Evaluation of Oral Administration of Lauric Acid Supplement on Fasting Blood Glucose Level and Pancreatic Histomorphological Studies in High Fat Diet/Streptozotocin-Induced Type 2 Diabetic Male Wistar Rats

E. Alex, A. Dubo, D. Ejiogu, KW Iyomo, KV Jerome, N. Aisha, AO Daikwo, J. Yahaya, RO Osiyemi, J. Yaro
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引用次数: 3

Abstract

Background: Diabetes mellitus is the most common serious metabolic disease in human with a hall-mark of an elevated blood glucose concentration caused by a number of biochemical and physiological alterations Aim: The aim of the study was to evaluate the effect oral administration of lauric acid supplement on fasting blood glucose level and pancreatic histomorphological studies in high fat diet/streptozotocin (STZ)-induced type 2 diabetic male Wistar rats. Study Design: Thirty-five apparently healthy male Wistar rats of 6-8 weeks, weighing between 70 g-90 g were grouped into seven groups of five animals each (n=5) and treated for a period of twenty-one days (21) with graded doses of lauric acid supplement after validation of diabetes. Group 1 and 3 were fed with normal rat feed while group 2, 4, 5, 6, 7 were fed with high fat diet for eight weeks after which low dose STZ was given to same groups. Methodology: Group 1: (Normal control), Group 2: (Diabetic control untreated), Groups 3: (Normoglycemic) received 125 mg/kg Lauric acid, Group 4, 5 and 6 were administered 125, 250 and 500 mg/kg body weight of lauric acid, Group 7: (Standard control) received metformin 100 mg/kg. Blood glucose level was determined at weekly intervals using glucose test strips and digital glucometer (Accu-Chek Advantage, Roche Diagnostic, Germany). At the end of twenty-one (21) days, rats were anaesthetized using ketamine and xylazine at 75 and 25 (mg/kg) respectively. The Pancreatic tissues were excised and subjected to routine histological investigation for histo-pathological changes. Result: The results showed that lauric acid at all doses significantly (P<0.05) decreased the fasting blood glucose level from (32.45 ± 0.54, 28.85 ± 1.81, 28.85 ± 2.52 mmo/L) to (7.9 ± 1.07, 5.27 ± 0.39 and 4.45 ± 0.48 mmol/L) after three weeks of treatment. And also, Subsequent histomorphological evaluation also showed necrosis and vacuolization of islet β-cells to be reasonably reduced in the diabetic treated rats Conclusion: This study has been able to demonstrate the Antidiabetic potential of graded doses of lauric acid supplementations for 21 days of administration and it has found out that it possesses strong Antihyperglycemic potencies and induced β-cell regeneration in high fat diet/streptozotocin induced type 2 diabetic rat models.
口服月桂酸对高脂饮食/链脲佐菌素诱导2型糖尿病雄性Wistar大鼠空腹血糖水平和胰腺组织形态学的影响
背景:糖尿病是人类最常见的严重代谢性疾病,以一系列生化和生理改变引起的血糖浓度升高为标志。目的:本研究的目的是评估口服月桂酸补充剂对高脂饮食/链脲佐菌素(STZ)诱导的2型糖尿病雄性Wistar大鼠空腹血糖水平和胰腺组织形态学的影响。研究设计:35只明显健康的6-8周雄性Wistar大鼠,体重在70 g-90 g之间,分为7组,每组5只(n=5),在确认糖尿病后,用月桂酸分级剂量补充治疗21天(21)。第1、3组饲喂正常大鼠饲料,第2、4、5、6、7组饲喂高脂饲料,连续8周后给予低剂量STZ。方法:1组(正常对照组)、2组(未治疗的糖尿病对照组)、3组(血糖正常者)给予月桂酸125 mg/kg, 4、5、6组分别给予月桂酸125、250、500 mg/kg, 7组(标准对照组)给予二甲双胍100 mg/kg。使用血糖试纸和数字血糖仪(Accu-Chek Advantage,罗氏诊断公司,德国)每隔一周测定一次血糖水平。21 d后,分别以75 mg/kg的氯胺酮和25 mg/kg的噻嗪麻醉大鼠。切除胰腺组织,进行常规组织学检查,观察组织病理变化。结果:各剂量月桂酸治疗3周后,空腹血糖由(32.45±0.54、28.85±1.81、28.85±2.52 mmol/L)降至(7.9±1.07、5.27±0.39、4.45±0.48 mmol/L),差异均有统计学意义(P<0.05)。结论:本研究在高脂饮食/链脲佐菌素诱导的2型糖尿病大鼠模型中,分级剂量月桂酸具有较强的降糖作用,并能诱导β细胞再生,证明了月桂酸给药21 d后胰岛β细胞坏死和空泡化程度明显降低。
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