File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Collagen studies in newborn rat kidneys with incomplete ureteric obstruction

TitleCollagen studies in newborn rat kidneys with incomplete ureteric obstruction
Authors
Issue Date1993
PublisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/ki/index.html
Citation
Kidney International, 1993, v. 44 n. 3, p. 593-605 How to Cite?
AbstractCollagen studies in newborn rats with incomplete ureteric obstruction were performed to describe and quantify changes in collagen deposition resulting from urinary tract obstruction at an early developmental age. Incomplete ureteric obstruction was created in three-day-old rats by placing the left ureter in a tunnel formed by the psoas muscle, and sham-operated controls underwent a laparotomy. The rats were sacrificed at 10, 17, 24 or 31 days. Collagen types I, III, IV, and V were localized by indirect immunofluorescence microscopy, the total collagen content of the kidney was quantitated using hydroxyproline analysis, and collagen types I and III were quantitated using cyanogen bromide (CNBr) peptide analysis. Increased immunofluorescent staining for all of the collagens was found in the diffusely widened medullary interstitium of the obstructed kidney, and more focally in the cortical interstitium. Collagen types I, III and V but not collagen type IV, were also found in bands in the interstitium at the junction of the cortex with the medulla. Increased staining for collagen type IV was found in thickened and tortuous tubular basement membranes (TBM) of the obstructed kidneys. The total collagen content of the obstructed kidney was significantly increased compared to the amounts in both the contralateral kidneys and in the kidneys from sham-operated controls at 24 and 31 days of age (P < 0.01 in each case, Wilcoxon matched pairs rank sum test and Mann Whitney U-test, respectively). The amount of collagen in the kidneys correlated with the degree of hydronephrosis (Spearman correlation test, r = 0.78, P < 0.02). CNBr peptide analysis demonstrated that over 50% of the collagen in the normal neonatal rat kidney was collagen type I and approximately 25% was collagen type III. In the obstructed kidneys most of the collagen was also collagen type I and collagen type III, although the proportion of total collagen comprised by these collagen types was decreased d with the controls. The amount of collagen type III in the contralateral kidneys was reduced compared to that in the controls. Thus, the neonatal renal response to obstruction resulted in increased amounts of a range of collagens in the interstitium and TBM, and the extent of this response was partially related to the degree of hydronephrosis.
Persistent Identifierhttp://hdl.handle.net/10722/147379
ISSN
2021 Impact Factor: 18.998
2020 SCImago Journal Rankings: 3.499
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHaralambousGasser, Aen_US
dc.contributor.authorChan, Den_US
dc.contributor.authorWalker, RGen_US
dc.contributor.authorPowell, HRen_US
dc.contributor.authorBecker, GJen_US
dc.contributor.authorJones, CLen_US
dc.date.accessioned2012-05-29T06:03:17Z-
dc.date.available2012-05-29T06:03:17Z-
dc.date.issued1993en_US
dc.identifier.citationKidney International, 1993, v. 44 n. 3, p. 593-605en_US
dc.identifier.issn0085-2538en_US
dc.identifier.urihttp://hdl.handle.net/10722/147379-
dc.description.abstractCollagen studies in newborn rats with incomplete ureteric obstruction were performed to describe and quantify changes in collagen deposition resulting from urinary tract obstruction at an early developmental age. Incomplete ureteric obstruction was created in three-day-old rats by placing the left ureter in a tunnel formed by the psoas muscle, and sham-operated controls underwent a laparotomy. The rats were sacrificed at 10, 17, 24 or 31 days. Collagen types I, III, IV, and V were localized by indirect immunofluorescence microscopy, the total collagen content of the kidney was quantitated using hydroxyproline analysis, and collagen types I and III were quantitated using cyanogen bromide (CNBr) peptide analysis. Increased immunofluorescent staining for all of the collagens was found in the diffusely widened medullary interstitium of the obstructed kidney, and more focally in the cortical interstitium. Collagen types I, III and V but not collagen type IV, were also found in bands in the interstitium at the junction of the cortex with the medulla. Increased staining for collagen type IV was found in thickened and tortuous tubular basement membranes (TBM) of the obstructed kidneys. The total collagen content of the obstructed kidney was significantly increased compared to the amounts in both the contralateral kidneys and in the kidneys from sham-operated controls at 24 and 31 days of age (P < 0.01 in each case, Wilcoxon matched pairs rank sum test and Mann Whitney U-test, respectively). The amount of collagen in the kidneys correlated with the degree of hydronephrosis (Spearman correlation test, r = 0.78, P < 0.02). CNBr peptide analysis demonstrated that over 50% of the collagen in the normal neonatal rat kidney was collagen type I and approximately 25% was collagen type III. In the obstructed kidneys most of the collagen was also collagen type I and collagen type III, although the proportion of total collagen comprised by these collagen types was decreased d with the controls. The amount of collagen type III in the contralateral kidneys was reduced compared to that in the controls. Thus, the neonatal renal response to obstruction resulted in increased amounts of a range of collagens in the interstitium and TBM, and the extent of this response was partially related to the degree of hydronephrosis.en_US
dc.languageengen_US
dc.publisherNature Publishing Group. The Journal's web site is located at http://www.nature.com/ki/index.htmlen_US
dc.relation.ispartofKidney Internationalen_US
dc.subject.meshAnimalsen_US
dc.subject.meshAnimals, Newbornen_US
dc.subject.meshCollagen - Metabolismen_US
dc.subject.meshDna - Metabolismen_US
dc.subject.meshDisease Models, Animalen_US
dc.subject.meshFemaleen_US
dc.subject.meshFluorescent Antibody Techniqueen_US
dc.subject.meshKidney - Metabolism - Pathologyen_US
dc.subject.meshNephritis, Interstitial - Etiology - Metabolism - Pathologyen_US
dc.subject.meshOrgan Sizeen_US
dc.subject.meshRatsen_US
dc.subject.meshRats, Sprague-Dawleyen_US
dc.subject.meshUreteral Obstruction - Complications - Metabolism - Pathologyen_US
dc.titleCollagen studies in newborn rat kidneys with incomplete ureteric obstructionen_US
dc.typeArticleen_US
dc.identifier.emailChan, D:chand@hkucc.hku.hken_US
dc.identifier.authorityChan, D=rp00540en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1038/ki.1993.286-
dc.identifier.pmid8231033-
dc.identifier.scopuseid_2-s2.0-0027293409en_US
dc.identifier.volume44en_US
dc.identifier.issue3en_US
dc.identifier.spage593en_US
dc.identifier.epage605en_US
dc.identifier.isiWOS:A1993LT42800016-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridHaralambousGasser, A=6507425517en_US
dc.identifier.scopusauthoridChan, D=7402216545en_US
dc.identifier.scopusauthoridWalker, RG=7404929257en_US
dc.identifier.scopusauthoridPowell, HR=7101711376en_US
dc.identifier.scopusauthoridBecker, GJ=7401553242en_US
dc.identifier.scopusauthoridJones, CL=7408260666en_US
dc.identifier.issnl0085-2538-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats