Literature DB >> 17626218

Lesions of the tegmentomammillary circuit in the head direction system disrupt the head direction signal in the anterior thalamus.

Joshua P Bassett1, Matthew L Tullman, Jeffrey S Taube.   

Abstract

Head direction (HD) cells in the rodent limbic system are believed to correspond to a cognitive representation of directional heading in the environment. Lesions of vestibular hair cells disrupt the characteristic firing patterns of HD cells, and thus vestibular afference is a critical contributor to the HD signal. A subcortical pathway that may convey this information includes the dorsal tegmental nucleus of Gudden (DTN) and the lateral mammillary nucleus (LMN). To test the hypothesis that the DTN and LMN are critical components for generating HD cell activity, we made electrolytic lesions of the DTN or LMN in rats and screened for HD cell activity in the anterior thalamus. Directional activity was absent in all animals with complete LMN lesions and in animals with complete DTN lesions, although a few HD cells were isolated in animals with incomplete lesions. Some DTN-lesioned animals contained cells whose firing rates were modulated by angular head velocity. Although cells with bursting patterns of activity have been observed in the anterior dorsal nucleus of the thalamus of animals with disruption of vestibular inputs, this pattern of activity was not observed in either the LMN- or DTN-lesioned animals. The general absence of direction-specific activity in the anterior thalamus of animals with DTN or LMN lesions is consistent with the view that the DTN-LMN circuit is essential for the generation of HD cell activity.

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Year:  2007        PMID: 17626218      PMCID: PMC6672597          DOI: 10.1523/JNEUROSCI.0268-07.2007

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  61 in total

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3.  Acetylcholine contributes to the integration of self-movement cues in head direction cells.

Authors:  Ryan M Yoder; Jeremy H M Chan; Jeffrey S Taube
Journal:  Behav Neurosci       Date:  2017-08       Impact factor: 1.912

4.  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

5.  Intact landmark control and angular path integration by head direction cells in the anterodorsal thalamus after lesions of the medial entorhinal cortex.

Authors:  Benjamin J Clark; Jeffrey S Taube
Journal:  Hippocampus       Date:  2010-11-03       Impact factor: 3.899

Review 6.  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

7.  Both visual and idiothetic cues contribute to head direction cell stability during navigation along complex routes.

Authors:  Ryan M Yoder; Benjamin J Clark; Joel E Brown; Mignon V Lamia; Stephane Valerio; Michael E Shinder; Jeffrey S Taube
Journal:  J Neurophysiol       Date:  2011-03-30       Impact factor: 2.714

8.  Active and passive movement are encoded equally by head direction cells in the anterodorsal thalamus.

Authors:  Michael E Shinder; Jeffrey S Taube
Journal:  J Neurophysiol       Date:  2011-05-25       Impact factor: 2.714

9.  Head direction cell activity in mice: robust directional signal depends on intact otolith organs.

Authors:  Ryan M Yoder; Jeffrey S Taube
Journal:  J Neurosci       Date:  2009-01-28       Impact factor: 6.167

10.  Head direction cell instability in the anterior dorsal thalamus after lesions of the interpeduncular nucleus.

Authors:  Benjamin J Clark; Asha Sarma; Jeffrey S Taube
Journal:  J Neurosci       Date:  2009-01-14       Impact factor: 6.167

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