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Deneysel Diyabetin Sıçan Böbreklerinde Meydana Getirdiği Histolojik Değişiklikler+

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dc.contributor.author Öztürk, Feral
dc.contributor.author Iraz, Mustafa
dc.contributor.author Eşrefoğlu, Mukaddes
dc.contributor.author Kuruş, Meltem
dc.contributor.author Gül, Mehmet
dc.contributor.author Otlu, Ali
dc.date.accessioned 2015-02-27T12:00:37Z
dc.date.available 2015-02-27T12:00:37Z
dc.date.issued 2006
dc.identifier.citation Öztürk, Feral ;Iraz, Mustafa ;Eşrefoğlu, Mukaddes ;Kuruş, Meltem ;Gül, Mehmet ;Otlu, Ali ;İnönü Üniversitesi Tıp Fakültesi Dergisi 12(1) 1-4 (2005) tr_TR
dc.identifier.uri http://www.totmdergisi.org/articles/2005/volume12/issue1/2005_12_1_1.pdf
dc.identifier.uri http://hdl.handle.net/11616/1383
dc.description İnönü Üniversitesi Tıp Fakültesi Dergisi 12(1) 1-4 (2005) tr_TR
dc.description.abstract This study was designed to detect and evaluate the histochemical and immunohistochemical alterations in rat kidney histology following streptozotocin (STZ)-induced and fructose-induced experimental diabetes. Material and Methods: Fifteen male Sprague-Dawley adult rats were divided into three groups as control, STZ and fructose groups. STZ group rats received a single dose of STZ (45mg/kg) intraperitoneally. Fructose group rats were fed by tap water containing 10 % D-fructose for 8 weeks. At the end of eight weeks rats were killed, left kidneys were removed. Following routine tissue process, kidneys were embedded in paraffin. Histochemical and immunohistochemical stains were applied and the specimens examined by light microscope. Results: In both STZ and fructose groups histological changes were observad in the cortex. Increase of Basal membrane thickness in glomerule capillary, mesangial matrix, thickness in parietal layer of Bowman’s capsule and rare tubular basal membrane thickness were detected in both groups. In fructose group arteriol walls also showed increased thickness. Conclusion: We concluded that both STZ and fructose induced experimental diabetes led to similar findings in rat kidneys and these findings probably occur as direct and/or indirect results of hyperglisemia. tr_TR
dc.description.abstract This study was designed to detect and evaluate the histochemical and immunohistochemical alterations in rat kidney histology following streptozotocin (STZ)-induced and fructose-induced experimental diabetes. Material and Methods: Fifteen male Sprague-Dawley adult rats were divided into three groups as control, STZ and fructose groups. STZ group rats received a single dose of STZ (45mg/kg) intraperitoneally. Fructose group rats were fed by tap water containing 10 % D-fructose for 8 weeks. At the end of eight weeks rats were killed, left kidneys were removed. Following routine tissue process, kidneys were embedded in paraffin. Histochemical and immunohistochemical stains were applied and the specimens examined by light microscope. Results: In both STZ and fructose groups histological changes were observad in the cortex. Increase of Basal membrane thickness in glomerule capillary, mesangial matrix, thickness in parietal layer of Bowman’s capsule and rare tubular basal membrane thickness were detected in both groups. In fructose group arteriol walls also showed increased thickness. Conclusion: We concluded that both STZ and fructose induced experimental diabetes led to similar findings in rat kidneys and these findings probably occur as direct and/or indirect results of hyperglisemia. tr_TR
dc.language.iso tur tr_TR
dc.publisher İnönü Üniversitesi Tıp Fakültesi Dergisi tr_TR
dc.rights Attribution 3.0 United States *
dc.rights.uri http://creativecommons.org/licenses/by/3.0/us/ *
dc.subject Deneysel diyabet tr_TR
dc.subject Sıçan tr_TR
dc.subject Böbrek tr_TR
dc.subject Işık mikroskopi tr_TR
dc.subject Experimental Diabetes tr_TR
dc.subject Rat tr_TR
dc.subject Kidney tr_TR
dc.subject Light Microscopy tr_TR
dc.title Deneysel Diyabetin Sıçan Böbreklerinde Meydana Getirdiği Histolojik Değişiklikler+ tr_TR
dc.title.alternative The Histologic Alterations of Experimental Diabetes on the Rat Kidneys tr_TR
dc.type Article tr_TR


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