Endothelial proliferation and increased blood-brain barrier permeability in the basal ganglia in a rat model of 3,4-dihydroxyphenyl-L-alanine-induced dyskinesia.
(2006) In JNeurosci 26(37). p.9448-9461- Abstract
- 3,4-Dihydroxyphenyl-(L)-alanine ((L)-DOPA)-induced dyskinesia is associated with molecular and synaptic plasticity in the basal ganglia, but the occurrence of structural remodeling through cell genesis has not been explored. In this study, rats with 6-hydroxydopamine lesions received injections of the thymidine analog 5-bromo-2'-deoxyuridine (BrdU) concomitantly with (L)-DOPA for 2 weeks. A large number of BrdU-positive cells were found in the striatum and its output structures (globus pallidus, entopeduncular nucleus, and substantia nigra pars reticulata) in (L)-DOPA-treated rats that had developed dyskinesia. The vast majority (60-80%) of the newborn cells stained positively for endothelial markers. This endothelial proliferation was... (More)
- 3,4-Dihydroxyphenyl-(L)-alanine ((L)-DOPA)-induced dyskinesia is associated with molecular and synaptic plasticity in the basal ganglia, but the occurrence of structural remodeling through cell genesis has not been explored. In this study, rats with 6-hydroxydopamine lesions received injections of the thymidine analog 5-bromo-2'-deoxyuridine (BrdU) concomitantly with (L)-DOPA for 2 weeks. A large number of BrdU-positive cells were found in the striatum and its output structures (globus pallidus, entopeduncular nucleus, and substantia nigra pars reticulata) in (L)-DOPA-treated rats that had developed dyskinesia. The vast majority (60-80%) of the newborn cells stained positively for endothelial markers. This endothelial proliferation was associated with an upregulation of immature endothelial markers (nestin) and a downregulation of endothelial barrier antigen on blood vessel walls. In addition, dyskinetic rats exhibited a significant increase in total blood vessel length and a visible extravasation of serum albumin in the two structures in which endothelial proliferation was most pronounced (substantia nigra pars reticulata and entopeduncular nucleus). The present study provides the first evidence of angiogenesis and blood-brain barrier dysfunction in an experimental model of (L)-DOPA-induced dyskinesia. These microvascular changes are likely to affect the kinetics of (L)-DOPA entry into the brain, favoring the occurrence of motor complications. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/160996
- author
- Westin, Jenny LU ; Lindgren, Hanna LU ; Gardi, Jonathan ; Nyengaard, Jens Randel ; Brundin, Patrik LU ; Mohapel, Paul LU and Cenci Nilsson, Angela LU
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- basal ganglia, blood-brain barrier, 6-OHDA, angiogenesis, proliferation, BrdU, Parkinson's disease, dyskinesia
- in
- JNeurosci
- volume
- 26
- issue
- 37
- pages
- 9448 - 9461
- publisher
- Society for Neuroscience
- external identifiers
-
- pmid:16971529
- wos:000240495500013
- scopus:33748711640
- ISSN
- 1529-2401
- DOI
- 10.1523/JNEUROSCI.0944-06.2006
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Neuronal Survival (013212041), Basal Ganglia (013212026), Wallenberg Neuroscience Centre, Lund (0131000110)
- id
- 47938515-1216-4076-bac7-b7abfb9d0dab (old id 160996)
- alternative location
- http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=16971529&dopt=Abstract
- date added to LUP
- 2016-04-01 15:33:23
- date last changed
- 2023-09-04 03:27:31
@article{47938515-1216-4076-bac7-b7abfb9d0dab, abstract = {{3,4-Dihydroxyphenyl-(L)-alanine ((L)-DOPA)-induced dyskinesia is associated with molecular and synaptic plasticity in the basal ganglia, but the occurrence of structural remodeling through cell genesis has not been explored. In this study, rats with 6-hydroxydopamine lesions received injections of the thymidine analog 5-bromo-2'-deoxyuridine (BrdU) concomitantly with (L)-DOPA for 2 weeks. A large number of BrdU-positive cells were found in the striatum and its output structures (globus pallidus, entopeduncular nucleus, and substantia nigra pars reticulata) in (L)-DOPA-treated rats that had developed dyskinesia. The vast majority (60-80%) of the newborn cells stained positively for endothelial markers. This endothelial proliferation was associated with an upregulation of immature endothelial markers (nestin) and a downregulation of endothelial barrier antigen on blood vessel walls. In addition, dyskinetic rats exhibited a significant increase in total blood vessel length and a visible extravasation of serum albumin in the two structures in which endothelial proliferation was most pronounced (substantia nigra pars reticulata and entopeduncular nucleus). The present study provides the first evidence of angiogenesis and blood-brain barrier dysfunction in an experimental model of (L)-DOPA-induced dyskinesia. These microvascular changes are likely to affect the kinetics of (L)-DOPA entry into the brain, favoring the occurrence of motor complications.}}, author = {{Westin, Jenny and Lindgren, Hanna and Gardi, Jonathan and Nyengaard, Jens Randel and Brundin, Patrik and Mohapel, Paul and Cenci Nilsson, Angela}}, issn = {{1529-2401}}, keywords = {{basal ganglia; blood-brain barrier; 6-OHDA; angiogenesis; proliferation; BrdU; Parkinson's disease; dyskinesia}}, language = {{eng}}, number = {{37}}, pages = {{9448--9461}}, publisher = {{Society for Neuroscience}}, series = {{JNeurosci}}, title = {{Endothelial proliferation and increased blood-brain barrier permeability in the basal ganglia in a rat model of 3,4-dihydroxyphenyl-L-alanine-induced dyskinesia.}}, url = {{http://dx.doi.org/10.1523/JNEUROSCI.0944-06.2006}}, doi = {{10.1523/JNEUROSCI.0944-06.2006}}, volume = {{26}}, year = {{2006}}, }