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[未提及的物质]对链脲佐菌素诱导的糖尿病Wistar白化大鼠的抗糖尿病活性证据。

Evidence of antidiabetic activity of against streptozotocin-induced diabetic Wistar albino rats.

作者信息

Simon Jerine Peter, Baskaran Udhaya Lavinya, Shallauddin Kadar Basha, Ramalingam Giridharan, Evan Prince Sabina

机构信息

School of Biosciences and Technology, VIT University, Vellore, Tamil Nadu 632014 India.

出版信息

3 Biotech. 2018 Feb;8(2):129. doi: 10.1007/s13205-018-1156-8. Epub 2018 Feb 13.

Abstract

The aim of our study is to investigate the protective effect of against streptozotocin-induced diabetes in Wistar albino rats. Rats were divided into five groups: group I was normal control, group II was diabetic control (50 mg/kg b.w. of streptozotocin, i.p.), group III was (400 mg/kg b.w., p.o.) treated diabetic rats; group IV was Glibenclamide (0. 6 mg/kg b.w., p.o.) treated diabetic rats and group V was treated with (400 mg/kg b.w., p.o.) alone. There was significant elevation in the levels of blood glucose, serum lipid profile and serum renal markers (total protein, urea, creatinine and uric acid) in the diabetic rats. Also, diabetic rats showed significantly ( < 0.05) reduced antioxidant status (reduced levels of superoxide dismutase, catalase, glutathione peroxidase, glutathione--transferase and reduced glutathione; increased levels of TBARS), impaired oral glucose tolerance and elevated HbA1C. was able to normalize the above mentioned parameters. Significant histopathological changes were found in the pancreas, liver and kidney sections of the diabetic control group while treatment with was able to minimize the extent of tissue damage. Current study shows that possesses significant antidiabetic and antihyperlipidemic effects in streptozotocin-induced diabetic rats by effectively reducing the rise in blood glucose levels and lipid profile.

摘要

我们研究的目的是调查[具体物质名称未给出]对链脲佐菌素诱导的Wistar白化大鼠糖尿病的保护作用。大鼠被分为五组:第一组为正常对照组,第二组为糖尿病对照组(腹腔注射50mg/kg体重的链脲佐菌素),第三组为用[具体物质名称未给出](口服400mg/kg体重)治疗的糖尿病大鼠;第四组为用格列本脲(口服0.6mg/kg体重)治疗的糖尿病大鼠,第五组仅用[具体物质名称未给出](口服400mg/kg体重)治疗。糖尿病大鼠的血糖水平、血清脂质谱和血清肾脏标志物(总蛋白、尿素、肌酐和尿酸)显著升高。此外,糖尿病大鼠的抗氧化状态显著降低(超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶、谷胱甘肽-S-转移酶和还原型谷胱甘肽水平降低;丙二醛水平升高),口服葡萄糖耐量受损,糖化血红蛋白升高(P<0.05)。[具体物质名称未给出]能够使上述参数正常化。糖尿病对照组的胰腺、肝脏和肾脏切片中发现了显著的组织病理学变化,而用[具体物质名称未给出]治疗能够将组织损伤程度降至最低。当前研究表明,[具体物质名称未给出]通过有效降低血糖水平和脂质谱的升高,对链脲佐菌素诱导的糖尿病大鼠具有显著的抗糖尿病和抗高血脂作用。

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