TY - JOUR
T1 - Effect of carbenoxolone on inflammatory cytokine levels, fasting blood sugar, and histopathology of pancreas on experimental autoimmune diabetes in C57BL/6 mice
AU - Rasouli, Mehdi
AU - Jafari-Khataylou, Yaser
AU - Ashrafi-Helan, Javad
N1 - Publisher Copyright:
© 2018, Mazandaran University of Medical Sciences. All rights reserved.
PY - 2018/6
Y1 - 2018/6
N2 - Background and purpose: Destruction of insulin-producing beta cells by T cells causes type-1 diabetes (T1D). Carbenoxolone has cytoprotective and anti-inflammatory effects, and has been shown to be capable of suppressing Th17 cells that are effectively involved in the pathogenesis of type 1 diabetes, therefore, we studied the effect of Carbenoxolone on T1D in C57BL/6 mice. Materials and methods: Forty male C57BL/6 inbred strain mice were randomly divided into four groups and in three groups diabetes was induced by streptozotocin. A positive control group was considered and two other groups received 50 mg/kg/day i.p. carbenoxolone (7 and 5 doses). Then, on days 7 and 14 after the disease induction, fasting blood sugar (FBS) level, anti-inflammatory cytokines IL-1β, IL-6 and TNF-α, and pathological changes of the pancreas were studied during the course of the disease. Results: Carbenoxolone increased the levels of IL-1β, IL-6, TNF-α, and FBS. Also, it significantly increased infiltration of inflammatory cells into the pancreatic islets (P <0.05). Conclusion: It seems that carbenoxolone triggers a breakdown in Treg/Th17 balance by increasing the levels of pro-inflammatory cytokines and increases the number of Th17 cells, thereby causing toxic effects on the pancreatic beta cells and increasing the severity of the disease.
AB - Background and purpose: Destruction of insulin-producing beta cells by T cells causes type-1 diabetes (T1D). Carbenoxolone has cytoprotective and anti-inflammatory effects, and has been shown to be capable of suppressing Th17 cells that are effectively involved in the pathogenesis of type 1 diabetes, therefore, we studied the effect of Carbenoxolone on T1D in C57BL/6 mice. Materials and methods: Forty male C57BL/6 inbred strain mice were randomly divided into four groups and in three groups diabetes was induced by streptozotocin. A positive control group was considered and two other groups received 50 mg/kg/day i.p. carbenoxolone (7 and 5 doses). Then, on days 7 and 14 after the disease induction, fasting blood sugar (FBS) level, anti-inflammatory cytokines IL-1β, IL-6 and TNF-α, and pathological changes of the pancreas were studied during the course of the disease. Results: Carbenoxolone increased the levels of IL-1β, IL-6, TNF-α, and FBS. Also, it significantly increased infiltration of inflammatory cells into the pancreatic islets (P <0.05). Conclusion: It seems that carbenoxolone triggers a breakdown in Treg/Th17 balance by increasing the levels of pro-inflammatory cytokines and increases the number of Th17 cells, thereby causing toxic effects on the pancreatic beta cells and increasing the severity of the disease.
KW - Carbenoxolone
KW - Histopathology of pancreas
KW - Pre-inflammatory cytokines
KW - Type 1 diabetes
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M3 - Article
AN - SCOPUS:85047809494
SN - 1735-9260
VL - 28
SP - 1
EP - 11
JO - Journal of Mazandaran University of Medical Sciences
JF - Journal of Mazandaran University of Medical Sciences
IS - 161
ER -