Dias, Cândida
Keimpema, Erik
Carvalho, Rui A.
Madeira, Daniela
Dias, Liliana
Ledo, Ana
Laranjinha, João
Cunha, Rodrigo A.
Agostinho, Paula
Harkany, Tibor
Köfalvi, Attila
Funding for this research was provided by:
COMPETE 2020 - Operational Programme for Competitiveness and Internationalisation
European Regional Development Fund
Centro 2020 Regional Operational Programme
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
FCT – Fundação para a Ciência e a Tecnologia (UIDB/04539/2020)
Article History
Received: 11 August 2025
Accepted: 8 February 2026
First Online: 9 April 2026
Declarations
:
: All studies were conducted in accordance with the principles and procedures outlined in the 3Rs guidelines of EU Directive 2010/63/EU (NC3Rs Reporting Guidelines Working Group, 2010), FELASA, and the ARRIVE guidelines (Percie du Sert et al. 2020). The experiments were approved by the Animal Care Committee of the Center for Neuroscience and Cell Biology, University of Coimbra, Portugal (ORBEA_167_2018_1911/2018 and ORBEA_238_2019/1410/2019), and certified by the Portuguese National Authority for Animal Health (DGAV; 0421/000/000/2020). We also followed the ARRIVE guidelines for the design and execution of in vitro pharmacological experiments (see below), as well as for data management and interpretation (Clark et al. ). Not applicable for consent to participate.
: All authors have read and approved the final manuscript and consent to its publication.
: The authors declare no competing interests.