Over the next 25 years, it is projected that over 72 million people will be 65 years and older in the United States representing 20% of the population. Age-related degeneration of the cranial muscles that culminate in reductions of muscle mass, strength, and function can contribute to swallowing deficits in over 15% of elderly people, negatively impacting health, nutrition, and quality of life. The tongue is crucial to adequate swallowing function. However, the processes primary to age-related decline in the cranial sensorimotor system have been understudied. Because swallowing disorders are so prevalent in the aging population, study of the underlying cellular mechanisms contributing to age-related muscular degeneration in the tongue is a clinical priority, as is the development of novel therapies that specifically target the pathways underlying these disorders. The proposed research will examine mechanisms that contribute to decline in satellite cell (SC; muscle-specific adult stem cells) regeneration and function, and the potential for an exercise-based treatment, similar to exercise tasks used now in the clinic, to reverse this age-induced cellular senescence. Specifically, we will study the effects of p16 expression, an aging biomarker associated with SC senescence in the limb, on SC activation, self-renewal, proliferation, and differentiation in aging rat lingual muscles. In addition, we will determine the immediate (2-week) and longer-term (8-week) effects of a tongue exercise treatment on p16 expression, SC regenerative capacity, and tongue muscle and swallowing function. We hypothesize that with age: (1) p16 expression will be up-regulated, (2) SC regenerative capacity will be reduced, and (3) tongue muscle and swallowing function will be impaired. With tongue exercise, we hypothesize that: (1) p16 expression will be down-regulated, (2) SC activation, self-renewal, proliferation, and differentiation will be enhanced following 2 weeks of exercise, (3) age-related reductions in SC regeneration will be rescued following 8 weeks of exercise, and (4) enhanced muscle regenerative processes will manifest in improved tongue muscle and swallowing function in aged rats. To address these hypotheses, this proposal has 2 specific aims: (1) to quantify putative underlying mechanisms of lingual muscle regeneration and tongue muscle SC populations in aging rats with and without exercise at multiple time points, (2) to determine the effects of age and exercise on tongue muscle and swallowing function. This research is highly significant because it is the first to examine the effects of the p16 aging biomarker on SC regenerative capacity and to isolate and quantify lingual muscle SCs with age and exercise, and determine whether improved SC regenerative processes manifest in functional gains. This proposal will be the first to elucidate and quantify underlying cellular mechanisms of age-related and exercise-induced muscle plasticity for the development of effective treatment and targeted delivery strategies for individuals with swallowing disorders.

Public Health Relevance

Swallowing problems increase with aging, but the mechanisms of decline in function of muscles involved in these actions are understudied and not well understood. This research will identify how cellular mechanisms contribute to decline in muscle function in the tongue and how tongue exercise may help rescue or restore muscle and swallowing function. This work is highly significant in exploring the effects of exercise therapy for the prevention and rehabilitation of swallowing disorders, and the potential for cell-based therapies as a future treatment of swallowing disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31AG054315-02
Application #
9479995
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Williams, John
Project Start
2017-04-01
Project End
2019-03-31
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Surgery
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Kletzien, Heidi; Macdonald, Cameron L; Orne, Jason et al. (2018) Comparison Between Patient-Perceived Voice Changes and Quantitative Voice Measures in the First Postoperative Year After Thyroidectomy: A Secondary Analysis of a Randomized Clinical Trial. JAMA Otolaryngol Head Neck Surg 144:995-1003
Kletzien, Heidi; Russell, John A; Leverson, Glen et al. (2018) Effect of neuromuscular electrical stimulation frequency on muscles of the tongue. Muscle Nerve 58:441-448
Kletzien, Heidi; Hare, Allison J; Leverson, Glen et al. (2018) Age-related effect of cell death on fiber morphology and number in tongue muscle. Muscle Nerve 57:E29-E37
Hoffman, Matthew R; Kletzien, Heidi; Dailey, Seth H et al. (2017) Simulation of KTP Laser-Based Zenker Diverticulotomy with a Porcine Model and Laryngeal Dissection Station. OTO Open 1: