Immune Response during Activation of Pre- and Postsynaptic Serotonin 5-HT1A Receptors in C57Bl/6J Mice at Various Stages of a Depression-Like State
- 48 Downloads
- 2 Citations
The development of a depression-like state in C57Bl/6J mice with repeated defeat experience (10 and 20 days) was accompanied by inhibition of the immune response (evaluated from the number of IgM antibody-producing cells). Activation of postsynaptic 5-HT1A receptors with a selective agonist 8-OH-DPAT (1.0 mg/kg) in these animals had no effect on the immune reaction. In mice without the experience of confrontations, stimulation of postsynaptic receptors caused a decrease in the number of IgM antibody-producing cells at the peak of the immune response induced by sheep erythrocytes (5 × 108 cells). However, the count of these cells remained unchanged in mice with a depression-like state (irrespective of the stage of disorder). Activation of presynaptic 5-HT1A receptors with 8-OH-DPAT (0.1 mg/kg) in control animals and mice with 10-day defeat experience was followed by immune stimulation. These changes were not observed in mice with a depression-like state caused by 20-day social stress.
Key Words
depression-like state serotoninergic system pre- and postsynaptic serotonin 5-HT1A receptors immune responsePreview
Unable to display preview. Download preview PDF.
References
- 1.D. F. Avgustinovich, O. V. Alekseenko, I. V. Bakshtanovskaya, et al., Uspekhi Fiziol. Nauk, 5, No. 4, 19–40 (2004).Google Scholar
- 2.E. L. Al’perina and T. A. Pavina, Byull. Eksp. Biol. Med., 122, No. 11, 541–543 (1996).Google Scholar
- 3.S. M. Davydova and G. V. Idova, Ros. Fiziol. Zh., 3, No. 10, 1156–1162 (2007).Google Scholar
- 4.L. V. Devoino, G. V. Idova, and E. L. Al’perina, Psychoneuroimmunomodulation: Behavior and Immunity. Role of the “Neurotransmitter State” of the Brain [in Russian], Novosibirsk (2009).Google Scholar
- 5.G. V. Idova, M. A. Cheido, E. N. Zhukova, et al., Byull. Eksp. Biol. Med., 132, No. 10, 432–434 (2001).Google Scholar
- 6.G. N. Kryzhanovskii, S. V. Magaeva, S. V. Makarov, and R. I. Sepiashvili, Neuroimmunopathology [in Russian], Moscow (2003).Google Scholar
- 7.N. N. Kudryavtseva and I. V. Bakshtanovskaya, Zh. Vyssh. Nervn. Deyat., 41, No. 3, 459–466 (1991).Google Scholar
- 8.V. Ya. Semke, T. P. Vetlugina, T. I. Nevidimova, et al., Clinical Neuroimmunopathology [in Russian], Tomsk (2003).Google Scholar
- 9.N. M. Barnes and T. Sharp, Neuropharmacology, 38, No. 8, 1083–1152 (1999).PubMedCrossRefGoogle Scholar
- 10.M. Boldrini, M. D. Underwood, J. J. Mann, and V. Arango, J. Psychiatr. Res., 42, No. 6, 433–442 (2008).PubMedCrossRefGoogle Scholar
- 11.L. Capuron, A. Miller, and M. R. Irwin, Psychoneuroimmunology, Ed. R. Ader, San Diego (2007), Vol. 1, pp. 509–530.Google Scholar
- 12.W. C. Drevets, M. E. Thase, E. L. Moses-Kolko, et al., Nucl. Med. Biol., 34, No. 7, 865–877 (2007).PubMedCrossRefGoogle Scholar
- 13.G. S. Ladics, J. Immunotoxicol., 4, No. 2, 149–152.Google Scholar