ライフサイエンスコーパス: basolateral amygdala

1 pus but did not prevent hyperactivity in the basolateral amygdala.

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

3 contralateral cortex, nucleus accumbens, and basolateral amygdala.

4 l hippocampus, and projection neurons in the basolateral amygdala.

5 mmunofluorescence, and RNA sequencing of the basolateral amygdala.

6 cortex via the paraventricular thalamus and basolateral amygdala.

7 ippocampal-entorhinal cortex network and the basolateral amygdala.

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

9 exclusively within excitatory neurons of the basolateral amygdala.

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

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

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

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

14 eceptors on output projection neurons of the basolateral amygdala.

15 enlargement is localized specifically to the basolateral amygdala.

16 ses and theta oscillations recorded from the basolateral amygdala.

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

18 ering protein expression within the adjacent basolateral amygdala.

19 rentially modulated through the vSub and the basolateral amygdala.

20 a direct pathway between anterior insula and basolateral amygdala.

21 h a marker of synaptic plasticity within the basolateral amygdala.

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

23 in GABA- and glutamate-positive cells in the basolateral amygdala.

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

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

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

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

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

29 d overlapping brain circuits and depended on basolateral amygdala activity for expression.

30 hancement was associated with an increase in basolateral amygdala activity.

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

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

33 cortical nucleus, whereas in the lateral and basolateral amygdala alpha1, alpha2, alpha5, beta1, beta

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

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

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

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

38 to the OFC, but not in projections from the basolateral amygdala and thalamus.

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

40 scillatory neuronal interactions between the basolateral amygdala and the rostral anterior cingulate

41 to the NAc shell and strengthens input from basolateral amygdala and ventral hippocampus.

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

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

44 e thalamus, bed nucleus of stria terminalis, basolateral amygdala, and medial prefrontal cortex as pr

45 Intra-basolateral amygdala antagonism of dopamine D1-receptors

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

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

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

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

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

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

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

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

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

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

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

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

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

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

60 ated with distinct oscillatory states in the basolateral amygdala (BLA) and medial prefrontal cortex

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

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

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

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

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

66 ions directly stimulate GIRK currents in the basolateral amygdala (BLA) and potentiate baclofen-induc

67 c properties of ventral hippocampus (vHipp), basolateral amygdala (BLA) and prefrontal cortex (PFC) i

68 ctions from the ventral hippocampus (vHipp,) basolateral amygdala (BLA) and prefrontal cortex (PFC) o

69 mbic (IL) cortex neurons that project to the basolateral amygdala (BLA) and reduced CD response compa

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

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

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

73 epend on functional interactions between the basolateral amygdala (BLA) and the nucleus accumbens cor

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

75 e of the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA) and their reciprocal inhibito

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

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

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

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

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

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

82 deling of relative excitatory drive from the basolateral amygdala (BLA) away from corticotropin relea

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

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

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

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

87 lcohol consumption, whereas knockdown in the basolateral amygdala (BLA) decreased alcohol consumption

88 glutamatergic terminals from the PeF to the basolateral amygdala (BLA) enhanced the acquisition, del

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

90 We first show that the rat basolateral amygdala (BLA) exhibits prominent gamma osci

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

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

93 pharmacological manipulations, we found that basolateral amygdala (BLA) glutamatergic activity tracks

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

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

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

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

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

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

100 young and aged rats to test the role of the basolateral amygdala (BLA) in intertemporal decision mak

101 nd (3) excitatory synaptic physiology in the basolateral amygdala (BLA) in male Sprague Dawley rats.

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

103 r insular cortex (aIC) that project into the basolateral amygdala (BLA) in response to conditioned ta

104 earch has established a crucial role for the basolateral amygdala (BLA) in social experiential learni

105 neurons of mice integrate auditory cues and basolateral amygdala (BLA) inputs non-linearly in a NMDA

106 The basolateral amygdala (BLA) integrates sensory input from

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

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

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

110 Extensive evidence indicates that the basolateral amygdala (BLA) interacts with other brain re

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

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

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

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

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

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

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

118 Basolateral amygdala (BLA) is critical for fear learning

119 The basolateral amygdala (BLA) is integral in mood and emoti

120 The basolateral amygdala (BLA) modulates the consolidation o

121 formed and stored in a genetically distinct basolateral amygdala (BLA) neuronal population that driv

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

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

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

125 e behavior and increase spine-density in the basolateral amygdala (BLA) of rats 10 days later.

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

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

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

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

130 and associated with anatomical variation in basolateral amygdala (BLA) perineuronal nets, which are

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

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

133 The basolateral amygdala (BLA) plays a critical role in fear

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

135 The basolateral amygdala (BLA) plays a vital role in associa

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

137 Basolateral amygdala (BLA) principal cells are capable o

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

139 version of diazepam (CD) that was tested on basolateral amygdala (BLa) pyramidal cells in mouse brai

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

141 The basolateral amygdala (BLA) receives input from subcortic

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

143 The basolateral amygdala (BLA) regulates conditioned respons

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

145 The basolateral amygdala (BLA) sends excitatory projections

146 Whole-cell recordings in basolateral amygdala (BLA) slices from rats revealed hig

147 Here, we show that stress increases basolateral amygdala (BLA) spike firing.

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

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

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

151 Y1R+ neurons projecting from the mPFC to the basolateral amygdala (BLA) this efferent population was

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

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

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

155 were analyzed with anterograde tracing from basolateral amygdala (BLA) to PFC to identify sex-specif

156 g factor (CRF) modulate the responses of the basolateral amygdala (BLA) to stress and are associated

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

158 s coeruleus (LC) neurons that project to the basolateral amygdala (BLA) using a DREADD (designer rece

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

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

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

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

163 r learning, disengaged mesolimbic circuitry, basolateral amygdala (BLA), and plasticity-related AMPA

164 ess effects on the dorsal hippocampus (HPC), basolateral amygdala (BLA), and somatosensory cortex (SS

165 This avoidance requires prelimbic (PL) PFC, basolateral amygdala (BLA), and ventral striatum (VS).

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

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

168 onmuscle myosin II inhibition (NMIIi) in the basolateral amygdala (BLA), but not dorsal hippocampus (

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

170 ties in the medial prefrontal cortex (mPFC), basolateral amygdala (BLA), dorsomedial striatum (DMS) a

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

172 and alteration of synaptic plasticity in the basolateral amygdala (BLA), in male rats.

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

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

175 ess in BLA.SIGNIFICANCE STATEMENT Within the basolateral amygdala (BLA), neuropeptide Y (NPY) is asso

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

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

178 ctivation in the prefrontal cortex (PFC) and basolateral amygdala (BLA), we examined electron microsc

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

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

181 In the present study, a basolateral amygdala (BLA)-prefrontal cortex (PFC)-peria

182 Here, we show that the mouse basolateral amygdala (BLA)-prelimbic prefrontal cortex (

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

184 s-induced norepinephrine (NE) release in the basolateral amygdala (BLA).

185 hat appears to project downstream to CA1 and basolateral amygdala (BLA).

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

187 ion, the medial prefrontal cortex (mPFC) and basolateral amygdala (BLA).

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

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

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

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

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

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

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

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

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

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

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

199 A particularly strong candidate is the basolateral amygdala (BLA).

200 solateral prefrontal cortex (dlPFC), and the basolateral amygdala (BLA).

201 A strong candidate is the basolateral amygdala (BLA).

202 tory synaptic proteins and physiology in the basolateral amygdala (BLA).

203 sity on parvalbumin (PV) interneurons in the basolateral amygdala (BLA).

204 ity within the anterior insula (aIC) and the basolateral amygdala (BLA).

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

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

207 n at inputs from the ventral hippocampus and basolateral amygdala but not from the mediodorsal nucleu

208 ex and increased immunoreactive cells in the basolateral amygdala compared with WT littermates.

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

210 xpression in the infralimbic cortex (IL) and basolateral amygdala complex (BLA) that were associated

211 The basolateral amygdala complex (BLA), extensively connecte

212 ck requires de novo protein synthesis in the basolateral amygdala complex (BLA), whereas consolidatio

213 lidation of conditioned fear memories in the basolateral amygdala complex (BLA).

214 y enhanced memory and heightened cFos in the basolateral amygdala complex (BLC) with retrieval of the

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

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

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

218 entromedial prefrontal cortex or hippocampal-basolateral amygdala connectivity-differentiated between

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

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

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

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

223 uding the locus coeruleus, and much later in basolateral amygdala, dorsal raphe nucleus, and the subs

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

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

226 show that increasing neural activity in the basolateral amygdala enhances both conditioned anticipat

227 without affecting anxiety-like behaviors and basolateral amygdala firing.

228 -2 in the mThal, prefrontal cortex (PFC), or basolateral amygdala from acute brain slices.

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

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

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

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

233 egions, namely the medial prefrontal cortex, basolateral amygdala, hippocampus, anterior cingulate co

234 sory cortex, and increased activation of the basolateral amygdala in response to repeated whisker sti

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

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

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

238 Intra-basolateral amygdala inhibition of CaMKII promoted memor

239 and medial prefrontal cortices as well as at basolateral amygdala inputs and striatal cholinergic int

240 ation were specific to MD inputs; activating basolateral amygdala inputs produced opposite effects.

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

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

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

244 The basolateral amygdala is the main entry site for sensory

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

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

247 The prelimbic (PL) area and basolateral amygdala (lateral [LA] and basolateral [BL]

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

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

250 unction of the ventral striatum, whereas the basolateral amygdala mediates processing of the threat c

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

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

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

254 revealed that these arrests are effected by basolateral amygdala neurons projecting to the central a

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

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

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

258 d that in vivo optogenetic activation of the basolateral amygdala-nucleus accumbens (BLA-NAc) glutama

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

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

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

262 ), with little AT(2)R-eGFP expression in the basolateral amygdala or lateral division of the central

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

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

265 lly into the ventromedial prefrontal cortex, basolateral amygdala, or hippocampal CA1 region.

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

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

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

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

270 mPFC projections to the NAcS, but not to the basolateral amygdala, partially reversed suppression of

271 The basolateral amygdala participates in this process, but p

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

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

274 The basolateral amygdala projection (BLAp) innervates broad

275 is a form of one-trial learning dependent on basolateral amygdala projection neurons (BLApn).

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

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

278 entation of anandamide hydrolysis within the basolateral amygdala reduces behavioral indices of stres

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

280 RNA sequencing of the basolateral amygdala revealed transcriptional divergence

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

282 sory cortex, and increased activation of the basolateral amygdala, suggesting that impaired somatosen

283 identified a distinct neural ensemble in the basolateral amygdala that encodes the negative affective

284 projection-defined neuronal ensemble in the basolateral amygdala that is active during self-paced be

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 The basolateral amygdala therefore facilitates cue-induced c

288 Here we show that basolateral amygdala to orbitofrontal cortex projections

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

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

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

292 projections to NAcS, or vmPFC projections to basolateral amygdala, to punished EtOH-SA.

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

294 l, and lateral shell; anterior and posterior basolateral amygdala; ventral pallidum; and periaqueduct

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

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

297 cortex, but not to the infralimbic cortex or basolateral amygdala, were more active to safety and com

298 trengthened the coupling between the cmA and basolateral amygdala, whereas LZP increased the interpla

299 ch as the nucleus accumbens shell (NAcS) and basolateral amygdala, which encode positive and negative

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