Interaction of Carthamus oil, chromium picolinate and glyburide in blood glucose and its impact on liver enzymes and lipid profile in diabetes-induced rats

Gisele Mara Silva Gonçalve, P. Barros, Gustavo Henrique Da Silva, Júlia Ferreira Watanabe, A. Eisinger
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Abstract

Introduction: Carthamus oil is a compound that has the potential to be used in numerous applications due to its anti-inflammatory, antioxidant, immunomodulatory and neuroprotective effects. Chromium picolinate has been indicated for the control of insulin resistance. Aim: To evaluate the effect of Carthamus oil (30 mg/kg) and chromium picolinate (5 µg/kg) interaction with oral glyburide in chemically diabetes-induced Wistar rats and its influence on drug therapy. Method: Diabetes mellitus was induced with streptozotocin, and the animals were randomized into experimental groups (n= 6/group), who received gastric gavage treatments for ten days, G1: control, G2: diabetic and received glyburide, G3: diabetic and received the interaction of Carthamus oil and chromium picolinate, G4: diabetic and received the interaction of glyburide, Carthamus oil and chromium picolinate. After the treatment period, fasting blood glucose, post-sucrose blood glucose, total cholesterol and triglyceride levels, alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in blood serum were compared, in addition to urine analysis. Results: In this study, the only altered parameters were the post-sucrose blood glucose measurement with the lowest result for G4 (P <0.05), and the ALT measurement, with lower values for G4 (P <0.05) compared to G1. Conclusion: It can be concluded that the unprecedented interaction of Carthamus oil, chromium picolinate and glyburide contributed to the reduction of blood glucose and serum levels of ALT in diabetic rats and is promising for future studies in humans.
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红花油、吡啶甲酸铬和格列本脲对糖尿病大鼠血糖的相互作用及其对肝酶和脂质谱的影响
介绍:红花油是一种化合物,由于其抗炎、抗氧化、免疫调节和神经保护作用,具有广泛应用的潜力。吡啶甲酸铬已被用于控制胰岛素抵抗。目的:观察红花油(30 mg/kg)和吡啶甲酸铬(5µg/kg)与口服格列本脲对化学性糖尿病Wistar大鼠的作用及其对药物治疗的影响。方法:采用链脲佐菌素诱导糖尿病,随机分为各组(n= 6/组),各组分别灌胃治疗10 d, G1组为对照组,G2组为糖尿病组,采用格列本脲组,G3组为糖尿病组,采用红花油与吡啶甲酸铬联用组,G4组为糖尿病组,采用格列本脲、红花油与吡啶甲酸铬联用组。治疗期结束后,比较各组空腹血糖、蔗糖后血糖、总胆固醇、甘油三酯水平、血清丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)水平,并进行尿液分析。结果:本研究中仅有蔗糖后血糖测量值发生变化,G4血糖最低(P <0.05), ALT测量值G4血糖较G1低(P <0.05)。结论:红花油、吡啶甲酸铬和格列本脲的相互作用可以降低糖尿病大鼠的血糖和血清ALT水平,具有良好的临床应用前景。
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