Nakakaawa Lilian, Gbala Ifeoluwa D, Bargul Joel L, Cheseto Xavier, Wesonga John M
Department of Molecular Biology and Biotechnology Pan African University Institute for Basic Sciences Technology, and Innovation (PAUSTI) Nairobi Kenya.
Department of Life and Physical Sciences Bugema University Kampala Uganda.
Food Sci Nutr. 2025 Jan 6;13(1):e4635. doi: 10.1002/fsn3.4635. eCollection 2025 Jan.
Microgreens of Brassica plants have attracted increasing research interest in the management of the prevailing epidemic of Type 2 diabetes mellitus (T2DM) because of their high nutritional value. This study evaluated the antidiabetic effects of Microgreens Ethanolic Extract (BMEE) in type-2 diabetic rats. For the normoglycemic assay, rats were divided into five groups and received a single oral dose of 100, 250, and 500 mg/kg of BMEE while the control groups received distilled water and Glibenclamide. Fasting blood glucose (FBG) levels were determined on a weekly basis for 28 days in diabetic rats after treatment with BMEE at 250 and 500 mg/kg dosage levels. Oral glucose tolerance test (OGTT), serum insulin levels, lipid profile and messenger RNA expression levels of Insulin receptor substrate 1 (), Glucose transporter 2 (), and Nuclear factor kappa light-chain enhancer of activated B cells () genes were determined. BMEE did not induce hypoglycemic effects in rats with normal blood glucose levels, but induced antidiabetic activities in the experimental type-2 diabetic rats. BMEE lowered FBG levels, increased oral glucose tolerance, increased insulin sensitization, and reduced insulin resistance. Treatment of diabetic rats with BMEE increased lipid metabolism and relatively higher expression levels of and genes, and led to reduced expression levels of in the liver. Overall, this study reports that BMEE has potential as a nutraceutical to be utilized in the management of T2DM.
十字花科植物的嫩苗因其高营养价值,在2型糖尿病(T2DM)流行的管理方面吸引了越来越多的研究兴趣。本研究评估了嫩苗乙醇提取物(BMEE)对2型糖尿病大鼠的抗糖尿病作用。对于正常血糖测定,将大鼠分为五组,分别单次口服100、250和500mg/kg的BMEE,而对照组给予蒸馏水和格列本脲。在以250和500mg/kg剂量水平用BMEE治疗后,对糖尿病大鼠每周测定一次空腹血糖(FBG)水平,持续28天。测定口服葡萄糖耐量试验(OGTT)、血清胰岛素水平、血脂谱以及胰岛素受体底物1()、葡萄糖转运蛋白2()和活化B细胞的核因子κ轻链增强子()基因的信使核糖核酸表达水平。BMEE在血糖正常的大鼠中未诱导低血糖作用,但在实验性2型糖尿病大鼠中诱导了抗糖尿病活性。BMEE降低了FBG水平,提高了口服葡萄糖耐量,增强了胰岛素敏感性,并降低了胰岛素抵抗。用BMEE治疗糖尿病大鼠增加了脂质代谢以及和基因相对较高的表达水平,并导致肝脏中表达水平降低。总体而言,本研究报告称BMEE作为一种营养保健品有潜力用于T2DM的管理。