Egleton Richard D, Campos Christopher C, Huber Jason D, Brown Rachel C, Davis Thomas P
Department of Pharmacology, College of Medicine, The University of Arizona, Tucson, AZ 85724, USA.
Diabetes. 2003 Jun;52(6):1496-501. doi: 10.2337/diabetes.52.6.1496.
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.
尽管糖尿病是一种伴有血管并发症的疾病,但人们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处。脉络丛是脑脊液(CSF)产生的主要部位,并表达多种离子转运体。先前的研究表明,糖尿病期间外周和大脑中的离子转运受到干扰。在本研究中,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体的影响。通过腹腔注射STZ(柠檬酸盐缓冲液中60 mg/kg,通过血糖分析确认:糖尿病大鼠601±22 mg/dl,年龄匹配的对照组181±46 mg/dl)在雄性Sprague-Dawley大鼠中诱导糖尿病;28天后,处死大鼠,采集脉络丛并提取蛋白质。使用针对离子转运体的抗体进行蛋白质印迹分析,包括Na(+)-K(+)-2Cl(-)共转运体和Na(+)-K(+)-ATP酶α1亚基。还研究了脉络丛中K(+)类似物(86)Rb(+)的流出情况。与年龄匹配的对照组相比,糖尿病大鼠Na(+)-K(+)-ATP酶α1亚基和Na(+)-K(+)-2Cl(-)共转运体的表达增加,Na(+)-H(+)交换体表达降低,Na(+)-K(+)-ATP酶β1或β2亚基无变化。这些变化的净效应是糖尿病脉络丛中(86)Rb(+)流出量比对照组增加66%。这些表达变化可能会影响脉络丛离子平衡,从而显著影响糖尿病大鼠的脑脊液生成。