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Angiotensin II receptor blocker inhibits p27Kip1 expression in glucose-stimulated podocytes and in diabetic glomeruli.

DC Field Value Language
dc.contributor.author강신욱-
dc.contributor.author류동열-
dc.contributor.author박형천-
dc.contributor.author유태현-
dc.contributor.author하성규-
dc.date.accessioned2017-10-26T06:41:25Z-
dc.date.available2017-10-26T06:41:25Z-
dc.date.issued2005-
dc.identifier.issn0085-2538-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/151180-
dc.description.abstractBACKGROUND: Diabetic nephropathy is characterized by glomerular and tubular hypertrophy, and angiotensin II receptor blockers (ARBs) are known to prevent renal hypertrophy in diabetic patients. METHODS: To determine the effect of ARB on podocyte p27(Kip1) mRNA and protein expression, podocytes were exposed to 5.6 mmol/L normal glucose or 25 mmol/L high glucose with or without ARB, 10(-7) mol/L L-158,809. For animal studies, streptozotocin-induced diabetic rats were left untreated or were treated with 1 mg/kg/day L-158,809 for 3 months (diabetes mellitus + ARB). Competitive reverse transcription-polymerase chain reaction (RT-PCR), Western blot, immunohistochemistry, and morphometric analyses were performed. RESULTS: p27(Kip1) mRNA and protein expression in podocytes exposed to high glucose and in 3-month diabetic glomeruli were significantly increased (P < 0.01). High glucose significantly increased angiotensin II levels both in cell lysates and in media compared with normal glucose (P < 0.05) and exogenous angiotensin II also increased p27(Kip1) mRNA and protein expression in podocytes. L-158,809 treatment in podocytes inhibited the increase in p27(Kip1) mRNA expression by 84%, and protein expression by 89% (P < 0.05). p27(Kip1) mRNA and protein expression in diabetic + ARB glomeruli were also significantly reduced by 78% and 85%, respectively, compared with diabetic glomeruli (P < 0.01). ARB treatment also significantly ameliorated increased glomerular p27(Kip1) expression in diabetes mellitus as assessed by immunohistochemistry (P < 0.01). The increase in glomerular volume in diabetes mellitus was also inhibited by 81% with ARB treatment (P < 0.05). CONCLUSION: p27(Kip1) mRNA and protein expression were increased in diabetic glomeruli as well as in high glucose-stimulated podocytes, and this increment in p27(Kip1) expression was ameliorated by ARB treatment. These findings indicate that ARB treatment has an additional effect on preventing renal hypertrophy in diabetes mellitus.-
dc.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherElsevier-
dc.relation.isPartOfKIDNEY INTERNATIONAL-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/2.0/kr/-
dc.subject.MESHAngiotensin II/analysis-
dc.subject.MESHAngiotensin Receptor Antagonists*-
dc.subject.MESHAnimals-
dc.subject.MESHCell Cycle Proteins/antagonists & inhibitors*-
dc.subject.MESHCell Cycle Proteins/genetics-
dc.subject.MESHCells, Cultured-
dc.subject.MESHCyclin-Dependent Kinase Inhibitor p27-
dc.subject.MESHDiabetes Mellitus, Experimental/metabolism*-
dc.subject.MESHDiabetic Nephropathies/prevention & control*-
dc.subject.MESHEpithelial Cells/metabolism-
dc.subject.MESHGlucose/pharmacology*-
dc.subject.MESHImidazoles/pharmacology*-
dc.subject.MESHKidney/pathology-
dc.subject.MESHKidney Glomerulus/cytology-
dc.subject.MESHKidney Glomerulus/metabolism*-
dc.subject.MESHMale-
dc.subject.MESHMice-
dc.subject.MESHRats-
dc.subject.MESHStreptozocin-
dc.subject.MESHTetrazoles/pharmacology*-
dc.subject.MESHTumor Suppressor Proteins/antagonists & inhibitors*-
dc.subject.MESHTumor Suppressor Proteins/genetics-
dc.titleAngiotensin II receptor blocker inhibits p27Kip1 expression in glucose-stimulated podocytes and in diabetic glomeruli.-
dc.typeArticle-
dc.publisher.locationUnited States-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorZHONG-GAO XU-
dc.contributor.googleauthorTAE-HYUN YOO-
dc.contributor.googleauthorDONG-RYEOL RYU-
dc.contributor.googleauthorHYEONG CHEON PARK-
dc.contributor.googleauthorSUNG KYU HA-
dc.contributor.googleauthorDAE SUK HAN-
dc.contributor.googleauthorSHARON G. ADLER-
dc.contributor.googleauthorRAMA NATARAJAN-
dc.contributor.googleauthorSHIN-WOOK KANG-
dc.identifier.doi10.1111/j.1523-1755.2005.00158.x-
dc.contributor.localIdA00053-
dc.contributor.localIdA01323-
dc.contributor.localIdA01759-
dc.contributor.localIdA02526-
dc.contributor.localIdA04252-
dc.relation.journalcodeJ01941-
dc.identifier.eissn1523-1755-
dc.identifier.pmid15698433-
dc.identifier.urlhttp://www.nature.com/ki/journal/v67/n3/full/4495127a.html-
dc.subject.keywordp27Kip1-
dc.subject.keywordangiotensin II receptor blocker-
dc.subject.keywordhigh glucose-
dc.subject.keyworddiabetic nephropathy-
dc.subject.keywordpodocytes-
dc.subject.keywordhypertrophy-
dc.contributor.alternativeNameKang, Shin Wook-
dc.contributor.alternativeNameRyu, Dong Ryeol-
dc.contributor.alternativeNamePark, Hyeong Cheon-
dc.contributor.alternativeNameYoo, Tae Hyun-
dc.contributor.alternativeNameHa, Sung Kyu-
dc.citation.volume67-
dc.citation.number3-
dc.citation.startPage944-
dc.citation.endPage952-
dc.identifier.bibliographicCitationKIDNEY INTERNATIONAL, Vol.67(3) : 944-952, 2005-
dc.date.modified2017-05-04-
dc.identifier.rimsid43513-
dc.type.rimsART-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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