 |
Previous Article | Next Article 
The Journal of Neuroscience, April 1, 2000, 20(7):2711-2718
Fos Imaging Reveals Differential Patterns of Hippocampal and
Parahippocampal Subfield Activation in Rats in Response to Different
Spatial Memory Tests
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 3YJ, United Kingdom
We compared neuronal activation, as measured by Fos staining,
during different spatial tasks in two experiments. The counts of
Fos-stained neurons in the hippocampus increased as the spatial demands
of the tasks increased, the tasks having been carefully matched for
other factors. In Experiment 1, matched groups of rats either ran a
standard eight-arm radial maze task or were trained to run up and down
just one arm of the maze; the number of runs and rewards was identical
in both conditions. In Experiment 2, rats were trained on the eight-arm
maze but in different rooms. On the critical test day, both groups were
run in the same room so that one group now performed with novel
landmarks. All hippocampal subfields (dentate gyrus, CA3, CA1, dorsal,
ventral, and caudal subiculum) showed a relative increases in
c-fos activation in the eight-arm (Experiment 1) and novel
room (Experiment 2) conditions, the sole exception being the ventral
subiculum in Experiment 2. Although increased c-fos
activation was found in both dorsal and ventral hippocampus, in
Experiment 2 the relative increase was significantly greater in the
dorsal hippocampus. Parahippocampal cortices responded heterogeneously:
the perirhinal cortex failed to show increased activation in both
experiments, in contrast to the entorhinal and postrhinal cortices.
Subsequent comparisons confirmed that the perirhinal and postrhinal
cortices responded in qualitatively different ways, the perirhinal
cortex differing from the rest of the hippocampal formation. These
experiments, which provide the first analysis of hippocampal Fos
production during tests of allocentric spatial working memory, reveal
that all components of the hippocampus are activated, but that under certain conditions the dorsal hippocampus is disproportionately involved.
Key words:
Fos; spatial memory; hippocampus; entorhinal cortex; dorsal hippocampus; parahippocampal cortex
Copyright © 2000 Society for Neuroscience 0270-6474/00/2072711-08$05.00/0
This article has been cited by other articles:

|
 |

|
 |
 
S. Trouche, B. Bontempi, P. Roullet, and C. Rampon
Recruitment of adult-generated neurons into functional hippocampal networks contributes to updating and strengthening of spatial memory
PNAS,
April 7, 2009;
106(14):
5919 - 5924.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
E. S. Carlson, I. Tkac, R. Magid, M. B. O'Connor, N. C. Andrews, T. Schallert, H. Gunshin, M. K. Georgieff, and A. Petryk
Iron Is Essential for Neuron Development and Memory Function in Mouse Hippocampus
J. Nutr.,
April 1, 2009;
139(4):
672 - 679.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. VanElzakker, R. D. Fevurly, T. Breindel, and R. L. Spencer
Environmental novelty is associated with a selective increase in Fos expression in the output elements of the hippocampal formation and the perirhinal cortex
Learn. Mem.,
December 2, 2008;
15(12):
899 - 908.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
A. C. H. Lee, V. L. Scahill, and K. S. Graham
Activating the Medial Temporal Lobe during Oddity Judgment for Faces and Scenes
Cereb Cortex,
March 1, 2008;
18(3):
683 - 696.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
G. L. Poirier, E. Amin, and J. P. Aggleton
Qualitatively Different Hippocampal Subfield Engagement Emerges with Mastery of a Spatial Memory Task by Rats
J. Neurosci.,
January 30, 2008;
28(5):
1034 - 1045.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
L. M. Talamini, M. Meeter, B. Elvevag, J. M. J. Murre, and T. E. Goldberg
Reduced Parahippocampal Connectivity Produces Schizophrenia-like Memory Deficits in Simulated Neural Circuits With Reduced Parahippocampal Connectivity
Arch Gen Psychiatry,
May 1, 2005;
62(5):
485 - 493.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. Wietrzych, H. Meziane, A. Sutter, N. Ghyselinck, P. F. Chapman, P. Chambon, and W. Krezel
Working memory deficits in retinoid X receptor {gamma}-deficient mice
Learn. Mem.,
May 1, 2005;
12(3):
318 - 326.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
M. C. Alvarado and J. Bachevalier
Comparison of the Effects of Damage to the Perirhinal and Parahippocampal Cortex on Transverse Patterning and Location Memory in Rhesus Macaques
J. Neurosci.,
February 9, 2005;
25(6):
1599 - 1609.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
C. Crosio, E. Heitz, C. D. Allis, E. Borrelli, and P. Sassone-Corsi
Chromatin remodeling and neuronal response: multiple signaling pathways induce specific histone H3 modifications and early gene expression in hippocampal neurons
J. Cell Sci.,
December 15, 2003;
116(24):
4905 - 4914.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. D. Vann and J. P. Aggleton
Evidence of a Spatial Encoding Deficit in Rats with Lesions of the Mammillary Bodies or Mammillothalamic Tract
J. Neurosci.,
April 15, 2003;
23(8):
3506 - 3514.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
P. J. Colombo, J. J. Brightwell, and R. A. Countryman
Cognitive Strategy-Specific Increases in Phosphorylated cAMP Response Element-Binding Protein and c-Fos in the Hippocampus and Dorsal Striatum
J. Neurosci.,
April 15, 2003;
23(8):
3547 - 3554.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
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]
|
 |
|

|
 |

|
 |
 
A. Stephan, S. Laroche, and S. Davis
Generation of Aggregated {beta}-Amyloid in the Rat Hippocampus Impairs Synaptic Transmission and Plasticity and Causes Memory Deficits
J. Neurosci.,
August 1, 2001;
21(15):
5703 - 5714.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. F. Guzowski, B. Setlow, E. K. Wagner, and J. L. McGaugh
Experience-Dependent Gene Expression in the Rat Hippocampus after Spatial Learning: A Comparison of the Immediate-Early Genes Arc, c-fos, and zif268
J. Neurosci.,
July 15, 2001;
21(14):
5089 - 5098.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
S. D. Vann, M. W. Brown, J. T. Erichsen, and J. P. Aggleton
Using Fos Imaging in the Rat to Reveal the Anatomical Extent of the Disruptive Effects of Fornix Lesions
J. Neurosci.,
November 1, 2000;
20(21):
8144 - 8152.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|

|