Author: Park HJ1, Shim HS2, An K3, Starkweather A4, Kim KS5, Shim I6.
Affiliation: 1Acupuncture and Meridian Science Research Center (AMSRC), Department of Science in Korean Medicine, Graduate School, College of Korean Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea ; Department of Psychology and Center for Neuroscience, Brigham Young University, Provo, UT 84602, USA. 2Acupuncture and Meridian Science Research Center (AMSRC), Department of Science in Korean Medicine, Graduate School, College of Korean Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea ; Department of Neuroscience and Cell Biology, University of Texas Medical Branch, Galveston, TX 77551, USA. 3Department of Adult Health and Nursing Systems, School of Nursing, Virginia Commonwealth University, Richmond, VA 23298-0567, USA. 4Center for Advancement in Managing Pain, School of Nursing, University of Connecticut, Storrs, CT 06269, USA. 5Department of Integrative Medicine and Research Center of Behavioral Medicine, College of Medicine, The Catholic University of Korea, Seoul 137-701, Republic of Korea. 6Acupuncture and Meridian Science Research Center (AMSRC), Department of Science in Korean Medicine, Graduate School, College of Korean Medicine, Kyung Hee University, 1 Hoegi-dong, Dongdaemun-gu, Seoul 130-701, Republic of Korea.
Conference/Journal: Mediators Inflamm.
Date published: 2015
Other:
Volume ID: 2015 , Special Notes: doi: 10.1155/2015/941413 , Word Count: 241
It has been known that activation of the central innate immune system or exposure to stress can disrupt balance of anti-/proinflammatory cytokines. The aim of the present study was to investigate the role of pro- and anti-inflammatory cytokines in the modulation of depressive-like behaviors, the hormonal and neurotransmitter systems in rats. We investigated whether centrally administered IL-1β is associated with activation of CNS inflammatory pathways and behavioral changes and whether treatment with IL-4 could modulate IL-1β-induced depressive-like behaviors and central neurotransmitter systems. Infusion of IL-4 significantly decreased IL-1β-induced anhedonic responses and increased social exploration and total activity. Treatment with IL-4 markedly blocked IL-1β-induced increase in PGE2 and CORT levels. Also, IL-4 reduced IL-1β-induced 5-HT levels by inhibiting tryptophan hydroxylase (TPH) mRNA and activating serotonin transporter (SERT) in the hippocampus, and levels of NE were increased by activating tyrosine hydroxylase (TH) mRNA expression. These results demonstrate that IL-4 may locally contribute to the regulation of noradrenergic and serotonergic neurotransmission and may inhibit IL-1β-induced behavioral and immunological changes. The present results suggest that IL-4 modulates IL-1β-induced depressive behavior by inhibiting IL-1β-induced central glial activation and neurotransmitter alterations. IL-4 reduced central and systemic mediatory inflammatory activation, as well as reversing the IL-1β-induced alterations in neurotransmitter levels. The present findings contribute a biochemical pathway regulated by IL-4 that may have therapeutic utility for treatment of IL-1β-induced depressive behavior and neuroinflammation which warrants further study.
PMID: 26417153