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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1990-6-4
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pubmed:abstractText |
Unchanged dextrans of graded size (28-60 A) were used to evaluate barrier size-selectivity in 56 proteinuric patients with diabetic glomerular disease. Transglomerular sieving was enhanced selectively for dextrans of greater than 46 A radius. A mathematical model of hindered solute transport through a porous membrane showed that this finding reflected the development in the glomerular barrier of a subset of enlarged, non-discriminatory pores. Although few in number, these enlarged pores accounted for both the magnitude and the composition of the observed proteinuria. We conclude that impaired barrier size-selectivity underlies the proteinuria of diabetic glomerular disease, and that impairment of barrier charge-selectivity need not be invoked in this circumstance.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0952-1178
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
S41-6
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:2332816-Biological Transport,
pubmed-meshheading:2332816-Capillary Permeability,
pubmed-meshheading:2332816-Diabetic Nephropathies,
pubmed-meshheading:2332816-Glomerular Filtration Rate,
pubmed-meshheading:2332816-Humans,
pubmed-meshheading:2332816-Kidney Glomerulus,
pubmed-meshheading:2332816-Particle Size,
pubmed-meshheading:2332816-Proteinuria
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pubmed:year |
1990
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pubmed:articleTitle |
Pathophysiology of proteinuria in diabetic glomerular disease.
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pubmed:affiliation |
Division of Nephrology, Stanford University School of Medicine, California 94305.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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