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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6 Pt 1
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pubmed:dateCreated |
1996-9-26
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pubmed:abstractText |
In the present study, we examined whether weight-bearing condition can regulate the sarcoplasmic reticulum (SR) Ca(2+)-release mechanism. Measurements of alpha 1-subunit dihydropyridine (alpha 1-DHP) and ryanodine receptor levels were made in hypertrophied fast-twitch plantaris muscles 5 wk after surgical removal of synergist muscles (increased weight bearing) and in atrophied slowtwitch soleus muscles (14 days of non-weight bearing) of the rat. Rates of AgNO3-induced SR Ca2+ release were measured with fura 2 as the Ca2+ indicator and pyrophosphate as the precipitating ion during vesicular Ca2+ loading. Ca(2+)-release rates were 38, 49, and 58% lower in vesicles from hypertrophied vs. control muscles at AgNO3 concentrations of 0.05, 0.5, and 5 microM, respectively (control = 18.2 +/- 1.4 microM.mg-1. min-1). Western blots showed no differences in the relative expression of alpha 1-DHP or ryanodine receptor when IIID5 (monoclonal) or GP3 (polyclonal) antibodies were used. There was also no difference in ryanodine (10 nM) binding in Ca(2+)-incubated SR vesicles from hypertrophied muscles, suggesting no difference in the number of channels. In contrast, expression of alpha 1-DHP and ryanodine receptors was increased by 144 and 157% in non-weight-bearing soleus muscles, respectively. Scatchard analysis of DHP binding showed a 40% increase in maximum binding capacity and no change in the dissociation constant with non-weight-bearing muscles. The direction of modification of the SR Ca(2+)-release mechanism is opposite with increased and decreased weight bearing, but the mechanism by which this is achieved appears to be different.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channels, L-Type,
http://linkedlifedata.com/resource/pubmed/chemical/Muscle Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Ryanodine Receptor Calcium Release...
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0002-9513
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
270
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
C1588-94
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:8764140-Adaptation, Physiological,
pubmed-meshheading:8764140-Animals,
pubmed-meshheading:8764140-Blotting, Western,
pubmed-meshheading:8764140-Calcium,
pubmed-meshheading:8764140-Calcium Channels,
pubmed-meshheading:8764140-Calcium Channels, L-Type,
pubmed-meshheading:8764140-Female,
pubmed-meshheading:8764140-Muscle, Skeletal,
pubmed-meshheading:8764140-Muscle Fibers, Fast-Twitch,
pubmed-meshheading:8764140-Muscle Fibers, Slow-Twitch,
pubmed-meshheading:8764140-Muscle Proteins,
pubmed-meshheading:8764140-Muscular Atrophy,
pubmed-meshheading:8764140-Rats,
pubmed-meshheading:8764140-Rats, Wistar,
pubmed-meshheading:8764140-Ryanodine Receptor Calcium Release Channel,
pubmed-meshheading:8764140-Sarcoplasmic Reticulum,
pubmed-meshheading:8764140-Weight-Bearing
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pubmed:year |
1996
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pubmed:articleTitle |
Adaptation of the skeletal muscle calcium-release mechanism to weight-bearing condition.
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pubmed:affiliation |
Department of Health Sciences, Boston University, Massachusetts 02215, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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