PPAR-γ has been proposed as a transcription factor that activates

PPAR-γ has been proposed as a transcription factor that activates the HO-1 gene in silico [5]. Studies have shown that PPAR-γ and HO-1 exert beneficial effects in neurodegenerative disorders. Interestingly, functional binding sites for the transcription factor C/EBPβ can be found in the promoter regions of PPAR-γ Compound Library datasheet and HO-1 [36, 37]. In the present study, IL-13 markedly abolishes LPS-induced C/EBP-β, PPAR-γ, and

HO-1 expressions. Consistent with previous studies using brain injury models, the results here demonstrate that C/EBP-β regulation provides a potential new avenue for the development of therapeutic strategies to prevent hyperactivated microglia-induced neuronal damage. Pathologic conditions and proinflammatory stimuli in the brain induce COX-2, a key enzyme in arachidonic acid metabolism. COX-2 mediates the production www.selleckchem.com/products/fg-4592.html of prostanoids, such as PGE2, which induce fever and pain, increase vascular permeability, and recruit inflammatory cells to sites of inflammation. In previous studies, Yang et al. [6] found that COX-2 and PGE2 appear to be involved in IL-13-induced death of activated microglia. Their findings

suggest that the death of activated microglia may act as an endogenous mechanism for the resolution and termination of brain inflammation [6]. The current study demonstrates that IL-13 enhances apoptosis in activated microglia and this plays a crucial role in reducing brain inflammation. C/EBP-α, a basic leucine zipper transcription factor, has been identified in many studies as playing a critical role in COX-2 expression in the Methisazone transcriptional activation of the COX-2 promoter [38]. C/EBP-α binds to C/EBP enhancer elements and is essential for inducing COX-2 expression by LPS, TNF-α, and IL-1β. Hsieh et al.

[39] showed that attenuated C/EBP-α expression in COX-2 activation in fat inflammation is important in the development of insulin resistance and fatty liver in high fat-induced obese rats. In addition, signaling cascade coupling of COX enzymes with PLA2s may be a key mechanism in the propagation of inflammatory reaction. Recently, PLA2s have been found to play a prominent role in the regulation of C/EBP-α gene expression. The activation of C/EBP-α is under the control of different signaling pathways and can be activated via PLA2 pathway more than the influence of COX-2 expression [40]. The hippocampus is part of a group of structures forming the limbic system and is also a part of the hippocampal formation, which also includes the dentate gyrus, subiculum, and entorhinal cortex. Different components of the limbic system play critical roles in various aspects of emotions, fear, learning, and memory [41-44].

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