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Differential effects of diabetes on rat choroid plexus ion transporter expression.

机译:糖尿病对大鼠脉络丛离子转运蛋白表达的差异作用。

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Though diabetes is a disease with vascular complications, little is known about its effects on the blood-brain barrier or the blood-cerebrospinal fluid barrier (BCSFB). The BCSFB is situated at choroid plexuses located in the lateral, third, and fourth ventricles. Choroid plexuses are the primary site of cerebrospinal fluid (CSF) production and express numerous ion transporters. Previous studies have shown a perturbation of ion transport in the periphery and brain during diabetes. In this study, we investigated the effect of diabetes on ion transporters in the choroid plexuses of streptozotocin (STZ)-induced diabetic rats. Diabetes was induced in male Sprague-Dawley rats by intraperitoneal injection of STZ (60 mg/kg in citrate buffer, confirmed by glucose analysis: 601 +/- 22 mg/dl diabetic rats, 181 +/- 46 mg/dl age-matched controls); and at 28 days, rats were killed, choroid plexuses harvested, and protein extracted. Western blot analyses were carried out using antibodies for ion transporters, including Na(+)-K(+)-2Cl(-) cotransporter and the Na(+)-K(+)-ATPase alpha1-subunit. The efflux of the K(+) analog (86)Rb(+) from choroid plexus was also studied. Diabetic rats showed an increase in expression of the Na(+)-K(+)-2Cl(-) cotransporter and the Na(+)-K(+)-ATPase alpha1-subunit, as compared with age-matched controls, a decrease in Na(+)-H(+) exchanger expression, and no change in Na(+)-K(+)-ATPase beta1- or beta2-subunit. The net effect of these changes was a 66% increase in (86)Rb(+) efflux from diabetic choroid plexus compared with controls. These changes in expression may affect choroid plexus ion balance and thus significantly affect CSF production in diabetic rats.
机译:尽管糖尿病是一种具有血管并发症的疾病,但对其对血脑屏障或血脑脊液屏障(BCSFB)的影响知之甚少。 BCSFB位于侧脑室,第三脑室和第四脑室的脉络丛中。脉络膜丛是脑脊液(CSF)产生的主要部位,并表达多种离子转运蛋白。先前的研究表明,在糖尿病期间,离子在周围和大脑中的传输受到干扰。在这项研究中,我们调查了糖尿病对链脲佐菌素(STZ)诱导的糖尿病大鼠脉络丛中离子转运蛋白的影响。腹膜内注射STZ(60 mg / kg柠檬酸盐缓冲液,经葡萄糖分析确认:601 +/- 22 mg / dl糖尿病大鼠,181 +/- 46 mg / dl年龄匹配)在雄性Sprague-Dawley大鼠中诱发糖尿病控件);在第28天,处死大鼠,收获脉络丛,并提取蛋白质。使用抗体的离子转运蛋白,包括Na(+)-K(+)-2Cl(-)共转运蛋白和Na(+)-K(+)-ATPaseα1-亚基,进行蛋白质印迹分析。还研究了脉络丛的K(+)类似物(86)Rb(+)的流出。与年龄匹配的对照组相比,糖尿病大鼠显示Na(+)-K(+)-2Cl(-)共转运蛋白和Na(+)-K(+)-ATPaseα1-亚基的表达增加。 Na(+)-H(+)交换子表达减少,并且Na(+)-K(+)-ATPase beta1-或beta2-亚基无变化。与对照组相比,这些变化的净效应是糖尿病脉络膜丛的(86)Rb(+)外排增加了66%。这些表达上的变化可能影响脉络丛离子平衡,从而显着影响糖尿病大鼠的CSF产生。

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