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Prolonged exercise potentiates sarcoplasmic reticulum Ca2+ uptake in rat diaphragm
Stasinos Stavrianeas1, Espen Spangenburg, Tim Batts
1Department of Exercise Science, Willamette University, 900 State St., Salem, OR 97301, USA. stas@willamette.edu
European Journal of Applied Physiology
|March 11, 2003
Summary
Prolonged exercise impairs sarcoplasmic reticulum (SR) function in rat leg muscles but enhances it in the diaphragm. This suggests exercise
Area of Science:
- Exercise Physiology
- Muscle Biology
- Cellular Physiology
Background:
- Sarcoplasmic reticulum (SR) plays a crucial role in muscle contraction and relaxation by regulating intracellular calcium (Ca2+).
- Previous studies indicate that prolonged exercise can negatively impact SR function in limb muscles.
Purpose of the Study:
- To investigate the differential effects of prolonged treadmill exercise on SR Ca2+ handling in rat diaphragm and red gastrocnemius muscles.
- To determine if exercise-induced adaptations in SR function vary based on muscle type and functional demands.
Main Methods:
- Isolated SR vesicles and muscle homogenates from rat diaphragm and red gastrocnemius were analyzed post-exercise.
- Measurements included SR Ca2+ ATPase activity, Ca2+ uptake, and Ca2+ release.
- Glycogen depletion was assessed to confirm muscle fiber recruitment.
Main Results:
- Prolonged exercise led to a significant decrease in SR Ca2+ ATPase activity, Ca2+ uptake, and Ca2+ release in the red gastrocnemius.
- In contrast, the diaphragm showed no change in SR Ca2+ ATPase activity or Ca2+ release, but exhibited a substantial increase (157-263%) in Ca2+ uptake.
- Glycogen depletion indicated significant fiber recruitment in both muscles.
Conclusions:
- The diaphragm's SR function is resistant to the negative effects of prolonged exercise observed in limb muscles.
- Prolonged exercise potentiates Ca2+ sequestration in the diaphragm SR without increasing energy cost.
- These findings necessitate a re-evaluation of exercise's role in regulating SR Ca2+ handling, highlighting muscle-specific responses.