| pubmed-article:10096881 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10096881 | lifeskim:mentions | umls-concept:C0679729 | lld:lifeskim |
| pubmed-article:10096881 | lifeskim:mentions | umls-concept:C0027869 | lld:lifeskim |
| pubmed-article:10096881 | lifeskim:mentions | umls-concept:C0206181 | lld:lifeskim |
| pubmed-article:10096881 | lifeskim:mentions | umls-concept:C0728940 | lld:lifeskim |
| pubmed-article:10096881 | lifeskim:mentions | umls-concept:C0015252 | lld:lifeskim |
| pubmed-article:10096881 | lifeskim:mentions | umls-concept:C0596235 | lld:lifeskim |
| pubmed-article:10096881 | lifeskim:mentions | umls-concept:C0446343 | lld:lifeskim |
| pubmed-article:10096881 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:10096881 | pubmed:dateCreated | 1999-5-7 | lld:pubmed |
| pubmed-article:10096881 | pubmed:abstractText | Stimulation-induced changes in presynaptic free calcium concentration ([Ca2+]i) were examined by fluorescent imaging at the spiny lobster excitor motor nerve terminals. The Ca2+ removal process in the terminal was analyzed based on a single compartment model, under the assumption that the Ca2+ removal rate from the terminal cytoplasm is proportional to nth power of [Ca2+]i. During 100 nerve stimuli at 10-100 Hz, [Ca2+]i reached a plateau that increased in a less-than-linear way with stimulation frequency, and the power index, n, was about 2. In the decay time course after stimulation, n changed with the number of stimuli from about 1.4 after 10 stimuli to about 2 after 100 stimuli. With the change of n from 1.4 to 2, the rate became larger at high [Ca2+]i (>1.5 microM), but was smaller at low [Ca2+]i (<1 microM). These results suggest that a cooperative Ca2+ removal mechanism of n = 2, such as mitochondria, may play an important role in the terminal. This view is supported by the gradual increase in the [Ca2+]i plateau during long-term stimulation at 20-50 Hz for 60 s and by the existence of a very slow [Ca2+]i recovery process after this stimulation, both of which may be due to accumulation of Ca2+ in the organelle. | lld:pubmed |
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| pubmed-article:10096881 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10096881 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10096881 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:10096881 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10096881 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:10096881 | pubmed:issn | 0006-3495 | lld:pubmed |
| pubmed-article:10096881 | pubmed:author | pubmed-author:OgawaSS | lld:pubmed |
| pubmed-article:10096881 | pubmed:author | pubmed-author:MiwaAA | lld:pubmed |
| pubmed-article:10096881 | pubmed:author | pubmed-author:SuzukiNN | lld:pubmed |
| pubmed-article:10096881 | pubmed:author | pubmed-author:OhnumaKK | lld:pubmed |
| pubmed-article:10096881 | pubmed:author | pubmed-author:KijimaHH | lld:pubmed |
| pubmed-article:10096881 | pubmed:author | pubmed-author:KazawaTT | lld:pubmed |
| pubmed-article:10096881 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10096881 | pubmed:volume | 76 | lld:pubmed |
| pubmed-article:10096881 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10096881 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10096881 | pubmed:pagination | 1819-34 | lld:pubmed |
| pubmed-article:10096881 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:10096881 | pubmed:meshHeading | pubmed-meshheading:10096881... | lld:pubmed |
| pubmed-article:10096881 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10096881 | pubmed:articleTitle | Cooperative Ca2+ removal from presynaptic terminals of the spiny lobster neuromuscular junction. | lld:pubmed |
| pubmed-article:10096881 | pubmed:affiliation | Department of Physics, School of Science, Nagoya University, Nagoya 464-8602, Japan. | lld:pubmed |
| pubmed-article:10096881 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:10096881 | pubmed:publicationType | Comparative Study | lld:pubmed |
| pubmed-article:10096881 | pubmed:publicationType | In Vitro | lld:pubmed |
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