Statins ameliorate endothelial barrier permeability changes in the cerebral tissue of streptozotocin-induced diabetic rats

被引:72
作者
Mooradian, AD
Haas, MJ
Batejko, O
Hovsepyan, M
Feman, SS
机构
[1] St Louis Univ, Sch Med, Div Endocrinol Diabet & Metab, Dept Internal Med, St Louis, MO 63104 USA
[2] St Louis Univ, Sch Med, Dept Ophthalmol, St Louis, MO 63104 USA
关键词
D O I
10.2337/diabetes.54.10.2977
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Statins may have favorable effects on endothelial barrier function. The effect of rosuvastatin and simvastatin therapy (10 mg/kg) for 5 weeks on blood-brain barrier (BBB), blood-retinal barrier (BRB), and cardiac muscle permeability of streptozotocin-induced. diabetic rats was studied. The size-selective permeability of different vascular beds to a group of fluorescein isothiocyanate dextrans of varying molecular weights was measured. The volume of distribution of 250-, 70-, and 40-kDa dextrans in the cerebral tissue of diabetic rats were significantly increased. The volume of distribution of these dextrans in cerebral tissue was normalized by both statins. Diabetes did not significantly alter the BRB, but both statins decreased the volume of distribution of 70- and 40-kDa dextrans in the retina. The volume of distribution of 40 kDa in cardiac muscle was increased in diabetes, and this change was prevented with statin treatment. Treatment with rosuvastatin and mevalonate (150 mg/kg in drinking water for 5 weeks) did not alter the volume of distribution measurements. We concluded that 1) diabetes in rats is associated with significant changes in the BBB permeability; 2) statin treatment improves the endothelial barrier function in cerebral tissue, retina, and cardiac muscled; and 3) this statin effect could not be attributed to HMGCoA reductase inhibition.
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收藏
页码:2977 / 2982
页数:6
相关论文
共 33 条
  • [1] Amerongen GPV, 2000, CIRCULATION, V102, P2803
  • [2] Diabetes downregulates GLUT1 expression in the retina and its microvessels but not in the cerebral cortex or its microvessels
    Badr, GA
    Tang, J
    Ismail-Beigi, F
    Kern, TS
    [J]. DIABETES, 2000, 49 (06) : 1016 - 1021
  • [3] Biochemistry and molecular cell biology of diabetic complications
    Brownlee, M
    [J]. NATURE, 2001, 414 (6865) : 813 - 820
  • [4] RhoA inactivation enhances endothelial barrier function
    Carbajal, JM
    Schaeffer, RC
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 277 (05): : C955 - C964
  • [5] Diabetes-related changes in rat cerebral occludin and zonula occludens-1 (ZO-1) expression
    Chehade, JM
    Haas, MJ
    Mooradian, AD
    [J]. NEUROCHEMICAL RESEARCH, 2002, 27 (03) : 249 - 252
  • [6] Role of endothelial dysfunction in atherosclerosis
    Davignon, J
    Ganz, P
    [J]. CIRCULATION, 2004, 109 (23) : 27 - 32
  • [7] Effect of simvastatin therapy on cell membrane cholesterol content and membrane function as assessed by polymorphonuclear cell NADPH oxidase activity
    Day, AP
    Bellavia, S
    Jones, OTG
    Stansbie, D
    [J]. ANNALS OF CLINICAL BIOCHEMISTRY, 1997, 34 : 269 - 275
  • [8] de Sotomayor MA, 2001, BIOCHEM BIOPH RES CO, V280, P486
  • [9] Lipid-lowering drug atorvastastin as an adjunct in the management of diabetic macular edema
    Gupta, A
    Gupta, V
    Thapar, S
    Bhansali, A
    [J]. AMERICAN JOURNAL OF OPHTHALMOLOGY, 2004, 137 (04) : 675 - 682
  • [10] Involvement of Rho GTPases in the transcriptional inhibition of preproendothelin-1 gene expression by simvastatin in vascular endothelial cells
    Hernández-Perera, O
    Pérez-Sala, D
    Soria, E
    Lamas, S
    [J]. CIRCULATION RESEARCH, 2000, 87 (07) : 616 - 622