A combined study of behavior and Fos expression in limbic structures after re-testing Wistar rats in the elevated plus-maze
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URI: http://hdl.handle.net/10818/27265Visitar enlace: https://www.ncbi.nlm.nih.gov/p ...
Visitar enlace: http://www.sciencedirect.com/s ...
ISSN: 0361-9230
DOI: 10.1016/j.brainresbull.2010.01.007
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Galvis Alonso, Orfa Yineth; García Becerra, Andrea Milena; Orejarena, M.J.; Lamprea Rodríguez, Marisol; Botelho De Oliveira, Silvia; Conde, C.A.; Moratoc, S.; Garcia Cairasco, NorbertoFecha
2010Resumen
The elevated plus-maze is an animal model used to study anxiety. In a second session, rats show a reduction
in the exploratory behavior even when the two sessions are separated by intervals as large as 7 days.
The aim of the present study was to investigate whether the reduction in the exploratory behavior is
maintained after intervals larger than 7 days. Additionally, we aimed at investigating eventual correlations
between behaviors in the plus-maze and activation of limbic structures as measured by Fos protein
expression after the second session. Rats were tested for 5 min in the elevated plus-maze and re-tested 3,
9 or 33 days later. Other groups were tested only once. The rat brains were processed for immunohistochemical
detection of Fos protein. The results show a decrease in the open arms exploration in the second
trial with intervals of 3, 9 and 33 days. The expression of Fos protein in the piriform cortex, septal nucleus
and paraventricular hypothalamic nucleus in the groups tested with intervals of 9 and 33 days were statistically
different from the other groups. The alterations observed in exploratory behavior in the second session
in the plus-maze did not correlate with Fos expression. In conclusion, although the specific test conditions
were sufficient to evoke behavioral alterations in exploration in the elevated plus-maze, they were
enough to induce significant Fos protein expression in piriform cortex, septal nucleus and thalamic and
hypothalamic paraventricular nuclei but not in other areas such as dorsomedial nucleus of the hypothalamus
and amygdala nuclei, known to be also active participants in circuits controlling fear and anxiety
Ubicación
Brain Res Bull. 2010 Apr 5;81(6):595-9
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