ライフサイエンスコーパス: lateral amygdala

1 from the hippocampus, thalamus, or the basal lateral amygdala.

2 at a CaMKII locus (GluA1-Ser831) in CeA and lateral amygdala.

3 expressed presynaptically by inputs from the lateral amygdala.

4 dala neurons and shunted excitation from the lateral amygdala.

5 oxazole-propionate receptors (AMPARs) in the lateral amygdala.

6 bed nucleus of the stria terminalis, LS, and lateral amygdala.

7 lar complex, in fear memory formation in the lateral amygdala.

8 arge fraction of postsynaptic neurons in the lateral amygdala, a brain structure essential for this l

9 sory-specific associations are stored in the lateral amygdala, allowing for their selective alteratio

10 In the basolateral and lateral amygdala, amphetamine or cocaine at home or expo

11 ir stereotypical locations encapsulating the lateral amygdala and BLA.

12 ephrine to open the BBB, lose neurons in the lateral amygdala and develop a behavioral disorder chara

13 rgic inhibition of projection neurons in the lateral amygdala and enables the induction of LTP at tha

14 t increased Fos-like immunoreactivity in the lateral amygdala and hippocampal area CA1.

15 location of fear memory to specific cells in lateral amygdala and suggest that neuronal excitability

16 latory protein, into dendritic spines in the lateral amygdala and that these spines undergo enlargeme

17 pression of a persistent phase of LTP in the lateral amygdala and that this late component requires t

18 ransgene was expressed at high levels in the lateral amygdala and the striatum but not other forebrai

19 were observed in the nucleus accumbens core, lateral amygdala, and anterior cingulate cortex in the P

20 nses to sensory stimuli are prevalent in the lateral amygdala, and are also prevalent in the medial a

21 he pathway from the auditory thalamus to the lateral amygdala, and during fear conditioning LTP-like

22 te and exhibited elevated dopamine in raphe, lateral amygdala, and medial amygdala but decreased dopa

23 culata, entorhinal cortex, central amygdala, lateral amygdala, arcuate nucleus, and central gray area

24 projections from the auditory cortex to the lateral amygdala are modified during the acquisition and

25 Cortical and thalamic inputs to the lateral amygdala are recruited during auditory fear cond

26 naptic plasticity underlying learning in the lateral amygdala, as they convey information about the u

27 N2A/GluN2B ratio in neurons of the basal and lateral amygdala (BLA) compared with weaker fear memorie

28 regulation of cholinergic input to the basal lateral amygdala (BLA).

29 t to a loud noise, whereas infusion into the lateral amygdala blocked freezing to a loud noise but no

30 ry have basally reduced CREB activity in the lateral amygdala but can be induced to perform at averag

31 The central lateral amygdala (CeL) is a key node in fear circuits, b

32 Recent studies indicate that the central lateral amygdala (CeL), in particular its somatostatin-e

33 , is gated via oxytocin acting in the centro-lateral amygdala (CeL).

34 studied how cell ensembles in the basal and lateral amygdala encode associations between conditioned

35 Is LTP in the lateral amygdala enduring, and, if so, does it require g

36 cal administration of methylphenidate in the lateral amygdala enhanced cue-reward learning through do

37 In the lateral amygdala, fear conditioning is associated with a

38 ociatively induced synaptic responses in the lateral amygdala following fear learning.

39 Synapses onto dendritic spines in the lateral amygdala formed by afferents from the auditory t

40 to be mediated by direct projections to the lateral amygdala from the auditory thalamus but mainly i

41 n as c-fos) in the auditory thalamus and the lateral amygdala in rewired mice, similar to the way aud

42 Here we combined intra-lateral amygdala in vivo pharmacology and ex vivo electr

43 al CA1 fibers with coincident stimuli of the lateral amygdala induces long-term potentiation of later

44 Thus, the encoding of memories in the lateral amygdala is mediated by AMPA receptor traffickin

45 channels in pyramidal cell dendrites in the lateral amygdala is required for associative LTP and the

46 Experience-driven synaptic plasticity in the lateral amygdala is thought to underlie the formation of

47 The lateral amygdala (LA) acquires differential coding of pr

48 xplore this hypothesis, we recorded from the lateral amygdala (LA) and auditory cortex (AC) before an

49 ciate auditory CS-evoked spike firing in the lateral amygdala (LA) and both conditional fear behavior

50 rly genes (IEGs) Arc/Arg3.1 and Egr-1 in the lateral amygdala (LA) and impairs the 'consolidation' of

51 oform that is expressed in the brain) in the lateral amygdala (LA) and that infusion to the LA of the

52 Previous work identified lateral amygdala (LA) calcium-permeable AMPA receptors (

53 umulate in dendritic spines of the adult rat lateral amygdala (LA) during consolidation of aversive p

54 that local infusion of garcinol into the rat lateral amygdala (LA) impairs the training and retrieval

55 ted in hippocampal areas CA1 and CA3 and the lateral amygdala (LA) in rats during and after chronic i

56 ation (LTP) at sensory input synapses to the lateral amygdala (LA) is a candidate mechanism for memor

57 iation (LTP) of synaptic transmission in the lateral amygdala (LA) is believed to underlie the format

58 The lateral amygdala (LA) is important for assigning emotion

59 ditioned stimulus (CS) representation in the lateral amygdala (LA) is not known.

60 The lateral amygdala (LA) is thought to be critical for the

61 nresolved, question regarding how particular lateral amygdala (LA) neurons are assigned to fear memor

62 ar conditioning, it is well established that lateral amygdala (LA) neurons potentiate their response

63 Although long-term potentiation (LTP) in the lateral amygdala (LA) plays an essential role in auditor

64 Activation of lateral amygdala (LA) pyramidal neurons by aversive stim

65 Neurons in the lateral amygdala (LA) receive glutamatergic sensory inpu

66 osphorylated (active) form of alphaCaMKII in lateral amygdala (LA) spines.

67 Here, we report that at lateral amygdala (LA) synapses (a storage site for fear

68 Changes in synaptic strength in the lateral amygdala (LA) that occur with fear learning are

69 ied a previously unexplored pathway from the lateral amygdala (LA) to the auditory cortex (ACx) and f

70 e (EC) provide feedforward inhibition in the lateral amygdala (LA), but how EC affects synaptic trans

71 ion of the immediate-early gene Egr-1 in the lateral amygdala (LA), hippocampus (CA1), and medial pre

72 In lateral amygdala (LA), neurons with increased excitabili

73 which is known to alter synaptic efficacy in lateral amygdala (LA), to study molecular mechanisms und

74 In the lateral amygdala (LA), training-induced increases in neu

75 this question, because a discrete region-the lateral amygdala (LA)-has been shown unambiguously to be

76 and morphological changes at synapses in the lateral amygdala (LA).

77 curs in several brain regions, including the lateral amygdala (LA).

78 ated with changes in synapse strength in the lateral amygdala (LA).

79 ducing stimulation of thalamic inputs to the lateral amygdala (LA).

80 ads to an increase in BDNF expression in the lateral amygdala (LA).

81 potentiation of some thalamic inputs to the lateral amygdala (LA).

82 s in the cortical and thalamic inputs to the lateral amygdala (LA); however, the specific roles of bo

83 was recorded in the dorsal subnucleus of the lateral amygdala (LAd) of freely behaving rats during Pa

84 receptor binding in the lateral septum (LS), lateral amygdala (LatAmyg), and central amygdala (CenAmy

85 y)-4H-chromen-4-one (XAP044), which inhibits lateral amygdala long term potentiation (LTP) in brain s

86 ings highlight a direct pathway by which the lateral amygdala may contribute to state-dependent corti

87 ormation about the unconditioned stimulus to lateral amygdala neurons during fear conditioning.

88 k NMDA receptor-mediated EPSCs is reduced in lateral amygdala neurons from fear-conditioned animals,

89 We manipulated CREB in a subset of lateral amygdala neurons in mice with a modified herpes

90 sured in vitro with whole-cell recordings in lateral amygdala neurons.

91 ICs were required for synaptic plasticity in lateral amygdala neurons.

92 ration was blocked in as few as 10 to 20% of lateral amygdala neurons.

93 SST-IR neurons were decreased in the lateral amygdala nucleus in BD (Nt, p = .003) and SZ (Nt

94 831 phosphorylation was increased in CeA and lateral amygdala of mice that lever-pressed for alcohol

95 med expression profiling of microRNAs in the lateral amygdala of rats 1 h after auditory fear conditi

96 ial amygdala on day 14 and in the medial and lateral amygdala on day 18.

97 ic activity were not observed in the septum, lateral amygdala, or hypothalamus, when males with eyesp

98 MDA-mediated transmission in the thalamic-to-lateral amygdala pathway is not facilitated after fear c

99 at, upon tetanic stimulation of afferents to lateral amygdala, presynaptic GABAbR-mediated inhibition

100 The protons activated ASICs in lateral amygdala pyramidal neurons, generating excitator

101 Overexpression of miR-182 within the lateral amygdala resulted in decreased expression of the

102 vels of alpha1d mRNA unaltered by ADX in the lateral amygdala, reticular thalamic nucleus, retrosplen

103 nucleus accumbens, medial amygdala, but not lateral amygdala, septum, and hypothalamus.

104 bipolar neurons, BLA stellate neurons or in lateral amygdala stellate neurons.

105 l was also seen in the neocortex, claustrum, lateral amygdala, ventral cochlear nucleus, raphe magnus

106 rthermore, knockdown of TRPC4 protein in the lateral amygdala via lentiviral-mediated gene delivery o

107 the dominant input to active neurons in the lateral amygdala was from the infralimbic cortex, wherea

108 The medial and lateral amygdala were then inactivated by local muscimol

109 in FOS levels in the medial and basolateral/lateral amygdala when either mPFC subdivision was inacti

110 osynaptic EPSCs evoked by stimulation in the lateral amygdala with EC50 values of 36 nM (control) and

111 microRNAs are endogenously expressed in the lateral amygdala, with 7 microRNAs upregulated and 32 do