Literature DB >> 11440795

Theta-rhythmically firing neurons in the anterior thalamus: implications for mnemonic functions of Papez's circuit.

R P Vertes1, Z Albo, G Viana Di Prisco.   

Abstract

In 1937 Papez described an anatomical circuit (or loop) beginning and ending in the hippocampal formation that he proposed subserved emotional experience (Papez, 1937). Specifically, the projections of the circuit were as follows: hippocampal formation--> mammillary bodies--> anterior thalamus--> cingulate cortex--> parahippocampal gyrus--> hippocampal formation. Although the circuit has been refined based on subsequent anatomical findings (Amaral and Witter, 1995; Shibata, 1992; Van Groen and Wyss, 1995), the major links of the circuit unquestionably represent a prominent system of connections in the mammalian brain. Hence, the enduring nature of 'Papez's circuit'. Unlike, however, its persistence as anatomical entity, the proposed functional role for the circuit has been less resilient. The early notion that Papez's circuit subserves emotional experience/expression has been abandoned (LeDoux, 1993) and replaced by the proposal that it is primarily involved in mnemonic functions (Aggleton and Brown, 1999). Lesions of each of the major components of the circuit have been shown to disrupt memory (Aggleton and Brown, 1999; Sutherland et al., 1988; Sziklas and Petrides, 1993). The mammillary bodies represent a major output from the hippocampus in Papez's circuit (Amaral and Witter, 1995). It has recently been shown that cells of mammillary body fire rhythmically in bursts synchronous with the theta rhythm of the hippocampus (Bland et al., 1995; Kirk et al., 1996; Kocsis and Vertes, 1994, 1997) and that this rhythmical activity is dependent upon the action of the hippocampus on the mammillary bodies (Bland et al., 1995; Kirk et al., 1996). It is well established that the mammillary bodies project massively to the anterior thalamus (Shibata, 1992), which taken together with the demonstration that mammillary body cells fire synchronously with theta, suggests that the mammillary bodies may act on the anterior thalamus, possibly in the manner that the hippocampus acts on the mammillary bodies, to rhythmically activate cells of the anterior thalamus at theta frequency. We demonstrated that approximately 75% of cells of the anterior ventral nucleus of the thalamus fire rhythmically synchronous with the hippocampal theta rhythm and the activity of 46% of these anterior ventral neurons was highly correlated with theta. These findings, together with demonstration of theta-rhythmically firing cells in other structures of Papez's circuit, indicate that a theta-rhythmic signal may resonate throughout Papez's circuit, possibly involved in the control of mnemonic functions of the circuit.

Entities:  

Mesh:

Year:  2001        PMID: 11440795     DOI: 10.1016/s0306-4522(01)00131-2

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  62 in total

1.  Oscillatory entrainment of thalamic neurons by theta rhythm in freely moving rats.

Authors:  Marian Tsanov; Ehsan Chah; Nick Wright; Seralynne D Vann; Richard Reilly; Jonathan T Erichsen; John P Aggleton; Shane M O'Mara
Journal:  J Neurophysiol       Date:  2010-10-20       Impact factor: 2.714

2.  Thickness of the human cerebral cortex is associated with metrics of cerebrovascular health in a normative sample of community dwelling older adults.

Authors:  Elizabeth C Leritz; David H Salat; Victoria J Williams; David M Schnyer; James L Rudolph; Lewis Lipsitz; Bruce Fischl; Regina E McGlinchey; William P Milberg
Journal:  Neuroimage       Date:  2010-10-28       Impact factor: 6.556

3.  The temporal context model in spatial navigation and relational learning: toward a common explanation of medial temporal lobe function across domains.

Authors:  Marc W Howard; Mrigankka S Fotedar; Aditya V Datey; Michael E Hasselmo
Journal:  Psychol Rev       Date:  2005-01       Impact factor: 8.934

4.  Interaction between neocortical and hippocampal networks via slow oscillations.

Authors:  Anton Sirota; György Buzsáki
Journal:  Thalamus Relat Syst       Date:  2005-12

5.  Conversion of a phase- to a rate-coded position signal by a three-stage model of theta cells, grid cells, and place cells.

Authors:  Hugh T Blair; Kishan Gupta; Kechen Zhang
Journal:  Hippocampus       Date:  2008       Impact factor: 3.899

Review 6.  Deep Brain Stimulation for Epilepsy: Biomarkers for Optimization.

Authors:  Katrina L Dell; Mark J Cook; Matias I Maturana
Journal:  Curr Treat Options Neurol       Date:  2019-09-26       Impact factor: 3.598

Review 7.  Distinct patterns of neuronal inputs and outputs of the juxtaparaventricular and suprafornical regions of the lateral hypothalamic area in the male rat.

Authors:  Joel D Hahn; Larry W Swanson
Journal:  Brain Res Rev       Date:  2010-02-17

8.  MAPBOT: Meta-analytic parcellation based on text, and its application to the human thalamus.

Authors:  Rui Yuan; Paul A Taylor; Tara L Alvarez; Durga Misra; Bharat B Biswal
Journal:  Neuroimage       Date:  2017-06-17       Impact factor: 6.556

9.  Distinct neural correlates of episodic memory among apolipoprotein E alleles in cognitively normal elderly.

Authors:  Hao Shu; Yongmei Shi; Gang Chen; Zan Wang; Duan Liu; Chunxian Yue; B Douglas Ward; Wenjun Li; Zhan Xu; Guangyu Chen; Qi-Hao Guo; Jun Xu; Shi-Jiang Li; Zhijun Zhang
Journal:  Brain Imaging Behav       Date:  2019-02       Impact factor: 3.978

Review 10.  Cellular dynamical mechanisms for encoding the time and place of events along spatiotemporal trajectories in episodic memory.

Authors:  Michael E Hasselmo; Lisa M Giocomo; Mark P Brandon; Motoharu Yoshida
Journal:  Behav Brain Res       Date:  2009-12-16       Impact factor: 3.332

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.