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. 2015 Jan 6:21:69-75.
doi: 10.12659/MSM.893159.

The effects of oxytocin on cognitive defect caused by chronic restraint stress applied to adolescent rats and on hippocampal VEGF and BDNF levels

Affiliations

The effects of oxytocin on cognitive defect caused by chronic restraint stress applied to adolescent rats and on hippocampal VEGF and BDNF levels

Ayfer Dayi et al. Med Sci Monit. .

Abstract

Background: Because brain development continues during adolescence, the effects of chronic stress on hippocampal changes that occur during that period are permanent. Oxytocin, which is synthesized in the hypothalamus and has many receptors in brain regions, including the hippocampus, may affect learning-memory. This study aimed to investigate chronic restraint stress on hippocampal functions, and hippocampal vascular endothelial growth factor (VEGF) and brain-derived neurotrophic factor (BDNF) levels in adolescent male and female rats and the role of oxytocin in these effects.

Material/methods: Experimental groups included control, stress+oxytocin, and stress+saline groups. Restraint stress was applied to all the stress groups for 1 h/day, for 7 days. Learning-memory tests were performed after the 7th day.

Results: In the stress+oxytocin groups, the process of finding the platform was shorter than in others groups. The stress+saline groups spent less time, whereas the stress+oxytocin groups spent more time, on the target quadrant in the probe trial. In the stress+oxytocin groups thigmotaxis time (indicating anxiety) decreased, but VEGF and BDNF levels increased. A positive correlation was found between VEGF and BDNF levels and the time spent within the target quadrant.

Conclusions: The results indicate that impaired hippocampal learning and memory loss due to chronic restraint stress can be positively affected by intranasal oxytocin.

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Figures

Figure 1
Figure 1
Effects of restraint stress on Morris Water Maze performance. Mean daily latencies to escape from the start point onto the hidden platform (A) in the male and (B) female rats. * p<0.05 compared to the other groups.
Figure 2
Figure 2
Time spent in the target and opposite quadrant in probe trial. (A) in the male and (B) female rats. * p<0.002 compared with control groups. ** p<0.001 compared to the stress+saline groups.
Figure 3
Figure 3
Thigmotaxis time in probe trial in the male and female rats. * p<0.001 compared to the other groups.
Figure 4
Figure 4
Hippocampal VEGF results. * p<0.002, ** p<0.001 compared to the other groups.
Figure 5
Figure 5
Hippocampal BDNF results. * p<0.05 compared to the other groups.

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