Source:http://linkedlifedata.com/resource/pubmed/id/10731483
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2000-6-1
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pubmed:abstractText |
The bikunin peptide chain of the protease inhibitor inter-alpha-inhibitor (IalphaI) has been reported to be an inhibitor of calcium oxalate (CaOx) crystallization, and hence has been proposed as having a role in CaOx kidney stone formation. However, further experimental evidence is required to assess if fragments of IalphaI other than bikunin may play a role in the regulation of crystallization events in stone formation. The aim of the present study was to assess the effects of IalphaI and several of its derivatives on CaOx crystallization in a seeded inorganic system and to compare these effects with those of a known inhibitor of crystallization, prothrombin. IalphaI was purified from a preparation of human plasma and fragmented by alkaline hydrolysis, and two of its peptide chains, bikunin and heavy chain 1 (H1), were purified further by HPLC. Their purity was confirmed by SDS/PAGE. Using Coulter counter and [(14)C]oxalate analysis and scanning electron microscopy, IalphaI, its H1 chain and bikunin from urine and from plasma were shown to be relatively weak inhibitors of CaOx crystallization in vitro at expected physiological concentrations. It was concluded that members of the IalphaI family may not be as important in kidney stone formation as has been generally proposed, although further studies are required before a possible role for IalphaI and its fragments in stone formation can be unambiguously discounted.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Alpha-Globulins,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Oxalate,
http://linkedlifedata.com/resource/pubmed/chemical/Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Prothrombin,
http://linkedlifedata.com/resource/pubmed/chemical/SPINT2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Serine Proteinase Inhibitors,
http://linkedlifedata.com/resource/pubmed/chemical/Trypsin Inhibitor, Kunitz Soybean,
http://linkedlifedata.com/resource/pubmed/chemical/inter-alpha-inhibitor
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0143-5221
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
98
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
471-80
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10731483-Alpha-Globulins,
pubmed-meshheading:10731483-Calcium Oxalate,
pubmed-meshheading:10731483-Chromatography, High Pressure Liquid,
pubmed-meshheading:10731483-Crystallization,
pubmed-meshheading:10731483-Glycoproteins,
pubmed-meshheading:10731483-Humans,
pubmed-meshheading:10731483-Membrane Glycoproteins,
pubmed-meshheading:10731483-Microscopy, Electron, Scanning,
pubmed-meshheading:10731483-Prothrombin,
pubmed-meshheading:10731483-Serine Proteinase Inhibitors,
pubmed-meshheading:10731483-Trypsin Inhibitor, Kunitz Soybean
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pubmed:year |
2000
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pubmed:articleTitle |
Effects of inter-alpha-inhibitor and several of its derivatives on calcium oxalate crystallization in vitro.
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pubmed:affiliation |
Department of Surgery, Flinders Medical Centre and the Flinders University of South Australia, Bedford Park, South Australia 5042, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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