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1 with previous reports supporting a role for perirhinal acetylcholine in object information acquisiti
3 her perspective is that both hippocampal and perirhinal activity are predictive of overall memory str
4 disproportionately on recollection, whereas perirhinal activity predicts recognition success when de
5 the underlying mechanisms, we recorded BLA, perirhinal and entorhinal neurons during an appetitive t
8 ial entorhinal cortex in humans, and between perirhinal and parahippocampal cortex as a function of i
9 al lobe (MTL), showing domain specificity in perirhinal and parahippocampal cortices (for object-proc
10 and the medial temporal lobe including both perirhinal and parahippocampal cortices and the posterio
12 temporal lobe cortical input structures, the perirhinal and posterior parahippocampal cortices, diffe
15 ns in the cortex (entorhinal, retrosplenial, perirhinal) and the amygdala could not be reactivated.
17 cingulate, prelimbic, infralimbic, insular, perirhinal, and entorhinal cortices as well as to CA1, d
19 o this end, we simultaneously recorded mPFC, perirhinal, and entorhinal neurons during the acquisitio
21 MTL), including the hippocampus, entorhinal, perirhinal, and parahippocampal cortices, forms a functi
23 tralateral side of the piriform, entorhinal, perirhinal, and parietal cortices as compared with the i
24 oning sessions for the piriform, entorhinal, perirhinal, and parietal cortices, and after the 4th ses
25 eminder session in the piriform, entorhinal, perirhinal, and parietal cortices, but not in the subicu
28 ital and medial prefrontal networks with the perirhinal (areas 35 and 36) and parahippocampal (areas
29 ns into the ATL: the temporal polar (n = 3), perirhinal (areas 35 and 36, n = 6), and inferotemporal
37 ITI, ITR, and more ventral cortex, including perirhinal cortex (group ITR+), with visual learning in
38 ludes signals that are largely unique to the perirhinal cortex (i.e., object familiarity), consistent
42 position that is comparable with that of the perirhinal cortex (PER) with regard to the lateral entor
48 the major white matter tracts converging on perirhinal cortex (PrC) and hippocampus (HC) would be di
49 edial temporal lobe (MTL), in particular the perirhinal cortex (PrC) and hippocampus (HC), are best c
50 merous studies support the importance of the perirhinal cortex (PRC) and parahippocampal cortex (PHC)
51 pal region are functionally divided into the perirhinal cortex (PRC) and the lateral entorhinal corte
52 emporal lobe cortex (MTLC), most notably the perirhinal cortex (PrC) and the parahippocampal cortex (
54 is well established that the hippocampus and perirhinal cortex (PrC) encode associative and item repr
59 s from each sensory stream are integrated in perirhinal cortex (PRc) of the anteromedial temporal lob
60 basis of episodic recollection, whereas the perirhinal cortex (PRc) supports familiarity for individ
62 subregions that connect differentially with perirhinal cortex (PRC) vs parahippocampal cortex (PHC)
63 elated fMRI to address the role of the human perirhinal cortex (PRC), and its interactions with the h
65 MTL), in particular the hippocampus (HC) and perirhinal cortex (PrC), play domain-sensitive roles in
70 responses in inferotemporal cortex (IT) and perirhinal cortex (PRH) as macaque monkeys performed a d
71 responses in inferotemporal cortex (IT) and perirhinal cortex (PRH) as macaque monkeys performed a t
76 ory strength is nonlinear in hippocampus and perirhinal cortex and also distinctly different in those
77 h taste and olfactory cortical areas and the perirhinal cortex and appears to be involved in assessme
79 ial memory are typically associated with the perirhinal cortex and hippocampal formation, respectivel
80 In particular, the effects in entorhinal and perirhinal cortex and hippocampus might be important for
81 by greater across-item pattern similarity in perirhinal cortex and in parahippocampal cortex, but gre
82 hese findings reach beyond simple notions of perirhinal cortex and lateral entorhinal cortex neurons
84 gardless of subsequent memory, we found that perirhinal cortex and parahippocampal cortex exhibited d
85 vel had higher c-fos activity in the rostral perirhinal cortex and the lateral entorhinal cortex.
88 e data indicate that behaviors requiring the perirhinal cortex are disrupted in advanced age, and sug
89 ding the hippocampus, entorhinal cortex, and perirhinal cortex are thought to be part of a unitary sy
90 ort that bilateral, excitoxic lesions of the perirhinal cortex attenuate rats' familiarity-based stim
91 tion and establish a functional homology for perirhinal cortex between species, although we propose t
92 dial temporal lobe, especially involving the perirhinal cortex Brodmann area 36 and entorhinal cortex
93 The discovery that bilateral lesions of the perirhinal cortex can leave configural (structural) lear
94 AD-67 immunohistochemistry, we show that the perirhinal cortex contains GABAergic neurons with long-r
95 ancy by demonstrating that both pSTS and the perirhinal cortex contribute to crossmodal binding in hu
96 al (especially spatial) information, whereas perirhinal cortex contributes to and is necessary for fa
97 perirhinal cortex, only damage to the caudal perirhinal cortex correlated significantly with recognit
99 human lesion studies have demonstrated that perirhinal cortex damage impairs complex object discrimi
100 of the sensitivity of object recognition to perirhinal cortex damage is not the result of standard h
104 ections, the density of PHAL(+) axons in the perirhinal cortex decreased steeply with rostrocaudal di
105 ceptor-mediated synaptic transmission within perirhinal cortex disrupted encoding for short- and long
106 There was no evidence that lesions of the perirhinal cortex disrupted the ability to learn the con
107 perception of places and paths, whereas the perirhinal cortex does so for objects and the contents o
108 obtained directly from human hippocampus and perirhinal cortex during a recognition paradigm and appl
109 receptor antagonist scopolamine into the rat perirhinal cortex during different stages (encoding, sto
110 cillations in the amygdala, hippocampus, and perirhinal cortex during this next-day memory test indic
111 the left posterior inferior frontal and left perirhinal cortex for words and objects, respectively, a
114 d points to a need to refine those models of perirhinal cortex function that emphasize its role in re
116 ories and add more weight to the role of the perirhinal cortex in associative encoding of objects.
119 These findings suggest a key role for the perirhinal cortex in representing and processing object-
120 results demonstrate a specific role for the perirhinal cortex in visual perception and establish a f
123 e identified regions in both hippocampus and perirhinal cortex in which activity varied as a function
124 gion for crossmodal perceptual features, and perirhinal cortex integrating these features into higher
125 by providing converging evidence that human perirhinal cortex is also critically involved in process
129 Previously it has been suggested that the perirhinal cortex is part of a pathway processing object
132 ated synaptic transmission (EPSC(KA) LTD) in perirhinal cortex layer II/III neurons that is distinct
135 ir differential exploration times, rats with perirhinal cortex lesions showed very poor discriminatio
140 nificant correlation was found between total perirhinal cortex loss and degree of recognition impairm
141 n supports the idea that the hippocampus and perirhinal cortex may be critical for the processing of
142 riments thus suggest that alterations in the perirhinal cortex may be responsible for reducing aged a
144 evidence to suggest that the hippocampus and perirhinal cortex may mediate processes beyond long-term
146 imental changes in the prefrontal cortex and perirhinal cortex occurred before metabolic syndrome or
149 lity or interneuron loss was observed in the perirhinal cortex of these aged, memory-impaired monkeys
150 we tested the effects of DPFE infusions into perirhinal cortex on meth-seeking under two different te
152 ion of short- and long-range inputs from the perirhinal cortex or temporal neocortex with perirhinal
153 anterior hippocampus, entorhinal cortex, and perirhinal cortex over the 30 s retention interval, with
154 s share common features, suggesting that the perirhinal cortex participates in perceptual discriminat
159 n contrast, activity in both hippocampus and perirhinal cortex positively correlated with the subsequ
160 induced pattern effects in orbitofrontal and perirhinal cortex predicted the magnitude of categorical
161 demonstrate that the level of engagement of perirhinal cortex predicts later memory for individual i
169 nhuman primates, and humans suggest that the perirhinal cortex represents information about objects f
171 s been implicated in spatial memory, whereas perirhinal cortex seems critical for object memory.
174 m one item presentation to the next, whereas perirhinal cortex signaled the conjunction of items and
176 Furthermore, there was a deficit of LTD in perirhinal cortex slices from virally transduced, recogn
177 chniques to provide strong evidence that the perirhinal cortex subserves perception and suggests that
179 Specifically, it has been suggested that the perirhinal cortex supports the perceptual abilities need
180 these two retrograde signalling cascades in perirhinal cortex synaptic plasticity and in visual reco
181 ll have to extend beyond the hippocampus and perirhinal cortex to incorporate a wider network of cort
183 ne transfer to these postsynaptic neurons in perirhinal cortex used a His tag antibody, as the peptid
184 ccelerated function and that activity in the perirhinal cortex was associated with a statistically di
185 iments, rats with excitotoxic lesions of the perirhinal cortex were found to be indistinguishable fro
186 dy highlights the critical importance of the perirhinal cortex within the temporal lobe for recogniti
187 ee MTL areas (hippocampus and entorhinal and perirhinal cortex) and visual area TE as monkeys perform
188 nation of the object recognition system (the perirhinal cortex) performs this critical function.
191 and facilitates long-term depression in the perirhinal cortex, a neural correlate of object recognit
192 tions implemented across the hippocampus and perirhinal cortex, allowing formal rejection of a single
193 n contrast, medial temporal lobe structures (perirhinal cortex, amygdala, hippocampus) and anterior i
194 iggered a switch in mechanisms of LTD in rat perirhinal cortex, an area critical for visual recogniti
195 levels of the ventral temporal neocortex or perirhinal cortex, and electron microscopic observations
196 Brain activity in the hippocampal region, perirhinal cortex, and parahippocampal cortex was associ
197 as for visual object representation, such as perirhinal cortex, and reward-guided learning, such as t
198 the entorhinal cortex, the hippocampus, the perirhinal cortex, and rostral parahippocampal cortex.
199 ced GAbeta accumulation in the subiculum and perirhinal cortex, both of which are brain regions requi
200 eciprocally connected to parahippocampal and perirhinal cortex, but evidence for functional subregion
201 study: Patients with lesions, including the perirhinal cortex, but not patients with damage restrict
202 ures other than the hippocampus, perhaps the perirhinal cortex, can support face recognition memory i
203 A signal in the anterior MTL, including perirhinal cortex, indicated the successful retrieval of
205 t, activity in a different group of regions (perirhinal cortex, parahippocampal cortex, and inferior
206 fore and after this exposure, and found that perirhinal cortex, parahippocampal cortex, subiculum, CA
207 ns of the left hippocampus, and in bilateral perirhinal cortex, predicted subsequent accuracy on the
209 uman memory: whether the hippocampus and the perirhinal cortex, two key components of the medial temp
210 rocess critical for the expression of LTD in perirhinal cortex, underlies visual recognition memory.
212 ns bilaterally in hippocampus, as well as in perirhinal cortex, where activity during learning increa
213 ted match and mismatch signals in the monkey perirhinal cortex, where match signals were selective fo
214 ted intrinsic functional connectivity of the perirhinal cortex, which is typically the first brain re
215 nterior medial temporal lobes, including the perirhinal cortex, which serve to integrate complex obje
216 c information is uniquely represented in the perirhinal cortex, which was also increasingly engaged f
217 e medial temporal lobe (MTL)--in particular, perirhinal cortex--support not just memory but certain k
218 not eCB-dependent signalling is important in perirhinal cortex-dependent visual recognition memory.
219 studies suggest that at least one component-perirhinal cortex-might also contribute to perceptual pr
239 ort that lower firing rates observed in aged perirhinal cortical principal cells are associated with
240 pocampus and surrounding parahippocampal and perirhinal cortices during the retrieval of episodic mem
241 e piriform cortex, subiculum, entorhinal and perirhinal cortices, and parietal and occipital cortices
242 ivity in the LEC is shaped by input from the perirhinal cortices, hippocampus, and amygdala, and thus
246 ent studies indicating that the formation of perirhinal-dependent memories requires activation of mus
248 etween a novel cue and meth-conditioned cue, perirhinal DPFE infusions shifted the pattern of respond
250 and related medial temporal lobe structures (perirhinal, entorhinal, and parahippocampal cortices) im
252 uring brief memory delays bilaterally in the perirhinal/entorhinal cortex, in the right posterior par
253 Together, these results provide evidence for perirhinal-hippocampal interactions in the selective con
254 mporal polar cortex and rostral parts of the perirhinal, inferotemporal, and anterior tip of the supe
257 on, dorsal and ventral auditory, ectorhinal, perirhinal, lateral entorhinal, and anteromedial, poster
259 Whereas LO, VLO, VO, and MO interact with perirhinal-LEC circuits, the interactions with postrhina
262 e water maze failed to provide evidence that perirhinal lesions disrupt overall levels of performance
263 results on the habituation experiments, the perirhinal lesions disrupted transfer performance on a c
266 ortex is critical for novelty detection, and perirhinal metabotropic glutamate 5 receptors (mGlu5) ar
268 verall, these results suggest that principal perirhinal neurons are subjected to significantly more i
269 ally stimulating channelrhodopsin-expressing perirhinal neurons at various frequencies while rats loo
270 njection of 17-beta-estradiol, the number of perirhinal neurons double-labeled for ER-beta/GABA was r
276 odor category-specific ensemble patterns in perirhinal, orbitofrontal, piriform, and insular cortice
277 poral lobe (MTL)-hippocampus and surrounding perirhinal, parahippocampal, and entorhinal cortical are
278 tudies in human subjects have demonstrated a perirhinal/parahippocampal division, such a division amo
279 n of emergent odor category codes within the perirhinal, piriform, orbitofrontal, and insular cortice
280 ilateral excitotoxic lesions of PRh or PPRh (perirhinal plus postrhinal cortices) in the rat would ca
281 oncholinergic projections from the BF to the perirhinal, postrhinal, and entorhinal cortex by using r
282 parahippocampal region, which comprises the perirhinal, postrhinal, and entorhinal cortices, as well
283 contrast, target the parahippocampal region (perirhinal, postrhinal, lateral and medial entorhinal co
284 to total projection neurons is higher in the perirhinal/postrhinal cases (26-48%) than in the entorhi
287 CMOR task requires functional integration of perirhinal (PRh) and posterior parietal (PPC) cortices,
288 Recognition of novelty depends upon intact perirhinal (pRh) cortex function, which is compromised b
289 ith damage to the parahippocampal (TH/TF) or perirhinal (PRh) cortex were tested on two sets of the t
291 representational similarity analysis of left perirhinal responses, semantic distances between entitie
292 ly labeled (PHAL(+)) axon terminals found at perirhinal sites adjacent to or rostrocaudally distant f
295 Furthermore, some of the neocortical and perirhinal terminals containing PHAL and GABA immunolabe
296 activity increased impulse transmission from perirhinal to entorhinal neurons and that this effect de
297 ly to affect feedforward inhibition from the perirhinal to the entorhinal cortex that gates the flow
298 However, for reasons that remain unclear, perirhinal transfer of neocortical inputs to the entorhi
299 long-range feedforward inhibition regulates perirhinal transfer of neocortical inputs to the entorhi
300 , physiological investigations indicate that perirhinal transmission of neocortical and EC inputs occ
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