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Disturbed emotionality in autoimmune MRL-lpr mice
B Sakić1, H Szechtman, H Talangbayan
1Department of Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada.
Physiology & Behavior
|September 1, 1994
Summary
Autoimmune MRL-lpr mice exhibit increased timidity and altered emotional reactivity compared to MRL +/+ mice. These behavioral changes may be linked to autoimmunity affecting the hypothalamic-pituitary-adrenal axis.
Area of Science:
- Neuroscience
- Immunology
- Behavioral Science
Background:
- MRL-lpr mice spontaneously develop autoimmune lupus-like disease earlier than MRL +/+ mice.
- Previous research suggests autoimmune MRL-lpr mice display altered emotional reactivity.
Purpose of the Study:
- To investigate the hypothesis that autoimmune MRL-lpr mice exhibit altered emotional reactivity.
- To identify behavioral measures that effectively differentiate MRL-lpr mice from MRL +/+ controls.
Main Methods:
- Comparison of male MRL-lpr and MRL +/+ mice (n=40/substrain, 3-4 months old) using a battery of behavioral tests.
- Tests included open field, elevated platform, novel object interaction, plus-maze, and Porsolt's swim test.
- Discriminant analysis was employed to identify key behavioral differences.
Main Results:
- MRL-lpr mice showed reduced exploration in the open field, increased time spent at home-base, and less defecation compared to MRL +/+ mice.
- MRL-lpr mice exhibited hesitation on an elevated platform, avoided novel objects, and spent less time on open arms of the plus-maze.
- Porsolt's swim test and the step-down test most effectively distinguished between the two substrains.
- In MRL-lpr mice, high antinuclear antibody titers correlated with impaired novel object exploration.
Conclusions:
- Results support the notion of increased timidity in autoimmune MRL-lpr mice, suggesting an immune system contribution to emotional reactivity.
- The observed behavioral disturbances in autoimmune MRL-lpr mice resemble those of stressed animals.
- It is speculated that altered emotional reactivity reflects autoimmunity's impact on the hypothalamic-pituitary-adrenal axis.