Literature DB >> 10102498

Perirhinal cortex projections to the amygdaloid complex and hippocampal formation in the rat.

C J Shi1, M D Cassell.   

Abstract

The differential efferent projections of the perirhinal cortex were traced by using anterograde and retrograde tracing techniques. The dorsal bank cortex (area 36) projected lightly to the lateral entorhinal cortex and more strongly to the lateral, posterolateral cortical, and posterior basomedial amygdaloid nuclei and amygdalostriatal transition zone. The ventral bank (dorsolateral entorhinal cortex) projected to the lateral entorhinal cortex, dorsal subiculum, and subfield CA1 and mainly targeted the basolateral amygdaloid nucleus. Corticocortical projections from the dorsal and ventral banks targeted different cortical areas. The fundus of the rhinal sulcus (area 35) projected to both lateral and medial entorhinal cortices, ventral subiculum, lateral and basolateral nuclei, and amygdalostriatal transition zone. Corticocortical projections targeted areas projected to by both dorsal and ventral banks and also by second somatosensory area, first temporal cortical area, and striate cortex. Neurons projecting to the lateral nucleus were distributed in all layers of the dorsal bank, wheras those projecting to CA1 and subiculum were found in superfical layers (mostly layer III) of the ventral bank. Projections to the basolateral nucleus arose from superfical layers (mostly layer II) of the fundus and deep layers of the ventral bank. Furthermore, projections to the amygdala mostly arose from rostral levels, whereas hippocampal projections primarily originated caudally. The rat perirhinal cortex is heterogeneous in its efferent connectivity, and distinct projections arise from the dorsal and ventral banks and fundus of the rhinal sulcus. The widespread cortical connectivity of the fundus suggests that only this part of the perirhinal cortex is similar to area 35 of the primate brain.

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Year:  1999        PMID: 10102498     DOI: 10.1002/(sici)1096-9861(19990412)406:3<299::aid-cne2>3.0.co;2-9

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  49 in total

1.  Propagation of neocortical inputs in the perirhinal cortex.

Authors:  M Martina; S Royer; D Paré
Journal:  J Neurosci       Date:  2001-04-15       Impact factor: 6.167

2.  Instability in the place field location of hippocampal place cells after lesions centered on the perirhinal cortex.

Authors:  G M Muir; D K Bilkey
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

3.  Dopamine attenuates prefrontal cortical suppression of sensory inputs to the basolateral amygdala of rats.

Authors:  J A Rosenkranz; A A Grace
Journal:  J Neurosci       Date:  2001-06-01       Impact factor: 6.167

4.  Regulation of synaptic plasticity genes during consolidation of fear conditioning.

Authors:  Kerry J Ressler; Gayla Paschall; Xiao-liu Zhou; Michael Davis
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

5.  Limited convergence of rhinal cortical and dopaminergic inputs in the rat basolateral amygdala: an ultrastructural analysis.

Authors:  Courtney R Pinard; Franco Mascagni; Jay F Muller; Alexander J McDonald
Journal:  Brain Res       Date:  2010-03-24       Impact factor: 3.252

Review 6.  Functional neuroanatomy of amygdalohippocampal interconnections and their role in learning and memory.

Authors:  Alexander J McDonald; David D Mott
Journal:  J Neurosci Res       Date:  2016-02-14       Impact factor: 4.164

7.  Cortical inputs innervate calbindin-immunoreactive interneurons of the rat basolateral amygdaloid complex.

Authors:  Gunes Unal; Jean-Francois Paré; Yoland Smith; Denis Paré
Journal:  J Comp Neurol       Date:  2014-06-01       Impact factor: 3.215

8.  Extrinsic origins of the somatostatin and neuropeptide Y innervation of the rat basolateral amygdala.

Authors:  A J McDonald; V Zaric
Journal:  Neuroscience       Date:  2015-03-10       Impact factor: 3.590

9.  Single-unit firing in rat perirhinal cortex caused by fear conditioning to arbitrary and ecological stimuli.

Authors:  Sharon C Furtak; Timothy A Allen; Thomas H Brown
Journal:  J Neurosci       Date:  2007-11-07       Impact factor: 6.167

Review 10.  Dual functions of perirhinal cortex in fear conditioning.

Authors:  Brianne A Kent; Thomas H Brown
Journal:  Hippocampus       Date:  2012-08-18       Impact factor: 3.899

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