Rahman Md Atiar, Chowdhury J M Kamirul Hasan, Aklima Jannatul, Azadi Mohammad Ali
Department of Biochemistry & Molecular Biology University of Chittagong Chittagong Bangladesh.
Department of Zoology University of Chittagong Chittagong Bangladesh.
Food Sci Nutr. 2018 Mar 30;6(4):943-952. doi: 10.1002/fsn3.625. eCollection 2018 Jun.
This research aims to investigate the protective effects Roxb polyphenols on streptozotocin-induced diabetic rats. Polyphenolic assays were undertaken through established methods. To conduct animal intervention study, forty Wistar albino male rats (average body weight 188.42 ± 7.13 g) of different groups were diabetized by streptozotocin (60 mg/kg) only in the animals of diabetic control (DC) and extract (LM) groups. At the end of 4 weeks of intervention, serum was analyzed for insulin, liver and cardiac enzymes, lipid profiles, uric acid, and creatinine using ELISA method. In vitro α-amylase inhibition of LM was evaluated and compared with reference drug acarbose. Pancreatic tissues were undertaken for histopathological screening. Food and fluid intake, weekly blood glucose level, liver glycogen, aspartate transaminase (AST), creatinine kinase (CK-MB), cholesterol, and lactate dehydrogenase (LDH) were significantly decreased, whereas oral glucose tolerance (OGTT) ability, serum insulin concentration, and pancreatic islets morphology were significantly improved in the LM300 treatment group compared to the DC group. Alpha-amylase inhibition was not found to be very promising for guiding the α-amylase inhibition pathway. Results suggest that can exert a potential effort to restore pancreatic β-cell damaged by streptozotocin induction.
本研究旨在探讨罗汉果多酚对链脲佐菌素诱导的糖尿病大鼠的保护作用。采用既定方法进行多酚含量测定。为进行动物干预研究,仅对糖尿病对照组(DC)和提取物(LM)组的动物用链脲佐菌素(60mg/kg)使不同组的40只雄性Wistar白化大鼠(平均体重188.42±7.13g)患糖尿病。干预4周结束时,采用酶联免疫吸附测定法分析血清中的胰岛素、肝酶和心肌酶、血脂谱、尿酸和肌酐。评估LM的体外α-淀粉酶抑制作用,并与参考药物阿卡波糖进行比较。对胰腺组织进行组织病理学筛查。与DC组相比,LM300治疗组的食物和液体摄入量、每周血糖水平、肝糖原、天冬氨酸转氨酶(AST)、肌酸激酶(CK-MB)、胆固醇和乳酸脱氢酶(LDH)显著降低,而口服葡萄糖耐量(OGTT)能力、血清胰岛素浓度和胰岛形态显著改善。未发现α-淀粉酶抑制作用对指导α-淀粉酶抑制途径非常有前景。结果表明,其可发挥潜在作用来恢复因链脲佐菌素诱导而受损的胰腺β细胞。