The Nature of the Glomerular Injury in Minimal Change and Focal Sclerosing Glomerulopathies
Glomerular barrier function was evaluated in 12 healthy human volunteers and in 16 proteinuric patients in whom the nephrotic syndrome was associated with alteration of glomerular epithelial cells alone (minimal change nephropathy [MCN]) or in combination with focal glomerular sclerosis (FGS). We de...
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Veröffentlicht in: | American journal of kidney diseases 1981-09, Vol.1 (2), p.91-98 |
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creator | Winetz, Jan A. Robertson, Channing R. Golbetz, Helen V. Carrie, Brian J. Salyer, William R. Myers, Bryan D. |
description | Glomerular barrier function was evaluated in 12 healthy human volunteers and in 16 proteinuric patients in whom the nephrotic syndrome was associated with alteration of glomerular epithelial cells alone (minimal change nephropathy [MCN]) or in combination with focal glomerular sclerosis (FGS). We determined the glomerular sieving coefficient for each of nine narrow dextran fractions (Einstein Stoke radius [ ESR ] = 30 to 46 Å), and directly measured, or indirectly estimated, values for the determinants of glomerular ultrafiltration. These quantities were then subjected to analysis based on an hydrodynamic theory of solute transport through an isoporous membrane. The results indicate that relative to normal subjects, effective pore radius is reduced from 59 to 55 and 53 Å in MCN and FGS, respectively; while the ratio, pore area to pore length (a measure of pore density) is correspondingly reduced from 21.7 x 106 to 10.1 x 106 and 4.7 x 106 cm, respectively. We suggest that collapse of the anionic glomerular membrane matrix in these proteinuric disorders may lead to pore shrinkage and reduced pore density, but that reduced electrostatic repulsion of anionic albumin (ESR = 36 Å) facilitates its permeation into Bowman's space. The qualitatively similar disorder of glomerular barrier function in MCN and FGS is consistent with a unitary pathogenesis, but may represent a nonspecific response to depletion of glomerular polyanion. |
doi_str_mv | 10.1016/S0272-6386(81)80035-2 |
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We determined the glomerular sieving coefficient for each of nine narrow dextran fractions (Einstein Stoke radius [ ESR ] = 30 to 46 Å), and directly measured, or indirectly estimated, values for the determinants of glomerular ultrafiltration. These quantities were then subjected to analysis based on an hydrodynamic theory of solute transport through an isoporous membrane. The results indicate that relative to normal subjects, effective pore radius is reduced from 59 to 55 and 53 Å in MCN and FGS, respectively; while the ratio, pore area to pore length (a measure of pore density) is correspondingly reduced from 21.7 x 106 to 10.1 x 106 and 4.7 x 106 cm, respectively. We suggest that collapse of the anionic glomerular membrane matrix in these proteinuric disorders may lead to pore shrinkage and reduced pore density, but that reduced electrostatic repulsion of anionic albumin (ESR = 36 Å) facilitates its permeation into Bowman's space. The qualitatively similar disorder of glomerular barrier function in MCN and FGS is consistent with a unitary pathogenesis, but may represent a nonspecific response to depletion of glomerular polyanion.</description><identifier>ISSN: 0272-6386</identifier><identifier>EISSN: 1523-6838</identifier><identifier>DOI: 10.1016/S0272-6386(81)80035-2</identifier><identifier>PMID: 6174043</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Dextrans - blood ; Dextrans - urine ; Glomerular Filtration Rate ; Glomerulonephritis - physiopathology ; Glomerulosclerosis, Focal Segmental - physiopathology ; Humans ; Inulin - blood ; Inulin - urine ; Kidney Glomerulus - physiopathology ; Middle Aged ; Nephrosis, Lipoid - physiopathology</subject><ispartof>American journal of kidney diseases, 1981-09, Vol.1 (2), p.91-98</ispartof><rights>1981 National Kidney Foundation, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c360t-fd4b30b2752585f6b97947d58a04eed6147b011ca3732eaf9464202c6a3216473</citedby><cites>FETCH-LOGICAL-c360t-fd4b30b2752585f6b97947d58a04eed6147b011ca3732eaf9464202c6a3216473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0272-6386(81)80035-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6174043$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Winetz, Jan A.</creatorcontrib><creatorcontrib>Robertson, Channing R.</creatorcontrib><creatorcontrib>Golbetz, Helen V.</creatorcontrib><creatorcontrib>Carrie, Brian J.</creatorcontrib><creatorcontrib>Salyer, William R.</creatorcontrib><creatorcontrib>Myers, Bryan D.</creatorcontrib><title>The Nature of the Glomerular Injury in Minimal Change and Focal Sclerosing Glomerulopathies</title><title>American journal of kidney diseases</title><addtitle>Am J Kidney Dis</addtitle><description>Glomerular barrier function was evaluated in 12 healthy human volunteers and in 16 proteinuric patients in whom the nephrotic syndrome was associated with alteration of glomerular epithelial cells alone (minimal change nephropathy [MCN]) or in combination with focal glomerular sclerosis (FGS). We determined the glomerular sieving coefficient for each of nine narrow dextran fractions (Einstein Stoke radius [ ESR ] = 30 to 46 Å), and directly measured, or indirectly estimated, values for the determinants of glomerular ultrafiltration. These quantities were then subjected to analysis based on an hydrodynamic theory of solute transport through an isoporous membrane. The results indicate that relative to normal subjects, effective pore radius is reduced from 59 to 55 and 53 Å in MCN and FGS, respectively; while the ratio, pore area to pore length (a measure of pore density) is correspondingly reduced from 21.7 x 106 to 10.1 x 106 and 4.7 x 106 cm, respectively. We suggest that collapse of the anionic glomerular membrane matrix in these proteinuric disorders may lead to pore shrinkage and reduced pore density, but that reduced electrostatic repulsion of anionic albumin (ESR = 36 Å) facilitates its permeation into Bowman's space. The qualitatively similar disorder of glomerular barrier function in MCN and FGS is consistent with a unitary pathogenesis, but may represent a nonspecific response to depletion of glomerular polyanion.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Dextrans - blood</subject><subject>Dextrans - urine</subject><subject>Glomerular Filtration Rate</subject><subject>Glomerulonephritis - physiopathology</subject><subject>Glomerulosclerosis, Focal Segmental - physiopathology</subject><subject>Humans</subject><subject>Inulin - blood</subject><subject>Inulin - urine</subject><subject>Kidney Glomerulus - physiopathology</subject><subject>Middle Aged</subject><subject>Nephrosis, Lipoid - physiopathology</subject><issn>0272-6386</issn><issn>1523-6838</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMlOwzAQhi0EglJ4BCSfEBwC3mK7J4QqWiqxHCgnDpbjTFpXWYqdIPXtSWnVK6fRzPz_LB9CV5TcUULl_QdhiiWSa3mj6a0mhKcJO0IDmjKeSM31MRocJGfoPMYVIWTEpTxFp5IqQQQfoK_5EvCbbbsAuClw22fTsqkgdKUNeFavurDBvsavvvaVLfF4aesFYFvneNK4vvDhSghN9PXiYGzWtl16iBfopLBlhMt9HKLPydN8_Jy8vE9n48eXxHFJ2qTIRcZJxlTKUp0WMhupkVB5qi0RALmkQmWEUme54gxsMRJSMMKctJxRKRQfouvd3HVovjuIral8dFCWtoami0ZxrShJRS9Md0LXXxwDFGYd-q_CxlBitlDNH1SzJWY0NX9QDet9V_sFXVZBfnDtKfb9h10f-i9_PAQTnYfaQe4DuNbkjf9nwy_dMoWT</recordid><startdate>198109</startdate><enddate>198109</enddate><creator>Winetz, Jan A.</creator><creator>Robertson, Channing R.</creator><creator>Golbetz, Helen V.</creator><creator>Carrie, Brian J.</creator><creator>Salyer, William R.</creator><creator>Myers, Bryan D.</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>198109</creationdate><title>The Nature of the Glomerular Injury in Minimal Change and Focal Sclerosing Glomerulopathies</title><author>Winetz, Jan A. ; Robertson, Channing R. ; Golbetz, Helen V. ; Carrie, Brian J. ; Salyer, William R. ; Myers, Bryan D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-fd4b30b2752585f6b97947d58a04eed6147b011ca3732eaf9464202c6a3216473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Dextrans - blood</topic><topic>Dextrans - urine</topic><topic>Glomerular Filtration Rate</topic><topic>Glomerulonephritis - physiopathology</topic><topic>Glomerulosclerosis, Focal Segmental - physiopathology</topic><topic>Humans</topic><topic>Inulin - blood</topic><topic>Inulin - urine</topic><topic>Kidney Glomerulus - physiopathology</topic><topic>Middle Aged</topic><topic>Nephrosis, Lipoid - physiopathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Winetz, Jan A.</creatorcontrib><creatorcontrib>Robertson, Channing R.</creatorcontrib><creatorcontrib>Golbetz, Helen V.</creatorcontrib><creatorcontrib>Carrie, Brian J.</creatorcontrib><creatorcontrib>Salyer, William R.</creatorcontrib><creatorcontrib>Myers, Bryan D.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of kidney diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Winetz, Jan A.</au><au>Robertson, Channing R.</au><au>Golbetz, Helen V.</au><au>Carrie, Brian J.</au><au>Salyer, William R.</au><au>Myers, Bryan D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Nature of the Glomerular Injury in Minimal Change and Focal Sclerosing Glomerulopathies</atitle><jtitle>American journal of kidney diseases</jtitle><addtitle>Am J Kidney Dis</addtitle><date>1981-09</date><risdate>1981</risdate><volume>1</volume><issue>2</issue><spage>91</spage><epage>98</epage><pages>91-98</pages><issn>0272-6386</issn><eissn>1523-6838</eissn><abstract>Glomerular barrier function was evaluated in 12 healthy human volunteers and in 16 proteinuric patients in whom the nephrotic syndrome was associated with alteration of glomerular epithelial cells alone (minimal change nephropathy [MCN]) or in combination with focal glomerular sclerosis (FGS). We determined the glomerular sieving coefficient for each of nine narrow dextran fractions (Einstein Stoke radius [ ESR ] = 30 to 46 Å), and directly measured, or indirectly estimated, values for the determinants of glomerular ultrafiltration. These quantities were then subjected to analysis based on an hydrodynamic theory of solute transport through an isoporous membrane. The results indicate that relative to normal subjects, effective pore radius is reduced from 59 to 55 and 53 Å in MCN and FGS, respectively; while the ratio, pore area to pore length (a measure of pore density) is correspondingly reduced from 21.7 x 106 to 10.1 x 106 and 4.7 x 106 cm, respectively. We suggest that collapse of the anionic glomerular membrane matrix in these proteinuric disorders may lead to pore shrinkage and reduced pore density, but that reduced electrostatic repulsion of anionic albumin (ESR = 36 Å) facilitates its permeation into Bowman's space. The qualitatively similar disorder of glomerular barrier function in MCN and FGS is consistent with a unitary pathogenesis, but may represent a nonspecific response to depletion of glomerular polyanion.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>6174043</pmid><doi>10.1016/S0272-6386(81)80035-2</doi><tpages>8</tpages></addata></record> |
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subjects | Adolescent Adult Dextrans - blood Dextrans - urine Glomerular Filtration Rate Glomerulonephritis - physiopathology Glomerulosclerosis, Focal Segmental - physiopathology Humans Inulin - blood Inulin - urine Kidney Glomerulus - physiopathology Middle Aged Nephrosis, Lipoid - physiopathology |
title | The Nature of the Glomerular Injury in Minimal Change and Focal Sclerosing Glomerulopathies |
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