens).

3 us), and limbic system (amygdala and nucleus accumbens).

4 orks and their connectivity with the nucleus accumbens.

5 at prefrontal cortex synapses in the nucleus accumbens.

6 tive change of the RPE signal in the nucleus accumbens.

7 1 dopamine receptor (D1-MSNs) in the nucleus accumbens.

8 A-dependent AMPA transmission in the nucleus accumbens.

9 ion of DA clearance in slices of the nucleus accumbens.

10 gions, particularly the striatum and nucleus accumbens.

11 the CNS such as the hippocampus and nucleus accumbens.

12 ing phasic dopamine signaling in rat nucleus accumbens.

13 ays and in vivo microdialysis in rat nucleus accumbens.

14 in the medial prefrontal cortex and nucleus accumbens.

15 e-induced release of dopamine in the nucleus accumbens.

16 icture evaluation in the caudate and nucleus accumbens.

17 n direct-pathway MSNs (dMSNs) in the nucleus accumbens.

18 ility of medium spiny neurons of the nucleus accumbens.

19 nse to anticipation of reward in the nucleus accumbens.

20 ocin were mediated by actions in the nucleus accumbens.

21 was modulated by D1 availability in nucleus accumbens.

22 nd higher D1-receptor density in the nucleus accumbens.

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

24 ine-enhanced extracellular DA in the nucleus accumbens.

25 depend on oxytocin signaling in the nucleus accumbens.

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

27 tal projection neurons (SPNs) of the nucleus accumbens.

28 or of gene expression, acting in the nucleus accumbens, a brain reward region, is capable of increasi

29 In the nucleus accumbens, a key region involved in reward processing, [

30 perties evoked activation within the nucleus accumbens, a subregion of the striatum.

31 We examined dopamine release in the nucleus accumbens across multiple time scales, using complementa

32 analyses convergently indicated that nucleus accumbens activity can support aggregate forecasts.

33 ved in striatum, olfactory tubercle, nucleus accumbens, amygdala, and neocortex, whereas in spinal co

34 ilateral subcortical structures: the nucleus accumbens, amygdala, caudate, hippocampus, pallidum, put

35 mes of eight subcortical structures (nucleus accumbens, amygdala, caudate, hippocampus, pallidum, put

36 conditions (i.e. prefrontal cortex, nucleus accumbens, amygdala, ventral tegmental area) is not well

37 es on the mesolimbic reward pathway (nucleus accumbens; amygdala) that receive OT projections and con

38 hermore, medium spiny neurons in the nucleus accumbens, an area implicated in development of OCD, dis

39 D2-type medium spiny neurons in the nucleus accumbens, an effect seen in male but not female mice.

40 duced more expression changes in the nucleus accumbens and amygdala.

41 omoter regions, was evaluated in the nucleus accumbens and dorsal striatum of rats using western blot

42 , the main projection neurons in the nucleus accumbens and dorsal striatum, and their function in rel

43 ased the expression of Zif268 in the nucleus accumbens and dorsolateral striatum of LgA rats.

44 ility, we focused on the core of the nucleus accumbens and examined expression and epigenetic regulat

45 itability of medium spiny neurons in nucleus accumbens and gating the compositional plasticity of alp

46 hanistic studies of gene networks in nucleus accumbens and gene regulatory mechanisms across a variet

47 e was preferentially associated with nucleus accumbens and medial orbitofrontal cortex activity, wher

48 ive emotionality potentially via the nucleus accumbens and miR-181.

49 ities between the ventral striatum's nucleus accumbens and olfactory tubercle (OT) suggests the distr

50 is crucial for processing of affect; nucleus accumbens and orbitofrontal cortex of the reward circuit

51 Patients showed smaller baseline accumbens and pallidal volumes than controls (P<0.05).

52 ite effects on TrkB signaling in the nucleus accumbens and prefrontal cortex, tat-cyclotraxin-B admin

53 d increased connectivity between the nucleus accumbens and the cingulo-opercular network.

54 h decreased connectivity between the nucleus accumbens and the default mode network and increased con

55 e 1 transporter observed in both the nucleus accumbens and the dorsolateral striatum.

56 functional connectivity between the nucleus accumbens and the midcingulate cortex in response to mon

57 The ventral striatum (nucleus accumbens) and its role in mood, reward, and motivation

58 y neurons (D1-/D2-MSNs) comprise the nucleus accumbens, and activity in D1-MSNs promotes, whereas act

59 within the caudate, ventral caudate/nucleus accumbens, and anterior and posterior insula, 2) to unex

60 regions, including the hippocampus, nucleus accumbens, and anterior cingulate cortex, in individuals

61 ets, including contralateral cortex, nucleus accumbens, and basolateral amygdala.

62 s were increased in the amygdala and nucleus accumbens, and decreased in the hippocampus, but not cau

63 n of Fgf2 in the dorsal hippocampus, nucleus accumbens, and dorsal striatum.

64 add new knowledge about bilateral amygdala, accumbens, and hippocampus reductions in ADHD.

65 ns studied, orbitofrontal cortex and nucleus accumbens, are not sequentially dependent during context

66 al and epigenetic alterations in the nucleus accumbens, are thought to contribute to this life-long d

67 s identify a functional role for the nucleus accumbens as a critical brain region whereby CBD can pro

68 o induce long-term depression in the nucleus accumbens, as well as increased potentiation at these sy

69 .892C>T (p.Arg298Trp) variant in the nucleus accumbens associated 1 (NACC1) gene in seven affected in

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

71 l core or caudal medial shell of the nucleus accumbens attenuated cocaine priming-induced reinstateme

72 A RP1-269M15.3 in frontal cortex and nucleus accumbens basal ganglia, respectively, were significantl

73 Subsequently, nucleus accumbens brain slices were prepared, and we tested for

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

75 tion in brain reward regions such as nucleus accumbens, but could not address gene expression in the

76 ted a more excitable ensemble in the nucleus accumbens, but not orbitofrontal cortex, compared with t

77 Activation of prefrontal inputs to the accumbens by cues initiates spillover of synaptic glutam

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

79 the dorsal medial prefrontal cortex-amygdala-accumbens circuit, as well as smaller amygdala volume, r

80 te reward, little is known about the nucleus accumbens circuitry underlying withdrawal.

81 The volumes of the accumbens (Cohen's d=-0.15), amygdala (d=-0.19), caudate

82 <15 years) versus adults (>21 years): in the accumbens (Cohen's d=-0.19 vs -0.10), amygdala (d=-0.18

83 Dopamine release in the nucleus accumbens core (NAc) is known to mediate the motivationa

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

85 n medium spiny neurons (MSNs) in the nucleus accumbens core (NAcore) and requires spillover of glutam

86 cortical terminals synapsing in the nucleus accumbens core (NAcore) to stimulate metabotropic glutam

87 nse factor 1 immunoreactivity in the nucleus accumbens core and anteromedial BNST in female mice but

88 for use-dependent inhibition in the nucleus accumbens core and dorsal striatum, is also minimal in t

89 gy to knock down GLT-1 or xCT in the nucleus accumbens core and examined the behavioral and molecular

90 ability of neuronal ensembles in the nucleus accumbens core and shell (NAc(core) and NAc(shell)), and

91 dorsal medial prefrontal cortex, and nucleus accumbens core and shell.

92 ed mode of dopamine signaling in the nucleus accumbens core and that such signaling relates to elemen

93 well as synaptic impairments in the nucleus accumbens core considered hallmarks of addiction.

94 to the anteromedial BNST but not the nucleus accumbens core increased social approach and decreased s

95 dorsomedial prefrontal cortex to the nucleus accumbens core makes it difficult to selectively enhance

96 f cortical glutamatergic synapses on nucleus accumbens core medium spiny neurons, but it is unknown h

97 opamine concentration changes in the nucleus accumbens core of rats throughout acquisition and perfor

98 zation stress, and 3 weeks later the nucleus accumbens core was examined for changes in glutamate tra

99 tly, by restoring glutamate transport in the accumbens core with ceftriaxone the capacity of acute st

100 l administration of OSU6162 into the nucleus accumbens core, but not dorsolateral striatum, selective

101 ggest that low D2 mRNA levels in the nucleus accumbens core, likely mediated via epigenetic modificat

102 hibit reduced Crem expression in the nucleus accumbens core.

103 unit of Sxc)/Sxc upregulation in the nucleus accumbens core.

104 46), amygdala (d=-0.31), thalamus (d=-0.31), accumbens (d=-0.25) and intracranial volumes (d=-0.12),

105 ng-lasting increase in extracellular nucleus accumbens DA, locomotion, and brain-stimulation reward.

106 coeruleus) and preference/aversion (nucleus accumbens) demonstrate the unique capabilities of these

107 ic plasticity in medium spiny neurons of the accumbens direct and indirect pathways.

108 We found in rats that nucleus accumbens dopamine following a reward-predicting cue was

109 PDM increased nucleus accumbens dopamine levels and facilitated electrical bra

110 ctivation of glutamatergic inputs to nucleus accumbens during cued reinstatement of cocaine seeking v

111 e-wide RNA expression in post-mortem nucleus accumbens from donors (N=26) with known loneliness measu

112 We show that inputs to the nucleus accumbens from medial prefrontal cortex and amygdala reg

113 studied (thalamus, caudate, putamen, nucleus accumbens, globus pallidus, and substantia nigra).

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

115 onse in the prefrontal cortex (PFC), nucleus accumbens, hippocampus, and amygdala.

116 the caudate, putamen, pallidum, and nucleus accumbens in 53 depressed patients (mean age: 44.1 years

117 of dopaminergic neurons in the mouse nucleus accumbens in a sensitized locomotor response to cocaine.

118 m and potentially its projections to nucleus accumbens in context-induced relapse after punishment-im

119 on of the orbitofrontal cortices and nucleus accumbens in patients with semantic dementia.

120 cross the rostral-caudal axis of the nucleus accumbens in the control of drug-induced negative affect

121 plored the role of astrocytes in the nucleus accumbens in the neural mechanisms underlying cocaine se

122 ults emphasize the centrality of the nucleus accumbens in the pathophysiology of reward deficits and

123 acquire the skill, the volume of the nucleus accumbens increased.

124 medial prefrontal cortex (mPFC) and nucleus accumbens, increased anxiety-like behavior, and decrease

125 , thus revealing an unsuspected hypothalamus-accumbens interplay in action selection.

126 odel that synaptic plasticity in the nucleus accumbens is central to age-related changes in voluntary

127 from the medial prefrontal cortex to nucleus accumbens is dynamically modulated to enhance females' a

128 om the prelimbic (PrL) cortex to the nucleus accumbens is implicated in reinstatement.

129 motivate continued drug use, and the nucleus accumbens is important for orchestrating both processes.

130 PS1 includes patterns of activity in nucleus accumbens, lateral prefrontal and parahippocampal cortic

131 thalamus as a prominent input to the nucleus accumbens mediating the expression of opiate-withdrawal-

132 rent understanding about the role of nucleus accumbens MSN subtypes in stress-related depression beha

133 assess molecular differences in the nucleus accumbens (NAc) (a specific brain nucleus postulated to

134 pus (male/female) and upregulated in nucleus accumbens (NAc) (male) in depressed human subjects and i

135 e histone dimethyltransferase G9a in nucleus accumbens (NAc) after chronic cocaine administration.

136 e mitochondrial fission mediator, in nucleus accumbens (NAc) after repeated cocaine exposure and in c

137 r the second extinction test and the nucleus accumbens (NAc) and dorsal striatum were collected to me

138 addiction cycle: the dopamine-dense nucleus accumbens (NAc) and norepinephrine-rich ventral bed nucl

139 tional and structural changes in the nucleus accumbens (NAc) and prefrontal cortex (PFC) associated w

140 sends excitatory projections to the nucleus accumbens (NAc) and regulates motivated behaviors partia

141 amine receptor (DRD)-1 and -2 in the nucleus accumbens (NAc) and with down-regulated Lepr in the vent

142 medial prefrontal cortex (mPFC) and nucleus accumbens (NAc) are both integral components of the cort

143 vation of cholinergic neurons in the nucleus accumbens (NAc) are inhibited by CB1 agonists and eCBs.

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

145 ium spiny neurons (MSNs) of the core nucleus accumbens (NAc) by combining patch-clamp recordings with

146 The nucleus accumbens (NAc) contains a hedonic hotspot in the rostra

147 ed real-time dopamine release in the nucleus accumbens (NAc) core or shell while rats received unsign

148 craving depends on strengthening of nucleus accumbens (NAc) core synapses through incorporation of C

149 reward regions, particularly in the nucleus accumbens (NAc) core.

150 Although dopamine in the nucleus accumbens (NAc) critically regulates motivation and alte

151 n medium spiny neurons (MSNs) of the nucleus accumbens (NAc) drives behavioral adaptations in addicti

152 ventral tegmental area (VTA) to the nucleus accumbens (NAc) fire in response to unpredicted rewards

153 Transcriptional profiling of the nucleus accumbens (NAc) from handled rats following repeated exp

154 The nucleus accumbens (NAc) gates motivated behaviors through the fu

155 57BL/6J mice to confirm the role for nucleus accumbens (NAC) glutamate/Homer2 expression in MA prefer

156 e medial prefrontal cortex (mPFC)-to-nucleus accumbens (NAc) glutamatergic transmission is selectivel

157 ion repeatedly showed stress-induced nucleus accumbens (NAc) hypertrophy.

158 a neutral amino acid transporter, in nucleus accumbens (NAc) in depression and stress susceptibility.

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

160 essing GABAergic interneurons of the nucleus accumbens (NAc) in the behavioral adaptations induced by

161 The nucleus accumbens (NAc) in the ventral striatum integrates many

162 owing evidence of Cdk5 expression in nucleus accumbens (NAc) influencing reward-related behaviors.

163 The nucleus accumbens (NAc) integrates dopaminergic and glutamatergi

164 itatory synaptic transmission in the nucleus accumbens (NAc) is a key biological substrate underlying

165 viously showed that DeltaFosB in the nucleus accumbens (NAc) is a key mediator of this cross-sensitiz

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

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

168 Although the nucleus accumbens (NAc) is required for behavioral flexibility,

169 term potentiation (theta-LTP) in the nucleus accumbens (NAc) is significantly impaired in slices take

170 The nucleus accumbens (NAc) mediates cue-triggered motivational resp

171 a dynamic role in cocaine action in nucleus accumbens (NAc) medium spiny neuron (MSN) subtypes, thos

172 lterations of synaptic strength onto nucleus accumbens (NAc) medium spiny neurons (MSN).

173 olecular and cellular adaptations in nucleus accumbens (NAc) medium spiny neurons (MSNs) underlie str

174 We examined adaptations in nucleus accumbens (NAc) neurons in mouse and rat peripheral nerv

175 al mPFC projections to a subfield of nucleus accumbens (NAc) neurons naturally encodes the decision t

176 spike timing-dependent plasticity in nucleus accumbens (NAc) neurons.

177 crease in dendritic spine density on nucleus accumbens (NAc) neurons.

178 tein expression are increased in the nucleus accumbens (NAc) of mice excessively consuming alcohol.

179 we measured phasic DA release in the nucleus accumbens (NAc) of rats during presentation of cues that

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

181 abnormal blood vessel morphology in nucleus accumbens (NAc) of stress-susceptible but not resilient

182 anisms of GLP-1R signaling on PVT-to-nucleus accumbens (NAc) projecting neurons.

183 in the basolateral amygdala (BLA) to nucleus accumbens (NAc) projection, and maturation of these sile

184 The nucleus accumbens (NAc) provides one of the most prominent proje

185 histone deacetylase 5 (HDAC5) in the nucleus accumbens (NAc) reduced cocaine reward-context associati

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

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

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

189 ressing neurons (D1+ neurons) in the nucleus accumbens (NAc) shell but not the core in mice, which re

190 ssive-like behavior through a common nucleus accumbens (NAc) shell calcium-permeable alpha-amino-3-hy

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

192 e studied the role of projections to nucleus accumbens (NAc) shell from ventral subiculum (vSub), bas

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

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

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

196 ist Ro25 was infused into IL-mPFC or nucleus accumbens (NAc) shell, another structure implicated in e

197 ulates the expression of Fosb in the nucleus accumbens (NAc) to promote the cell-type-specific accumu

198 creases dopamine (DA) release in the nucleus accumbens (NAc) via inhibition of local VTA GABAergic ne

199 ses in dopamine concentration in the nucleus accumbens (NAc) while discrete aversive stimuli elicit p

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

201 her impaired dopamine release in the nucleus accumbens (NAc), a brain region critical to goal-directe

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

203 n medium spiny neurons (MSNs) in the nucleus accumbens (NAc), a critical brain region for cocaine cra

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

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

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

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

208 is also highly expressed within the nucleus accumbens (NAc), a pivotal brain region underlying rewar

209 ited preferential D2R changes in the nucleus accumbens (NAc), a striatal region that critically regul

210 n implicated in social behavior: the nucleus accumbens (NAc), amygdala, and ventral tegmental area.

211 tive knockdown of Tlr4 mRNA in mouse nucleus accumbens (NAc), and (3) injection of the TLR4 antagonis

212 d by the basolateral amygdala (BLA), nucleus accumbens (NAc), and medial prefrontal cortex (mPFC).

213 d-related brain regions, such as the nucleus accumbens (NAc), are linked to the pathophysiology of de

214 s the basolateral amygdala (BLA) and nucleus accumbens (NAc), as important to valence encoding.

215 n in brain reward regions, including nucleus accumbens (NAc), contribute to persistent functional cha

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

217 increases levels of dopamine in the nucleus accumbens (nAc), facilitating behavioural reinforcement

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

219 ine generates silent synapses in the nucleus accumbens (NAc), whose eventual unsilencing/maturation b

220 the serotonergic projections to the nucleus accumbens (NAc).

221 /kg) on oxygen and glucose levels in nucleus accumbens (NAc).

222 ns in medium spiny neurons (MSNs) of nucleus accumbens (NAc).

223 conveying upstream signals from the nucleus accumbens (NAc).

224 ough remodeling neurocircuits in the nucleus accumbens (NAc).

225 ease in terminal regions such as the nucleus accumbens (NAc).

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

227 bic system structures, including the nucleus accumbens (NAc).

228 ncrease dopaminergic transmission in nucleus accumbens (NAc).

229 e-induced neuronal activation in the nucleus accumbens (NAc).

230 ions in key brain areas, such as the nucleus accumbens (NAc).

231 e transporter 1 (EAAT2/GLT-1) in the nucleus accumbens (NAc).

232 as the basolateral amygdala (BLA) or nucleus accumbens (NAc).

233 the ventral tegmental area (VTA) and nucleus accumbens (NAc); however, direct neuroanatomical evidenc

234 ned Slc6a15 in the ventral striatum [nucleus accumbens (NAc)] in depression.

235 Deep brain stimulation of the nucleus accumbens (NAc-DBS) is an emerging therapy for diverse,

236 varenicline (0.3 mul/side) into the nucleus accumbens (NAc; 0 or 3.5 mug), but not the ventral tegme

237 subcortical reward-related regions (nucleus accumbens, NAC) mediates the selection of appropriate be

238 mined functional connectivity of the nucleus accumbens (NAcc) - a hub of the reward network - focusin

239 neuroimaging research indicates that nucleus accumbens (NAcc) and anterior insula (AIns) activity inv

240 Although activity in both the nucleus accumbens (NAcc) and medial prefrontal cortex predicted

241 ve value-related activity within the nucleus accumbens (NAcc) during inter-temporal choice and with w

242 rmal reward-related responses in the nucleus accumbens (NAcc) have been reported for major depressive

243 e kappa-opioid receptor (KOR) in the nucleus accumbens (NAcc) powerfully mediates negative affective

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

245 d in MDD more generally, include the nucleus accumbens (NAcc), lateral prefrontal cortex (LPFC), insu

246 nts and the connectivity between the nucleus accumbens (NAcc), the amygdala, and the medial prefronta

247 tivity in the shell subregion of the nucleus accumbens (NASh).

248 log Kmt2b, in adult ventral striatum/nucleus accumbens neurons markedly increased anxiety scores in m

249 eward by controlling the activity of nucleus accumbens neurons.

250 nd an alternate neurofeedback group (nucleus accumbens), none sustained activation in target regions

251 ltered extracellular dopamine in the nucleus accumbens nor maintained self-administration.

252 n areas such as the prelimbic cortex and the accumbens nucleus.

253 s also upregulated postmortem in the nucleus accumbens of male human cocaine addicts.

254 opamine signaling in the core of the nucleus accumbens of rats to determine the relationship between

255 g to their axonal projections to the nucleus accumbens or dorsal striatum in mice.

256 sula activity, but no differences in nucleus accumbens or orbitofrontal activation, compared with ine

257 al orbitofrontal cortex (P=0.01) and nucleus accumbens (P=0.08).

258 ce-induced neural adaptations in the nucleus accumbens, prefrontal cortex, and ventral tegmental area

259 reveal that spontaneous activity of nucleus accumbens-projecting VTA (VTA-NAc) neurons is selectivel

260 Rs) to synapses in subregions of the nucleus accumbens promotes cocaine seeking.

261 1b in human brain and blood, greater nucleus accumbens reactivity to positive emotional stimuli and e

262 he processes described above) in the nucleus accumbens reduced wheel running.

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

264 romatin remodeling complexes, in the nucleus accumbens regulates reward-related behaviors in response

265 ntaining AMPARs in subregions of the nucleus accumbens reinstates cocaine seeking.

266 l within a key neural substrate, the nucleus accumbens, remains elusive.

267 tion with SMAD3 are increased in the nucleus accumbens, resulting in increased binding of BRG1 to the

268 nent of this network is the anterior nucleus accumbens shell (aNAcSh), which sends GABAergic projecti

269 ptogenetic stimulation of infralimbic cortex-accumbens shell (ILC-NAc shell) inputs or treatment with

270 evated mRNA expression in the medial nucleus accumbens shell (NAcSh) and caudate nucleus in postmorte

271 h prominent morphological changes in nucleus accumbens shell (NACsh) neurons, including increases in

272 U) is a neuropeptide enriched in the nucleus accumbens shell (NAcSh), a brain region associated with

273 mPFC and/or vmPFC projections to the nucleus accumbens shell allows the chemogenetic exploitation of

274 otein expression (HSV miSAP97) in the medial accumbens shell attenuated cocaine seeking.

275 tal cortex (vmPFC) projection to the nucleus accumbens shell is important for extinction of cocaine s

276 a nigra, entopeduncular nucleus, and nucleus accumbens shell measured using brain mapping analyses of

277 ckade of PKA binding to AKAPs in the nucleus accumbens shell of Sprague-Dawley rats attenuates reinst

278 ke dopamine receptors (D1DRs) in the nucleus accumbens shell promoted cocaine seeking through a proce

279 ed only in neuronal ensembles of the nucleus accumbens shell that are related to associative learning

280 ne to induce dopamine release in the nucleus accumbens shell, a brain area believed to underlie nicot

281 undantly to cingulate cortex and the nucleus accumbens shell, and moderately to medial amygdala, locu

282 C neurons that project to the medial nucleus accumbens shell, confirming that these neurons are respo

283 ress-induced relapse, comprising the nucleus accumbens shell, the dorsal raphe nucleus and the medial

284 opamine concentration in the rostral nucleus accumbens shell.

285 al subiculum neurons that project to nucleus accumbens shell.

286 y in SPNs from the shell part of the nucleus accumbens, specifically.

287 sioned patients had decreased volumes of the accumbens subregion of the ventral striatum.

288 ortex, hippocampus, caudate-putamen, nucleus accumbens, thalamus, and hypothalamus) of BAC aldh1l1-tr

289 The nucleus accumbens (the pleasure and reward 'hub' in the brain) i

290 ne to elevate dopamine levels in the nucleus accumbens, the ability of cocaine to establish a conditi

291 ated with reward responsivity in the nucleus accumbens, the default mode network, and the cingulo-ope

292 ithin the striatum, the shell of the nucleus accumbens, the hippocampal projection zone, and the amyg

293 ontinue to grow ectopically from the nucleus accumbens to the PFC and profoundly change PFC structura

294 , in cross-sectional analyses, right nucleus accumbens volume was inversely related to anhedonia seve

295 ilateral hippocampus, amygdala, thalamus and accumbens volumes as well as intracranial volume, but la

296 nnabinoid/mGlu5-mediated LTD in the mPFC and accumbens was abolished in adult n-3-deficient mice.

297 Spine density in MSNs in the accumbens was also increased, but the increase did not c

298 ticular brain regions, including the nucleus accumbens, where oxytocin receptor signaling facilitates

299 duce stable synaptic rewiring in the nucleus accumbens, which will likely influence responses to subs

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