Increasing the Permeability of the Blood–brain Barrier in Three Different Models in vivo. (17th May 2015)
- Record Type:
- Journal Article
- Title:
- Increasing the Permeability of the Blood–brain Barrier in Three Different Models in vivo. (17th May 2015)
- Main Title:
- Increasing the Permeability of the Blood–brain Barrier in Three Different Models in vivo
- Authors:
- Liu, Wei‐Ye
Wang, Zhi‐Bin
Wang, Yue
Tong, Ling‐Chang
Li, Ya
Wei, Xin
Luan, Ping
Li, Ling - Abstract:
- <abstract abstract-type="main" id="cns12405-abs-0001"> <title>Summary</title> <sec id="cns12405-sec-0001" sec-type="section"> <title>Aims</title> <p>Blood–brain barrier (BBB) plays significant roles in the circumstance maintains for the central nervous system (CNS). The dysfunction of the BBB could occur in all pathological conditions of CNS diseases, such as ischemic stroke, cerebral edema, or inflammatory disorders. However, the comparisons among different animal models with a broken BBB <italic>in vivo</italic> are still need to be further studied.</p> </sec> <sec id="cns12405-sec-0002" sec-type="section"> <title>Methods</title> <p>Here we used three different mice models <italic>in vivo</italic>, including MCAO induce, LPS treatment, and cold injury to mimic the situation in clinic. The permeability of BBB in three models was detected by perfusion of Evan's blue dye. The functional proteins of the BBB including claudin‐5, VE‐cadherin, and caveolin‐1 were compared in three different models <italic>in vivo</italic>.</p> </sec> <sec id="cns12405-sec-0003" sec-type="section"> <title>Results</title> <p>With the hyperpermeability of Evan's blue in the three models, both claudin‐5 and VE‐cadherin were decreased, while the expression of caveolin‐1 was increased. Our study showed that BBB dysfunction induced by MCAO in mice was relatively stable, reliable, and moderate compared with LPS or cold injury‐induced BBB permeability models, although the procedural time was generally<abstract abstract-type="main" id="cns12405-abs-0001"> <title>Summary</title> <sec id="cns12405-sec-0001" sec-type="section"> <title>Aims</title> <p>Blood–brain barrier (BBB) plays significant roles in the circumstance maintains for the central nervous system (CNS). The dysfunction of the BBB could occur in all pathological conditions of CNS diseases, such as ischemic stroke, cerebral edema, or inflammatory disorders. However, the comparisons among different animal models with a broken BBB <italic>in vivo</italic> are still need to be further studied.</p> </sec> <sec id="cns12405-sec-0002" sec-type="section"> <title>Methods</title> <p>Here we used three different mice models <italic>in vivo</italic>, including MCAO induce, LPS treatment, and cold injury to mimic the situation in clinic. The permeability of BBB in three models was detected by perfusion of Evan's blue dye. The functional proteins of the BBB including claudin‐5, VE‐cadherin, and caveolin‐1 were compared in three different models <italic>in vivo</italic>.</p> </sec> <sec id="cns12405-sec-0003" sec-type="section"> <title>Results</title> <p>With the hyperpermeability of Evan's blue in the three models, both claudin‐5 and VE‐cadherin were decreased, while the expression of caveolin‐1 was increased. Our study showed that BBB dysfunction induced by MCAO in mice was relatively stable, reliable, and moderate compared with LPS or cold injury‐induced BBB permeability models, although the procedural time was generally long and operation complexity was hard. Moreover, our study also found that the model of the increased BBB permeability by cold injury was severe in the regional cerebral tissue and the model treated with LPS was mild in the global cerebral tissue. The operation of the two models <italic>in vivo</italic> was easy, quick, and stable.</p> </sec> <sec id="cns12405-sec-0004" sec-type="section"> <title>Conclusion</title> <p>The MCAO model was the most suitable for studying the permeability of BBB among the three models <italic>in vivo</italic>.</p> </sec> </abstract> … (more)
- Is Part Of:
- CNS neuroscience & therapeutics. Volume 21:Number 7(2015)
- Journal:
- CNS neuroscience & therapeutics
- Issue:
- Volume 21:Number 7(2015)
- Issue Display:
- Volume 21, Issue 7 (2015)
- Year:
- 2015
- Volume:
- 21
- Issue:
- 7
- Issue Sort Value:
- 2015-0021-0007-0000
- Page Start:
- 568
- Page End:
- 574
- Publication Date:
- 2015-05-17
- Subjects:
- Neuropharmacology -- Periodicals
Central nervous system -- Diseases -- Effect of drugs on -- Periodicals
612.8 - Journal URLs:
- http://www.blackwell-synergy.com/loi/cnsnt ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cns.12405 ↗
- Languages:
- English
- ISSNs:
- 1755-5930
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 9830.140000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3072.xml