Literature DB >> 8930786

Organization of connections between the amygdaloid complex and the perirhinal and parahippocampal cortices in macaque monkeys.

L Stefanacci1, W A Suzuki, D G Amaral.   

Abstract

Neuroanatomical studies in macaque monkeys have demonstrated that the perirhinal and parahippocampal (PRPH) cortices are strongly interconnected with the hippocampal formation. Recent behavioral evidence indicates that these cortical regions are importantly involved in normal recognition memory function. The PRPH cortices are also interconnected with the amygdaloid complex, although comparatively little is known about the precise topography of these connections. We investigated the topographic organization of reciprocal connections between the amygdala and the PRPH cortices by placing anterograde and retrograde tracers throughout these three regions. We found that there was an organized arrangement of connections between the amygdala and the PRPH cortices and that the deep (lateral, basal, and accessory basal) nuclei of the amygdaloid complex were the source of most connections between the amygdala and the PRPH cortices. The temporal polar regions of the perirhinal cortex had the strongest and most widespread interconnections with the amygdala. Connections from more caudal levels of the perirhinal cortex had a more discrete pattern of termination. Perirhinal inputs to the amygdala terminated primarily in the lateral nucleus, the magnocellular and parvicellular divisions of the basal nucleus, and the magnocellular division of the accessory basal nucleus. Return projections originated predominately in the lateral nucleus, the intermediate and parvicellular divisions of the basal nucleus, and the magnocellular division of the accessory basal nucleus. The interconnections between the amygdala and the parahippocampal cortex were substantially less robust than those with the perirhinal cortex and mainly involved the basal nucleus. Area TF was more strongly interconnected with the amygdala than was area TH. Input from the parahippocampal cortex terminated predominantly in the lateral half of the parvicellular division of the basal nucleus but also to a lesser extent in the magnocellular division of the basal nucleus and the lateral nucleus. Return projections originated predominantly in the magnocellular division of the basal nucleus and were directed almost exclusively to area TF.

Mesh:

Year:  1996        PMID: 8930786     DOI: 10.1002/(SICI)1096-9861(19961125)375:4<552::AID-CNE2>3.0.CO;2-0

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


  72 in total

1.  Damage to the lateral and central, but not other, amygdaloid nuclei prevents the acquisition of auditory fear conditioning.

Authors:  K Nader; P Majidishad; P Amorapanth; J E LeDoux
Journal:  Learn Mem       Date:  2001 May-Jun       Impact factor: 2.460

2.  DNA targeting of rhinal cortex D2 receptor protein reversibly blocks learning of cues that predict reward.

Authors:  Zheng Liu; Barry J Richmond; Elisabeth A Murray; Richard C Saunders; Sara Steenrod; Barbara K Stubblefield; Deidra M Montague; Edward I Ginns
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-09       Impact factor: 11.205

3.  Effects of HIV and early life stress on amygdala morphometry and neurocognitive function.

Authors:  Uraina S Clark; Ronald A Cohen; Lawrence H Sweet; Assawin Gongvatana; Kathryn N Devlin; George N Hana; Michelle L Westbrook; Richard C Mulligan; Beth A Jerskey; Tara L White; Bradford Navia; Karen T Tashima
Journal:  J Int Neuropsychol Soc       Date:  2012-05-24       Impact factor: 2.892

4.  Abstract Context Representations in Primate Amygdala and Prefrontal Cortex.

Authors:  A Saez; M Rigotti; S Ostojic; S Fusi; C D Salzman
Journal:  Neuron       Date:  2015-08-19       Impact factor: 17.173

Review 5.  Emotion, cognition, and mental state representation in amygdala and prefrontal cortex.

Authors:  C Daniel Salzman; Stefano Fusi
Journal:  Annu Rev Neurosci       Date:  2010       Impact factor: 12.449

6.  Reward-spatial view representations and learning in the primate hippocampus.

Authors:  Edmund T Rolls; Jian-Zhong Xiang
Journal:  J Neurosci       Date:  2005-06-29       Impact factor: 6.167

7.  Sequence of information processing for emotions based on the anatomic dialogue between prefrontal cortex and amygdala.

Authors:  H T Ghashghaei; C C Hilgetag; H Barbas
Journal:  Neuroimage       Date:  2006-11-27       Impact factor: 6.556

8.  Neurotrophin receptor heterozygosity causes deficits in catecholaminergic innervation of amygdala and hippocampus in aged mice.

Authors:  O von Bohlen Und Halbach; L Minichiello
Journal:  J Neural Transm (Vienna)       Date:  2006-06-01       Impact factor: 3.575

9.  Evidence for direct projections from the basal nucleus of the amygdala to retrosplenial cortex in the Macaque monkey.

Authors:  J A Buckwalter; C M Schumann; G W Van Hoesen
Journal:  Exp Brain Res       Date:  2007-11-30       Impact factor: 1.972

10.  Selective impairment of reasoning about social exchange in a patient with bilateral limbic system damage.

Authors:  Valerie E Stone; Leda Cosmides; John Tooby; Neal Kroll; Robert T Knight
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-12       Impact factor: 11.205

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