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  • Journal of Experimental and Clinical Medicine
  • Volume:39 Issue:3
  • Effects of beta-1,3-D glucan on systemic bortezomib treated rat pancreas

Effects of beta-1,3-D glucan on systemic bortezomib treated rat pancreas

Authors : Nurhan ERKAYA, Seçil Nazife PARLAK
Pages : 743-748
View : 42 | Download : 11
Publication Date : 2022-08-30
Article Type : Research Paper
Abstract :Bortezomib, selective inhibitor of the 26S proteasome, is used for treatment of some types of cancer and immunosuppressive therapies. B-1,3-insert ignore into journalissuearticles values(D);-glucan, a synthetic antioxidant is used complementary medical treatment for human. This study was conducted to investigate the effects of the antioxidant Beta-1,3-D glucan on rat pancreas treated with systemic bortezomib. In the study, 36 Sprague-Dawley adult male rats were divided into four groups: control insert ignore into journalissuearticles values(C);, bortezomib insert ignore into journalissuearticles values(BZ);, β-1, 3-D-glucan insert ignore into journalissuearticles values(BD); and bortezomib + β-1,3- insert ignore into journalissuearticles values(D); –glukan insert ignore into journalissuearticles values(BZ+BD);. Each group was divided into two subgroups insert ignore into journalissuearticles values(48 or 72 hours);, depending on the time of sacrification. After experiments, immunohistochemical, stereological and histopathological changes in all rat pancreatic tissues were examined. It was determined increased degenerative, vacuolated serous acini cells and inflammatory cell infiltrations in the groups of BZ and BZ+BG. In immunohistochemical analysis, densities of insulin positive cells were decreased in the groups of BZ and BZ+BG. Furthermore, in stereological mean volume of serous acinus analysis, significantly increases were detected in the groups of BZ and BZ+BG insert ignore into journalissuearticles values(p<0.05);. BZ treatment had the detrimental effects on pancreas tissues. Also, administration of BG was insufficient to prevent injury induced by BZ treatment in the pancreas tissues.
Keywords : Bortezomib, Beta glucan, pancreas, İnsulin, oxidative stress

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