Learning, memory and blood-brain barrier pathology in Duchenne muscular dystrophy mice lacking Dp427, or Dp427 and Dp140.

Autor: Verhaeg M; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Adamzek K; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., van de Vijver D; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Putker K; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Engelbeen S; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Wijnbergen D; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Overzier M; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., Suidgeest E; C.J. Gorter MRI Center, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands., van der Weerd L; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.; C.J. Gorter MRI Center, Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands., Aartsma-Rus A; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands., van Putten M; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Jazyk: angličtina
Zdroj: Genes, brain, and behavior [Genes Brain Behav] 2024 Jun; Vol. 23 (3), pp. e12895.
DOI: 10.1111/gbb.12895
Abstrakt: Duchenne muscular dystrophy is a severe neuromuscular disorder that is caused by mutations in the DMD gene, resulting in a disruption of dystrophin production. Next to dystrophin expression in the muscle, different isoforms of the protein are also expressed in the brain and lack of these isoforms leads to cognitive and behavioral deficits in patients. It remains unclear how the loss of the shorter dystrophin isoform Dp140 affects these processes. Using a variety of behavioral tests, we found that mdx and mdx 4cv mice (which lack Dp427 or Dp427 + Dp140, respectively) exhibit similar deficits in working memory, movement patterns and blood-brain barrier integrity. Neither model showed deficits in spatial learning and memory, learning flexibility, anxiety or spontaneous behavior, nor did we observe differences in aquaporin 4 and glial fibrillary acidic protein. These results indicate that in contrast to Dp427, Dp140 does not play a crucial role in processes of learning, memory and spontaneous behavior.
(© 2024 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd.)
Databáze: MEDLINE
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