Blood-Brain Barrier Alterations in MDX Mouse, An Animal Model of the Duchenne Muscular Dystrophy

2005 ◽  
Vol 2 (1) ◽  
pp. 47-54 ◽  
Author(s):  
Beatrice Nico ◽  
Luisa Roncali ◽  
Domenica Mangieri ◽  
Domenico Ribatti
PEDIATRICS ◽  
1982 ◽  
Vol 69 (3) ◽  
pp. 255-259 ◽  
Author(s):  
Rodney L. Levine ◽  
Wendy R. Fredericks ◽  
Stanley I. Rapoport

A potential animal model of kernicterus has been developed. The blood-brain barrier was opened on one side of the brain, by brief infusion of a hypertonic solution into the carotid artery. Upon peripheral infusion of bilirubin, the animals developed unilateral yellow staining of the brain: the treated side was stained whereas the control side was not. This cerebral icterus resulted from the entry of albumin-bound bilirubin into the brain, and not from the passage of free bilirubin.


2017 ◽  
Vol 19 (suppl_3) ◽  
pp. iii101-iii101
Author(s):  
S. Aasen ◽  
H. Espedal ◽  
O. Keunen ◽  
C. Holte ◽  
H. Baghirov ◽  
...  

PLoS ONE ◽  
2011 ◽  
Vol 6 (3) ◽  
pp. e16601 ◽  
Author(s):  
Svitlana Garbuzova-Davis ◽  
Michael K. Louis ◽  
Edward M. Haller ◽  
Hiranya M. Derasari ◽  
Ashley E. Rawls ◽  
...  

Nanoscale ◽  
2016 ◽  
Vol 8 (15) ◽  
pp. 7866-7870 ◽  
Author(s):  
Chia-Hao Su ◽  
Ching-Yi Tsai ◽  
Boguslaw Tomanek ◽  
Wei-Yu Chen ◽  
Fong-Yu Cheng

A novel BBB-stealth nanocomposite show the antitumor activity in in vivo and in situ glioblastoma animal model, MRI, and IVIS® Spectrum.


Author(s):  
H.D. Geissinger ◽  
L.D. Rhodes

Since the ‘mdx’ mouse appears to have the same basic defect as sufferers of human Duchenne Muscular Dystrophy (DMD), much recent interest in this possible animal model for the human disease has been generated. Perforations in the sarcolemma have been reported recently in the necrotic tibialis anterior (TA) of 35-days-old and the extensor digitorum longus muscles of 39-days-old ‘mdx’ mice. It is the purpose of this communication to find out if these lesions occur not only in necrotic, but also in unaffected, or in centronucleated fibers of the TA of mice which are younger than 35, or older than 39 days.METHODS: TA from 22-, 25-, 41-, 61- and 99-days-old C57BL/10ScSn/MDX and C57BL/lOScSn control mice were pinned on corkboard in a relaxed state, prefixed for 30 minutes in 2.5% glutaraldehyde followed by routine processing for TEM. Appropriate micrographs were evaluated for a more detailed morphological analysis of the sarcolemma (SL) and the basal lamina (BL).RESULTS: It should be stated beforehand that in all muscles examined the BL appeared to be intact. In the muscles of a 25-days-old control mouse the SL appeared quite intact (FIG. 1). In contrast to this small perforations or large tears in the SL could be seen in otherwise unaffected muscles of 22- (FIG. 2), 25- and 41-days-old ‘mdx’ mice, as well as in necrotic and regenerating fibers of mice from these ages.


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