pubmed-article:7646555 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C0026239 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C1882726 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C0010592 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C0304348 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C1442080 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C0205263 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C1704666 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C1517892 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C2346927 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C1515926 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C0871161 | lld:lifeskim |
pubmed-article:7646555 | lifeskim:mentions | umls-concept:C0208973 | lld:lifeskim |
pubmed-article:7646555 | pubmed:issue | 4 | lld:pubmed |
pubmed-article:7646555 | pubmed:dateCreated | 1995-9-20 | lld:pubmed |
pubmed-article:7646555 | pubmed:abstractText | The alterations in rat liver mitochondria induced by acetylsalicylate in the presence of low concentrations of Ca2+ (large amplitude swelling, permeability to 14C]sucrose, collapse of transmembrane potential and effluxes of endogenous Mg2+ and accumulated Ca2+) were fully prevented by either cyclosporin A or Mg2+. Cyclosporin A and Mg2+ were also capable of restoring transmembrane potential upon its decrease induced by acetylsalicylate. The loss of endogenous Mg2+ was the primary effect promoted by acetylsalicylate; the other noxious effects followed. These results indicate that Mg2+ are fundamental components of the mitochondrial permeability barrier and that their loss might be responsible for the membrane transition induced by acetylsalicylate. | lld:pubmed |
pubmed-article:7646555 | pubmed:language | eng | lld:pubmed |
pubmed-article:7646555 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7646555 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:7646555 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7646555 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7646555 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7646555 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7646555 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:7646555 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:7646555 | pubmed:month | Aug | lld:pubmed |
pubmed-article:7646555 | pubmed:issn | 0006-2952 | lld:pubmed |
pubmed-article:7646555 | pubmed:author | pubmed-author:SiliprandiNN | lld:pubmed |
pubmed-article:7646555 | pubmed:author | pubmed-author:SiliprandiDD | lld:pubmed |
pubmed-article:7646555 | pubmed:author | pubmed-author:ToninelloAA | lld:pubmed |
pubmed-article:7646555 | pubmed:author | pubmed-author:BibanCC | lld:pubmed |
pubmed-article:7646555 | pubmed:author | pubmed-author:TassaniVV | lld:pubmed |
pubmed-article:7646555 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:7646555 | pubmed:day | 8 | lld:pubmed |
pubmed-article:7646555 | pubmed:volume | 50 | lld:pubmed |
pubmed-article:7646555 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:7646555 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:7646555 | pubmed:pagination | 497-500 | lld:pubmed |
pubmed-article:7646555 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:meshHeading | pubmed-meshheading:7646555-... | lld:pubmed |
pubmed-article:7646555 | pubmed:year | 1995 | lld:pubmed |
pubmed-article:7646555 | pubmed:articleTitle | The alterations in the energy linked properties induced in rat liver mitochondria by acetylsalicylate are prevented by cyclosporin A or Mg2+. | lld:pubmed |
pubmed-article:7646555 | pubmed:affiliation | Dipartimento di Chimica Biologica, Universitá id Padova, Italy. | lld:pubmed |
pubmed-article:7646555 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:7646555 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:7646555 | lld:pubmed |