苦瓜对链脲佐菌素诱导糖尿病大鼠空腹血糖水平的影响

S. Mohal, D. Mondal, P. Chowdhury, A. Khanom, K. Shamim
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摘要

背景:科学研究揭示了苦瓜的降糖特性。本研究旨在显微镜下观察苦瓜(karela)是否对糖尿病患者的空腹血糖(FBG)有降低作用。研究类型:实验研究。单位:前身为孟加拉谢赫·穆吉布医科大学(BSMMU)和孟加拉国糖尿病、内分泌和代谢疾病研究与康复研究所(BIRDEM)的研究生医学研究所(IPGMR)解剖学系。实验对象:选取10 ~ 12周龄、体重150 ~ 280gm的健康雄性朗埃文斯幼鼠65只。方法:根据大鼠不同的饮食、喂养方式和药物治疗方式,将大鼠分为4组。主要观察指标:各组大鼠差异FBG水平变化。结果:对照组(a组)空腹血糖(FBG)初始和终期(注射链脲佐菌素/载药第7天和第51天)平均值分别为7.872±0.60和8.55±0.82。因此,平均值(FBG)增加了约13% (P = 0.022*),高于初始值。糖尿病未治疗组平均初始(FBG)水平为25.95±8.90,最终(FBG)水平为24.02±4.08。因此,在这里,(FBG)水平下降了约13% (P = 0.557)。另一方面,胰岛素组糖尿病大鼠初始FBG均值为24.35±6.81,终值均值为8.38±5.02,较胰岛素组低(P = 0.000*); karela组糖尿病大鼠初始FBG均值为23.03±5.70,终值均值为5.65±1.29,较胰岛素组低(P = 0.000*)。胰岛素治疗组和karela治疗组的数值分别显著低于未治疗组(P= 0.007)和(P= 0.005)。而胰岛素组与karela组在这方面差异无统计学意义(P = 0.605)。结论:卡累拉对链脲佐菌素所致糖尿病的高血糖作用有一定的抑制作用。然而,建议进一步的研究来确定卡累拉作为一种安全、有用、有效的抗高血糖药物和抗糖尿病药物。关键词:糖尿病;高血糖;Momordica charantia (karela) DOI: http://dx.doi.org/ 10.3329/bja.v9i1.8148孟加拉解剖学杂志2011年1月,Vol. 9 No. 1 pp 45-48
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Momordica Charantia (Karela) on the Fasting Blood Glucose level in the Streptozotocin-Induced Diabetic Rats
Context: Scientific studies revealed the hypoglycaemic properties of momordica charantia. The present study was carried out to find out microscopically whether Momordica charantia (karela) has got any impact lowering of FBG (Fasting Blood Glucose) level in diabetes mellitus. Study type: an experiemental study. Setting: Anatomy department of the then IPGMR (Institute of Post Graduate Medicine and Research) at present BSMMU (Bangabandhu Sheikh Mujib Medical University) and BIRDEM (Bangladesh Institute of Research and Rehabilitation in Diabetes, Endocrine & Metabolic Disorders). Subjects: Sixty five healthy young Long Evans rats of male sex weighing 150 to 280gm aged between 10 to 12 weeks were used in this study. Methods: The rats were divided into four equal groups depending on their different sorts of dietry feeding and drug treatment. Main outcome measures: variation of differential FBG level in different groups of rat. Result: Mean 'initial' and 'final' (on day 7 and day 51 from Streptozotocin/vehicle injection) fasting blood glucose (FBG) level in the control group (Group-A) was 7.872 ± 0.60 and 8.55 ± 0.82 respectively. Therefore the mean (FBG) increased by about 13% (P = 0.022*) which is higher than that of the initial value. In untreated diabetic group the mean initial (FBG) level was 25.95 ± 8.90 and the mean final was 24.02 ± 4.08. So here, the (FBG) level decreased by about 13% (P = 0.557). On the other hand, in the insulintreated diabetic rats the mean initial (FBG) level was 24.35 ± 6.81 and the mean final was 8.38 ± 5.02, which is lower (P = 0.000*) & in the karela–treated diabetic rats, the initial (FBG) level was 23.03 ± 5.70 and the mean final was 5.65 ± 1.29 which is lower* (P = 0.000*). The value in the insulin-treated diabetic rats & in the karela-treated diabetic rats were significantly lower than that of the untreated diabetic rats (P = 0.007) & (P= 0.005) respectively. But there was no significant difference between the insulin-treated diabetic rats & the karela-treated diabetic rats (P = 0.605) in this regard. Conclusion: Karela showed a tendency of acting against hyperglycemic effects of Streptozotocin-induced diabetes mellitus. However, further investigations are recommended for establishing karela as a safe, useful effective anti- hyperglycemic agent as well as antidiabetogenic agent. Key words: Diabetes mellitus; Hyperglycemia; Momordica charantia (karela) DOI: http://dx.doi.org/ 10.3329/bja.v9i1.8148 Bangladesh Journal of Anatomy January 2011, Vol. 9 No. 1 pp 45-48
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