Morphological changes induced in the pig kidney by extracorporeal shock wave lithotripsy: Nephron injury
While shock wave lithotripsy (SWL) is known to cause significant damage to the kidney, little is known about the initial injury to cells along the nephron. In this study, one kidney in each of six juvenile pigs (6–7 weeks old) was treated with 1,000 shock waves (at 24 kV) directed at a lower pole ca...
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Veröffentlicht in: | The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology Discoveries in molecular, cellular, and evolutionary biology, 2003-11, Vol.275A (1), p.979-989 |
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container_title | The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology |
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description | While shock wave lithotripsy (SWL) is known to cause significant damage to the kidney, little is known about the initial injury to cells along the nephron. In this study, one kidney in each of six juvenile pigs (6–7 weeks old) was treated with 1,000 shock waves (at 24 kV) directed at a lower pole calyx with an unmodified HM‐3 lithotripter. Three pigs were utilized as sham‐controls. Kidneys were fixed by vascular perfusion immediately after SWL or sham‐SWL. Three of the treated kidneys were used to quantitate lesion size. Cortical and medullary samples for light (LM) and transmission electron microscopy (TEM) were taken from the focal zone for the shock waves (F2), the contralateral kidney, and the kidneys of sham‐SWL pigs. Because preservation of the tissue occurred within minutes of SWL, the initial injury caused by the shock waves could be separated from secondary changes. No tissue damage was observed in contralateral sham‐SWL kidneys, but treated kidneys showed signs of injury, with a lesion of 0.2% ± 0.1% of renal volume. Intraparenchymal hemorrhage and injury to tubules was found at F2 in both the cortex and medulla of SWL‐treated kidneys. Tubular injury was always associated with intraparenchymal bleeding, and the range of tissue injury included total destruction of tubules, focal cellular fragmentation, necrosis, cell vacuolization, and membrane blebbing. The initial injury caused by SWL was cellular fragmentation and necrosis. Cellular vacuolization, membrane blebbing, and disorganization of apical brush borders appear to be secondary changes related to hypoxia. Anat Rec Part A 275A:979–989, 2003. © 2003 Wiley‐Liss, Inc. |
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In this study, one kidney in each of six juvenile pigs (6–7 weeks old) was treated with 1,000 shock waves (at 24 kV) directed at a lower pole calyx with an unmodified HM‐3 lithotripter. Three pigs were utilized as sham‐controls. Kidneys were fixed by vascular perfusion immediately after SWL or sham‐SWL. Three of the treated kidneys were used to quantitate lesion size. Cortical and medullary samples for light (LM) and transmission electron microscopy (TEM) were taken from the focal zone for the shock waves (F2), the contralateral kidney, and the kidneys of sham‐SWL pigs. Because preservation of the tissue occurred within minutes of SWL, the initial injury caused by the shock waves could be separated from secondary changes. No tissue damage was observed in contralateral sham‐SWL kidneys, but treated kidneys showed signs of injury, with a lesion of 0.2% ± 0.1% of renal volume. Intraparenchymal hemorrhage and injury to tubules was found at F2 in both the cortex and medulla of SWL‐treated kidneys. Tubular injury was always associated with intraparenchymal bleeding, and the range of tissue injury included total destruction of tubules, focal cellular fragmentation, necrosis, cell vacuolization, and membrane blebbing. The initial injury caused by SWL was cellular fragmentation and necrosis. Cellular vacuolization, membrane blebbing, and disorganization of apical brush borders appear to be secondary changes related to hypoxia. Anat Rec Part A 275A:979–989, 2003. © 2003 Wiley‐Liss, Inc.</description><identifier>ISSN: 1552-4884</identifier><identifier>EISSN: 1552-4892</identifier><identifier>DOI: 10.1002/ar.a.10115</identifier><identifier>PMID: 14533172</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; cell fragmentation ; extracorporeal shock wave lithotripsy ; Female ; Hemorrhage - etiology ; Hemorrhage - pathology ; Kidney Cortex - injuries ; Kidney Cortex - pathology ; Kidney Cortex - ultrastructure ; Kidney Cortex Necrosis - etiology ; Kidney Cortex Necrosis - pathology ; Kidney Medulla - injuries ; Kidney Medulla - pathology ; Kidney Medulla - ultrastructure ; Lithotripsy - adverse effects ; lithotripsy injury ; nephron injury ; Nephrons - injuries ; Nephrons - pathology ; Nephrons - ultrastructure ; pig model ; renal morphology ; Swine</subject><ispartof>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology, 2003-11, Vol.275A (1), p.979-989</ispartof><rights>Copyright © 2003 Wiley‐Liss, Inc.</rights><rights>Copyright 2003 Wiley-Liss, Inc.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4255-62dbd3cf0fed07396a35ed6bc3d6f83b860473f7e80c26d0aba7c0544f8943273</citedby><cites>FETCH-LOGICAL-c4255-62dbd3cf0fed07396a35ed6bc3d6f83b860473f7e80c26d0aba7c0544f8943273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Far.a.10115$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Far.a.10115$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14533172$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shao, Youzhi</creatorcontrib><creatorcontrib>Connors, Bret A.</creatorcontrib><creatorcontrib>Evan, Andrew P.</creatorcontrib><creatorcontrib>Willis, Lynn R.</creatorcontrib><creatorcontrib>Lifshitz, David A.</creatorcontrib><creatorcontrib>Lingeman, James E.</creatorcontrib><title>Morphological changes induced in the pig kidney by extracorporeal shock wave lithotripsy: Nephron injury</title><title>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology</title><addtitle>Anat Rec A Discov Mol Cell Evol Biol</addtitle><description>While shock wave lithotripsy (SWL) is known to cause significant damage to the kidney, little is known about the initial injury to cells along the nephron. In this study, one kidney in each of six juvenile pigs (6–7 weeks old) was treated with 1,000 shock waves (at 24 kV) directed at a lower pole calyx with an unmodified HM‐3 lithotripter. Three pigs were utilized as sham‐controls. Kidneys were fixed by vascular perfusion immediately after SWL or sham‐SWL. Three of the treated kidneys were used to quantitate lesion size. Cortical and medullary samples for light (LM) and transmission electron microscopy (TEM) were taken from the focal zone for the shock waves (F2), the contralateral kidney, and the kidneys of sham‐SWL pigs. Because preservation of the tissue occurred within minutes of SWL, the initial injury caused by the shock waves could be separated from secondary changes. No tissue damage was observed in contralateral sham‐SWL kidneys, but treated kidneys showed signs of injury, with a lesion of 0.2% ± 0.1% of renal volume. Intraparenchymal hemorrhage and injury to tubules was found at F2 in both the cortex and medulla of SWL‐treated kidneys. Tubular injury was always associated with intraparenchymal bleeding, and the range of tissue injury included total destruction of tubules, focal cellular fragmentation, necrosis, cell vacuolization, and membrane blebbing. The initial injury caused by SWL was cellular fragmentation and necrosis. Cellular vacuolization, membrane blebbing, and disorganization of apical brush borders appear to be secondary changes related to hypoxia. Anat Rec Part A 275A:979–989, 2003. © 2003 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>cell fragmentation</subject><subject>extracorporeal shock wave lithotripsy</subject><subject>Female</subject><subject>Hemorrhage - etiology</subject><subject>Hemorrhage - pathology</subject><subject>Kidney Cortex - injuries</subject><subject>Kidney Cortex - pathology</subject><subject>Kidney Cortex - ultrastructure</subject><subject>Kidney Cortex Necrosis - etiology</subject><subject>Kidney Cortex Necrosis - pathology</subject><subject>Kidney Medulla - injuries</subject><subject>Kidney Medulla - pathology</subject><subject>Kidney Medulla - ultrastructure</subject><subject>Lithotripsy - adverse effects</subject><subject>lithotripsy injury</subject><subject>nephron injury</subject><subject>Nephrons - injuries</subject><subject>Nephrons - pathology</subject><subject>Nephrons - ultrastructure</subject><subject>pig model</subject><subject>renal morphology</subject><subject>Swine</subject><issn>1552-4884</issn><issn>1552-4892</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMlOwzAURS0EYihs-ADkFQukFie2M7CrKiaJQUKwthz7pTFN42AnlPw9Lq1gx-rdxblHeheh04hMIkLiS-kmMqQo4jvoMOI8HrMsj3d_c8YO0JH374FNCEv30UHEOKVRGh-i6tG6trK1nRsla6wq2czBY9PoXoEOF3cV4NbM8cLoBgZcDBi-OidV6FkHoeMrqxZ4JT8B16arbOdM64cr_ARt5WwTHO-9G47RXilrDyfbO0JvN9evs7vxw_Pt_Wz6MFYs5nycxLrQVJWkBE1SmieSctBJoahOyowW2foDWqaQERUnmshCpopwxsosZzRO6Qidb7ytsx89-E4sjVdQ17IB23uR8pTnOcsDeLEBlbPeOyhF68xSukFERKx3FdIJKX52DfDZ1toXS9B_6HbIAFxugJWpYfhHJaYvG-U3UV6Dug</recordid><startdate>200311</startdate><enddate>200311</enddate><creator>Shao, Youzhi</creator><creator>Connors, Bret A.</creator><creator>Evan, Andrew P.</creator><creator>Willis, Lynn R.</creator><creator>Lifshitz, David A.</creator><creator>Lingeman, James E.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</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>200311</creationdate><title>Morphological changes induced in the pig kidney by extracorporeal shock wave lithotripsy: Nephron injury</title><author>Shao, Youzhi ; Connors, Bret A. ; Evan, Andrew P. ; Willis, Lynn R. ; Lifshitz, David A. ; Lingeman, James E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4255-62dbd3cf0fed07396a35ed6bc3d6f83b860473f7e80c26d0aba7c0544f8943273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>cell fragmentation</topic><topic>extracorporeal shock wave lithotripsy</topic><topic>Female</topic><topic>Hemorrhage - etiology</topic><topic>Hemorrhage - pathology</topic><topic>Kidney Cortex - injuries</topic><topic>Kidney Cortex - pathology</topic><topic>Kidney Cortex - ultrastructure</topic><topic>Kidney Cortex Necrosis - etiology</topic><topic>Kidney Cortex Necrosis - pathology</topic><topic>Kidney Medulla - injuries</topic><topic>Kidney Medulla - pathology</topic><topic>Kidney Medulla - ultrastructure</topic><topic>Lithotripsy - adverse effects</topic><topic>lithotripsy injury</topic><topic>nephron injury</topic><topic>Nephrons - injuries</topic><topic>Nephrons - pathology</topic><topic>Nephrons - ultrastructure</topic><topic>pig model</topic><topic>renal morphology</topic><topic>Swine</topic><toplevel>online_resources</toplevel><creatorcontrib>Shao, Youzhi</creatorcontrib><creatorcontrib>Connors, Bret A.</creatorcontrib><creatorcontrib>Evan, Andrew P.</creatorcontrib><creatorcontrib>Willis, Lynn R.</creatorcontrib><creatorcontrib>Lifshitz, David A.</creatorcontrib><creatorcontrib>Lingeman, James E.</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>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shao, Youzhi</au><au>Connors, Bret A.</au><au>Evan, Andrew P.</au><au>Willis, Lynn R.</au><au>Lifshitz, David A.</au><au>Lingeman, James E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Morphological changes induced in the pig kidney by extracorporeal shock wave lithotripsy: Nephron injury</atitle><jtitle>The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology</jtitle><addtitle>Anat Rec A Discov Mol Cell Evol Biol</addtitle><date>2003-11</date><risdate>2003</risdate><volume>275A</volume><issue>1</issue><spage>979</spage><epage>989</epage><pages>979-989</pages><issn>1552-4884</issn><eissn>1552-4892</eissn><abstract>While shock wave lithotripsy (SWL) is known to cause significant damage to the kidney, little is known about the initial injury to cells along the nephron. In this study, one kidney in each of six juvenile pigs (6–7 weeks old) was treated with 1,000 shock waves (at 24 kV) directed at a lower pole calyx with an unmodified HM‐3 lithotripter. Three pigs were utilized as sham‐controls. Kidneys were fixed by vascular perfusion immediately after SWL or sham‐SWL. Three of the treated kidneys were used to quantitate lesion size. Cortical and medullary samples for light (LM) and transmission electron microscopy (TEM) were taken from the focal zone for the shock waves (F2), the contralateral kidney, and the kidneys of sham‐SWL pigs. Because preservation of the tissue occurred within minutes of SWL, the initial injury caused by the shock waves could be separated from secondary changes. No tissue damage was observed in contralateral sham‐SWL kidneys, but treated kidneys showed signs of injury, with a lesion of 0.2% ± 0.1% of renal volume. Intraparenchymal hemorrhage and injury to tubules was found at F2 in both the cortex and medulla of SWL‐treated kidneys. Tubular injury was always associated with intraparenchymal bleeding, and the range of tissue injury included total destruction of tubules, focal cellular fragmentation, necrosis, cell vacuolization, and membrane blebbing. The initial injury caused by SWL was cellular fragmentation and necrosis. Cellular vacuolization, membrane blebbing, and disorganization of apical brush borders appear to be secondary changes related to hypoxia. Anat Rec Part A 275A:979–989, 2003. © 2003 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>14533172</pmid><doi>10.1002/ar.a.10115</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals cell fragmentation extracorporeal shock wave lithotripsy Female Hemorrhage - etiology Hemorrhage - pathology Kidney Cortex - injuries Kidney Cortex - pathology Kidney Cortex - ultrastructure Kidney Cortex Necrosis - etiology Kidney Cortex Necrosis - pathology Kidney Medulla - injuries Kidney Medulla - pathology Kidney Medulla - ultrastructure Lithotripsy - adverse effects lithotripsy injury nephron injury Nephrons - injuries Nephrons - pathology Nephrons - ultrastructure pig model renal morphology Swine |
title | Morphological changes induced in the pig kidney by extracorporeal shock wave lithotripsy: Nephron injury |
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