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[Untitled]
- Source :
- Molecular and Cellular Biochemistry. 224:91-102
- Publication Year :
- 2001
- Publisher :
- Springer Science and Business Media LLC, 2001.
-
Abstract
- To investigate the hypothesis that prolonged partial ischemia would result in a depression in homogenate sarcoplasmic reticulum (SR) Ca2+-sequestering and mechanical properties in muscle, a cuff was placed around the hindlimb of 8 adult Sprague–Dawley rats (267 ± 5.8 g; × ± S.E.) and partially inflated (315 mm Hg) for 2 h. Following occlusion, the EDL was sampled both from the ischemic (I) and contralateral control (C) leg and SR properties compared with the EDL muscles extracted from rats (n = 8) immediately following anaesthetization (CC). Ischemia was indicated by a lower (p < 0.05) concentration (mmol.kg dry wt–1) of ATP (19.0 ± 0.7 vs. 16.7 ± 0.7) and phosphocreatine (58.1 ± 5.7 vs. 35.0 ± 4.6) in I compared to C. Although Ca2+-ATPase activity (μmol·g protein–1.sec–1 ), both maximal and submaximal, was not different between C and I (19.7 ± 0.4 vs. 18.5 ± 1.3), reductions (p < 0.05) in Ca2+-uptake (mmol·g protein–1.sec–1 ) of between 18.2 and 24.7% across a range of submaximal free Ca2+-levels were observed in I compared to C. Lower submaximal Ca2+-ATPase activity and Ca2+-uptake were also observed in the EDL in C compared to CC animals. Time dependent reductions (p < 0.05) were found in peak twitch and maximal tetanic tension in EDL from I but not C. It is concluded that partial ischemia, resulting in modest reductions in energy state in EDL, induces a reduction in Ca2+-uptake independent of changes in Ca2+-ATPase activity. These changes reduce the coupling ratio and the efficiency of Ca2+-transport by SR.
- Subjects :
- medicine.medical_specialty
Endoplasmic reticulum
Ca2 transport
Clinical Biochemistry
Ischemia
Cell Biology
General Medicine
Hindlimb
Anatomy
medicine.disease
Coupling ratio
Phosphocreatine
chemistry.chemical_compound
Endocrinology
chemistry
Internal medicine
Mole
medicine
Molecular Biology
Ca2 cycling
Subjects
Details
- ISSN :
- 03008177
- Volume :
- 224
- Database :
- OpenAIRE
- Journal :
- Molecular and Cellular Biochemistry
- Accession number :
- edsair.doi...........a5a64559240f8447fba9545dc09b8f81
- Full Text :
- https://doi.org/10.1023/a:1011930502758