Streptozotocin-induced diabetes progressively increases blood-brain barrier permeability in specific brain regions in rats

Department of Basic Pharmaceutical Sciences, West Virginia University, Morgantown, West Virginia Submitted 12 May 2006 ; accepted in final form 24 August 2006 This study investigated the effects of streptozotocin-induced diabetes on the functional integrity of the blood-brain barrier in the rat at 7...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 2006-12, Vol.291 (6), p.H2660-H2668
Hauptverfasser: Huber, Jason D, VanGilder, Reyna L, Houser, Kimberly A
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container_title American journal of physiology. Heart and circulatory physiology
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creator Huber, Jason D
VanGilder, Reyna L
Houser, Kimberly A
description Department of Basic Pharmaceutical Sciences, West Virginia University, Morgantown, West Virginia Submitted 12 May 2006 ; accepted in final form 24 August 2006 This study investigated the effects of streptozotocin-induced diabetes on the functional integrity of the blood-brain barrier in the rat at 7, 28, 56, and 90 days, using vascular space markers ranging in size from 342 to 65,000 Da. We also examined the effect of insulin treatment of diabetes on the formation and progression of cerebral microvascular damage and determined whether observed functional changes occurred globally throughout the brain or within specific brain regions. Results demonstrate that streptozotocin-induced diabetes produced a progressive increase in blood-brain barrier permeability to small molecules from 28 to 90 days and these changes in blood-brain barrier permeability were region specific, with the midbrain most susceptible to diabetes-induced microvascular damage. In addition, results showed that insulin treatment of diabetes attenuated blood-brain barrier disruption, especially during the first few weeks; however, as diabetes progressed, it was evident that microvascular damage occurred even when hyperglycemia was controlled. Overall, results of this study suggest that diabetes-induced perturbations to cerebral microvessels may disrupt homeostasis and contribute to long-term cognitive and functional deficits of the central nervous system. in situ; endothelial; cerebral blood flow; neurovascular; dementia Address for reprint requests and other correspondence: J. D. Huber, Dept. of Basic Pharmaceutical Sciences, West Virginia Univ. School of Pharmacy, PO Box 9530, Morgantown, WV 26506 ( jhuber{at}hsc.wvu.edu )
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We also examined the effect of insulin treatment of diabetes on the formation and progression of cerebral microvascular damage and determined whether observed functional changes occurred globally throughout the brain or within specific brain regions. Results demonstrate that streptozotocin-induced diabetes produced a progressive increase in blood-brain barrier permeability to small molecules from 28 to 90 days and these changes in blood-brain barrier permeability were region specific, with the midbrain most susceptible to diabetes-induced microvascular damage. In addition, results showed that insulin treatment of diabetes attenuated blood-brain barrier disruption, especially during the first few weeks; however, as diabetes progressed, it was evident that microvascular damage occurred even when hyperglycemia was controlled. Overall, results of this study suggest that diabetes-induced perturbations to cerebral microvessels may disrupt homeostasis and contribute to long-term cognitive and functional deficits of the central nervous system. in situ; endothelial; cerebral blood flow; neurovascular; dementia Address for reprint requests and other correspondence: J. D. Huber, Dept. of Basic Pharmaceutical Sciences, West Virginia Univ. 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Heart and circulatory physiology</title><addtitle>Am J Physiol Heart Circ Physiol</addtitle><description>Department of Basic Pharmaceutical Sciences, West Virginia University, Morgantown, West Virginia Submitted 12 May 2006 ; accepted in final form 24 August 2006 This study investigated the effects of streptozotocin-induced diabetes on the functional integrity of the blood-brain barrier in the rat at 7, 28, 56, and 90 days, using vascular space markers ranging in size from 342 to 65,000 Da. We also examined the effect of insulin treatment of diabetes on the formation and progression of cerebral microvascular damage and determined whether observed functional changes occurred globally throughout the brain or within specific brain regions. Results demonstrate that streptozotocin-induced diabetes produced a progressive increase in blood-brain barrier permeability to small molecules from 28 to 90 days and these changes in blood-brain barrier permeability were region specific, with the midbrain most susceptible to diabetes-induced microvascular damage. In addition, results showed that insulin treatment of diabetes attenuated blood-brain barrier disruption, especially during the first few weeks; however, as diabetes progressed, it was evident that microvascular damage occurred even when hyperglycemia was controlled. Overall, results of this study suggest that diabetes-induced perturbations to cerebral microvessels may disrupt homeostasis and contribute to long-term cognitive and functional deficits of the central nervous system. in situ; endothelial; cerebral blood flow; neurovascular; dementia Address for reprint requests and other correspondence: J. D. Huber, Dept. of Basic Pharmaceutical Sciences, West Virginia Univ. 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Heart and circulatory physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huber, Jason D</au><au>VanGilder, Reyna L</au><au>Houser, Kimberly A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Streptozotocin-induced diabetes progressively increases blood-brain barrier permeability in specific brain regions in rats</atitle><jtitle>American journal of physiology. Heart and circulatory physiology</jtitle><addtitle>Am J Physiol Heart Circ Physiol</addtitle><date>2006-12-01</date><risdate>2006</risdate><volume>291</volume><issue>6</issue><spage>H2660</spage><epage>H2668</epage><pages>H2660-H2668</pages><issn>0363-6135</issn><eissn>1522-1539</eissn><coden>AJPPDI</coden><abstract>Department of Basic Pharmaceutical Sciences, West Virginia University, Morgantown, West Virginia Submitted 12 May 2006 ; accepted in final form 24 August 2006 This study investigated the effects of streptozotocin-induced diabetes on the functional integrity of the blood-brain barrier in the rat at 7, 28, 56, and 90 days, using vascular space markers ranging in size from 342 to 65,000 Da. We also examined the effect of insulin treatment of diabetes on the formation and progression of cerebral microvascular damage and determined whether observed functional changes occurred globally throughout the brain or within specific brain regions. Results demonstrate that streptozotocin-induced diabetes produced a progressive increase in blood-brain barrier permeability to small molecules from 28 to 90 days and these changes in blood-brain barrier permeability were region specific, with the midbrain most susceptible to diabetes-induced microvascular damage. In addition, results showed that insulin treatment of diabetes attenuated blood-brain barrier disruption, especially during the first few weeks; however, as diabetes progressed, it was evident that microvascular damage occurred even when hyperglycemia was controlled. Overall, results of this study suggest that diabetes-induced perturbations to cerebral microvessels may disrupt homeostasis and contribute to long-term cognitive and functional deficits of the central nervous system. in situ; endothelial; cerebral blood flow; neurovascular; dementia Address for reprint requests and other correspondence: J. D. Huber, Dept. of Basic Pharmaceutical Sciences, West Virginia Univ. School of Pharmacy, PO Box 9530, Morgantown, WV 26506 ( jhuber{at}hsc.wvu.edu )</abstract><cop>United States</cop><pub>American Physiological Society</pub><pmid>16951046</pmid><doi>10.1152/ajpheart.00489.2006</doi></addata></record>
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subjects Animals
Blood-Brain Barrier - pathology
Blood-Brain Barrier - physiopathology
Brain - blood supply
Brain - physiopathology
Capillary Permeability
Carbon Radioisotopes
Central Nervous System - blood supply
Central Nervous System - physiopathology
Cognition Disorders - physiopathology
Coloring Agents
Diabetes
Diabetes Mellitus, Experimental - metabolism
Diabetes Mellitus, Experimental - pathology
Diabetes Mellitus, Experimental - physiopathology
Disease Models, Animal
Endothelium, Vascular - physiopathology
Evans Blue
Hyperglycemia
Hypoglycemic Agents - pharmacology
Insulin
Insulin - pharmacology
Male
Microcirculation - physiopathology
Nervous system
Permeability
Rats
Rats, Sprague-Dawley
Regional Blood Flow - physiology
Studies
Sucrose - metabolism
Tight Junctions - pathology
Tight Junctions - physiology
Tritium
title Streptozotocin-induced diabetes progressively increases blood-brain barrier permeability in specific brain regions in rats
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