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Interleukin-6 (IL-6) in addition to its role in the immune system has the potential to modulate several brain functions including learning and memory processes. In the present study we investigated the role of IL-6 in CNS function in male mice not expressing IL-6 (C57BL/6J IL6-/-tm 1 Kopf) and wild type mice (WT) used as controls. The animals were kept in standard conditions with water and food available ad libitum except during experiments. All testing took place between 8.30 AM and 12.30 PM. Each group consisted of 13 animals. In order to evaluate a role of endogenous IL-6 in cognitive functions “object recognition test” for the evaluation of recognition memory was used. In an attempt to evaluate whether observed effect was memory specifi c, the level of anxiety and psychomotor activity of mice was evaluated in an “elevated plus maze” test and in an open fi eld, respectively. Recognition memory, measured by the difference in exploration of the new object and a duplicate of the familiar one, presented 1 h earlier, was impaired in IL-6 defi cient mice. Moreover, lack of IL-6 signifi cantly attenuated locomotor and exploratory activity measured in an open fi eld test and enhanced anxiety evaluated in an “elevated plus maze” test. Results of this study indicate that IL-6 defi ciency impairs recognition memory, attenuates locomotor and exploratory activity and enhances anxiety in mice. The study was supported by the Polish Ministry of Science grant Nr 2P05B01826.
Interleukin 6 (IL-6) is a cytokine playing an important pleiotropic role in the immune system. IL-6 is also involved in stress response, etiology of the age-related diseases and plays a role of mediator between the central nervous system and the immune system. To study effects of IL-6 on behavior during aging we examined aged (13 to 15 months) IL-6 deficient and wild type (WT) mice. Behavior was tested using the open field test, elevated plus maze test and registration of spontaneous activity in the individual home cages for 72 hours. These registrations showed that IL-6 deficient animals were less active than WT mice. The difference was more distinct during the dark phase. Interestingly, in the open field IL-6 deficient mice displayed higher locomotor activity than control WT mice and spent more time in the central part of the arena. In the elevated plus maze IL-6 deficient mice spent more time exploring open arms than WT mice. We conclude that IL-6 deficient aging animals show lower level of anxiety than WT control animals. After tests mice were perfused and brains were cut into 40 μm sections. Brain sections were immunohistochemically labeled for IL-6 and its receptor (IL-6R), also known as CD126. We found that cells immunopositive for both IL-6 and CD126 were present in the hippocampus and other brain structures. Supported by the National Science Center grant No 1577.
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