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1 bed nucleus of the stria terminalis, LS, and lateral amygdala.
2 lar complex, in fear memory formation in the lateral amygdala.
3 te neurons in the insular cortex and rostral lateral amygdala.
4 use auditory cortex receives inputs from the lateral amygdala.
5 hreatening signals to the insular cortex and lateral amygdala.
6 d synaptic plasticity are enhanced in Fmr1KO lateral amygdala.
7 from the hippocampus, thalamus, or the basal lateral amygdala.
8 at a CaMKII locus (GluA1-Ser831) in CeA and lateral amygdala.
9 expressed presynaptically by inputs from the lateral amygdala.
10 dala neurons and shunted excitation from the lateral amygdala.
11 oxazole-propionate receptors (AMPARs) in the lateral amygdala.
12 arge fraction of postsynaptic neurons in the lateral amygdala, a brain structure essential for this l
14 PTSD symptoms, was associated with increased lateral amygdala activation in response to an aversive s
15 sory-specific associations are stored in the lateral amygdala, allowing for their selective alteratio
18 ephrine to open the BBB, lose neurons in the lateral amygdala and develop a behavioral disorder chara
19 rgic inhibition of projection neurons in the lateral amygdala and enables the induction of LTP at tha
21 location of fear memory to specific cells in lateral amygdala and suggest that neuronal excitability
22 latory protein, into dendritic spines in the lateral amygdala and that these spines undergo enlargeme
23 pression of a persistent phase of LTP in the lateral amygdala and that this late component requires t
24 ransgene was expressed at high levels in the lateral amygdala and the striatum but not other forebrai
25 were observed in the nucleus accumbens core, lateral amygdala, and anterior cingulate cortex in the P
26 nses to sensory stimuli are prevalent in the lateral amygdala, and are also prevalent in the medial a
27 he pathway from the auditory thalamus to the lateral amygdala, and during fear conditioning LTP-like
28 te and exhibited elevated dopamine in raphe, lateral amygdala, and medial amygdala but decreased dopa
29 gram ensembles supporting a threat memory in lateral amygdala, and this engram ensemble was reactivat
30 culata, entorhinal cortex, central amygdala, lateral amygdala, arcuate nucleus, and central gray area
31 blished that cortical auditory inputs to the lateral amygdala are exclusively excitatory and that cor
32 projections from the auditory cortex to the lateral amygdala are modified during the acquisition and
34 naptic plasticity underlying learning in the lateral amygdala, as they convey information about the u
35 N2A/GluN2B ratio in neurons of the basal and lateral amygdala (BLA) compared with weaker fear memorie
37 t to a loud noise, whereas infusion into the lateral amygdala blocked freezing to a loud noise but no
38 ry have basally reduced CREB activity in the lateral amygdala but can be induced to perform at averag
40 ve (SOM(+)) GABAergic neurons of the central lateral amygdala (CeL), and its activity modulates actio
41 Recent studies indicate that the central lateral amygdala (CeL), in particular its somatostatin-e
44 ndicates that a neural population within the lateral amygdala, defined by the expression of mWAKE, fu
46 studied how cell ensembles in the basal and lateral amygdala encode associations between conditioned
48 cal administration of methylphenidate in the lateral amygdala enhanced cue-reward learning through do
52 to be mediated by direct projections to the lateral amygdala from the auditory thalamus but mainly i
53 onfirmed the significance of the central and lateral amygdala, hippocampal body, and prefrontal corte
54 n as c-fos) in the auditory thalamus and the lateral amygdala in rewired mice, similar to the way aud
56 al CA1 fibers with coincident stimuli of the lateral amygdala induces long-term potentiation of later
57 g retrogradely on parvalbumin-positive (PV+) lateral amygdala interneurons in the formation of a less
59 channels in pyramidal cell dendrites in the lateral amygdala is required for associative LTP and the
60 Experience-driven synaptic plasticity in the lateral amygdala is thought to underlie the formation of
62 xplore this hypothesis, we recorded from the lateral amygdala (LA) and auditory cortex (AC) before an
63 ciate auditory CS-evoked spike firing in the lateral amygdala (LA) and both conditional fear behavior
64 rly genes (IEGs) Arc/Arg3.1 and Egr-1 in the lateral amygdala (LA) and impairs the 'consolidation' of
65 oform that is expressed in the brain) in the lateral amygdala (LA) and that infusion to the LA of the
67 umulate in dendritic spines of the adult rat lateral amygdala (LA) during consolidation of aversive p
69 that local infusion of garcinol into the rat lateral amygdala (LA) impairs the training and retrieval
70 ted in hippocampal areas CA1 and CA3 and the lateral amygdala (LA) in rats during and after chronic i
71 ation (LTP) at sensory input synapses to the lateral amygdala (LA) is a candidate mechanism for memor
72 iation (LTP) of synaptic transmission in the lateral amygdala (LA) is believed to underlie the format
73 we show that an extra-SCN oscillator in the lateral amygdala (LA) is defined by expression of the cl
77 nresolved, question regarding how particular lateral amygdala (LA) neurons are assigned to fear memor
78 ar conditioning, it is well established that lateral amygdala (LA) neurons potentiate their response
79 Although long-term potentiation (LTP) in the lateral amygdala (LA) plays an essential role in auditor
85 uli by conveying auditory information to the lateral amygdala (LA) through long-range excitatory glut
86 ied a previously unexplored pathway from the lateral amygdala (LA) to the auditory cortex (ACx) and f
87 AC) by providing auditory information to the lateral amygdala (LA) via long-range excitatory glutamat
89 on terminals that were mainly located in the lateral amygdala (La), and slight innervations in other
90 e (EC) provide feedforward inhibition in the lateral amygdala (LA), but how EC affects synaptic trans
91 ion of the immediate-early gene Egr-1 in the lateral amygdala (LA), hippocampus (CA1), and medial pre
93 which is known to alter synaptic efficacy in lateral amygdala (LA), to study molecular mechanisms und
95 this question, because a discrete region-the lateral amygdala (LA)-has been shown unambiguously to be
102 s in the cortical and thalamic inputs to the lateral amygdala (LA); however, the specific roles of bo
103 was recorded in the dorsal subnucleus of the lateral amygdala (LAd) of freely behaving rats during Pa
104 receptor binding in the lateral septum (LS), lateral amygdala (LatAmyg), and central amygdala (CenAmy
105 y)-4H-chromen-4-one (XAP044), which inhibits lateral amygdala long term potentiation (LTP) in brain s
106 ings highlight a direct pathway by which the lateral amygdala may contribute to state-dependent corti
108 k NMDA receptor-mediated EPSCs is reduced in lateral amygdala neurons from fear-conditioned animals,
113 a sharp spatial border between the basal and lateral amygdala nuclei, and identified continuous spati
115 831 phosphorylation was increased in CeA and lateral amygdala of mice that lever-pressed for alcohol
116 med expression profiling of microRNAs in the lateral amygdala of rats 1 h after auditory fear conditi
118 ic activity were not observed in the septum, lateral amygdala, or hypothalamus, when males with eyesp
119 MDA-mediated transmission in the thalamic-to-lateral amygdala pathway is not facilitated after fear c
120 at, upon tetanic stimulation of afferents to lateral amygdala, presynaptic GABAbR-mediated inhibition
122 ex, can dynamically affect the output of the lateral amygdala, providing a general mechanism for fear
123 , and knocking down cannabinoid receptors in lateral amygdala PV+ neurons restored threat memory spec
125 Here, for the first time, we show that the lateral amygdala receives long-range GABAergic projectio
127 or the development of trauma symptoms, while lateral amygdala responding to aversive events after tra
129 vels of alpha1d mRNA unaltered by ADX in the lateral amygdala, reticular thalamic nucleus, retrosplen
133 ry communication from auditory cortex to the lateral amygdala, suggesting that the timing and ratio o
134 have demonstrated that plasticity at thalamo-lateral amygdala (T-LA) synapses is critically involved
135 fied functional connectivity with medial and lateral amygdala, the temporal order of these connection
136 ed us to identify two previously undescribed lateral amygdala to auditory cortex (LAC) GABAergic proj
137 l was also seen in the neocortex, claustrum, lateral amygdala, ventral cochlear nucleus, raphe magnus
138 rthermore, knockdown of TRPC4 protein in the lateral amygdala via lentiviral-mediated gene delivery o
139 the dominant input to active neurons in the lateral amygdala was from the infralimbic cortex, wherea
141 in FOS levels in the medial and basolateral/lateral amygdala when either mPFC subdivision was inacti
142 osynaptic EPSCs evoked by stimulation in the lateral amygdala with EC50 values of 36 nM (control) and
143 microRNAs are endogenously expressed in the lateral amygdala, with 7 microRNAs upregulated and 32 do