Mishra Chetna, Khalid Monowar Alam, Fatima Nazmin, Singh Babita, Tripathi Dinesh, Waseem Mohammad, Mahdi Abbas Ali
Department of Biochemistry, King George's Medical University, Lucknow-226003, Uttar Pradesh, India.
Department of Environmental Science, Integral University, Lucknow-226021, Uttar Pradesh, India.
Iran J Basic Med Sci. 2019 Jan;22(1):49-57. doi: 10.22038/ijbms.2018.26889.6574.
Phytochemicals such as polyphenols, alkaloids, and terpenoids, protect against the development of early stages and complications of diabetes mellitus according to various reports. The aim of this study was to measure the anti-dyslipidemic and anti-diabetic effects of Citral on high-fat-diet (HFD) and streptozotocin (STZ) induced diabetic dyslipidemic rats and to see also its effect on carbohydrate metabolic regulatory enzymes in the liver.
Rats were kept on a high-fat diet for 2 weeks, then diabetes was induced by a single dose of STZ (35 mg/kg/BW, intraperitoneally), Citral was administered orally at a dose of 45 mg/kg/BW for 28 days to diabetic rats. Blood glucose, plasma insulin, and lipid profile in blood were studied. Antioxidant activities were assayed in the liver, pancreas, and adipose tissues. Carbohydrate metabolic enzymes of the liver were also studied in diabetic dyslipidemic rats.
The results of this study confirmed that administration of Citral significantly (<0.05) decreased the blood glucose level and increased plasma insulin in diabetic rats. Citral also improved oxidative markers along with anti-oxidative enzymes of the liver, adipose tissue, and pancreas in the HFD/STZ group. Citral also regulated the activity of the glucose-metabolic enzymes in the liver. The results of the present study were compared to Glibenclamide, which is a standard oral drug for lowering the blood sugar.
Results may show that Citral possesses anti-dyslipidemic activity as well as anti-diabetic activity and also regulates the enzyme activity of glycolytic and gluconeogenic processes in the liver.
根据各种报告,多酚、生物碱和萜类等植物化学物质可预防糖尿病早期阶段的发展及其并发症。本研究的目的是测定柠檬醛对高脂饮食(HFD)和链脲佐菌素(STZ)诱导的糖尿病血脂异常大鼠的抗血脂异常和抗糖尿病作用,并观察其对肝脏碳水化合物代谢调节酶的影响。
大鼠高脂饮食喂养2周,然后单次腹腔注射STZ(35mg/kg体重)诱导糖尿病,给糖尿病大鼠口服柠檬醛,剂量为45mg/kg体重,持续28天。研究血糖、血浆胰岛素和血液中的血脂谱。测定肝脏、胰腺和脂肪组织中的抗氧化活性。还研究了糖尿病血脂异常大鼠肝脏中的碳水化合物代谢酶。
本研究结果证实,给予柠檬醛可显著(<0.05)降低糖尿病大鼠的血糖水平并增加血浆胰岛素。柠檬醛还改善了HFD/STZ组肝脏、脂肪组织和胰腺的氧化标志物以及抗氧化酶。柠檬醛还调节了肝脏中葡萄糖代谢酶的活性。本研究结果与格列本脲(一种降低血糖的标准口服药物)进行了比较。
结果可能表明,柠檬醛具有抗血脂异常活性和抗糖尿病活性,还可调节肝脏中糖酵解和糖异生过程的酶活性。