ライフサイエンスコーパス: basolateral amygdala

1 y transmission in the PFC at inputs from the basolateral amygdala.

2 gulation of AMPA-receptor endocytosis in the basolateral amygdala.

3 in emotion-related circuits anchored in the basolateral amygdala.

4 d striatum and remained intact in cortex and basolateral amygdala.

5 eceptors on output projection neurons of the basolateral amygdala.

6 enlargement is localized specifically to the basolateral amygdala.

7 ses and theta oscillations recorded from the basolateral amygdala.

8 ion, and these effects are most prominent in basolateral amygdala.

9 ering protein expression within the adjacent basolateral amygdala.

10 rentially modulated through the vSub and the basolateral amygdala.

11 a direct pathway between anterior insula and basolateral amygdala.

12 ocial interaction-specific expression in the basolateral amygdala.

13 mmunohistochemical staining for c-Fos in the basolateral amygdala.

14 of NPS to modulate neuronal activity in the basolateral amygdala.

15 contralateral cortex, nucleus accumbens, and basolateral amygdala.

16 e in initiating asymmetric activation of the basolateral amygdala.

17 put sampled from only the right but not left basolateral amygdala.

18 rected actions has been found to involve the basolateral amygdala.

19 and complexity of neurites of neurons in the basolateral amygdala.

20 e medial prefrontal cortex, hippocampus, and basolateral amygdala.

21 alcium/calmodulin-dependent kinase II in the basolateral amygdala.

22 mmunofluorescence, and RNA sequencing of the basolateral amygdala.

23 cortex via the paraventricular thalamus and basolateral amygdala.

24 ippocampal-entorhinal cortex network and the basolateral amygdala.

25 INs, and principal excitatory neurons in the basolateral amygdala.

26 exclusively within excitatory neurons of the basolateral amygdala.

27 mbens, the medial prefrontal cortex, and the basolateral amygdala.

28 lective potentiator CIQ bilaterally into the basolateral amygdala (3, 10, or 30 mug/side) following e

29 focused on the primary output neurons of the basolateral amygdala, a brain region that plays a key ro

30 chronized theta oscillations between V2L and basolateral amygdala, a physiological correlate of succe

31 dal neurons such as hippocampal area CA1 and basolateral amygdala, a slow afterhyperpolarization (sAH

32 eported neural correlates of salience in the basolateral amygdala (ABL) of rats during learning in an

33 en found in reward-responsive neurons in the basolateral amygdala (ABL).

34 Additionally, we found that intra-basolateral amygdala administration of the NPY Y(1) rece

35 In contrast, within the basolateral amygdala afferents, presynaptic Pr was not s

36 norepinephrine (NE) administration into the basolateral amygdala after training on an inhibitory avo

37 cingulate, thalamus, nucleus accumbens, and basolateral amygdala-all regions involved in motivated b

38 In addition, basolateral amygdala AMPA, but not NMDA glutamate recept

39 ortex (mPFC), ventral hippocampus (vHIP) and basolateral amygdala (AMY).

40 ess-mediated increases in GABA efflux in the basolateral amygdala, an event accompanied by no changes

41 As in other species, the OFC projects to the basolateral amygdala and dorsal striatum in mice.

42 42 had increased c-Fos expression within the basolateral amygdala and in serotonergic neurons in the

43 et, PTEN, colocalized with miR-144-3p in the basolateral amygdala and showed functional downregulatio

44 ted decreases were also observed between the basolateral amygdala and the rACC.

45 s (accumbens shell, ventral hippocampus, and basolateral amygdala) and differences (medial prefrontal

46 268 expression in the infralimbic cortex and basolateral amygdala, and elevated c-Fos or Zif268 expre

47 terior cingulate cortex, infralimbic cortex, basolateral amygdala, and habenula inhibited social play

48 le sources, including the prefrontal cortex, basolateral amygdala, and midline thalamus.

49 synaptic properties of ventral hippocampus, basolateral amygdala, and prefrontal cortex input to the

50 om the midline thalamus, contralateral mPFC, basolateral amygdala, and ventral hippocampus.

51 revealed that functional Hcn channels in the basolateral amygdala are necessary for conditioned fear

52 macology, revealing that Hcn channels in the basolateral amygdala are required for fear acquisition a

53 negative and positive representations in the basolateral amygdala are unknown.

54 The basolateral amygdala (BL) is involved in fear and anxiet

55 We recorded basolateral amygdala (BL) neurons in a seminaturalistic

56 valbumin-expressing (PV) interneurons in the basolateral amygdala (BLA) a dedicated role in the selec

57 he dorsomedial prefrontal cortex (dmPFC) and basolateral amygdala (BLA) and altered synaptic transmis

58 The basolateral amygdala (BLA) and centromedial amygdala (CM

59 ing the intrinsic functional connectivity of basolateral amygdala (BLA) and centromedial amygdala (CM

60 question, we recorded activity in the mPFC, basolateral amygdala (BLA) and dorsal and ventral hippoc

61 We also assessed the role of basolateral amygdala (BLA) and dorsal medial prefrontal

62 this hypothesis directly, as neurons in both basolateral amygdala (BLA) and gustatory cortex (GC)-ana

63 aversive unconditioned stimuli (USs) in the basolateral amygdala (BLA) and have examined their role

64 that NgR1 expression is required in both the basolateral amygdala (BLA) and infralimbic (IL) cortex t

65 The effects of inactivation of the basolateral amygdala (BLA) and ketamine administration o

66 itioned fear requires neural activity in the basolateral amygdala (BLA) and medial prefrontal cortex

67 ation of specific brain regions, such as the basolateral amygdala (BLA) and nucleus accumbens (NAc),

68 , we investigate causal contributions of the basolateral amygdala (BLA) and orbitofrontal cortex (OFC

69 ered activity in brain systems including the basolateral amygdala (BLA) and orbitofrontal cortex (OFC

70 The basolateral amygdala (BLA) and orbitofrontal cortex (OFC

71 e examined the role of a pathway linking the basolateral amygdala (BLA) and pDMS in such goal-directe

72 agonistic relationship may exist between the basolateral amygdala (BLA) and PFC during emotional proc

73 gion of the dorsal hippocampus (CA1) and the basolateral amygdala (BLA) and that of dopaminergic, nor

74 Although the basolateral amygdala (BLA) and the gustatory region of i

75 nderlie learning and memory deficits via the basolateral amygdala (BLA) and the hippocampus; however,

76 in the higher-order auditory cortex Te2 and basolateral amygdala (BLA) and their crosstalk during th

77 The basolateral amygdala (BLA) and ventral hippocampus (vHPC

78 We therefore evaluated the contribution of basolateral amygdala (BLA) and ventral hippocampus (vHPC

79 The perirhinal cortex (PRh) and basolateral amygdala (BLA) appear to mediate distinct as

80 l cortex (OFC) and its interactions with the basolateral amygdala (BLA) are critical for goal-directe

81 The neuronal circuits of the basolateral amygdala (BLA) are crucial for acquisition,

82 (vHPC), medial prefrontal cortex (mPFC), and basolateral amygdala (BLA) are each required for the exp

83 Reciprocal circuits between the mPFC and basolateral amygdala (BLA) are particularly important fo

84 depression (LTD) in principal neurons of the basolateral amygdala (BLA) are thought to underlie the a

85 eir synaptic connections with neurons in the basolateral amygdala (BLA) at neonatal to adult developm

86 had stronger functional connectivity of the basolateral amygdala (BLA) complex with the pregenual an

87 The orbitofrontal cortex (OFC) and basolateral amygdala (BLA) constitute part of a neural c

88 The basolateral amygdala (BLA) contributes to emotion-relate

89 Given the basolateral amygdala (BLA) contributes to these behavior

90 Neuropeptide Y (NPY) administration into the basolateral amygdala (BLA) decreases anxiety-like behavi

91 s-Tyr-d-Trp-Orn-Thr-Pen-Thr-NH(2)), into the basolateral amygdala (BLA) during posttraining, nonconti

92 a dampening of neuronal excitability in the basolateral amygdala (BLA) ex vivo and in vivo, and were

93 ts with bilateral excitotoxic lesions of the basolateral amygdala (BLA) failed to display such cue-po

94 by miR-19b, Adrb1 levels were reduced in the basolateral amygdala (BLA) following chronic stress.

95 We provide a cellular mechanism in the basolateral amygdala (BLA) for the rapid stress regulati

96 Basolateral amygdala (BLA) function is critical for flex

97 The basolateral amygdala (BLA) has a crucial role in emotion

98 imbic medial prefrontal cortex (PL-mPFC) and basolateral amygdala (BLA) have been implicated in the e

99 By contrast, inhibitory Gi-DREADDs in the basolateral amygdala (BLA) impaired the acquisition of b

100 rtance of the orbitofrontal cortex (OFC) and basolateral amygdala (BLA) in acquisition of the rGT and

101 udies implicate cholinergic signaling in the basolateral amygdala (BLA) in behaviors related to stres

102 the FAAH inhibitor URB597, directly into the basolateral amygdala (BLA) in conjunction with memory re

103 n addition, we infused mifepristone into the basolateral amygdala (BLA) in ethanol-seeking animals as

104 we identified a role for miR-34a within the basolateral amygdala (BLA) in fear memory consolidation.

105 n between the roles of the central (CeA) and basolateral amygdala (BLA) in regulating social behavior

106 nts has demonstrated a critical role for the basolateral amygdala (BLA) in such reward-seeking action

107 Considerable evidence implicates the basolateral amygdala (BLA) in the formation of outcome r

108 from the ventral hippocampus (vHipp) and the basolateral amygdala (BLA) in the medial prefrontal cort

109 Infusion of URB597 into the basolateral amygdala (BLA) increased social play behavio

110 e 5-HT(2C)R agonist CP-809101 in the lateral/basolateral amygdala (BLA) increases shock-elicited fear

111 minalis (jcBNST) is activated in response to basolateral amygdala (BLA) inputs through the stria term

112 The basolateral amygdala (BLA) integrates sensory input from

113 is structure, and the insular cortex and the basolateral amygdala (BLA) interact during CTA formation

114 The prefrontal cortex (PFC) and basolateral amygdala (BLA) interact to control emotional

115 e is dependent on orbitofrontal cortex (OFC)-basolateral amygdala (BLA) interactions.

116 Previous work showed that the basolateral amygdala (BLA) is a critical substrate for d

117 s of E2 signaling.SIGNIFICANCE STATEMENT The basolateral amygdala (BLA) is a key structure of the fea

118 The basolateral amygdala (BLA) is a site of convergence of n

119 The basolateral amygdala (BLA) is an important structure for

120 The basolateral amygdala (BLA) is central to fear generation

121 Oscillatory activity in the basolateral amygdala (BLA) is critical for emotional beh

122 Neuronal synchrony in the basolateral amygdala (BLA) is critical for emotional beh

123 The basolateral amygdala (BLA) is critical for encoding the

124 Basolateral amygdala (BLA) is critical for fear learning

125 The basolateral amygdala (BLA) is critically involved in the

126 The basolateral amygdala (BLA) is thought to be essential fo

127 The basolateral amygdala (BLA) mediates the facilitating eff

128 tual meaning of the LFH call in responses of basolateral amygdala (BLA) neurons from awake, freely mo

129 ted regions, it is reasonable to expect that basolateral amygdala (BLA) neurons should produce a rich

130 dator) induces long-lasting sensitization of basolateral amygdala (BLA) noradrenergic (NE) receptors

131 either central nucleus of amygdala (CeA) or basolateral amygdala (BLA) of female rats with one parti

132 ve onto excitatory projection neurons in the basolateral amygdala (BLA) of juvenile Fmr1(-/y) knockou

133 nxiety-like behavior and spinogenesis in the basolateral amygdala (BLA) of rats.

134 nist actions on synaptic transmission in the basolateral amygdala (BLA) of the rat were examined usin

135 by specifically overexpressing FKBP51 in the basolateral amygdala (BLA) or central amygdala resulted

136 divergent downstream structures such as the basolateral amygdala (BLA) or nucleus accumbens (NAc).

137 memory but was ineffective when given in the basolateral amygdala (BLA) or the ventral medial prefron

138 ore, this effect was not mediated via the LC-basolateral amygdala (BLA) pathway, because BLA inactiva

139 ow that neuropeptide-receptor systems in the basolateral amygdala (BLA) play an important role in the

140 The basolateral amygdala (BLA) plays a central role in such

141 The basolateral amygdala (BLA) plays a key role in many affe

142 The basolateral amygdala (BLA) plays an integral role in the

143 Ibotenate lesions of the basolateral amygdala (BLA) prevent stress dampening by s

144 Basolateral amygdala (BLA) principal cells are capable o

145 The lateral orbitofrontal cortex (lOFC) and basolateral amygdala (BLA) promote cocaine-seeking behav

146 Dopamine (DA) in the basolateral amygdala (BLA) promotes fear learning by dis

147 as negatively related to both aggression and basolateral amygdala (BLA) reactivity to angry faces, wh

148 The basolateral amygdala (BLA) receives input from subcortic

149 ions between the prefrontal cortex (PFC) and basolateral amygdala (BLA) regulate emotional behaviors.

150 Western blot analysis of the basolateral amygdala (BLA) revealed an increase in the G

151 The basolateral amygdala (BLA) sends excitatory projections

152 Rodent research suggests that the basolateral amygdala (BLA) subserves instrumental behavi

153 that an increase in calcineurin (CaN) in the basolateral amygdala (BLA) supports the shift from fear

154 emporally precise optogenetic stimulation of basolateral amygdala (BLA) terminals in the central nucl

155 tified distinct neuronal circuits within the basolateral amygdala (BLA) that differentially mediate f

156 ing measuring freezing have demonstrated the basolateral amygdala (BLA) to be critical to both fear l

157 f the medial prefrontal cortex (mPFC) or the basolateral amygdala (BLA) to examine the effects of bet

158 supports unidirectional gustatory input from basolateral amygdala (BLA) to hypothalamus in sated subj

159 AMPAR)-silent excitatory synapses within the basolateral amygdala (BLA) to nucleus accumbens (NAc) pr

160 t involve activation of projections from the basolateral amygdala (BLA) to the medial prefrontal cort

161 postsynaptic principal neurons (PNs) of the basolateral amygdala (BLA) were performed.

162 Theta oscillations synchronize the basolateral amygdala (BLA) with the hippocampus (HPC) an

163 cannabinoid 1 receptor (Cnr1) and CCK in the basolateral amygdala (BLA), a brain region critical for

164 at activation of efferent projections of the basolateral amygdala (BLA), a brain region implicated in

165 the BLA evokes norepinephrine release in the basolateral amygdala (BLA), alters BLA neuronal activity

166 fy the roles of the dorsal hippocampus (DH), basolateral amygdala (BLA), and medial prefrontal cortex

167 king the medial prefrontal cortex (PFC), the basolateral amygdala (BLA), and nucleus accumbens (NAc)

168 ginate from medial prefrontal cortex (mPFC), basolateral amygdala (BLA), and ventral subiculum of the

169 ehavior, with a focus on the NACc and on the basolateral amygdala (BLA), another important locus for

170 gonist) of pain-related hyperactivity in the basolateral amygdala (BLA), but not central amygdala (Ce

171 ommunication between the hippocampus and the basolateral amygdala (BLA), but the mechanisms of this p

172 When expressed in the basolateral amygdala (BLA), ERGR reduced anxiety, as tes

173 egion of the hippocampus, dentate gyrus, and basolateral amygdala (BLA), GFP immunofluorescence coinc

174 s, including those examining the role of the basolateral amygdala (BLA), have traditionally used tech

175 with changes in the synaptic circuits of the basolateral amygdala (BLA), in which emotional learning

176 Within the basolateral amygdala (BLA), LAC did not reduce, but slig

177 excitatory input from pyramidal cells of the basolateral amygdala (BLA), neurons that are activated b

178 ue-guided alcohol seeking is mediated by the basolateral amygdala (BLA), nucleus accumbens (NAc), and

179 omous receptor of neuregulin 1 (NRG1) in the basolateral amygdala (BLA), was expressed in GABAergic n

180 we visualized robust c-fos expression in the basolateral amygdala (BLA), which was reduced in mice pr

181 ronal activity in one key limbic region, the basolateral amygdala (BLA), whose activity fluctuates ac

182 Using viral-mediated basolateral amygdala (BLA)-specific deletion of Mecp2 in

183 Here, we identify a basolateral amygdala (BLA)-ventral striatum (NAc) pathwa

184 ntext and require glutamate signaling in the basolateral amygdala (BLA).

185 educed fear-evoked theta oscillations in the basolateral amygdala (BLA).

186 ories, including both dorsal hippocampus and basolateral amygdala (BLA).

187 ight on the synaptic organization of the rat basolateral amygdala (BLA).

188 from the ventral hippocampus (vHipp) and the basolateral amygdala (BLA).

189 imbic cortex (IL), ventral striatum (VS), or basolateral amygdala (BLA).

190 diversity of GABAergic neurons in the rodent basolateral amygdala (BLA).

191 ntly activating phospholipase C (PLC) in the basolateral amygdala (BLA).

192 ted in-field was mediated by inputs from the basolateral amygdala (BLA).

193 (PFC and OFC), nucleus accumbens (NAC), and basolateral amygdala (BLA).

194 interactions between the hippocampus and the basolateral amygdala (BLA).

195 endent electrophysiological responses in the basolateral amygdala (BLA).

196 apid mobilization of endocannabinoids in the basolateral amygdala (BLA).

197 he nucleus (DRN) neurons that project to the basolateral amygdala (BLA).

198 ronic stress contributes to hyperactivity of basolateral amygdala (BLA; comprised of basal, lateral,

199 e, selectively control PCs projecting to the basolateral amygdala (BLAPC) compared to those projectin

200 Conversely, naloxone infused into the basolateral amygdala blocked food deprivation-induced ch

201 The basolateral amygdala complex (BLA) has been identified a

202 The basolateral amygdala complex (BLA) is considered an esse

203 Synaptic plasticity in the basolateral amygdala complex (BLA) mediates the acquisit

204 soform protein levels in the hippocampus and basolateral amygdala complex (BLA).

205 disruption by actin depolymerization in the basolateral amygdala complex (BLC).

206 gests that these changes limited only to the basolateral amygdala complex may not be sufficient to in

207 , including the lateral nucleus (LAT) of the basolateral amygdala complex, is sensitive to stress.

208 ere we tested whether neural activity in rat basolateral amygdala conforms to this pattern by recordi

209 ur results indicate that anterior insula and basolateral amygdala constitute a network part that is p

210 on how distinct interneuron subtypes in the basolateral amygdala contribute to the acquisition and e

211 ese regions, the prefrontal cortex (PFC) and basolateral amygdala, convey executive control and affec

212 ion in the nucleus accumbens and central and basolateral amygdala correlated with genotype-related di

213 NAc core DA as being important for allowing basolateral amygdala-dependent information to gain contr

214 In contrast, reward-paired stimulation of basolateral amygdala did not hijack choice.

215 lutamatergic signaling mechanisms within the basolateral amygdala differentially and dissociably medi

216 d abolition of the signal by inactivation of basolateral amygdala disrupted this change in orienting

217 o the nucleus accumbens core, but not in the basolateral amygdala, dorsal hippocampus, infralimbic or

218 intracellular signaling pathways within the basolateral amygdala during stress-induced reinstatement

219 insic functional connectivity, with the left basolateral amygdala emerging as the strongest predictor

220 ions of the core (but not the shell) and the basolateral amygdala enhanced context-specific locomotor

221 -2 in the mThal, prefrontal cortex (PFC), or basolateral amygdala from acute brain slices.

222 ctify this, we monitored, in near-real time, basolateral amygdala glutamate concentration changes dur

223 e we combined chemogenetic excitation of rat basolateral amygdala glutamatergic neurons with a variet

224 ndamide and CRF1 signaling exhibited blunted basolateral amygdala habituation, which further mediated

225 Surprisingly, lesions of the basolateral amygdala had minimal effects on associative

226 that activation of Galphas signaling in the basolateral amygdala has a role in anxiety.

227 Neural activity in basolateral amygdala has recently been shown to reflect

228 ere discussed in the context of roles of the basolateral amygdala in coding and using reward predicti

229 st this, we recorded single unit activity in basolateral amygdala in rats with 6-hydroxydopamine or s

230 ning and GluN2A-containing NMDARs within the basolateral amygdala in the memory destabilization and r

231 s of infralimbic neurons that project to the basolateral amygdala in these groups.

232 he roles of the ventral subiculum (vSub) and basolateral amygdala in this process.

233 anyl induced similar oxygen decreases in the basolateral amygdala, indicating that brain hypoxia coul

234 Intra-basolateral amygdala inhibition of CaMKII promoted memor

235 in response to ventral hippocampal, but not basolateral amygdala, inputs.

236 tral amygdala, but MJN110 infusions into the basolateral amygdala, interfered with the naloxone-preci

237 The basolateral amygdala is critical for generating anxiety,

238 as not examined whether neuron number in the basolateral amygdala is stable through this period.

239 nduction of beta-adrenergic signaling in the basolateral amygdala is sufficient to induce acute and s

240 The basolateral amygdala is the main entry site for sensory

241 Activation of noradrenergic circuitry in the basolateral amygdala is thought to have a role in stress

242 Compound 6c was not efficacious in the basolateral amygdala kindling rat model of temporal lobe

243 ate gyrus, we find that knockdown of PTEN in basolateral amygdala leads to a significant decrease in

244 nnection of the medial prefrontal cortex and basolateral amygdala led rats to become more impulsive b

245 D1 neuron projections implicates the medial basolateral amygdala (mBLA) as a downstream target of th

246 The findings also suggest that the basolateral amygdala modulates memory consolidation via

247 fect of acute stress occurred independent of basolateral amygdala neural input and was mimicked by tr

248 ircuit revealed enlarged dendritic arbors in basolateral amygdala neurons in S1, but normal infralimb

249 ed the effects of shRNA knockdown of PTEN in basolateral amygdala neurons on synaptic spine density a

250 nsic excitability and synaptic plasticity in basolateral amygdala neurons that give rise to temporall

251 itioning, which does not involve infralimbic-basolateral amygdala neurons.

252 prediction errors and attentional signals in basolateral amygdala neurons.

253 re) produces a long-lasting sensitization of basolateral amygdala noradrenergic substrates [via a cor

254 In the basolateral amygdala of fear-naive mice PAR1 couples to

255 In contrast, FosB remained elevated in the basolateral amygdala of mice with resolved nociception a

256 was also seen in the infralimbic cortex and basolateral amygdala of stress-susceptible male mice aft

257 sions of the NAc core, NAc medial shell, and basolateral amygdala on context-specific locomotor sensi

258 e, we examined the effects of lesions of the basolateral amygdala on the occurrence of unblocking whe

259 togenetically stimulated mPFC projections to basolateral amygdala or nucleus accumbens, two subcortic

260 There was no increase in IL-1beta in the basolateral amygdala or the perirhinal cortex.

261 e found in the dorsal striatum, hippocampus, basolateral amygdala, or prefrontal cortex.

262 statory neocortex, medial prefrontal cortex, basolateral amygdala, or the central nucleus of the amyg

263 umber of Fos-positive neurons in central and basolateral amygdala, orbitofrontal cortex, ventral and

264 Intra-CeA (but not intra-basolateral amygdala) PACAP dose-dependently induced ano

265 s (NAc) shell from ventral subiculum (vSub), basolateral amygdala, paraventricular thalamus, and vent

266 The basolateral amygdala participates in this process, but p

267 complex, and local plasticity in excitatory basolateral amygdala principal neurons is considered to

268 nstrate that C1ql3-expressing neurons in the basolateral amygdala project to the medial prefrontal co

269 we found that local injection of NPS in the basolateral amygdala promotes anxiolysis after chronic e

270 Furthermore, behavioral analysis of basolateral amygdala PTEN knockdown suggests that these

271 underling the sAHP or excitability of CA1 or basolateral amygdala pyramidal neurons.

272 miR-144-3p overexpression in the basolateral amygdala rescued impaired fear extinction in

273 contrast with hippocampus, cell grafts into basolateral amygdala rescued the hyperactivity deficit,

274 DA synthesis to DA neurons projecting to the basolateral amygdala restored short-term memory but not

275 and pharmacological manipulations of GC and basolateral amygdala revealed the role of top-down input

276 RNA sequencing of the basolateral amygdala revealed transcriptional divergence

277 These results suggest that basolateral amygdala serves a critical function in atten

278 tent with findings that the NAc core and the basolateral amygdala share a variety of behavioral funct

279 idate, miR-144-3p, robustly expressed in the basolateral amygdala, showed specific extinction-induced

280 per side) into the CeA, but not the adjacent basolateral amygdala, significantly attenuated binge-lik

281 ences in monoamine levels were observed (the basolateral amygdala, subregions of the hippocampus and

282 tions from the midbrain dopamine system into basolateral amygdala, suggests that the PKH signal in am

283 an anxiety-related dorsal raphe nucleus (DR)-basolateral amygdala system to pharmacological challenge

284 ial isolation of female rats sensitizes a DR-basolateral amygdala system to stress-related stimuli, w

285 malian brain, such as the hippocampus or the basolateral amygdala, the clustering of the scaffolding

286 ns of a protein synthesis inhibitor into the basolateral amygdala, the subsequent fear response was a

287 nsfers conditioned information formed in the basolateral amygdala to brain structures that generate e

288 thesized that the mPFC communicates with the basolateral amygdala to disrupt learning in females afte

289 Here we show that basolateral amygdala to orbitofrontal cortex projections

290 ogical investigation of projections from the basolateral amygdala to the medial prefrontal cortex and

291 absent or labile, in the projection from the basolateral amygdala to the NAc in incubation of cocaine

292 olateral prefrontal cortex, hippocampus, and basolateral amygdala) to identify imaging predictors of

293 , we report that transient inhibition of the basolateral amygdala triggered a profound increase in so

294 strocytes depressed excitatory synapses from basolateral amygdala via A1 adenosine receptor activatio

295 ectivity between the anterior insula and the basolateral amygdala was strongly related to state anxie

296 sing paired recordings obtained in the mouse basolateral amygdala, we found that AACs powerfully inhi

297 ine concentrations in the left but not right basolateral amygdala were elevated in groups presented w

298 Anandamide levels in the basolateral amygdala were increased by extinction traini

299 estraint stress increased GABA efflux in the basolateral amygdala, whereas central amygdala efflux re

300 became silent with time, engram cells in the basolateral amygdala, which were necessary for fear memo