Search

Background. Both fasting and ageing processes lead to muscle wasting. We studied the effect of single 48 h fasting on soleus skeletal muscle mass and force in young and old mice. Methods. The study involved 18 young and 13 old mice. Body and soleus (SOL) muscle mass were measured followed by assessment of peak and specific SOL force under ex vivo conditions. SOL muscle half-relaxation time and 20 Hz to 100 Hz force ratio were also measured. Results. After fasting, weight loss was greater (p < .05) in young mice compared to old mice (17.0 ± 2.6 versus 12.0 ± 1.7%, respectively). Fasted young, but not old mice showed reduction (p < .05) in SOL mass compared to the control values. On the other hand, specific SOL force was reduced (p < .05) only in old mice, while 20 Hz to 100 Hz force ratio decreased (p < .05) only in young mice after fasting. Conclusions. Our results showed that 48 h fasting caused lower SOL muscle peak and specific force in old but not young mice. [ABSTRACT FROM AUTHOR]

Phenotypic diversity between laboratory mouse strains provides a model for studying the underlying genetic mechanisms. The A/J strain performs poorly in various endurance exercise models. The aim of the study was to test if endurance capacity and contractility of the fast- and slow-twitch muscles are affected by the genes on mouse chromosome 10. The C57BL/6J (B6) strain and C57BL/6J-Chr 10A/J/NaJ (B6.A10) consomic strain which carries the A/J chromosome 10 on a B6 strain background were compared. The B6.A10 mice compared to B6 were larger in body weight (p < 0.02): 27.2 ± 1.9 vs. 23.8 ± 2.7 and 23.4 ± 1.9 vs. 22.9 ± 2.3 g, for males and females, respectively, and in male soleus weight (p < 0.02): 9.7 ± 0.4 vs. 8.6 ± 0.9 mg. In the forced running test the B6.A10 mice completed only 64% of the B6 covered distance (p < 0.0001). However, there was no difference in voluntary wheel running (p = 0.6) or in fatigability of isolated soleus (p = 0.24) or extensor digitorum longus (EDL, p = 0.7) muscles. We conclude that chromosome 10 of the A/J strain contributes to reduced endurance performance. We also discuss physiological mechanisms and methodological aspects relevant to interpretation of these findings. [ABSTRACT FROM AUTHOR]

Background. Mouse strains differ in body and skeletal muscle mass. It is commonly believed that specific force is a constant value irrespective of muscle mass. We hypothesised that excessive muscle hypertrophy might compromise force output. Methods. We studied force generating capacity and muscle mass of isolated soleus (SOL) and extensor digitorum longus (EDL) muscles in 14-15-week-old males of C57BL/6J, BEH+/+ and DUH mice (n = 7 per strain). In addition, muscles of young (4-5 weeks old, n = 7 per strain) BEH+/+ and DUH mice were also studied. Specific forces were calculated as isometric tetanic force divided by the estimated physiological cross-section area (PCSA) of the muscles. Results. DUH strain generated lower specific force (p < .01- .001) than both C57BL/6J and BEH+/+ strains in SOL (110 ± 20 vs. 146 ± 28 and 164 ± 8 mN/mm², respectively) and EDL muscles (74 ± 18 vs. 101 ± 19 and 95 ± 11 mN/mm², respectively). There were no differences between muscles of young and adult mice (p > .05). C57BL/6J and BEH+/+ generated similar specific force. Conclusions. Our results show that body mass is not associated with reduction in specific force of skeletal muscles in mice. It seems that age did not affect specific force either. However, the heaviest DUH mice had lower specific force in both slow twitch SOL and fast twitch EDL compared to BEH+/+ and C57BL/6J mice. It appears that DUH strain could be a useful model in studying factors limiting specific force of skeletal muscle. [ABSTRACT FROM AUTHOR]

Fasting improves metabolic health, but is also associated with loss of lean body mass. We investigated if old mice are less resistant to fasting-induce muscle wasting than adult mice. We compared changes in skeletal muscles and fat distribution in C57BL/6J mice subjected to 48-hour fasting at adult (6-month old) or old (24-month old) age. Old mice lost less weight (11.9 ± 1.5 vs 16.9 ± 2.8%, p < 0.001) and showed less (p < 0.01) pronounced muscle wasting than adult mice. Extensor digitorum longus (EDL) muscle force decreased only in adult mice after fasting. Serum IGF-1 levels were higher (p < 0.01) and showed greater (p < 0.01) decline in adult mice compared to old mice. Phosphorylation of 4EBP1 was reduced in the gastrocnemius muscles of adult mice only. Energy expenditure was slower in old mice and showed smaller fasting-induced decline than in adult mice when adjusted for variations in physical activity. There was a loss of fat mass in both age groups, but it was more pronounced in adult mice than old mice. Our results suggest that ageing-related decrease in metabolic rate protects old mice from skeletal muscle wasting during fasting. • We investigated effects of fasting on body composition of adult and old C57BL/6J mice. • 48-hour fasting was associated with low physical activity and greater decrease serum IGF-1 in adult compared to old mice. • Fasting induced significant muscle wasting and force loss only in adult mice. • Reduced metabolic rate protects old mice from excessive muscle wasting during fasting. [ABSTRACT FROM AUTHOR]

Myostatin is an inhibitor of skeletal muscle growth and might be involved in adaptations to caloric restriction (CR). We compared responses to 12-week 30% CR in male mice of Berlin high strain with myostatin dysfunction (BEH) and wild-type myostatin (BEH+/+). BEH mice were heavier than BEH+/+ mice (58.8 ± 2.0 versus 53.1 ± 2.7 g, p < 0.001), had 1.8-fold greater hind limb muscle mass and were less (p < 0.05) physically active when fed ad libitum. After CR, BEH and BEH+/+ strains experienced similar weight loss (24.7 ± 5.7 versus 20.6 ± 6.5%, p > 0.05, respectively) and decreases (p < 0.001) in plasma IGF-1 and total cholesterol, but loss of hind limb muscle mass was greater (p < 0.001) in BEH mice than BEH+/+ mice. BEH mice had better (p < 0.001) glucose tolerance and showed smaller (p < 0.05) improvements of it than BEH+/+ mice after CR (1038.2 ± 174.7 versus 744.4 ± 95.8 glucose mM× 120 min, p < 0.01 for BEH; 1365.8 ± 218.5 versus 831.5 ± 134.4 glucose mM ×120 min, p < 0.001, for BEH+/+, respectively). In summary, myostatin dysfunction is associated with muscle hypertrophy and high glucose tolerance, but greater muscle wasting and smaller improvements in glucose tolerance in response to CR. • We investigated effects of myostatin dysfunction and caloric restriction in Berlin high mouse strain. • 12 weeks of 30% caloric restriction induced loss of fat and muscle mass, lowered plasma triacylglycerol and cholesterol. • Myostatin dysfunction was associated with greater loss of hind limb muscle mass and attenuated improvements in glucose tolerance of mice • Myostatin dysfunction does not protect from muscle wasting during caloric restrriction. [ABSTRACT FROM AUTHOR]