4.5 Article

The Changing Sensory and Sympathetic Innervation of the Young, Adult and Aging Mouse Femur

Journal

NEUROSCIENCE
Volume 387, Issue -, Pages 178-190

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2018.01.047

Keywords

skeletal; nociceptors; pediatric; genetic disorders; geriatric

Categories

Funding

  1. National Institutes of Health [CA154550, CA157449, NS023970]
  2. Abbott (Abbott Park, IL)
  3. Adolor (Exton, PA)
  4. Array BioPharma (Boulder, CO)
  5. Johnson and Johnson (New Brunswick, NJ)
  6. Merck (White Plains, New York)
  7. Pfizer (New York, NY)
  8. Plexxikon (Berkeley, CA)
  9. Rinat (South San Francisco, CA)
  10. Roche (Palo Alto, CA)

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Although bone is continually being remodeled and ultimately declines with aging, little is known whether similar changes occur in the sensory and sympathetic nerve fibers that innervate bone. Here, immunohistochemistry and confocal microscopy were used to examine changes in the sensory and sympathetic nerve fibers that innervate the young (10 days post-partum), adult (3 months) and aging (24 months) C57Bl/6 mouse femur. In all three ages examined, the periosteum was the most densely innervated bone compartment. With aging, the total number of sensory and sympathetic nerve fibers clearly declines as the cambium layer of the periosteum dramatically thins. Yet even in the aging femur, there remains a dense sensory and sympathetic innervation of the periosteum. In cortical bone, sensory and sympathetic nerve fibers are largely confined to vascularized Haversian canals and while there is no significant decline in the density of sensory fibers, there was a 75% reduction in sympathetic nerve fibers in the aging vs. adult cortical bone. In contrast, in the bone marrow the overall density/unit area of both sensory and sympathetic nerve fibers appeared to remain largely unchanged across the lifespan. The preferential preservation of sensory nerve fibers suggests that even as bone itself undergoes a marked decline with age, the nociceptors that detect injury and signal skeletal pain remain relatively intact. (C) 2018 The Author(s). Published by Elsevier Ltd on behalf of IBRO.

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