ライフサイエンスコーパス: amygdaloid

1 eus, and the magnocellular part of the basal amygdaloid.

2 by combining anterograde labeling of thalamo-amygdaloid afferents with postembedding immunoelectron m

3 usality methods to evaluate task-based intra-amygdaloid and extra-amygdaloid connectivity with the ne

4 mmunoreactive cells were detected in several amygdaloid and hypothalamic nuclei.

5 pothalamic VN target-sites and also in a few amygdaloid and hypothalamic sites outside the traditiona

6 d and sustained expression was noted in most amygdaloid and hypothalamic VN target-sites and also in

7 express neither CRF-R, including the central amygdaloid and paraventricular hypothalamic nuclei, and

8 To determine whether discrete components of amygdaloid and striatal memory systems could interact to

9 tical, olfactory, hippocampal, hypothalamic, amygdaloid and visual structures.

10 nuclei; and in a number of septal, thalamic, amygdaloid, and brainstem nuclei.

11 ntral medial prefrontal cortex and thalamic, amygdaloid, and hippocampal sources.

12 PA and NMDA receptor properties at cortical, amygdaloid, and hippocampal synapses.

13 affected twin had markedly smaller caudate, amygdaloid, and hippocampal volumes, and smaller cerebel

14 the caudal sublenticular region and anterior amygdaloid area (cSLR/AAA) differ from other basal foreb

15 by 70% in the PVN and by 50% in the anterior amygdaloid area, a control region of the brain.

16 ral cortex, hypothalamus, thalamus, cortical amygdaloid area, and white matter tracts did not show an

17 uclei (including anterior cortical, anterior amygdaloid area, periamygdaloid cortex, medial, posterio

18 of the lateral olfactory tract, the anterior amygdaloid area, the posterolateral cortical amygdaloid

19 apsule tracts carried GDNF into the anterior amygdaloid area.

20 ngulate cortex, project to medially situated amygdaloid areas such as the cortical and medial nuclei

21 lar cortex, orbital cortex, and all cortical amygdaloid areas.

22 The amygdaloid basal nuclei (BA) receive convergent input fr

23 is study investigated the involvement of the amygdaloid BDNF system in molecular mechanisms underlyin

24 , and neuropeptide Y (NPY) expression in the amygdaloid brain regions of rats.

25 e ELS demonstrated atypical intra- and extra-amygdaloid CeA-dominant paths with compensatory modulati

26 Furthermore, evidence suggests that the amygdaloid central nucleus (ACe) may influence cardiovas

27 rch sought to determine if activation of the amygdaloid central nucleus (ACe) modulates the activity

28 rostral ventromedial medulla) and forebrain (amygdaloid central nucleus and nucleus parafascicularis

29 These results reveal a novel role for amygdaloid chromatin remodeling in the process of alcoho

30 the amygdalo-hypothalamic projections, intra-amygdaloid circuitry and afferents from the lateral cort

31 essential for controlling the development of amygdaloid circuitry.

32 ey limbic-related cortical/thalamic/striatal/amygdaloid circuits, and the promise of subtle modulatio

33 ange rests on a rather small arcopallial and amygdaloid cluster of neurons.

34 amygdala complex as well as subsequent extra-amygdaloid communication.

35 adult human subjects was used to investigate amygdaloid complex (AC) activity associated with the sto

36 The amygdaloid complex (AC), a key component of the limbic s

37 hypothalamus, the lateral hypothalamus (LH), amygdaloid complex (AD) and thalamus (TH), and to a less

38 ily deactivated sites within the basolateral amygdaloid complex (BLA) or central amygdaloid region (C

39 esent study examined whether the basolateral amygdaloid complex (BLA) participates in the expression

40 Within the basolateral amygdaloid complex (BLA), neuropeptide Y (NPY) buffers a

41 ateral lesions restricted to the basolateral amygdaloid complex (i.e., not including the Ce) did not

42 080411 genotype by sex was found in the left amygdaloid complex (male risk allele carriers showed les

43 e) plus adjacent portions of the basolateral amygdaloid complex (with either the excitotoxin NMDA or

44 cleus 0.36, remaining nuclei 3.33, and total amygdaloid complex 12.21.

45 with bilateral ibotenic acid lesions of the amygdaloid complex and the hippocampus or were sham oper

46 s mediating anxiety responses, including the amygdaloid complex and the paraventricular hypothalamic

47 ta-opioid receptors is also decreased in the amygdaloid complex and ventral putamen of Alzheimer's di

48 Projection neurons of the basolateral (BL) amygdaloid complex are regulated by an intrinsic inhibit

49 n animals implicates stress hormones and the amygdaloid complex as key, interacting modulators of mem

50 f neurons was estimated in the control human amygdaloid complex by using stereological sampling.

51 The intact amygdaloid complex from one hemisphere of 10 brains was

52 hological changes in neuronal density in the amygdaloid complex have been associated with various neu

53 Single-unit activity was recorded from the amygdaloid complex in freely moving rats during an infus

54 as well as the critical contribution of the amygdaloid complex in modulation of memory by emotional

55 The amygdaloid complex is a prominent temporal lobe region t

56 To investigate whether activity in the amygdaloid complex is altered with anxiolytic effects of

57 The rodent amygdaloid complex is composed of numerous subnuclei imp

58 evelopmental profile of ER expression in the amygdaloid complex is not available.

59 The amygdaloid complex is thought to be a major site of acti

60 azabemide to MAO-B was measured in the right amygdaloid complex of 15 major depressive subjects and 1

61 ns by injecting anterograde tracers into the amygdaloid complex of Macaca fascicularis monkeys and ex

62 V1 by injecting anterograde tracers into the amygdaloid complex of Macaca fascicularis monkeys.

63 ine (DA) transporter and D2 receptors in the amygdaloid complex of subjects with major depression ind

64 nd D2/D3 receptors have been observed in the amygdaloid complex of subjects with major depression.

65 The primate amygdaloid complex projects to a number of visual cortic

66 We conclude from these observations that the amygdaloid complex provides an excitatory input to areas

67 The amygdaloid complex represents a group of telencephalic n

68 ing magnetic resonance imaging guidance, the amygdaloid complex was lesioned bilaterally in six rhesu

69 The entire amygdaloid complex was outlined and then further partiti

70 The amygdaloid complex was outlined on coronal sections then

71 x (Brodmann area 11/32) bilaterally, and the amygdaloid complex were affected, but no significant atr

72 tion could be relayed from the cortex to the amygdaloid complex were investigated by using the antero

73 lesions of the hippocampal formation or the amygdaloid complex were tested on concurrent discriminat

74 l, basal, and accessory basal) nuclei of the amygdaloid complex were the source of most connections b

75 SREB2 expression (hippocampal formation and amygdaloid complex).

76 s found in limbic system areas: (1) extended amygdaloid complex, (2) lateral septum, and (3) infralim

77 PH cortices are also interconnected with the amygdaloid complex, although comparatively little is kno

78 The neostriatum, amygdaloid complex, and most hypothalamic areas express

79 Brain areas analyzed were caudate, putamen, amygdaloid complex, hippocampal formation and various ce

80 on of NK(1) receptor immunoreactivity in the amygdaloid complex, induction of NK(1) receptor endocyto

81 he medial temporal polar cortex, most of the amygdaloid complex, most or all of the entorhinal cortex

82 euniens and anterior medial thalamic nuclei, amygdaloid complex, piriform cortex and subfornical orga

83 which include the lateral hypothalamic area, amygdaloid complex, septal-ventral striatal areas, and i

84 the components of the basal ganglia and the amygdaloid complex, the alar and basal hypothalamic regi

85 In the basolateral (BL) amygdaloid complex, the excitability of projection cells

86 shed afferent to the ventral striatum is the amygdaloid complex, which projects throughout the shell

87 f sensory information that occurs within the amygdaloid complex.

88 to the lateral nucleus of the macaque monkey amygdaloid complex.

89 ly involved in feedback inhibition in the BL amygdaloid complex.

90 nerable brain regions of the hippocampus and amygdaloid complex.

91 nd innervate interneurons in the basolateral amygdaloid complex.

92 the bed nucleus of the stria terminalis and amygdaloid complex.

93 gdala (CEm), the major output nucleus of the amygdaloid complex.

94 incides with altered volume and shape of the amygdaloid complex.

95 cleus (Me) is a superficial component of the amygdaloid complex.

96 ods used to define subdivisions of the human amygdaloid complex.

97 btained for the basal ganglia and septal and amygdaloid complexes in amphibians (anamniotic tetrapods

98 een suggested to play a role in cochlear and amygdaloid complexes.

99 The cortical, thalamic, and amygdaloid connections of the rodent temporal cortices w

100 aluate task-based intra-amygdaloid and extra-amygdaloid connectivity with the network underlying impl

101 onal relationships for both intra- and extra-amygdaloid connectivity, while ELS demonstrated atypical

102 orbitofrontal cortex (OFC)-CeA-driven extra-amygdaloid connectivity.

103 The role of amygdaloid corticotropin-releasing factor (CRF) in alcoh

104 Neonatal amygdaloid damage mildly impaired acquisition at the 24-

105 ults provide evidence for the involvement of amygdaloid dopamine in regulating surprise in fear and t

106 In conclusion, these results suggest that amygdaloid dopamine transmission at D2 receptors contrib

107 Modularity analysis identified amygdaloid elements consistent with the main anatomical

108 olved in high-order functions in prefrontal, amygdaloid, entorhinal, and perirhinal cortex, to which

109 he surface of the telencephalic vesicles, an amygdaloid group of cells originated in the caudal pole

110 Acute ethanol exposure decreased amygdaloid HDAC activity and HDAC2 protein levels, incre

111 We measured amygdaloid HDAC activity, levels of HDAC isoforms, and h

112 tudy examined the effects of bilateral intra-amygdaloid infusions of the D2 receptor antagonist, etic

113 investigated the effects of bilateral intra-amygdaloid infusions of the selective D1 receptor antago

114 Animals received intra-amygdaloid injection of kainic acid (KA) to induce seizu

115 , caudal ventral striatal areas that receive amygdaloid inputs also receive significant innervation b

116 he AMPA/NMDA ratio increased at cortical and amygdaloid inputs but not at hippocampal inputs.

117 There are also amygdaloid inputs to CaBP-positive areas outside the she

118 Amygdaloid inputs to the CaBP-poor zone in the lateral a

119 Evidence based on cortical, thalamic, and amygdaloid inputs to the striatum suggests a medio-later

120 nterior insula, which integrates sensory and amygdaloid inputs, projects to the classic ventral stria

121 rea and charted the distribution of specific amygdaloid inputs.

122 ons (< 1%), we focused on cortical and intra-amygdaloid inputs.

123 APDC, were tested on both the development of amygdaloid kindling and on fully developed stage 5 amygd

124 The development of amygdaloid kindling was significantly retarded in 2R,4R-

125 The lateral amygdaloid (LA) nucleus is the main input station of the

126 No amygdaloid labeling was observed.

127 LTP, and genetic modifications that disrupt amygdaloid LTP eliminate fear conditioning.

128 antagonists of the NMDA receptor block both amygdaloid LTP induction and fear conditioning, fear con

129 hypothalamic arcuate and dorsomedial nuclei, amygdaloid medial and centromedial nuclei, thalamic cent

130 uated for 0-90 min in rats receiving central amygdaloid microinjection of RX 77368 (0.1, 0.5 or 1.0 m

131 d the bed n of the stria terminalis), medial amygdaloid n; the thalamus (anteromedial thal. n; reunie

132 reverse the amphetamine-induced increase in amygdaloid neuronal activity and required more than 20 m

133 trates that a small group of arcopallial and amygdaloid neurons constitute a wide range of contralate

134 reduce anxiety and dendritic arborization of amygdaloid neurons of adult male Wistar rats.

135 for glutamate and aspartate to determine if amygdaloid neurons projecting to different targets in th

136 ls of glutamate and aspartate in basolateral amygdaloid neurons projecting to the prefrontal cortex a

137 However, the great majority of amygdaloid neurons with projections to the mediodorsal n

138 ted calcium channels in acutely isolated rat amygdaloid neurons.

139 vation in GC secretion might directly affect amygdaloid neurons.

140 for fear conditioning in rats trained under amygdaloid NMDA receptor blockade.

141 animals suggests that structures within the amygdaloid nuclear complex (ANC) are critical for acquir

142 nal cortex of the inferior colliculis (2.1), amygdaloid nuclei (1.5-2.1), cingulate cortex (1.8), CA1

143 sory olfactory tract, and innervates several amygdaloid nuclei (nucleus of the accessory olfactory tr

144 unts for the amygdala and each of four major amygdaloid nuclei (the lateral, basal, accessory basal,

145 rolateral cortical, and posterior basomedial amygdaloid nuclei and amygdalostriatal transition zone.

146 Anatomically, individual amygdaloid nuclei are connected with many neural systems

147 Individual amygdaloid nuclei have been shown to project to various

148 levation in binding to MAO-B observed in all amygdaloid nuclei in major depressive subjects as compar

149 dala and to assess the separate roles of the amygdaloid nuclei in social behavior in primates.

150 t distinct neural systems involving separate amygdaloid nuclei mediate different types of conditioned

151 but no double labeled cells were seen in the amygdaloid nuclei or the hypothalamic region.

152 sed in the amygdala (lateral and basolateral amygdaloid nuclei) and hippocampal formation (pyramidal

153 reflect the known neurobiology of individual amygdaloid nuclei, allowing for human imaging studies to

154 nterior hypothalamus, the medial and central amygdaloid nuclei, and the lateral septum.

155 nd in cortical regions, central and anterior amygdaloid nuclei, and the olfactory bulb.

156 lexus of Meynert, basolateral and basomedial amygdaloid nuclei, anterior pretectal and interpeduncula

157 presubiculum, parasubiculum, CA1-CA4 fields, amygdaloid nuclei, basal forebrain, thalamus, hypothalam

158 r nucleus, zona incerta, medial and cortical amygdaloid nuclei, cerebellum, nucleus of the solitary t

159 omotor cortices, the limbic system including amygdaloid nuclei, hippocampus and septum, the basal gan

160 of the stria terminalis, medial and cortical amygdaloid nuclei, preoptic area, lateral habenula, peri

161 l formation, presubiculum and parasubiculum, amygdaloid nuclei, thalamic nuclei, locus coeruleus, and

162 agonal band of Broca, the basal and cortical amygdaloid nuclei, the entopeduncular nucleus, the subth

163 These include two amygdaloid nuclei, the horizontal limb of the diagonal b

164 brain regions connected to the BSTL are the amygdaloid nuclei, the paraventricular and ventromedial

165 The activation of amygdaloid nuclei, the ventral perirhinal cortex (vPRh),

166 ells were present in the cortical and medial amygdaloid nuclei, which are known to have strong recipr

167 leus, with little or no innervation of other amygdaloid nuclei.

168 basal forebrain regions, thalamic nuclei and amygdaloid nuclei.

169 serotonergic input, such as hypothalamic and amygdaloid nuclei.

170 e seen in the parabrachial nucleus or in the amygdaloid nuclei.

171 arse labeling in the lateral and basolateral amygdaloid nuclei.

172 nces were found in the medial or basolateral amygdaloid nuclei.

173 The anterior cortical amygdaloid nucleus (ACo) is a chemosensory area of the c

174 tly higher in female rats, and in the medial amygdaloid nucleus (Am), GAD(67) mRNA was higher in male

175 Induction in the central amygdaloid nucleus (CeA) and in the bed nucleus of the s

176 The central amygdaloid nucleus (CeA) is a key limbic structure invol

177 x (PR), and moderate labeling in the lateral amygdaloid nucleus (L).

178 The medial amygdaloid nucleus (Me) is a key nodal point in the neur

179 iform cortex (Pir), posteriolateral cortical amygdaloid nucleus (PLCo), and the amygdalopiriform tran

180 piriform cortex and posterolateral cortical amygdaloid nucleus (PLCo).

181 area of the hypothalamus and also the medial amygdaloid nucleus and CA1 subfield of the hippocampus.

182 l in naked mole-rats include the basolateral amygdaloid nucleus and dentate gyrus, but the septohippo

183 nuclei, hippocampal CA3 region, centromedial amygdaloid nucleus and thalamic paraventricular and reun

184 mporal lobe was associated with the cortical amygdaloid nucleus and the pyramidal cells of the hippoc

185 n neocortex and magnocellular cells in basal amygdaloid nucleus are also intensely CRF(1)-ir.

186 monkeys (orbitofrontal region) or in the BL amygdaloid nucleus in cats.

187 intaining a central role for the basolateral amygdaloid nucleus in the acquisition and storage of thi

188 ing increased c-fos expression in the medial amygdaloid nucleus of both DOM and SUB males as well as

189 striatal area is more related to the central amygdaloid nucleus than to the striatum.

190 ampus and magnocellular cells in basolateral amygdaloid nucleus were also intensely FLNa immunoreacti

191 levels of mRNA of DA receptors in the basal amygdaloid nucleus were measured postmortem in subjects

192 olus vulgaris-leucoagglutinin in the central amygdaloid nucleus were shown to contact cSLR/AAA cholin

193 s-expression by 3.7-times in the basolateral amygdaloid nucleus, 1.2-times in the supraoptic nucleus

194 c area, several hypothalamic nuclei, central amygdaloid nucleus, amygdalohippocampal area, dorsal per

195 followed by moderate labeling of the medial amygdaloid nucleus, amygdalostriatal zone and caudoputam

196 amygdaloid area, the posterolateral cortical amygdaloid nucleus, and the dorsolateral part of the lat

197 al parvocellular part of the basal accessory amygdaloid nucleus, and the magnocellular part of the ba

198 alon: IRP-LI was concentrated in the central amygdaloid nucleus, bed nucleus of stria terminalis and

199 al ventricular ridge, PDVR, and dorsolateral amygdaloid nucleus, DLA) subdivisions.

200 at in Cape mole-rats include the basolateral amygdaloid nucleus, hippocampal CA3 subfield, and dentat

201 specifically, the lateral septum and medial amygdaloid nucleus, indicate greater c-fos mRNA inductio

202 ory tubercle, nucleus accumbens, basolateral amygdaloid nucleus, rostroventrolateral medulla and nucl

203 in the lateral septal nucleus and the medial amygdaloid nucleus, which have numerous Fos-stained nucl

204 is remarkably similar to that of the medial amygdaloid nucleus.

205 ed to be a possible homologue of the central amygdaloid nucleus.

206 is theorized to be homologous to the medial amygdaloid nucleus.

207 ield CA1 and mainly targeted the basolateral amygdaloid nucleus.

208 us, and the dorsolateral part of the lateral amygdaloid nucleus.

209 GABAergic, and project to the medial CEA (an amygdaloid output region), this may be a novel mechanism

210 chanism whereby conditioned fear potentiates amygdaloid output.

211 brachial area (part of the spino-parabrachio-amygdaloid pain pathway) in brain slices from control ra

212 monstrated narrowly defined BLA-driven intra-amygdaloid paths and concise orbitofrontal cortex (OFC)-

213 and robust CeA-facilitated intra- and extra-amygdaloid paths.

214 e pathway, the spino-(trigemino)-parabrachio-amygdaloid pathway, was performed using an alpha-herpes

215 The fear component is regulated by amygdaloid pathways, while the contextual component is,

216 Amygdaloid projections from the posterior insular cortex

217 Cortical, thalamic, and amygdaloid projections of the rat anterior and posterior

218 Amygdaloid projections targeted the ventromedial subdivi

219 We examined the organization of amygdaloid projections to visual cortical areas TE and V

220 Interestingly, only arcopallial and amygdaloid projections were reciprocally organized, and

221 olateral amygdaloid complex (BLA) or central amygdaloid region (CeA) via GABA(A) agonist (muscimol) i

222 higher FLI than the tested groups in all the amygdaloid regions and in the hypothalamic paraventricul

223 ntal motor cortex, hippocampus, thalamus and amygdaloid) regions based on their relevance to ASD.

224 artially overlapping brain mechanisms (i.e., amygdaloid-reticular projections) mediate these effects.

225 as higher in 6ByJ relative to 6J mice in the amygdaloid ridge, hypothalamus, and midbrain.

226 CI, Pandey and colleagues identify a central amygdaloid signaling pathway involved in anxiety-like an

227 t is expressed in the majority of in thalamo-amygdaloid spines and that within these spines, the vari

228 he prevalence of the NR2B subunit in thalamo-amygdaloid spines provides morphological evidence suppor

229 A high percentage of thalamo-amygdaloid spines was immunoreactive for GluR2 (80%), Gl

230 ratios of GluRs were measured within thalamo-amygdaloid spines.

231 lamic 'attack' site in the absence of medial amygdaloid stimulation suppressed predatory attack, thus

232 ttack, thus simulating the effects of medial amygdaloid stimulation.

233 in anxiety levels or on CREB function in the amygdaloid structures of NP rats.

234 Among the nonchemosensory amygdaloid structures, the PDVR receives afferents from

235 define a unique set of molecular markers for amygdaloid subnuclei and provide tools to genetically di

236 ields, dysfunctional pulvinar, claustrum and amygdaloid subnuclei of the amygdala, the latter progres

237 ellular and neurochemical composition of the amygdaloid subnuclei suggests their clustering into subu

238 pes of DA receptor mRNA were detected in all amygdaloid subnuclei, although D1, D2, and D4 receptor m

239 ivate) or bicuculline (to activate) to these amygdaloid subregions.

240 ovide support for the hypothesis that medial amygdaloid suppression of lateral hypothalamically elici

241 second limb of the pathway subserving medial amygdaloid suppression of predatory attack behavior proj

242 Drug infusion produced a blockade of medial amygdaloid suppression of predatory attack in a time- an

243 sent study tested the hypothesis that medial amygdaloid suppression of predatory attack is mediated,

244 ning, fear conditioning induces increases in amygdaloid synaptic transmission that resemble LTP, and

245 d anxiolysis was measured in adult rats, and amygdaloid tissues were used for miRNA profiling by micr