Erratum to ‘Melatonin improves methamphetamine-induced blood brain barrier impairment through NADPH oxidase-2 in primary rat brain microvascular endothelium cells’ [Br. Ecol. Soc. 1646 (2016) 393–401]

2016 ◽  
Vol 1646 ◽  
pp. R1
Keyword(s):  
Nadph Oxidase ◽  
Rat Brain ◽  
Blood Brain Barrier ◽  
Brain Barrier ◽  
Microvascular Endothelium ◽  
Blood Brain ◽  
Nadph Oxidase 2 ◽  
Endothelium Cells

scholarly journals Analysis of Biotinylated Generation 4 Poly(amidoamine) (PAMAM) Dendrimer Distribution in the Rat Brain and Toxicity in a Cellular Model of the Blood-Brain Barrier

Molecules ◽  
2013 ◽  
Vol 18 (9) ◽  
pp. 11537-11552 ◽  
Author(s):  
Ruth Hemmer ◽  
Andrew Hall ◽  
Robert Spaulding ◽  
Brett Rossow ◽  
Michael Hester ◽  
...  
Keyword(s):  
Rat Brain ◽  
Blood Brain Barrier ◽  
Pamam Dendrimer ◽  
Brain Barrier ◽  
Cellular Model ◽  
Blood Brain

scholarly journals Blood—Brain Barrier Genomics

2001 ◽  
Vol 21 (1) ◽  
pp. 61-68 ◽  
Author(s):  
Jian Yi Li ◽  
Ruben J. Boado ◽  
William M. Pardridge
Keyword(s):  
Gene Expression ◽  
Blood Brain Barrier ◽  
Brain Barrier ◽  
Specific Gene ◽  
Microvascular Endothelium ◽  
Tissue Specific ◽  
Tissue Specific Gene ◽  
Specific Gene Expression ◽  
Blood Brain ◽  
Tester Cdna

The blood–brain barrier (BBB) is formed by the brain microvascular endothelium, and the unique transport properties of the BBB are derived from tissue-specific gene expression within this cell. The current studies developed a gene microarray approach specific for the BBB by purifying the initial mRNA from isolated rat brain capillaries to generate tester cDNA. A polymerase chain reaction–based subtraction cloning method, suppression subtractive hybridization (SSH), was used, and the BBB cDNA was subtracted with driver cDNA produced from mRNA isolated from rat liver and kidney. Screening 5% of the subtracted tester cDNA resulted in identification of 50 gene products and more than 80% of those were selectively expressed at the BBB; these included novel gene sequences not found in existing databases, ESTs, and known genes that were not known to be selectively expressed at the BBB. Genes in the latter category include tissue plasminogen activator, insulin-like growth factor-2, PC-3 gene product, myelin basic protein, regulator of G protein signaling 5, utrophin, IκB, connexin-45, the class I major histocompatibility complex, the rat homologue of the transcription factors hbrm or EZH1, and organic anion transporting polypeptide type 2. Knowledge of tissue-specific gene expression at the BBB could lead to new targets for brain drug delivery and could elucidate mechanisms of brain pathology at the microvascular level.

Neural precursor cell influences on blood–brain barrier characteristics in rat brain endothelial cells

2007 ◽  
Vol 1159 ◽  
pp. 67-76 ◽  
Author(s):  
Joseph C. Lim ◽  
Adam J. Wolpaw ◽  
Maeve A. Caldwell ◽  
Stephen B. Hladky ◽  
Margery A. Barrand
Keyword(s):  
Endothelial Cells ◽  
Rat Brain ◽  
Blood Brain Barrier ◽  
Precursor Cell ◽  
Brain Barrier ◽  
Neural Precursor ◽  
Brain Endothelial Cells ◽  
Neural Precursor Cell ◽  
Blood Brain ◽  
Rat Brain Endothelial Cells

Studies on DNA fragmentation and disruption of the blood-brain barrier in delayed radiation injuries in the rat brain

1997 ◽  
Vol 17 (4) ◽  
pp. 277-283 ◽  
Author(s):  
Shinichi Toyonaga ◽  
Tatsuo Mima ◽  
Masahiro Kurisaka ◽  
Koreaki Mori ◽  
Yasuhiro Ogawa
Keyword(s):  
Rat Brain ◽  
Dna Fragmentation ◽  
Blood Brain Barrier ◽  
Brain Barrier ◽  
Radiation Injuries ◽  
Blood Brain
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