English

dc.contributor.authorCavusoglu, TG
dc.contributor.authorDariverenli, E
dc.contributor.authorVural, K
dc.contributor.authorEkerbicer, N
dc.contributor.authorUlman, C
dc.contributor.authorÖlmez, E
dc.contributor.authorUysal, N
dc.date.accessioned2024-07-18T11:57:44Z
dc.date.available2024-07-18T11:57:44Z
dc.description.abstractWALTER DE GRUYTER GMBH
dc.identifier.issn1303-829X
dc.identifier.urihttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/7148
dc.language.isoArticle
dc.publisher0250-4685
dc.subjectObjectives: Type 2 diabetes is a common metabolic disease and anxiety disorders are very common among diabetics. Buspirone is used in the treatment of anxiety, also having blood glucose-lowering effects. The aim of the study was to investigate the effects of buspirone on the glucose and lipid metabolism as well as vascular function in type 2 diabetic rats. Methods: A type 2-diabetic model was induced through a high-fat diet for eight weeks followed by the administration of low-dose streptozotocin (35 mg/kg, intraperitoneal) in rats. Buspirone was given at two different doses (1.5 mg/kg/d and 5 mg/kg/d) and combined with metformin (300 mg/kg/d). The fasting glucose and insulin levels, lipid profile were analyzed, and vascular response measured from the thoracic aorta was also evaluated. Results: Both doses of buspirone caused a significant improvement in fasting blood glucose levels. In particular, the buspirone treatment, combined with metformin, improved endothelial dysfunction and was found to be correlated with decreased nitrate/nitrite levels. Conclusions: Buspirone may be effective in the treatment of type 2 diabetes, either alone or in combination with other treatments, particularly in terms of endothelial dysfunction, inflammation and impaired blood glucose, and insulin levels.
dc.titleEnglish
dc.typeINSULIN-RESISTANCE
dc.typePLASMA-GLUCOSE
dc.typeNITRIC-OXIDE
dc.typeSTREPTOZOTOCIN
dc.typeCHOLESTEROL
dc.typeMECHANISMS
dc.typeSEROTONIN
dc.typeSTRESS
dc.type5-HT

Files