Department of Pharmacy, Medical Faculty, University of Novi Sad, 2100 Novi Sad, Serbia.
J Diabetes Res. 2013;2013:598603. doi: 10.1155/2013/598603. Epub 2013 Mar 13.
Major problem for diabetic patients represents damage of blood vessels and the oxidative stress of the brain cells due to increased concentration of free radicals and poor nutrition of brain cells. Gliclazide has antioxidative properties and poor blood brain barrier (BBB) penetration. Bile acids are known for their hypoglycemic effect and as promoters of drug penetration across biological membranes. Accordingly, the aim of this study is to investigate whether the bile acid (deoxycholic acid) can change the permeation of gliclazide, through the blood brain barrier of a rat model type-1 diabetes. Twenty-four male Wistar rats were randomly allocated to four groups, of which, two were given alloxan intraperitoneally (100 mg/kg) to induce diabetes. One diabetic group and one healthy group were given a bolus gliclazide intra-arterially (20 mg/kg), while the other two groups apart from gliclazide got deoxycholic acid (4 mg/kg) subcutaneously. Blood samples were collected 30, 60, 150, and 240 seconds after dose, brain tissues were immediately excised and blood glucose and gliclazide concentrations were measured. Penetration of gliclazide in groups without deoxycholic acid pretreatment was increased in diabetic animals compared to healthy animals. Also in both, the healthy and diabetic animals, deoxycholic acid increased the permeation of gliclazide through that in BBB.
糖尿病患者的主要问题是由于自由基浓度增加和脑细胞营养不足,导致血管和脑细胞的氧化应激损伤。格列齐特具有抗氧化特性,但血脑屏障(BBB)穿透能力差。胆汁酸以其降血糖作用和促进药物穿透生物膜而闻名。因此,本研究旨在研究胆汁酸(脱氧胆酸)是否可以改变格列齐特通过 1 型糖尿病大鼠模型的血脑屏障的渗透。24 只雄性 Wistar 大鼠随机分为四组,其中两组腹腔内给予(100mg/kg)链脲佐菌素诱导糖尿病。一组糖尿病组和一组健康组经动脉内给予格列齐特(20mg/kg),而另外两组除给予格列齐特外,还皮下给予脱氧胆酸(4mg/kg)。在给予药物后 30、60、150 和 240 秒采集血样,立即切除脑组织并测量血糖和格列齐特浓度。未用脱氧胆酸预处理的组中,糖尿病动物的格列齐特渗透增加,与健康动物相比。在健康和糖尿病动物中,脱氧胆酸均增加了格列齐特通过 BBB 的渗透。