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https://hdl.handle.net/11499/4287
Title: | Effect of insufficient insulin treatment in streptozotocin-induced diabetes mellitus | Authors: | Ozmen, O. Topsakal, Şenay. Sahinduran, S. Ozcelik, M. |
Keywords: | Immunohistochemistry Insufficient insulin treatment Insulin-dependent diabetes mellitus Pathology Streptozotocin insulin lispro animal cell animal experiment animal model animal tissue article controlled study drug effect female glucose blood level histopathology hyperglycemia immunohistochemistry ketonuria nonhuman pancreas islet beta cell priority journal streptozocin diabetes Animals Diabetes Mellitus, Experimental Dose-Response Relationship, Drug Female Hyperglycemia Insulin Islets of Langerhans Pancreas Proinsulin Rats Rats, Sprague-Dawley |
Abstract: | OBJECTIVES: In this study, we investigated clinically, pathologically, and immunohistochemically the effect of insufficient short-acting insulin treatment on streptozotocin (STZ)-induced diabetes mellitus in rats. METHODS: Three groups composed of 10 rats each were studied as follows: (1) a group that received only STZ (50 mg/kg) (STZ group); (2) a group that received 50 mg/kg STZ and, after 12 hours, 8 IU of short-acting insulin treatment (STZ + INS group), repeated every night for 5 days; and (3) a control group. Ketonuria and blood glucose levels were examined every day. Blood was obtained from 2 rats from each group, and necropsy was performed every day during the 5-day period. RESULTS: Hyperglycemia was observed in the STZ and STZ + INS groups 24 hours after, but levels were higher in the STS + INS group than those in the STZ-only group. Histopathology was similar in the STZ and STZ + INS groups, and degeneration was observed in both groups, but immunohistochemistry revealed a more severe reduction in insulin-secreting cells in the STZ + INS group than that in the STZ group. There were no hyperglycemia and histopathological or immunochemical alteration in the control group. CONCLUSIONS: This study showed that insufficient short-acting insulin treatment can increase the diabetogenic effect of STZ in rats. © 2007 Lippincott Williams & Wilkins, Inc. | URI: | https://hdl.handle.net/11499/4287 https://doi.org/10.1097/MPA.0b013e31802f082f |
ISSN: | 0885-3177 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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