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 |
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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 ) |
doi_str_mv | 10.1152/ajpheart.00489.2006 |
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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 )</description><identifier>ISSN: 0363-6135</identifier><identifier>EISSN: 1522-1539</identifier><identifier>DOI: 10.1152/ajpheart.00489.2006</identifier><identifier>PMID: 16951046</identifier><identifier>CODEN: AJPPDI</identifier><language>eng</language><publisher>United States: American Physiological Society</publisher><subject>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</subject><ispartof>American journal of physiology. Heart and circulatory physiology, 2006-12, Vol.291 (6), p.H2660-H2668</ispartof><rights>Copyright American Physiological Society Dec 2006</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c519t-f23706d4e58b194e6c1216227c4c7c70ce5b030174baa309cf97ebdcd737b5fa3</citedby><cites>FETCH-LOGICAL-c519t-f23706d4e58b194e6c1216227c4c7c70ce5b030174baa309cf97ebdcd737b5fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3039,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16951046$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huber, Jason D</creatorcontrib><creatorcontrib>VanGilder, Reyna L</creatorcontrib><creatorcontrib>Houser, Kimberly A</creatorcontrib><title>Streptozotocin-induced diabetes progressively increases blood-brain barrier permeability in specific brain regions in rats</title><title>American journal of physiology. 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. School of Pharmacy, PO Box 9530, Morgantown, WV 26506 ( jhuber{at}hsc.wvu.edu )</description><subject>Animals</subject><subject>Blood-Brain Barrier - pathology</subject><subject>Blood-Brain Barrier - physiopathology</subject><subject>Brain - blood supply</subject><subject>Brain - physiopathology</subject><subject>Capillary Permeability</subject><subject>Carbon Radioisotopes</subject><subject>Central Nervous System - blood supply</subject><subject>Central Nervous System - physiopathology</subject><subject>Cognition Disorders - physiopathology</subject><subject>Coloring Agents</subject><subject>Diabetes</subject><subject>Diabetes Mellitus, Experimental - metabolism</subject><subject>Diabetes Mellitus, Experimental - pathology</subject><subject>Diabetes Mellitus, Experimental - physiopathology</subject><subject>Disease Models, Animal</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Evans Blue</subject><subject>Hyperglycemia</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Insulin</subject><subject>Insulin - pharmacology</subject><subject>Male</subject><subject>Microcirculation - physiopathology</subject><subject>Nervous system</subject><subject>Permeability</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regional Blood Flow - physiology</subject><subject>Studies</subject><subject>Sucrose - metabolism</subject><subject>Tight Junctions - pathology</subject><subject>Tight Junctions - physiology</subject><subject>Tritium</subject><issn>0363-6135</issn><issn>1522-1539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV1rFDEUhoModq3-AkEGL7ybbT4myQSvpFgrFLywXod8nNnNMjsZk0x1--udcdcqgngVOOd5X3J4EHpJ8JoQTi_MbtyCSWWNcdOqNcVYPEKreUNrwpl6jFaYCVYLwvgZepbzDmPMpWBP0RkRihPciBW6_1wSjCXexxJdGOow-MmBr3wwFgrkakxxkyDncAf9oQqDS2DyPLd9jL62yYShsialAKkaIe3B2NCHsqBVHsGFLrjqiCXYhDjkZZNMyc_Rk870GV6c3nP05er97eV1ffPpw8fLdze140SVuqNMYuEb4K0lqgHhCCWCUukaJ53EDrjFDBPZWGMYVq5TEqx3XjJpeWfYOXpz7J1P-TpBLnofsoO-NwPEKWvREqpaRv8LEiVaodQCvv4L3MUpDfMRmlIlBFO8mSF2hFyKOSfo9JjC3qSDJlgvAvUvgfqnQL0InFOvTtWT3YP_nTkZm4G3R2AbNttvIYEet4ccYh83B3019f0tfC8P1VQRLfQ1FQLr0Xdz-uLf6Yf__JFiPwDhPMH-</recordid><startdate>20061201</startdate><enddate>20061201</enddate><creator>Huber, Jason D</creator><creator>VanGilder, Reyna L</creator><creator>Houser, Kimberly A</creator><general>American Physiological Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20061201</creationdate><title>Streptozotocin-induced diabetes progressively increases blood-brain barrier permeability in specific brain regions in rats</title><author>Huber, Jason D ; VanGilder, Reyna L ; Houser, Kimberly A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c519t-f23706d4e58b194e6c1216227c4c7c70ce5b030174baa309cf97ebdcd737b5fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Blood-Brain Barrier - pathology</topic><topic>Blood-Brain Barrier - physiopathology</topic><topic>Brain - blood supply</topic><topic>Brain - physiopathology</topic><topic>Capillary Permeability</topic><topic>Carbon Radioisotopes</topic><topic>Central Nervous System - blood supply</topic><topic>Central Nervous System - physiopathology</topic><topic>Cognition Disorders - physiopathology</topic><topic>Coloring Agents</topic><topic>Diabetes</topic><topic>Diabetes Mellitus, Experimental - metabolism</topic><topic>Diabetes Mellitus, Experimental - pathology</topic><topic>Diabetes Mellitus, Experimental - physiopathology</topic><topic>Disease Models, Animal</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Evans Blue</topic><topic>Hyperglycemia</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Insulin</topic><topic>Insulin - pharmacology</topic><topic>Male</topic><topic>Microcirculation - physiopathology</topic><topic>Nervous system</topic><topic>Permeability</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Regional Blood Flow - physiology</topic><topic>Studies</topic><topic>Sucrose - metabolism</topic><topic>Tight Junctions - pathology</topic><topic>Tight Junctions - physiology</topic><topic>Tritium</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huber, Jason D</creatorcontrib><creatorcontrib>VanGilder, Reyna L</creatorcontrib><creatorcontrib>Houser, Kimberly A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. 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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source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
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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