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百里醌对链脲佐菌素诱导的糖尿病肾病的保护作用。

Protective effects of thymoquinone on streptozotocin-induced diabetic nephropathy.

作者信息

Kanter Mehmet

机构信息

Department of Histology and Embryology, Faculty of Medicine, Trakya University, 22030 Edirne, Turkey.

出版信息

J Mol Histol. 2009 Apr;40(2):107-15. doi: 10.1007/s10735-009-9220-7. Epub 2009 May 31.

Abstract

The aim of this study was designed to investigate the possible beneficial effects of the thymoquinone (TQ) in streptozotocine (STZ)-induced diabetes in rats. The rats were randomly allotted into one of three experimental groups: A (control), B (diabetic untreated), and C (diabetic treated with TQ); each group contain ten animals. B and C groups received STZ. Diabetes was induced in two groups by a single intra-peritoneal (i.p) injection of STZ (50 mg/kg, freshly dissolved in 5 mmol/l citrate buffer, pH 4.5). Two days after STZ treatment, development of diabetes in two experimental groups was confirmed by measuring blood glucose levels in a tail vein blood samples. Rats with blood glucose levels of 250 mg/dl or higher were considered to be diabetic. The rats in TQ treated groups were given TQ (50 mg/kg body weight) once a day orally by using intra gastric intubation for 12 weeks starting 2 days after STZ injection. Treatment of TQ reduced the glomerular size, thickening of capsular, glomerular and tubular basement membranes, increased amounts of mesangial matrix and tubular dilatation and renal function as compared with diabetics untreated. We conclude that TQ therapy causes renal morphologic and functional improvement after STZ-induced diabetes in rats. We believe that further preclinical research into the utility of TQ treatment may indicate its usefulness as a potential treatment in diabetic nephropathy.

摘要

本研究旨在探讨百里醌(TQ)对链脲佐菌素(STZ)诱导的大鼠糖尿病可能产生的有益作用。大鼠被随机分为三个实验组之一:A组(对照组)、B组(未治疗的糖尿病组)和C组(用TQ治疗的糖尿病组);每组包含10只动物。B组和C组接受STZ。通过单次腹腔注射STZ(50 mg/kg,新鲜溶解于5 mmol/l柠檬酸盐缓冲液,pH 4.5)在两组中诱导糖尿病。STZ治疗两天后,通过测量尾静脉血样中的血糖水平来确认两个实验组中糖尿病的发生。血糖水平在250 mg/dl或更高的大鼠被认为患有糖尿病。从STZ注射后两天开始,用TQ治疗的组中的大鼠通过胃内插管每天口服一次TQ(50 mg/kg体重),持续12周。与未治疗的糖尿病大鼠相比,TQ治疗减少了肾小球大小、包膜、肾小球和肾小管基底膜增厚、系膜基质数量增加、肾小管扩张以及改善了肾功能。我们得出结论,TQ治疗可使STZ诱导的糖尿病大鼠的肾脏形态和功能得到改善。我们认为,对TQ治疗效用的进一步临床前研究可能表明其作为糖尿病肾病潜在治疗方法的有用性。

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