aging and rehab of muscle Flashcards
men vs women
Difference in muscle volume and physical strength between men and women continues throughout the life span.
Physical activity also lower in women than men throughout adulthood.
muscle vol
peaks at 25 - 35 yrs
Muscle atrophy associated with disuse, reduced number of satellite cells
reduced ability to repair
Sarcopenia:
Loss of lean body mass & muscle weakness associated with advancing age
Muscle strength predictor
Muscle strength is a strong predictor of: severe mobility limitation, slow gait speed, increased fall risk, risk of hospitalization, and high mortality rate.
older = increase fat, decrease muscle mass
The aging-associated loss of muscle mass:
• coincides with the onset of menopause in women
• accelerates during the transition into menopause
• then proceeds slower in women than in men
> 35 years, a healthy person:
• Loses 1%-2% muscle mass per year
• 1.5% annual decline in strength (increases to ~3%
per year @ 60 years)
The age-associated decline in muscle mass affects everyone, even master-athletes
While losing lean body mass, an ‘average’ adult will gain approximately 0.5 kg of fat per year between 30-60 years
The modification in body composition is frequently masked by unchanging body weight Advanced age (80 yr and older), periods of inactivity, and disease accelerate the process
Neural factors that contribute to sarcopenia:
Changes in central nervous system drive (optimising neural drive comes with use/practice)
- Altered neuromuscular junction structure and function (whether changes in the NMJ precede or follow the decline of muscle mass and strength remains unresolved)
Neural factors that contribute to sarcopenia:
- Satellite cells
- reduced number
- less responsive ti injury - Muscle Fibre
- decrease in no.
- decrease in size - predominantly type 2 - fibre type transformation
- fast to slow twitch fibre type shift
(2 > 1 )
Neural factors that contribute to sarcopenia: 2
- Excitation - contraction coupling
- disruption or uncoupling
- deficts in calcium release - Adipocyte infiltration
- Mitochondria
- reduce no
- loss of enzyme content - Myofilaments
- reduced single fibre max force
- reduction in myosin protein content and function
- reduction in elasticity
have motor neuron death
satellite cells
- Satellite cells maintain skeletal muscle homeostasis and enable - skeletal muscle regeneration
Stimulated by damage or stress to muscle tissue - With aging, muscle tissue homeostasis is progressively disrupted and the ability of muscle stem cells to repair injured muscle markedly declines.
Satellite cells can fuse to form new muscle fibers or self-renew and replenish the satellite cell pool, that will be used in the future
Muscle hypertrophy and the 4 stages of the satellite cell cycle
resting myofiber > (myotrauma) satellite activation and proliferation > (can also do self-renewal so goes back to start or) migration to injured fibre > fusion to damaged myofibers (hyperplasia) > regenerated myofiber and added nuclei
satellite - 2
age-related decline in satellite cell function compromises recovery capacity of sarcopenic muscles in response to injury
• satellite cell number loss contributes to age- dependent muscle fibrosis (excess fibrous connective tissue)
• Greater reduction of satellite
cells in type II (fast) fibers –
large force, fatigue resistant fibres
muscle fibre aging ***
~35% decrease in muscle fiber number between the 20 - 80
- type II muscle fiber myonuclear was only significantly lower in healthy elderly (>70 years) men.”
- The reduction in muscle fiber size is fiber type specific, with 10%–40% smaller type II fibers in elderly compared with young
Type I muscle fiber size is largely unaffected
“… fibrotic tissue replaces the functional muscle”
IF DAMAGED T2 IN AGING, HARDER TO REPAIR
motor neurons
Motor neurons die with increasing age
Denervation of type II muscle fibers with collateral re-innervation of type I muscle fiber neurons
AGE CHARACTERISTICS
- Young adulthood: intermingling of fibres belonging to different motor units.
Adulthood to old age: repeating cycles of denervation-reinnervation that result in fibres of the same type being beside one another (fibre type grouping) when viewed in cross-section.
Very old age is characterized by increasing frequency of axonal degeneration and/or motor neuron death leading to grouped fibre atrophy when viewed in cross-section.
- In particular denervation of type II muscle
fibers with collateral re-innervation of type I muscle fiber neurons
DECREASE CA2+ RELEASE
- There are receptors in the T-tubule which are needed to activate calcium release from the sarcoplasmic reticulum.
- Once calcium is released, it binds to troponin C and allows actin-myosin cross bridging
- Calcium is then pumped back into the sarcoplasmic reticulum
- Aging is associated with a reduction in # of receptors in the T-tubule and therefore deficits in calcium release
Structural alterations of myosin (reduction in myosin protein content)
• Reduces total # actin-myosin cross-bridges
• Greater % of cross-bridges in a weak- binding state