ライフサイエンスコーパス: insular cortex

1 he pial surface to form layers (2-6a) of the insular cortex.

2 th low-fat meals on the hypothalamus and the insular cortex.

3 y portion of the thalamus, and the gustatory insular cortex.

4 me reduction in orbitofrontal, cingulate and insular cortex.

5 and conditioned taste aversion memory in the insular cortex.

6 by brain mechanisms that do not require the insular cortex.

7 ilar finding involving NMDA receptors in the insular cortex.

8 but also in auditory, visual, entorhinal and insular cortex.

9 cleus of the stria terminalis but not in the insular cortex.

10 lateral hypothalamus, central amygdala, and insular cortex.

11 lose to the external capsule and deep in the insular cortex.

12 e thalamus, second somatosensory cortex, and insular cortex.

13 reactivity (FLI) in the central amygdala and insular cortex.

14 ut decreased NGF and BDNF mRNA levels in the insular cortex.

15 stributions of neurons in the prefrontal and insular cortex.

16 to restore hunger-like response patterns in insular cortex.

17 tatory responses to stimulation of the human insular cortex.

18 ion and lysine acetyltransferase activity in insular cortex.

19 ctivities along with the ERK/MAPK cascade in insular cortex.

20 rgets of the gustatory system, including the insular cortex.

21 he anterior extreme capsule white matter and insular cortex.

22 e amygdala arise in the dysgranular parietal insular cortex.

23 rojected heavily to the dysgranular anterior insular cortex.

24 cerebellar hemisphere to activity in Sylvian-insular cortex.

25 led dendrite-like processes in the agranular insular cortex.

26 y covered by the Nr4a2-negative cells of the insular cortex.

27 ecting that of long-term potentiation in the insular cortex.

28 ng signal (prediction error) in the anterior insular cortex.

29 ns, like the putamen with connections to the insular cortex.

30 rs the signature of autonomic arousal in the insular cortex.

31 taste memory and AMPA receptor expression in insular cortex.

32 he parabrachial nucleus, and projects to the insular cortex.

33 , subgenual anterior cingulate, and anterior insular cortex.

34 NMDAR-dependent CaMKII- AMPAR pathway in the insular cortex.

35 he lateral pallium at the site of the future insular cortex.

36 gating of cardiac-related information in the insular cortex.

37 mapping of vestibular responses in the human insular cortex.

38 ecially within adjacent posterior regions of insular cortex.

39 not AM251, infusions into the interoceptive insular cortex (a region known to be activated in acute

40 We hypothesized that the right mid-insular cortex, a central recipient of viscerosensory in

41 tivated protein kinase (MAPK)/RSK cascade in insular cortex, a CNS region known to be crucial for the

42 ral and functional abnormalities in the left insular cortex, a region also implicated in individuals

43 d 10% to 15% of the variance in amygdala and insular cortex activation to emotional faces.

44 ls related to subclinical anxiety levels and insular cortex activation.

45 ctivation in both regions; however, only the insular cortex activations are significantly associated

46 l regions in rats, the agranular/dysgranular insular cortex (AIC) and the ventromedial prefrontal cor

47 foundation for a role of the human anterior insular cortex (AIC) in emotional awareness, defined as

48 Consistent with an anterior insular cortex (AIC) involvement in storing taste memori

49 The right anterior insular cortex (AIC) was identified as the principal are

50 l-dependent (BOLD) responses in the anterior insular cortex (AIC), a core hub of the "salience networ

51 d to be expressed across the olfactory bulb, insular cortex, amygdala, and dorsal hippocampus.

52 ronal ensembles in the orbitofrontal cortex, insular cortex, amygdala, and nucleus accumbens while ra

53 ial temporal lobe, with values of 1.6 in the insular cortex and 0.7-1.0 in other cortical regions.

54 order) and with increased limbic activation (insular cortex and amygdala) during emotion processing (

55 D2 receptor binding in the salience network (insular cortex and anterior cingulate cortex [ACC] and t

56 on group exhibited regional CBF increases in insular cortex and anterior cingulate gyrus; increases i

57 erior temporal area extending to include the insular cortex and basal ganglia, lateralizing to the si

58 ness of Ce output neurons to inputs from the insular cortex and BLA.

59 body and to the modulation of pain (anterior insular cortex and brainstem, respectively) determines w

60 assessed high-signal-intensity areas in the insular cortex and extreme capsule on coronal MR images

61 rCBF in the vicinity of the hypothalamus and insular cortex and in additional paralimbic and limbic a

62 ontrol was associated with reduced volume in insular cortex and increased volume of caudate nucleus.

63 resentation has been demonstrated within the insular cortex and lateralization has been previously in

64 insula is an interface between the posterior insular cortex and motor cortex and is connected with mo

65 ack of layer IV, was defined as the temporal insular cortex and named as area TI after Beck.

66 ing of the multiple sensory functions of the insular cortex and of the cortical processing of vestibu

67 , caudate nucleus, anterior cingulate gyrus, insular cortex and orbitofrontal cortex).

68 labeling of the subjacent agranular parietal insular cortex and strong labeling of fibers and termina

69 lation of neurons in this structure, and the insular cortex and the basolateral amygdala (BLA) intera

70 ersus neutral stimuli were found in the left insular cortex and the left anterior cingulate.

71 re distributed most densely in the agranular insular cortex and the paraventricular nuclei of the tha

72 thalamus, as well as metabolic decreases in insular cortex and the periaqueductal gray, were noted.

73 e posterior insula, that is, in the granular insular cortex and the postcentral insular gyrus.

74 ocentric paralimbic regions of interest, the insular cortex and the temporal pole, were evaluated.

75 s, such as the primary somatosensory cortex, insular cortex, and ACC.

76 lateral hypothalamus, orbitofrontal cortex, insular cortex, and amygdala of hungry rats that volunta

77 ivated sites within the medial frontal lobe, insular cortex, and cerebellum distinct from, but close

78 er volume in medial prefrontal cortex (PFC), insular cortex, and subgenual anterior cingulate regions

79 ial prefrontal cortices, anterior cingulate, insular cortex, and superior temporal gyrus.

80 ate, the dorsolateral prefrontal cortex, the insular cortex, and the nucleus accumbens.

81 btained in patients with MDD in the anterior insular cortex, anterior and posterior thalamus, ventral

82 Amygdaloid projections from the posterior insular cortex appear to be organized in a feedforward p

83 hes, including viral vector transfections of insular cortex, arc fluorescence in situ hybridization (

84 e ventromedial prefrontal cortex (vmPFC) and insular cortex are implicated in distributed neural circ

85 s to determine whether NMDA receptors in the insular cortex are involved in this experience-dependent

86 ns supports the conclusion that amygdala and insular cortex are necessary, but not sufficient, for th

87 eural activity in the visual, cerebellar and insular cortex areas compared with a resting condition.

88 , anterior temporal, anterior cingulate, and insular cortex, as well as caudate, lenticulate, and amy

89 served decreased binding specifically in the insular cortex bilaterally.

90 the posterolateral orbitofrontal cortex and insular cortex bilaterally.

91 Electrolytic lesions of insular cortex blocked behavioral expression of a condit

92 ld expressions of disgust activated anterior insular cortex but not the amygdala; strong disgust also

93 evate FLI expression in central amygdala and insular cortex, but also failed to induce stronger taste

94 his pattern was seen in central amygdala and insular cortex, but not in basolateral amygdala, parabra

95 ain areas, the anterior cingulate cortex and insular cortex, but not in the spinal cord.

96 beling of the subjacent dysgranular parietal insular cortex, but only sparse labeling in the basolate

97 covery of von Economo neurons within macaque insular cortex by Evrard et al. described in this issue

98 Damage to the insular cortex can profoundly disrupt tobacco addiction

99 th posterior parietal areas 7a, 7ip, and 7b, insular cortex, caudal superior temporal sulcus (STS), c

100 The insular cortex cells, which are born later and which are

101 atosensory representation in caudal granular insular cortex (CGIC) in the rat, either before or after

102 satiety-related visceral signals converge in insular cortex, chemogenetic activation of hypothalamic

103 ding dorsolateral prefrontal cortex (dlPFC), insular cortex, cingular cortex, and the basal ganglia d

104 signated histogenetic unit gives rise to the insular cortex/claustrum and should therefore be conside

105 ing seven clusters across frontoparietal and insular cortex comparable to human MD regions and one un

106 esponses to disgusted faces in the bilateral insular cortex compared with healthy controls.

107 The insular cortex contains a site of cardiovascular represe

108 ed by anterograde tracer injections into the insular cortex, corticothalamic projections in the VPMpc

109 unctionally dissociable effects of vmPFC and insular cortex damage.

110 um, consistent with classical definitions of insular cortex dating back to Rose.

111 s that this is dissociable from the adjacent insular cortex-dependent taste aversion memory.

112 essing, they make evident that the region of insular cortex destroyed is not necessary for the normal

113 ene blue increased response in the bilateral insular cortex during a psychomotor vigilance task (Z =

114 regions within the human frontal cortex and insular cortex during food desirability choices, combine

115 alamic activity and the interaction with the insular cortex elicited by fat may contribute to an effi

116 odel of awareness proposes that the anterior insular cortex engenders feelings that provide an amodal

117 propose that inflammation restricted to the insular cortex enhances associative taste memory through

118 cortex in auditory processing, with the left insular cortex especially responsive to linguistic stimu

119 terior dorsal insula, such that a portion of insular cortex forms an isolated pocket medial to the Sy

120 rminals in granular and dysgranular parietal insular cortex from bregma to 3.8 mm behind bregma but o

121 g approaches to delineate the likely area of insular cortex given to gustatory function and to charac

122 A bilateral volume reduction in insular cortex gray matter was specific to first-episode

123 The insular cortex has been implicated as a region of cortic

124 g were placed in caudal granular/dysgranular insular cortex (IC) alone or in conjunction with the pos

125 The anterior insular cortex (IC) and the nucleus accumbens (NAc) core

126 Lesions of the insular cortex (IC) attenuate acquisition of conditioned

127 Insular cortex (IC) contributes to a variety of complex

128 l amygdala (BLA) and the gustatory region of insular cortex (IC) have been implicated in these proces

129 e present study investigated the role of the insular cortex (IC) in morphine-induced conditioned tast

130 Insular cortex (IC) is recognized as a potential site fo

131 We examined the influence of insular cortex (IC) lesions on morphine-induced suppress

132 present experiment examined the influence of insular cortex (IC) lesions on the intake of a taste sti

133 the influence of excitotoxic lesions of the insular cortex (IC) on taste-potentiated odor aversion (

134 strate that partial depletion of 5-HT in the insular cortex (IC) prevents LiCl-induced conditioned di

135 tudies suggest that the anterior part of the insular cortex (IC) serves as primary taste cortex, wher

136 the posterior half of GC in addition to the insular cortex (IC) that is just dorsal and caudal to th

137 a significant increase in ACh release in the insular cortex (IC), a highly relevant structure for tas

138 stronger Fos-like immunoreactivity (FLI) in insular cortex (IC), amygdala, and brainstem than famili

139 The insular cortex (IC), an area largely studied in rodents

140 Prior studies suggest that the insular cortex (IC), and particularly its posterior regi

141 To that aim, insular cortex (IC)-dependent positive and negative form

142 nucleus of the stria terminalis (BNST), and insular cortex (IC).

143 extracellular acetylcholine (ACh) levels in insular cortex (IC).

144 s designed to examine whether lesions of the insular cortex (IC; Experiment 1), the basolateral amygd

145 In the insular cortex, IL1beta enhanced IL6 mRNA and TNFalpha i

146 r-bound protons, within a discrete region of insular cortex implicated in representing internal physi

147 The specific role of insular cortex in acquisition and expression of a condit

148 tion of those stimuli and implicate anterior insular cortex in auditory processing, with the left ins

149 nvestigated the functional properties of the insular cortex in behaving monkeys using intracortical m

150 es have challenged the necessary role of the insular cortex in both awareness and feeling by showing

151 tion, supporting a critical role of anterior insular cortex in empathetic pain processing.

152 olinergic neurotransmission in the posterior insular cortex in neuropathic pain condition and the inv

153 onnectivity, and fALFF converged in the left insular cortex in patients with FXS.

154 ds of winning, consistent with a role of the insular cortex in signalling the probability of aversive

155 However, the role of the insular cortex in such modulatory processes remains poor

156 ior cingulate cortex (ACC) and the posterior insular cortex in the anxiodepressive, sensory, and affe

157 nversely, we report a signal in the anterior insular cortex in the highest earners that precedes the

158 Involvement of insular cortex in the induction of c-Fos-immunoreactivit

159 suggests a prominent role of dorsal anterior insular cortex in the parasympathetic control of cardiac

160 pite numerous studies suggesting the role of insular cortex in the processing of gustatory and olfact

161 uroimaging studies in humans have implicated insular cortex in these phenomena.

162 tion on visual awareness and the role of the insular cortex in this process remain unclear.

163 h the thinness of the anterior region of the insular cortex, in which highly impulsive (HI) rats expr

164 s and were distributed widely throughout the insular cortex including anterior areas not previously t

165 f the intralaminar complex (PINT) and caudal insular cortex (INS) block acquisition but not expressio

166 functional areas of the brain including the insular cortex (involved in enteroceptive monitoring) an

167 secondary somatosensory (SII) and agranular insular cortex ipsilaterally, as well as the homotopic a

168 As the insular cortex is a well-established region in pain proc

169 We suggest that fusion between temporal and insular cortex is an example of a relatively rare neuroa

170 The insular cortex is anatomically positioned to serve as on

171 The rostral perirhinal border with insular cortex is at the extreme caudal limit of the cla

172 The insular cortex is fundamentally involved in the processi

173 QR2 mRNA expression in the insular cortex is inversely correlated with mAChR activa

174 al conditioning, the gustatory region of the insular cortex is involved in encoding the taste of food

175 The insular cortex is involved in the perception of interoce

176 Additional activation observed in the insular cortex is proposed to be involved in conveying a

177 The insular cortex is required for CTA memory formation and

178 e processing of interoceptive signals in the insular cortex is thought to underlie self-awareness.

179 thalamus, putamen, and pallidum), as well as insular cortex, is associated with greater change in bel

180 the left IFG and left pallidum, putamen, and insular cortex, is associated with reduced change in bel

181 the gustatory cortex, including parts of the insular cortex, is crucial for the processing of food it

182 an assemblage of taste-responsive neurons in insular cortex, is widely regarded as integral to condit

183 ons in middle to caudal dysgranular parietal insular cortex labeled only the posterior nucleus.

184 in rostral granular and dysgranular parietal insular cortex labeled the ventral posterior and parvice

185 Expression in insular cortex, lateral septal nucleus, medial preoptic

186 ces of pain remained present after posterior insular cortex lesion, even though the mechanical allody

187 In the present experiment, insular cortex-lesioned (ICX) rats showed normal respons

188 Patients with focal anterior insular cortex lesions displayed decreased discriminatio

189 In contrast, patients with insular cortex lesions failed to adjust their bets by th

190 findings reveal that only discrete anterior insular cortex lesions, but not anterior cingulate corte

191 lved in cardiovascular control; (2) the left insular cortex may be chiefly concerned with parasympath

192 Volume reduction in insular cortex may constitute an important neuropatholog

193 Conversely, the right posterior insular cortex may regulate both cardiac and vasomotor s

194 exercise in humans, suggesting that the left insular cortex may serve as a site for cortical regulati

195 stable lesions to the vmPFC (n = 20) and the insular cortex (n = 13) were compared against healthy su

196 Insular cortex neurons demonstrate food-cue-biased respo

197 d to activate limbic/paralimbic regions (eg, insular cortex, nucleus accumbens, and parahippocampal g

198 roach to monitor visual cue responses in the insular cortex of behaving mice across hunger states.

199 In the hypothalamus and granular insular cortex of mice with type 1 diabetes, bone marrow

200 analyses of the neuronal connections of the insular cortex of the macaque monkey using modern high-r

201 gulation within the right and left posterior insular cortex of the rat, suggest the possibility of tr

202 parahippocampal gyrus and frontal operculum/insular cortex of the right hemisphere and, to a lesser

203 The anterior insular cortex of the right hemisphere, in particular it

204 eral areas, including the prefrontal cortex, insular cortex, olfactory bulb, amygdala, and hippocampu

205 lesions aimed at the gustatory region of the insular cortex on instrumental conditioning in rats.

206 lateral or bilateral electrolytic lesions of insular cortex or 'sham' operations.

207 ns whose locations matched with the anterior insular cortex or anterior cingulate cortex clusters ide

208 on of others' pain in patients with anterior insular cortex or anterior cingulate cortex lesions whos

209 ding the piriform cortex, entorhinal cortex, insular cortex, orbital cortex, and all cortical amygdal

210 n including the nucleus accumbens, striatum, insular cortex, orbitofrontal cortex, and medial forebra

211 The vmPFC and insular cortex patients showed selective and distinctive

212 nular insular (AId) and regions of posterior insular cortex (PI-comprising the agranular, dysgranular

213 choline has been evidenced in the posterior insular cortex (pIC) of neuropathic animal, which was si

214 r vestibular cortex (PIVC) and the posterior insular cortex (PIC).

215 Animal and human studies suggest that the insular cortex plays an important role in subjective awa

216 in the medial and lateral frontal cortices, insular cortex, posterior cingulate cortex, precuneus, a

217 al functional connectivity with parietal and insular cortex, predicted individual variability in stra

218 ation of the secondary somatosensory cortex, insular cortex, prefrontal cortex, inferior parietal lob

219 ded the olfactory system, nucleus accumbens, insular cortex, prefrontal cortex, ventral tegmental are

220 that acute microinfusion of MK-801 into the insular cortex prevented the attenuation of gustatory ne

221 ices received extensive projections from the insular cortex, primarily from its agranular areas.

222 Biocytin injections into granular parietal insular cortex produced a heavy labeling of the subjacen

223 in the temporal pole, anterior cingulate and insular cortex project to the hypothalamus.

224 Dysgranular anterior insular cortex projected to lateral agranular frontal co

225 Agranular posterior insular cortex projected to medial mediodorsal nucleus,

226 Agranular anterior insular cortex projected to the dysgranular anterior and

227 nd they suggest that discrete modules within insular cortex provide the basis for its polymodal integ

228 The rostral agranular insular cortex (RAIC) has recently been identified as a

229 The rostral agranular insular cortex (RAIC) of rats has opioid receptors and h

230 oid-responsive site in the rostral agranular insular cortex (RAIC) of the rat and characterize the an

231 by painful stimuli is the rostral agranular insular cortex (RAIC) where, as in other parts of the co

232 inhibitor GBR-12935 in the rostral agranular insular cortex (RAIC), a cortical area that receives a d

233 touch, but evidence suggests involvement of insular cortex rather than parietal somatosensory cortic

234 In contrast, bilateral insular cortex responded to pain stimulation regardless

235 iocytin injections into dysgranular parietal insular cortex resulted in heavy labeling of the subjace

236 Finally, in Experiment 3, lesions of the insular cortex retarded CTA acquisition but had no influ

237 approximately 20% less c-fos ir-cells in the insular cortex, retrosplenial cortex, and dentate gyrus.

238 a third network comprising the right fronto-insular cortex (rFIC) and anterior cingulate cortex (ACC

239 The right fronto-insular cortex (rFIC) is a critical component of a salie

240 The major targets are granular insular cortex, secondary somatosensory cortex and sever

241 an unanticipated long-lasting activation of insular cortex signal transduction cascades in novel tas

242 al component of the functional topography of insular cortex; such an approach could have general appl

243 in activity in the vicinity of the anterior insular cortex, suggesting that this region participates

244 alimbic areas such as anterior cingulate and insular cortex, supplementary motor area (SMA) and parie

245 , bilateral lesions to a region of posterior insular cortex, termed the "sensory insula," prevented t

246 in cortical areas such as the prefrontal and insular cortex that are associated limbic structures.

247 fic VMpo projection area in dorsal posterior insular cortex that provides the basis for a somatotopic

248 he endopiriform nucleus and claustrum of the insular cortex, the globus pallidus, the ventromedial hy

249 aterally, the middle frontal gyrus, the left insular cortex, the left middle temporal gyrus, and the

250 reward and emotion encompassing the anterior insular cortex, the nucleus accumbens, and the amygdala.

251 lum together with the anterior and posterior insular cortex, the putamen, as well as subcortical whit

252 fferences in the extent of the damage to the insular cortex, three findings were common to both indiv

253 terior suprasylvian cortex (vPS) and temporo-insular cortex (TI) lesions on complex visual and audito

254 ptic glutamatergic projections from anterior insular cortex to central amygdala is critical to relaps

255 ardiac nervous system, from the level of the insular cortex to the intrinsic cardiac nervous system,

256 ected pathway extending bilaterally from the insular cortex to the prefrontal cortex.

257 pendent on glutamatergic transmission in the insular cortex, to investigate the behavioral and cellul

258 We identified the anterior insular cortex-to-central amygdala projection as a new a

259 n the ventromedial prefrontal cortex and the insular cortex, two regions that have been shown to be r

260 e studied the auditory thalamic input to the insular cortex using mice as a model system.

261 in the amygdala, frontal operculum-anterior insular cortex, ventromedial prefrontal cortex, and the

262 tions uncover a pathway from AgRP neurons to insular cortex via the paraventricular thalamus and baso

263 t investigation was to determine whether the insular cortex was activated during volitional dynamic e

264 The prefrontal and insular cortex was evaluated microscopically for overlap

265 mu-OR binding in the left insular cortex was less in bulimic subjects than in cont

266 pression in both nucleus accumbens shell and insular cortex was positively associated with risk-takin

267 r performance for both the angular gyrus and insular cortex was reliably enhanced by the addition of

268 using high-resolution fMRI revealed that the insular cortex was sensitive to both visible and invisib

269 Furthermore, fALFF in the left insular cortex was significantly positively correlated w

270 The ipsilateral insular cortex was stimulated both electrically (0.5 mA,

271 in Mandarin lexical tones, the left anterior insular cortex was the most active.

272 e bilateral superior parietal lobes and left insular cortex were less activated.

273 greater connectivity between the DMN and the insular cortex, which is a brain region known to process

274 The insular cortex, which receives sensory inputs from both

275 rkers of myeloarchitectural integrity of the insular cortex, while affective empathy was predicted by

276 nd other areas of the frontal cortex and the insular cortex with hypothalamic, ventral, and dorsal st

277 The association of dysgranular parietal insular cortex with the posterior thalamus suggests it m

278 sentation of sensorimotor information in the insular cortex, with possible involvement of limbic area

279 ucture enclosed between the striatum and the insular cortex, with widespread reciprocal connections w