WWW.JNEUROSCI.ORG
-
The Journal of Neuroscience
 QUICK SEARCH:   [advanced]


     
-


HOME
  |  
SEARCH  |   ARCHIVE  |   SUBSCRIBE  |   CONTACT  |   HELP

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Submit an eLetter
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (34)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vann, S. D.
Right arrow Articles by Aggleton, J. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vann, S. D.
Right arrow Articles by Aggleton, J. P.

 Previous Article  |  Next Article 

The Journal of Neuroscience, November 1, 2000, 20(21):8144-8152

Using Fos Imaging in the Rat to Reveal the Anatomical Extent of the Disruptive Effects of Fornix Lesions

Seralynne D. Vann1, Malcolm W. Brown2, Jonathan T. Erichsen3, and John P. Aggleton1

1 School of Psychology, Cardiff University, Cardiff, CF10 3YG, United Kingdom, 2 Department of Anatomy, University of Bristol, Medical School, Bristol BS8 1TD, United Kingdom, and 3 Department of Optometry and Vision Sciences, Cardiff University, Cardiff CF10 3NB, United Kingdom

Activity of the immediate early gene c-fos was compared across hemispheres in rats with unilateral fornix lesions. To engage Fos production, rats first performed a radial arm maze task that is severely disrupted by bilateral fornix lesions. Using immunohistochemical techniques, Fos-positive cells were visualized and counted in 39 sites in both hemispheres. Fornix lesions led to a significant reduction in Fos in all ipsilateral hippocampal subfields, as well as the entorhinal cortex and most of the subicular complex. Other sites that showed reduced activity included the ipsilateral retrosplenial, anterior cingulate, and postrhinal cortices. Subcortical regions showing significant Fos decreases included the anterior thalamic nuclei, supramammillary nucleus, diagonal band of Broca, and lateral septum. Thus, the effects of fornix lesions extended beyond the hippocampal formation and included sites not directly innervated by the tract. These changes were nevertheless selective, as shown by the lack of hemispheric difference in any of the preselected control sites, the perirhinal cortex, or nucleus accumbens. Furthermore, there were no hemispheric differences in an additional group of animals with unilateral fornix lesions that were killed directly from the home cage. The location of Fos changes closely corresponded to those brain regions that when lesioned disrupt spatial working memory. Moreover, there was a correspondence between those brain regions that show increased Fos production in normal animals performing the radial arm maze task and those affected by fornix lesions. These results show that fornix transection has widespread, but selective, effects on a network of structures normally activated by spatial memory processes, with these effects extending beyond the hippocampal formation.

Key words: amnesia; fornix; hippocampus; immediate early genes; limbic cortices; rat; spatial memory; thalamus


Copyright © 2000 Society for Neuroscience  0270-6474/00/20218144-09$05.00/0


This article has been cited by other articles:


Home page
J. Neurosci.Home page
T. Miyashita, S. Kubik, N. Haghighi, O. Steward, and J. F. Guzowski
Rapid Activation of Plasticity-Associated Gene Transcription in Hippocampal Neurons Provides a Mechanism for Encoding of One-Trial Experience
J. Neurosci., January 28, 2009; 29(4): 898 - 906.
[Abstract] [Full Text] [PDF]


Home page
Learn. Mem.Home page
A. Haijima and Y. Ichitani
Anterograde and retrograde amnesia of place discrimination in retrosplenial cortex and hippocampal lesioned rats
Learn. Mem., July 14, 2008; 15(7): 477 - 482.
[Abstract] [Full Text] [PDF]


Home page
Learn. Mem.Home page
S. Kubik, T. Miyashita, and J. F. Guzowski
Using immediate-early genes to map hippocampal subregional functions
Learn. Mem., November 15, 2007; 14(11): 758 - 770.
[Abstract] [Full Text] [PDF]


Home page
Cereb CortexHome page
L. M. Saksida, T. J. Bussey, C. A. Buckmaster, and E. A. Murray
Impairment and Facilitation of Transverse Patterning after Lesions of the Perirhinal Cortex and Hippocampus, Respectively
Cereb Cortex, January 1, 2007; 17(1): 108 - 115.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. D. Runyan, A. N. Moore, and P. K. Dash
A Role for Prefrontal Cortex in Memory Storage for Trace Fear Conditioning
J. Neurosci., February 11, 2004; 24(6): 1288 - 1295.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
T. A. Jenkins, R. Dias, E. Amin, M. W. Brown, and J. P. Aggleton
Fos Imaging Reveals that Lesions of the Anterior Thalamic Nuclei Produce Widespread Limbic Hypoactivity in Rats
J. Neurosci., June 15, 2002; 22(12): 5230 - 5238.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
A. S. Mitchell, J. C. Dalrymple-Alford, and M. A. Christie
Spatial Working Memory and the Brainstem Cholinergic Innervation to the Anterior Thalamus
J. Neurosci., March 1, 2002; 22(5): 1922 - 1928.
[Abstract] [Full Text] [PDF]



-
-

Home  |   Search  |   Archive  |   Subscribe  |   Contact  |   Help

-
Copyright 2009 by Society for Neuroscience ONLINE ISSN: 1529-2401
-