The effects of resistance training on denervated myofibers, senescent cells, and associated protein markers in middle‐aged adults

Author:

Ruple Bradley A.1,Mattingly Madison L.1,Godwin Joshua S.1,McIntosh Mason C.1,Kontos Nicholas J.1,Agyin‐Birikorang Anthony1,Michel J. Max1,Plotkin Daniel L.1,Chen Shao‐Yung2,Ziegenfuss Tim N.3,Fruge Andrew D.4,Gladden L. Bruce1,Robinson Austin T.1,Mobley C. Brooks1,Mackey Abigail L.56ORCID,Roberts Michael D.1ORCID

Affiliation:

1. School of Kinesiology Auburn University Auburn Alabama USA

2. Seer, Inc. Redwood City California USA

3. The Center for Applied Health Sciences Canfield Ohio USA

4. College of Nursing Auburn University Auburn Alabama USA

5. Department of Clinical Medicine, Faculty of Health and Medical Sciences University of Copenhagen Copenhagen Denmark

6. Department of Orthopaedic Surgery, Institute of Sports Medicine Copenhagen Copenhagen University Hospital – Bispebjerg and Frederiksberg Copenhagen Denmark

Abstract

AbstractDenervated myofibers and senescent cells are hallmarks of skeletal muscle aging. However, sparse research has examined how resistance training affects these outcomes. We investigated the effects of unilateral leg extensor resistance training (2 days/week for 8 weeks) on denervated myofibers, senescent cells, and associated protein markers in apparently healthy middle‐aged participants (MA, 55 ± 8 years old, 17 females, 9 males). We obtained dual‐leg vastus lateralis (VL) muscle cross‐sectional area (mCSA), VL biopsies, and strength assessments before and after training. Fiber cross‐sectional area (fCSA), satellite cells (Pax7+), denervated myofibers (NCAM+), senescent cells (p16+ or p21+), proteins associated with denervation and senescence, and senescence‐associated secretory phenotype (SASP) proteins were analyzed from biopsy specimens. Leg extensor peak torque increased after training (p < .001), while VL mCSA trended upward (interaction p = .082). No significant changes were observed for Type I/II fCSAs, NCAM+ myofibers, or senescent (p16+ or p21+) cells, albeit satellite cells increased after training (p = .037). While >90% satellite cells were not p16+ or p21+, most p16+ and p21+ cells were Pax7+ (>90% on average). Training altered 13 out of 46 proteins related to muscle–nerve communication (all upregulated, p < .05) and 10 out of 19 proteins related to cellular senescence (9 upregulated, p < .05). Only 1 out of 17 SASP protein increased with training (IGFBP‐3, p = .031). In conclusion, resistance training upregulates proteins associated with muscle–nerve communication in MA participants but does not alter NCAM+ myofibers. Moreover, while training increased senescence‐related proteins, this coincided with an increase in satellite cells but not alterations in senescent cell content or SASP proteins. These latter findings suggest shorter term resistance training is an unlikely inducer of cellular senescence in apparently healthy middle‐aged participants. However, similar study designs are needed in older and diseased populations before definitive conclusions can be drawn.

Publisher

Wiley

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