Why Do Levels Of Anti-inflammatory Cytokines Increase During Memory Acquisition?
Neuroscience, ISSN: 0306-4522, Vol: 473, Page: 159-169
2021
- 12Citations
- 25Captures
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Metrics Details
- Citations12
- Citation Indexes12
- 12
- Captures25
- Readers25
- 25
Review Description
The role of anti-inflammatory cytokines in the mechanisms of learning and memory, modulation of synaptic plasticity in the mammalian brain has not received sufficient attention. These issues are discussed in this review, and among the many cytokines, attention is paid to the most studied in this respect IL-10, IL-4, IL-13 and TGF-β. The level of anti-inflammatory cytokines in the brain tends to increase during memory acquisition, but the significance of such an increase is unclear. We hypothesize that anti-inflammatory cytokines primarily protect and optimize the functioning of neuronal circuits involved in information processing. The increased local activity of neurons during memory acquisition activates many signaling molecules, and some of them can trigger unwanted processes (including neuroinflammation), but increased levels of anti-inflammatory cytokines prevent this triggering. Each of the anti-inflammatory cytokines plays a specific role in supporting information processing. For example, the role of IL-4 and IL-13 in recruiting T cells to the meninges during training in healthy animals has been most studied. It has also been shown that TGF-β is able to optimize late stage LTP in the hippocampus and support the consolidation of memory traces in behavioral studies. Cytokines have an effect on learning and memory through their influence on neuroplasticity, neurogenesis in the hippocampus and regulation of the neurovascular unit. Experiments have shown such an effect, and the data obtained create the prerequisites for new therapeutic approaches to the correction of cognitive impairments.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0306452221004139; http://dx.doi.org/10.1016/j.neuroscience.2021.08.007; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85114326619&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/34418518; https://linkinghub.elsevier.com/retrieve/pii/S0306452221004139; https://dx.doi.org/10.1016/j.neuroscience.2021.08.007
Elsevier BV
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