姜黄提取物对链脲佐菌素所致糖尿病小鼠肾、肝、胰器官功能障碍的保护作用

Y. Nindita, Astika Widy Utomo, Nani Maharani, Endang Mahati, Ilham Fernando Kristiandi, Irfan Kesumayadi, E. Kurniawati, M. A. Sobirin, N. Wijayahadi
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引用次数: 0

摘要

印度尼西亚的糖尿病(DM)并发症仍需引起重视。姜黄常被用作抗糖尿病的补充药物。目前尚未发现姜黄提取物(Curcuma domestica extract, CDE)和姜黄提取物(Curcuma xanthorza extract, CXE)对链脲佐菌素(STZ)诱导的DM小鼠肾、肝、胰腺功能障碍进展的影响。本研究是比较姜黄提取物和CXE对肾、肝、胰腺等多器官功能障碍进展的影响的实验研究。以100克纯碱和300毫升70%乙醇浸渍法制备提取物。小鼠腹腔注射180 mg/kgBW STZ诱导。CDE和CXE分别给予100 mg/kgBW口服21 d。在第0、1和21天用血糖仪测量血糖。治疗后第21天行肾、肝、胰腺组织病理检查。数据分析采用单因素方差分析和Kruskal-Wallis检验(P <0.05)。结果显示,治疗21天后,血糖水平显示CDE和CXE没有显著降低。组织病理学检查显示,CDE组和CXE组对肾脏炎症、肾脏纤维化和胰腺炎症均有显著保护作用(P =0.001, P =0.013, P =0.027)。肝脏炎症、肝纤维化、胰腺炎症无显著性差异(P =0.184、P =0.498、P =0.193)。然而,CXE治疗对肝脏炎症有显著改善(P =0.041)。与CDE相比,CXE具有更大的肝保护作用潜力。关键词:姜黄提取物,器官功能障碍,炎症,糖尿病,小鼠
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Protective Effect of Curcuma domestica and Curcuma xanthorrhiza Extracts toward Kidney, Liver, and Pancreatic Organ Dysfunction in Streptozotocin-Induced Diabetes Mellitus Mice
The complications of Diabetes mellitus (DM) in Indonesia still need attention. Curcuma are often used as complementary medicine for antidiabetic. There is no study has been found comparing the effect of Curcuma domestica extracts (CDE) and Curcuma xanthorrhiza extracts (CXE) on the progression of the kidney, liver, and pancreas dysfunction in the mice with streptozotocin (STZ)-induced DM. This study was an experimental study to compare the effect of CDE and CXE on the progression of multi-organ dysfunction such as kidney, liver, and pancreas. The extract was produced by a maceration process with composition 100 gr simplicial and 300 ml ethanol 70%. The mice were induced with 180 mg/kgBW STZ intraperitoneally. The CDE and CXE were given 100 mg/kgBW orally for 21 days. A blood glucose was measured by a glucose meter on days 0, 1, and 21. The histopathological examination of the kidney, liver and pancreas were done on 21 days after the treatment. Data were analyzed using One Way ANOVA and Kruskal-Wallis tests (P <0.05). The results revealed that blood glucose levels showed no significant reduction of CDE and CXE after 21 days of the treatment. Histopathological examination showed a significant protection in kidney inflammation, kidney fibrosis, and pancreatic inflammation (P =0.001, P =0.013, P =0.027 respectively) in CDE and CXE groups. No significant differences were examined in liver inflammation, liver fibrosis, and pancreatic inflammation (P =0.184, P =0.498, P =0.193 respectively). However, there was a significant improvement in liver inflammation by CXE treatment (P =0.041). CXE has a greater potential for hepatoprotective effect compared to CDE. Keywords: Curcuma extract, Organ dysfunction, Inflammation, Diabetes mellitus, Mice
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