pubmed-article:9020865 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0035820 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0030274 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0521449 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0086045 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0015127 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0021547 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0038734 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0442805 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0030011 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C1996904 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0596235 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C1698986 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C1880497 | lld:lifeskim |
pubmed-article:9020865 | lifeskim:mentions | umls-concept:C0045257 | lld:lifeskim |
pubmed-article:9020865 | pubmed:dateCreated | 1997-2-26 | lld:pubmed |
pubmed-article:9020865 | pubmed:abstractText | 2,2'-Dithiodipyridine (2,2'-DTDP), a reactive disulphide that mobilizes Ca2+ from ryanodine-sensitive Ca2+ stores in muscle, induced a biphasic increase in cytoplasmic free Ca2+ concentration ([Ca2+]i) in pancreatic beta-cells loaded with fura 2. This increase consisted of an early transient followed by a second, slower, rise. The [Ca2+]i transient was dependent on extracellular Ca2+ and disappeared on treatment with nimodipine. The reactive disulphide caused plasma membrane depolarization, as studied by the perforated-patch configuration of the patch-clamp technique. Hence membrane depolarization and opening of the L-type voltage-gated Ca2+ channels were responsible for the first transient in [Ca2+]i. The second slower increase in [Ca2+]i was prolonged but readily reversed by the disulphide-reducing agent 1,4-dithiothreitol. This increase in [Ca2+]i was not decreased by nimodipine or by omission of extracellular Ca2+, but was eliminated when the Ins(1,4,5)P3-sensitive Ca2+ pool was first depleted by carbachol. Ryanodine or its beta-alanyl analogue did not release Ca2+ from intracellular stores, and a high concentration of ryanodine did not inhibit Ca2+ release by 2,2'-DTDP. The disulphide compound suppressed glucose metabolism and decreased the mitochondrial inner-membrane potential. We conclude that thiol oxidation by 2,2'-DTDP affects Ca2+ homeostasis in beta-cells by multiple mechanisms. However, unlike the situation in muscle, in beta-cells 2,2'-DTDP releases Ca2+ from intracellular pools by mechanisms that do not involve activation of ryanodine receptors. Instead, in these cells the Ins(1,4,5)P3-sensitive intracellular Ca2+ store comprises an alternative target for the Ca(2+)-mobilizing action of the reactive disulphide compound. | lld:pubmed |
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pubmed-article:9020865 | pubmed:language | eng | lld:pubmed |
pubmed-article:9020865 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9020865 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:9020865 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9020865 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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pubmed-article:9020865 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:9020865 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:9020865 | pubmed:month | Jan | lld:pubmed |
pubmed-article:9020865 | pubmed:issn | 0264-6021 | lld:pubmed |
pubmed-article:9020865 | pubmed:author | pubmed-author:IslamM SMS | lld:pubmed |
pubmed-article:9020865 | pubmed:author | pubmed-author:LarssonOO | lld:pubmed |
pubmed-article:9020865 | pubmed:author | pubmed-author:BerggrenP OPO | lld:pubmed |
pubmed-article:9020865 | pubmed:author | pubmed-author:KindmarkHH | lld:pubmed |
pubmed-article:9020865 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:9020865 | pubmed:day | 15 | lld:pubmed |
pubmed-article:9020865 | pubmed:volume | 321 ( Pt 2) | lld:pubmed |
pubmed-article:9020865 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:9020865 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:9020865 | pubmed:pagination | 347-54 | lld:pubmed |
pubmed-article:9020865 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:9020865 | pubmed:year | 1997 | lld:pubmed |
pubmed-article:9020865 | pubmed:articleTitle | Thiol oxidation by 2,2'-dithiodipyridine causes a reversible increase in cytoplasmic free Ca2+ concentration in pancreatic beta-cells. Role for inositol 1,4,5-trisphosphate-sensitive Ca2+ stores. | lld:pubmed |