Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Browse
New in RUL
About RUL
In numbers
Help
Sign in
Transporters involved in adult rat cortical astrocyte dopamine uptake : kinetics, expression and pharmacological modulation
ID
Sočan, Vesna
(
Author
),
ID
Dolinar, Klemen
(
Author
),
ID
Kržan, Mojca
(
Author
)
PDF - Presentation file,
Download
(1,54 MB)
MD5: DA93DE0A5E1F44B8563FBBDF30035442
URL - Source URL, Visit
https://onlinelibrary.wiley.com/doi/10.1111/ejn.16202
Image galllery
Abstract
Astrocytes, glial cells in the central nervous system, perform a multitude of homeostatic functions and are in constant bidirectional communication with neuronal cells, a concept named the tripartite synapse; however, their role in the dopamine homeostasis remains unexplored. The aim of this study was to clarify the pharmacological and molecular characteristics of dopamine transport in cultured cortical astrocytes of adult rats. In addition, we were interested in the expression of mRNA of dopamine transporters as well as dopamine receptors D1 and D2 and in the effect of dopaminergic drugs on the expression of these transporters and receptors. We have found that astrocytes possess both Na$^+$-dependent and Na$^+$-independent transporters. Uptake of radiolabelled dopamine was time-, temperature- and concentration-dependent and was inhibited by decynium-22, a plasma membrane monoamine transporter inhibitor, tricyclic antidepressants desipramine and nortriptyline, both inhibitors of the norepinephrine transporter. Results of transporter mRNA expression indicate that the main transporters involved in cortical astrocyte dopamine uptake are the norepinephrine transporter and plasma membrane monoamine transporter. Both dopamine receptor subtypes were identified in cortical astrocyte cultures. Twenty-four-hour treatment of astrocyte cultures with apomorphine, a D1/D2 agonist, induced upregulation of D1 receptor, norepinephrine transporter and plasma membrane monoamine transporter, whereas the latter was downregulated by haloperidol and L-DOPA. Astrocytes take up dopamine by multiple transporters and express dopamine receptors, which are sensitive to dopaminergic drugs. The findings of this study could open a promising area of research for the fine-tuning of existing therapeutic strategies.
Language:
English
Keywords:
astrocytes
,
dopamine
,
rats
,
central nervous system
,
adult rat
,
cortical astrocytes
,
dopamine uptake
,
NET
,
PMAT
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2024
Number of pages:
Str. 1296–1310
Numbering:
Vol. 59, iss. 6
PID:
20.500.12556/RUL-155346
UDC:
612
ISSN on article:
1460-9568
DOI:
10.1111/ejn.16202
COBISS.SI-ID:
177881091
Publication date in RUL:
27.03.2024
Views:
500
Downloads:
45
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
Share:
Record is a part of a journal
Title:
European journal of neuroscience
Shortened title:
EJN, Eur. j. neurosci.
Publisher:
Wiley, Federation of European Neuroscience Societies
ISSN:
1460-9568
COBISS.SI-ID:
517706521
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
astrociti
,
dopamin
,
podgane
,
centralni živčni sistem
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
P3-0067
Name:
Farmakologija in farmakogenomika
Funder:
ARRS - Slovenian Research Agency
Funding programme:
Young researchers
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back