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Published on: May 22, 2018
Adenosine receptor neurobiology: overview
Jiang-Fan Chen1, Chien-fei Lee2, Yijuang Chern2
1Department of Neurology, Boston University School of Medicine, Boston, Massachusetts, USA.
Adenosine receptors (ARs) are crucial for brain function, modulating everything from sleep to neuroinflammation. New research highlights their structure, signaling, and potential as therapeutic targets for neurological and psychiatric diseases.
Area of Science:
- Neuroscience
- Pharmacology
- Molecular Biology
Background:
- Adenosine is a ubiquitous nucleoside acting as a key neuromodulator in the brain.
- Adenosine receptors (ARs), a family of G-protein-coupled receptors, regulate diverse brain functions including synaptic plasticity, cognition, sleep, motor activity, neuroinflammation, and cell death.
Purpose of the Study:
- To review recent advancements in understanding adenosine receptor (AR) structure, signaling, and function in the brain.
- To highlight novel developments in AR neurobiology and their therapeutic implications for neurological and psychiatric diseases.
Main Methods:
- Review of gene and genome structure and expression patterns of ARs.
- Analysis of canonical and noncanonical AR signaling pathways.
- Integration of findings from genetic-knockout and pharmacological studies.
- Highlighting recent breakthroughs in AR structural biology and receptor interactions.
Main Results:
- Detailed overview of AR gene/genome structure and expression.
- Characterization of novel AR signaling pathways, including noncanonical pathways.
- Insights from genetic and pharmacological studies on AR's role in brain function.
- Recent advances in understanding AR structure, heterodimerization, glial function, and druggability.
Conclusions:
- Adenosine A1 and A2A receptors (A1ARs and A2ARs) are strongly supported as therapeutic targets for neurological and psychiatric disorders.
- Emerging research on ARs, including structural biology and signaling, solidifies their importance in brain function and disease treatment.
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