Publication:
Long-term treatment with a beta-blocker timolol attenuates renal-damage in diabetic rats via enhancing kidney antioxidant-defense system

dc.contributor.coauthorGökturk, Hilal
dc.contributor.coauthorGök, Müslüm
dc.contributor.coauthorTuncay, Erkan
dc.contributor.coauthorCan, Belgin
dc.contributor.coauthorTuran, Belma
dc.contributor.kuauthorUlusu, Nuriye Nuray
dc.contributor.kuprofileFaculty Member
dc.contributor.schoolcollegeinstituteSchool of Medicine
dc.contributor.yokid6807
dc.date.accessioned2024-11-09T23:51:41Z
dc.date.issued2014
dc.description.abstractThe factors with increasing diabetes-prevalence lead to significant global increases in chronic kidney disease. Since hyperglycemia generates more ROS and attenuates cellular antioxidant-defense mechanisms, numerous studies demonstrated that hyperglycemia-induced oxidative stress played a major role in the extracellular matrix expansion in tissues. Although no direct relation between activation of beta-adrenergic (beta-AR) system and kidney disease in diabetes and since beta-blockers demonstrate marked beneficial effects due to their scavenging free radicals and/or acting as an antioxidant in diabetic animal studies, the eventual objective of the present study was to determine whether timolol-treatment of streptozotocin-induced diabetic rats (5 mg/kg, daily following diabetes-induction, for 12-week) has advantage to prevent hyperglycemia-induced renal-damage via enhancing the depressed antioxidant defense in the kidney. Light microscopy data and their quantification demonstrated that timolol-treatment prevented basically glomerular hypertrophy, expansion in mesangium cell size, thickening and fibrosis in glomerular basement membrane, and accumulation of glycogen into tubular epithelial cells. Additionally, electron microscopy data demonstrated that timolol-treatment could also prevent diabetes-induced changes in the kidney tissue such as hypertrophy in podocytes, lost of filtration gaps and slit-diaphragms, and vacuolization in the distal tubular cells. Biochemical analysis basically on enzymes of antioxidant-defense system, including glutathione-S-transferase, glutathione reductase, and glucose-6-phosphate dehydrogenase, further supported that diabetes-induced damage in the kidney is mostly dependent on the increased oxidative stress and timolol, having an antioxidant-like action, could protect the kidney against hyperglycemia-induced damage without normalization of high-blood glucose level. Consequently, it can be suggested that although beta-blockers are widely used for the treatment of cardiovascular diseases, beta-blocker therapy of diabetics seems to be a new therapeutic approach against hyperglycemia-induced kidney damage in diabetic patients.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue44958
dc.description.openaccessNO
dc.description.publisherscopeInternational
dc.description.sponsorshipTUBITAK[SBAG-111S042] This work has been supported partially by grant from TUBITAKSBAG-111S042.
dc.description.volume395
dc.identifier.doi10.1007/s11010-014-2123-2
dc.identifier.eissn1573-4919
dc.identifier.issn0300-8177
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-84906320900
dc.identifier.urihttp://dx.doi.org/10.1007/s11010-014-2123-2
dc.identifier.urihttps://hdl.handle.net/20.500.14288/14757
dc.identifier.wos340550000017
dc.keywordsDiabetes
dc.keywordsAntioxidants
dc.keywordsBeta-blockers
dc.keywordsKidney oxidative stress
dc.keywordsCarbohydrate-metabolism
dc.keywordsKey enzymes
dc.keywordsNebivolol
dc.keywordsNephropathy
dc.keywordsActivation
dc.keywordsCarvedilol
dc.keywordsReceptor
dc.keywordsCells
dc.keywordsHeart
dc.languageEnglish
dc.publisherSpringer
dc.sourceMolecular and Cellular Biochemistry
dc.subjectCell biology
dc.titleLong-term treatment with a beta-blocker timolol attenuates renal-damage in diabetic rats via enhancing kidney antioxidant-defense system
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0002-3173-1389
local.contributor.kuauthorUlusu, Nuriye Nuray

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