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The Interaction of Selective A1 and A2A Adenosine Receptor Antagonists with Magnesium and Zinc Ions in Mice: Behavioural, Biochemical and Molecular Studies

The purpose of the study was to investigate whether the co-administration of Mg(2+) and Zn(2+) with selective A1 and A2A receptor antagonists might be an interesting antidepressant strategy. Forced swim, tail suspension, and spontaneous locomotor motility tests in mice were performed. Further, bioch...

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Detalles Bibliográficos
Autores principales: Szopa, Aleksandra, Bogatko, Karolina, Herbet, Mariola, Serefko, Anna, Ostrowska, Marta, Wośko, Sylwia, Świąder, Katarzyna, Szewczyk, Bernadeta, Wlaź, Aleksandra, Skałecki, Piotr, Wróbel, Andrzej, Mandziuk, Sławomir, Pochodyła, Aleksandra, Kudela, Anna, Dudka, Jarosław, Radziwoń-Zaleska, Maria, Wlaź, Piotr, Poleszak, Ewa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7918707/
https://www.ncbi.nlm.nih.gov/pubmed/33673282
http://dx.doi.org/10.3390/ijms22041840
Descripción
Sumario:The purpose of the study was to investigate whether the co-administration of Mg(2+) and Zn(2+) with selective A1 and A2A receptor antagonists might be an interesting antidepressant strategy. Forced swim, tail suspension, and spontaneous locomotor motility tests in mice were performed. Further, biochemical and molecular studies were conducted. The obtained results indicate the interaction of DPCPX and istradefylline with Mg(2+) and Zn(2+) manifested in an antidepressant-like effect. The reduction of the BDNF serum level after co-administration of DPCPX and istradefylline with Mg(2+) and Zn(2+) was noted. Additionally, Mg(2+) or Zn(2+), both alone and in combination with DPCPX or istradefylline, causes changes in Adora1 expression, DPCPX or istradefylline co-administered with Zn(2+) increases Slc6a15 expression as compared to a single-drug treatment, co-administration of tested agents does not have a more favourable effect on Comt expression. Moreover, the changes obtained in Ogg1, MsrA, Nrf2 expression show that DPCPX-Mg(2+), DPCPX-Zn(2+), istradefylline-Mg(2+) and istradefylline-Zn(2+) co-treatment may have greater antioxidant capacity benefits than administration of DPCPX and istradefylline alone. It seems plausible that a combination of selective A1 as well as an A2A receptor antagonist and magnesium or zinc may be a new antidepressant therapeutic strategy.