ライフサイエンスコーパス: central nucleus of the amygdala

1 have developed a model to disrupt GR in the central nucleus of the amygdala.

2 projects back to the anterior BLA and to the central nucleus of the amygdala.

3 ) electrophysiological responsiveness in the central nucleus of the amygdala.

4 s in several brain sites such as the PVH and central nucleus of the amygdala.

5 rentially activated by administration in the central nucleus of the amygdala.

6 ial border of the lateral subdivision of the central nucleus of the amygdala.

7 R) neurons in the lateral subdivision of the central nucleus of the amygdala.

8 al (CeL) or medial (CeM) subdivisions of the central nucleus of the amygdala.

9 icular nucleus but lower basal levels in the central nucleus of the amygdala.

10 both CRF and glucocorticoid receptors in the central nucleus of the amygdala.

11 leus of the stria terminalis (BNST), and the central nucleus of the amygdala.

12 eus, bed nucleus of the stria terminalis and central nucleus of the amygdala.

13 nistration, reduced CRF immunodensity in the central nucleus of the amygdala.

14 d GR mRNA in the NAc core, ventral BNST, and central nucleus of the amygdala.

15 val-related afferent input was absent in the central nucleus of the amygdala.

16 frontal cortex, basolateral amygdala, or the central nucleus of the amygdala.

17 shows particularly robust expression in the central nucleus of the amygdala.

18 , nucleus accumbens, olfactory tubercle, and central nucleus of the amygdala.

19 striatum, and reduced Dlx5 expression in the central nucleus of the amygdala.

20 icotropin-releasing factor (CRF) mRNA in the central nucleus of the amygdala, a critical node in the

21 delivery and direct administration into the central nucleus of the amygdala, a critical stress-relat

22 These included central nucleus of the amygdala (ACe) and bed nucleus of

23 Whether damage to the central nucleus of the amygdala (Ace) contributes to the

24 esigned to determine the extent to which the central nucleus of the amygdala (ACe) contributes to thi

25 The hypothesis that the central nucleus of the amygdala (ACe) is an essential pa

26 og, 5 microg, and 10 microg) into either the central nucleus of the amygdala (ACe) or nucleus parafas

27 om the caudate-putamen (CPu) and 23 from the central nucleus of the amygdala (ACE).

28 s [that received electrolytic lesions of the central nucleus of the amygdala (ACe)] and control anima

29 Electrical stimulation of the central nucleus of the amygdala also modulated the respo

30 Electrical stimulation of the central nucleus of the amygdala altered the basal firing

31 and PVN, and/or CRF mRNA in the PVN and the central nucleus of the amygdala (AMY).

32 , a significant proportion of neurons in the central nucleus of the amygdala and in the hippocampal C

33 , and elevated c-Fos or Zif268 expression in central nucleus of the amygdala and medial paracapsular

34 e, MK-801 increased FLI in cingulate cortex, central nucleus of the amygdala and nucleus accumbens (N

35 , cortical pyramidal neurons, neurons of the central nucleus of the amygdala and parvocellular neuron

36 FosB expression was elevated in the central nucleus of the amygdala and spinal cord dorsal h

37 Elevated activity in the central nucleus of the amygdala and the anterior hippoca

38 expression in the parabrachial nucleus, the central nucleus of the amygdala and the basolateral amyg

39 results implicate Barrington's nucleus, the central nucleus of the amygdala and the bed nucleus of t

40 mediated by different brain structures, the central nucleus of the amygdala and the bed nucleus of t

41 everal other regions surveyed, including the central nucleus of the amygdala and the dorsal striatum.

42 ical and functional relationship between the central nucleus of the amygdala and the dorsal vagal com

43 The central nucleus of the amygdala and the supraoptic nucle

44 lary and pontine neurons that project to the central nucleus of the amygdala and to the lateral bed n

45 ebrain regions including olfactory tubercle, central nucleus of the amygdala, and bed nucleus of the

46 s of the stria terminalis, ventral pallidum, central nucleus of the amygdala, and cingulate cortex.

47 ary-adrenal axis, CRF mRNA expression in the central nucleus of the amygdala, and CRF(1) mRNA express

48 in the piriform cortex, supraoptic nucleus, central nucleus of the amygdala, and nucleus of the soli

49 ral and paraventricular hypothalamic nuclei, central nucleus of the amygdala, and periaqueductal gray

50 the basolateral nucleus of the amygdala, the central nucleus of the amygdala, and the bed nucleus of

51 tures, especially in the lateral part of the central nucleus of the amygdala, and the CA1 region of t

52 the bed nucleus of the stria terminalis, the central nucleus of the amygdala, and the parvocellular d

53 aventricular nucleus of the hypothalamus and central nucleus of the amygdala, and this was inhibited

54 medial prefrontal cortex, nucleus accumbens, central nucleus of the amygdala, and ventral tegmental a

55 roject to the laterocapsular division of the central nucleus of the amygdala as forming a functionall

56 of the hypothalamus and, importantly, in the central nucleus of the amygdala, as measured by solid ph

57 following KA and in the piriform cortex, and central nucleus of the amygdala at 120 min after KA.

58 hat lacked BDNF mRNA (e.g., medial habenula, central nucleus of the amygdala, bed nucleus of stria te

59 cumbens core, dorsomedial prefrontal cortex, central nucleus of the amygdala, bed nucleus of stria te

60 tems in the extended amygdala, including the central nucleus of the amygdala, bed nucleus of the stri

61 tion of c-fos expression in the hippocampus, central nucleus of the amygdala, bed nucleus of the stri

62 he paraventricular nucleus, arcuate nucleus, central nucleus of the amygdala, bed nucleus of the stri

63 tems in the extended amygdala, including the central nucleus of the amygdala, bed nucleus of the stri

64 At the cellular level, in the central nucleus of the amygdala, beta-gal was found in c

65 Infusions into the central nucleus of the amygdala blocked fear-potentiated

66 the medial zona incerta (MZI) project to the central nucleus of the amygdala (cAMY), horizontal diago

67 locus coeruleus (LC) and an increase in the central nucleus of the amygdala (CAMY), supporting a ton

68 nucleus of the hypothalamus (PVN) and in the central nucleus of the amygdala (cAMY).

69 ed tonic oxytocin receptor expression in the central nucleus of the amygdala (cAmyg) through activati

70 optic area (MPO), lateral hypothalamus (LH), central nucleus of the amygdala (Ce) and bed nucleus of

71 reflect dissociable circuits centered on the central nucleus of the amygdala (Ce) and the bed nucleus

72 onents of the central extended amygdala, the central nucleus of the amygdala (Ce) and the lateral bed

73 Studies have identified the central nucleus of the amygdala (Ce) as an essential com

74 ies of AT in young monkeys revealed that the central nucleus of the amygdala (Ce) is a key environmen

75 o imaging in young monkeys demonstrated that central nucleus of the amygdala (Ce) metabolism is relat

76 Unilateral inactivation of the central nucleus of the amygdala (Ce) plus adjacent porti

77 Microinjection of PRV into the central nucleus of the amygdala (Ce) resulted in progres

78 Low levels of c-Fos expression in the central nucleus of the amygdala (CE) were observed throu

79 ntricular nucleus of the hypothalamus (PVN), central nucleus of the amygdala (Ce), periaqueductal gra

80 IL has prominent projections to the central nucleus of the amygdala (Ce), the mediodorsal nu

81 expression, the LA is thought to engage the central nucleus of the amygdala (CE), which serves as th

82 CRH mRNA levels were observed in the PVN and central nucleus of the amygdala (ceA) 4-6 hr after SEB a

83 ticotropin-releasing factor (CRF) within the central nucleus of the amygdala (CeA) and bed nucleus of

84 The central nucleus of the amygdala (CeA) and its connection

85 , and the preoptic area (POA) as well as the central nucleus of the amygdala (CeA) and nucleus of the

86 In the central nucleus of the amygdala (CEA) and oval subnucleu

87 n-releasing hormone (CRH) are located in the central nucleus of the amygdala (CeA) and paraventricula

88 norepinephrine (NE) transmission within the central nucleus of the amygdala (CeA) and the bed nucleu

89 n (r/h)] and Urocortin I (Ucn I), within the central nucleus of the amygdala (CeA) and the lateral se

90 The central nucleus of the amygdala (CeA) and the nucleus of

91 -aspartate (NMDA) receptor antagonism in the central nucleus of the amygdala (CeA) and the posterior

92 kappa-opioid receptor (KOR) signaling in the central nucleus of the amygdala (CeA) and these neuroada

93 (MCP-1) that colocalize in neurons from the central nucleus of the amygdala (CeA) and ventral tegmen

94 the solitary tract (NTS)/area postrema (AP), central nucleus of the amygdala (CeA) and, to a smaller

95 cognitive function and overactivation of the central nucleus of the amygdala (CeA) are key factors th

96 C), lateral parabrachial nucleus (lPBN), and central nucleus of the amygdala (CeA) as potential sites

97 ype II glucocorticoid receptors (GRs) in the central nucleus of the amygdala (CeA) by delivering lent

98 tral periventricular nucleus (AVPe), and the central nucleus of the amygdala (CeA) contained few LepR

99 no-5-phosphonovalerate (APV) into the BLA or central nucleus of the amygdala (CEA) during fear condit

100 The central nucleus of the amygdala (CeA) has a critical rol

101 The central nucleus of the amygdala (CeA) has been identifie

102 The central nucleus of the amygdala (CeA) has been implicate

103 The central nucleus of the amygdala (CeA) has been shown to

104 The central nucleus of the amygdala (CeA) has been tradition

105 The central nucleus of the amygdala (CeA) helps translate le

106 antly increased EGR-1 mRNA expression in the central nucleus of the amygdala (CeA) in a dose-dependen

107 ristics of visceral afferent pathways to the central nucleus of the amygdala (CeA) in brainstem slice

108 To examine the role of the central nucleus of the amygdala (CeA) in mediating the b

109 enes in the prefrontal cortex area (PFC) and central nucleus of the amygdala (CeA) in monkeys.

110 amma-aminobutyric acid (GABA) release in the central nucleus of the amygdala (CeA) in Nf1 heterozygou

111 iated with the recruitment of neurons in the central nucleus of the amygdala (CeA) in nondependent ra

112 ctic response to insulin injections into the central nucleus of the amygdala (CeA) in these animals.

113 Lesion studies have implicated the central nucleus of the amygdala (CeA) in this process, p

114 tion-induced bladder pain, we found that the central nucleus of the amygdala (CeA) is a critical site

115 The central nucleus of the amygdala (CeA) is an important in

116 -9, extracellularly operating enzyme) in the central nucleus of the amygdala (CeA) is crucial for app

117 ases in ethanol intake, CRF signaling in the central nucleus of the amygdala (CeA) is engaged during

118 The central nucleus of the amygdala (CEA) is required for th

119 The central nucleus of the amygdala (CeA) mediates several a

120 The central nucleus of the amygdala (CeA) mediates stress- a

121 We hypothesized that the central nucleus of the amygdala (CeA) mediates this vari

122 a2 siRNA vector (pHSVsiLA2) infused into the central nucleus of the amygdala (CeA) of alcohol-preferr

123 The CRF neurons in the central nucleus of the amygdala (CeA) of P rats and HAD

124 C) receptors within the basolateral (BLA) or central nucleus of the amygdala (CeA) on acute fear-like

125 (CGRP; p<0.05, one tailed) processes in the central nucleus of the amygdala (CeA) on PND 198.

126 The central nucleus of the amygdala (CeA) plays a critical r

127 The GABAergic system in the central nucleus of the amygdala (CeA) plays an important

128 Neurones in the central nucleus of the amygdala (CeA) projecting to the

129 t a newly identified GABA circuit within the central nucleus of the amygdala (CeA) promotes cataplexy

130 Because GABAergic neurons of the central nucleus of the amygdala (CeA) target brainstem r

131 ulation of locally projecting neurons in the central nucleus of the amygdala (CeA) that produce the n

132 high glucocorticoid levels may act upon the central nucleus of the amygdala (CeA) to alter normally

133 al recordings of GABAA-mediated IPSPs in the central nucleus of the amygdala (CeA) to explore functio

134 dy, we retrogradely transported dye from the central nucleus of the amygdala (CeA) to identify CeA-pr

135 minobutyric acid (GABA)ergic fibers from the central nucleus of the amygdala (CeA) to the BNST.

136 ar nucleus of the hypothalamus (PVN) and the central nucleus of the amygdala (CeA) was observed durin

137 e CB(1) receptor mRNA and the protein in the central nucleus of the amygdala (CeA) were also investig

138 f [9-41]-alpha-helical CRH into the adjacent central nucleus of the amygdala (CEA) were ineffective,

139 e course of Fox expression in neurons in the central nucleus of the amygdala (CeA) were studied in en

140 This study focuses on the central nucleus of the amygdala (CeA), a brain region th

141 iating the anorexia produced by PACAP in the central nucleus of the amygdala (CeA), a limbic structur

142 In the central nucleus of the amygdala (CeA), a rostrocaudal gr

143 ABAergic synaptic activity in neurons of the central nucleus of the amygdala (CeA), an important brai

144 hanol drinking reduced NPY and Y1R IR in the central nucleus of the amygdala (CeA), and 24 h of ethan

145 bed nucleus of the stria terminalis (BNST), central nucleus of the amygdala (CeA), and lateral hypot

146 bed nucleus of the stria terminalis (BNST), central nucleus of the amygdala (CeA), and lateral hypot

147 hypothalamic paraventricular nucleus (PVN), central nucleus of the amygdala (CeA), and nucleus of th

148 s Fos-like immunoreactivity (FLI) within the central nucleus of the amygdala (CeA), bed nucleus of th

149 ns containing the lateral hypothalamus (LH), central nucleus of the amygdala (CeA), bed nucleus of th

150 been relatively unexplored compared with the central nucleus of the amygdala (CeA), despite the fact

151 he brain sites within the extended amygdala [central nucleus of the amygdala (CeA), lateral bed nucle

152 o the bed nucleus of stria terminalis (BST), central nucleus of the amygdala (CEA), paraventricular n

153 nspecific antagonists, administered into the central nucleus of the amygdala (CeA), selectively decre

154 gonist R121919 (0, 0.5, 1.5 mug/side) in the central nucleus of the amygdala (CeA), the basolateral n

155 ar nucleus of the hypothalamus (PVN) and the central nucleus of the amygdala (CEA), through complex m

156 n-releasing factor (CRF) is expressed in the central nucleus of the amygdala (CeA), where the CRF rec

157 In this study of the central nucleus of the amygdala (CeA), which is critical

158 neurones in the latero-capsular part of the central nucleus of the amygdala (CeA), which is now defi

159 IP3K-A expression is highly enriched in the central nucleus of the amygdala (CeA), which plays a piv

160 basolateral amygdala (BLA) terminals in the central nucleus of the amygdala (CeA)--achieved by viral

161 tide (CGRP) projections from the lPBN to the central nucleus of the amygdala (CeA).

162 A potential DYN/CRF afferent is the central nucleus of the amygdala (CeA).

163 into a variety of brain sites including the central nucleus of the amygdala (CeA).

164 l voltage-clamp recordings of neurons in the central nucleus of the amygdala (CeA).

165 f GLP-1 to induce visceral illness is in the central nucleus of the amygdala (CeA).

166 Alcohol dependence recruits neurons in the central nucleus of the amygdala (CeA).

167 pin-releasing factor (CRF) mRNA level in the central nucleus of the amygdala (CeA).

168 lamic (LHA) areas; and the extrahypothalamic central nucleus of the amygdala (CeA).

169 9)-PKCepsilon levels in both the NAc and the central nucleus of the amygdala (CeA).

170 sion mediated via GABAA receptors in the rat central nucleus of the amygdala (CeA).

171 s and certain signaling molecules within the central nucleus of the amygdala (CeA).

172 increasing histone H4 acetylation in the rat central nucleus of the amygdala (CeA).

173 ute stress increases glutamate efflux in the central nucleus of the amygdala (CeA).

174 by overexpression of exogenous MMP-9 in the central nucleus of the amygdala (CeA).

175 ctive activation of GABAergic neurons in the central nucleus of the amygdala (CeA).

176 ide (LiCl) increases c-Fos expression in the central nucleus of the amygdala (CeA).

177 15%), lateral hypothalamic area (LHA, 25%), central nucleus of the amygdala (CeA, 77%), sublenticula

178 dorsal hippocampus (CA1 pyramidal layer) and central nucleus of the amygdala (CeA; Experiment 3).

179 erally augments nociceptive amygdala (in the central nucleus of the amygdala [CeA]) PACAP immunoreact

180 The lateral central nucleus of the amygdala (CeAL) and the dorsolate

181 The lateral division of the central nucleus of the amygdala (CEAl) and the oval nucl

182 rons of the lateral/capsular division of the central nucleus of the amygdala (CEAl/c) and oval divisi

183 ticity in the laterocapsular division of the central nucleus of the amygdala (CeLC) generates emotion

184 ticity in the laterocapsular division of the central nucleus of the amygdala (CeLC) in brain slices f

185 eurons in the laterocapsular division of the central nucleus of the amygdala (CeLC).

186 C), the medial posteroventral portion of the central nucleus of the amygdala (CeMPV), and the Edinger

187 entral extended amygdala [CEA; including the central nucleus of the amygdala (CN), ventral bed nucleu

188 nd LY34 into the basal amygdala (BA) and the central nucleus of the amygdala (CNA) and recorded sleep

189 The central nucleus of the amygdala (CNA) and the nucleus of

190 ar nucleus of the hypothalamus (PVN) and the central nucleus of the amygdala (CNA) are two forebrain

191 s neurons and tracts, microinjected into the central nucleus of the amygdala (CNA) during the light p

192 nucleus paragigantocellularis (PGi) and the central nucleus of the amygdala (CNA) in rat brain.

193 cFos-IR in the central nucleus of the amygdala (CNA) increased in respo

194 The central nucleus of the amygdala (CNA) is a component of

195 e implanted with bilateral cannulas into the central nucleus of the amygdala (CNA) or control area an

196 o in the parabrachial nucleus (PBN), and the central nucleus of the amygdala (CNA), regions thought t

197 rce of ENK and CRF in the dorsal pons is the central nucleus of the amygdala (CNA).

198 expression of c-Fos immunoreactivity in the central nucleus of the amygdala (CNA).

199 ly labeled CRF-immunoreactive neurons in the central nucleus of the amygdala colocalized glucocortico

200 Post-training lesions of the central nucleus of the amygdala completely blocked both

201 ing the bed nucleus of the stria terminalis, central nucleus of the amygdala, diagonal band of Broca,

202 f these beta-adrenergic antagonists into the central nucleus of the amygdala did not block the dexame

203 ess adult neurogenesis, while lesions of the central nucleus of the amygdala do not.

204 Electrical stimulation of the central nucleus of the amygdala during REM sleep increas

205 nd rats with BLA lesions, and imply that the central nucleus of the amygdala encodes CS-US associatio

206 n in the basolateral region of the amygdala, central nucleus of the amygdala, gustatory portion of th

207 cotropin-releasing factor infusions into the central nucleus of the amygdala had no effect when given

208 mice, we found that GABAergic neurons in the central nucleus of the amygdala heavily innervate neuron

209 in-releasing hormone (Crh) expression in the central nucleus of the amygdala in anhedonic rats, and t

210 Here, we reveal a critical role for the central nucleus of the amygdala in predatory hunting.

211 The roles of the dorsal hippocampus and the central nucleus of the amygdala in the expression of con

212 labeling in the nucleus accumbens shore and central nucleus of the amygdala, independent of the adre

213 These results suggest that the central nucleus of the amygdala influences gut-related n

214 training and pretesting experiments with the central nucleus of the amygdala infusions.

215 ncreased significantly Fos expression in the central nucleus of the amygdala (lateral part), parabrac

216 in a number of anxiety-related brain areas (central nucleus of the amygdala, locus ceruleus, ventrol

217 ly reported that electrolytic lesions of the central nucleus of the amygdala, made 6 or 30 days after

218 recent studies suggesting that PACAP in the central nucleus of the amygdala may impact the emotional

219 plasticity within other brain regions (i.e., central nucleus of the amygdala) may be crucial for fear

220 circuit from the parabrachial nucleus to the central nucleus of the amygdala mediates appetite suppre

221 noreactivity in the paraventricular nucleus, central nucleus of the amygdala, nucleus of the solitary

222 Higher binding in the central nucleus of the amygdala of C. sociabilis was con

223 as corticotropin-releasing factor neurons in central nucleus of the amygdala or bed nucleus of the st

224 the hypothalamic paraventricular nucleus and central nucleus of the amygdala, OX, and another orexige

225 rtices, bed nucleus of the stria terminalis, central nucleus of the amygdala, periaqueductal gray, la

226 istration and that neuronal ensembles in the central nucleus of the amygdala play a critical role in

227 bed nucleus of the stria terminalis, and the central nucleus of the amygdala, prairie voles had highe

228 e tract-tracing techniques revealed that the central nucleus of the amygdala projects to the dorsal v

229 ot control short hairpin RNA, given into the central nucleus of the amygdala reversed CES-induced anh

230 eus, ventrolateral periaqueductal gray area, central nucleus of the amygdala, sublenticular extended

231 ctivation of these neurons projecting to the central nucleus of the amygdala suppresses appetite.

232 The LV system comprises the neurons in the central nucleus of the amygdala that excite DA cells.

233 t underlies early-life anxiety including the central nucleus of the amygdala, the anterior hippocampu

234 the bed nucleus of the stria terminalis, the central nucleus of the amygdala, the anteroventral, ante

235 dorsomedial nuclei of the hypothalamus, the central nucleus of the amygdala, the oval nucleus of the

236 r cell counts of CRH containing cells in the central nucleus of the amygdala to be lower in 24-month-

237 We identify an inhibitory pathway from the central nucleus of the amygdala to the ventrolateral per

238 bed nucleus of the stria terminalis, and the central nucleus of the amygdala, together referred to as

239 play activated Crh-expressing neurons in the central nucleus of the amygdala, typically involved in a

240 of acetylcholine (ACh) were measured in the central nucleus of the amygdala using microdialysis in 2

241 ing hormone (TRH) analog, RX 77368, into the central nucleus of the amygdala was examined in fasted,

242 ntration of [(3)H]DAMGO binding sites in the central nucleus of the amygdala was very low, the concen

243 omplex, retrogradely labelled neurons in the central nucleus of the amygdala were clustered in the ce

244 Significant changes in Fos expression in the central nucleus of the amygdala were not observed at any

245 Indeed, the central nucleus of the amygdala, which is essential for

246 ala, we combined retrograde tracing from the central nucleus of the amygdala with immunohistochemistr