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An Atlas of Brain-Bone Sympathetic Neural Circuits. | LitMetric

AI Article Synopsis

  • The sympathetic nervous system (SNS) plays a significant role in bone metabolism, with nerves found in the periosteum and bone marrow showing evidence of noradrenergic fibers.
  • Recent research using pseudorabies (PRV) tracing has identified 87 brain nuclei that send efferent SNS signals to bone, highlighting the complexity of this communication.
  • Specific regions, like the raphe magnus and periaqueductal gray, exhibit varying levels of SNS activity, leading to new insights into how these neural pathways could be linked to bone health and pain management.

Article Abstract

There is clear evidence that the sympathetic nervous system (SNS) mediates bone metabolism. Histological studies show abundant SNS innervation of the periosteum and bone marrow--these nerves consist of noradrenergic fibers that immunostain for tyrosine hydroxylase, dopamine beta hydroxylase, or neuropeptide Y. Nonetheless, the brain sites that send efferent SNS outflow to bone have not yet been characterized. Using pseudorabies (PRV) viral transneuronal tracing, we report, for the first time, the identification of central SNS outflow sites that innervate bone. We find that the central SNS outflow to bone originates from 87 brain nuclei, sub-nuclei and regions of six brain divisions, namely the midbrain and pons, hypothalamus, hindbrain medulla, forebrain, cerebral cortex, and thalamus. We also find that certain sites, such as the raphe magnus (RMg) of the medulla and periaqueductal gray (PAG) of the midbrain, display greater degrees of PRV152 infection, suggesting that there is considerable site-specific variation in the levels of central SNS outflow to bone. This comprehensive compendium illustrating the central coding and control of SNS efferent signals to bone should allow for a greater understanding of the neural regulation of bone metabolism, and importantly and of clinical relevance, mechanisms for central bone pain.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10871366PMC
http://dx.doi.org/10.1101/2024.02.07.579382DOI Listing

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