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Aging profoundly delays functional recovery from gustatory nerve injury

*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

The peripheral taste system remains plastic during adulthood. Sectioning the chorda tympani (CT) nerve, which sends sensory information from the anterior tongue to the central nervous system, causes degeneration of distal fibers and target taste buds. However, taste function is restored after about 40 days in young adult rodents. We tested whether aging impacts the reappearance of neural responses after unilateral CT nerve injury. Taste bud regeneration was minimal at day 50-65 after denervation, and most aged animals died before functional recovery could be assessed. A subset (n=3/5) of old rats exhibited normal CT responses at day 85 postsectioning, suggesting the potential for efficient recovery. The aged taste system is fairly resilient to sensory receptor loss and major functional changes in normal aging. However, injury to the taste system reveals a surprising vulnerability in old rodents. The gustatory system provides an excellent model to study mechanisms underlying delayed recovery from peripheral nerve injury. Strategies to accelerate recovery and restore normal function will be of interest, as the elderly population continues to grow.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 208-218 (11 pages)

Journal (Volume, Issue Number)

Neuroscience (Volume 209)

Publication milestones

  • Published - 05/03/2012

Publication status

Published - 05/03/2012

ISSN

0306-4522

Publication IDs

  • Scopus: 84859270677
  • PubMed: 22387273

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
0.36
SciVal
Author count
4
SciVal
citations
12
SciVal
Paper percentile
69
Fractional count
1
Fractional count
0.25
Fractional count
3
Fractional count
0.75
Fractional count
1
Fractional count
1

PlumX, opens in new tab

Captures
19
Citation count
21

Funding Details

This work was funded by NIDCD ( DC005811 ) to L.P.M. We are also grateful to the Dean's Student Summer Research Program (A.Y.) and the Institute of Molecular Medicine and Genetics (S.S.) at Georgia Health Sciences University for stipend support.
FunderFunding number
NIDCD
R01DC005811