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Change in P-glycoprotein and caveolin protein expression in brain striatum capillaries in New Zealand Obese mice with type 2 diabetes

Journal
Life Sciences
Journal Volume
85
Journal Issue
23-26
Pages
775
Date Issued
2009-12-16
Author(s)
Wu, Kuo-Chen
Pan H.-J.
HSIANG-SHU YIN  
MEI-RU CHEN  
SHAO-CHUN LU 
CHUN-JUNG LIN 
DOI
10.1016/j.lfs.2009.10.014
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-70649112119&doi=10.1016%2fj.lfs.2009.10.014&partnerID=40&md5=6409dc54e4b5a4e64c06376102b0e69f
https://scholars.lib.ntu.edu.tw/handle/123456789/465054
Abstract
Aims: To investigate the expression of P-gp and caveolins in brain striatum capillaries in inbred mice with type 2 diabetes. Main methods: Inbred mice with type 2 diabetes (male New Zealand obese; NZO) were compared with related mice without diabetes (female NZO and New Zealand White). Protein expression of P-gp and caveolins in capillaries of the brain striatum was examined by immunohistochemical analysis. P-gp efflux pump activity in the blood-brain barrier (BBB) was measured by in vivo brain microdialysis. Regulation of P-gp and caveolin expression was examined in cultured adult rat brain endothelial cells (ARBEC). Key findings: In capillaries in the brain striatum, expression of P-gp and caveolins was higher and lower, respectively, in mice with type 2 diabetes compared with non-diabetic mice. Brain extracellular concentrations of intravenously injected rhodamine 123 were more than 50-60% lower in type 2 diabetic mice. Insulin and PMA treatments significantly increased P-gp expression, whereas the same treatments decreased caveolin expression in ARBEC. Significance: Protein expression of P-gp and caveolins can be regulated in animals with type 2 diabetes. These changes may be important in modulating P-gp activity in the BBB in type 2 diabetes. ? 2009 Elsevier Inc. All rights reserved.
SDGs

[SDGs]SDG3

Other Subjects
caveolin 1; caveolin 2; glycoprotein P; insulin; rhodamine 123; animal experiment; animal model; animal tissue; article; blood brain barrier; brain capillary; brain cell; cell culture; controlled study; corpus striatum; diabetic obesity; endothelium cell; extracellular fluid; female; immunohistochemistry; male; microdialysis; mouse; New Zealand black mouse; non insulin dependent diabetes mellitus; nonhuman; protein expression; protein localization; regulatory mechanism; Animals; Blotting, Western; Capillaries; Caveolins; Cells, Cultured; Corpus Striatum; Diabetes Mellitus, Experimental; Diabetes Mellitus, Type 2; Down-Regulation; Female; Gene Expression Regulation; Glucose Transport Proteins, Facilitative; Immunohistochemistry; Male; Mice; Mice, Inbred Strains; Mice, Obese; P-Glycoprotein; Rats; Reference Standards; Up-Regulation; Animalia; Mus; Rattus
Type
journal article

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