Núria Nadal-Gratacós

@nurianadalg.bsky.social

Assistant Professor at UB. Interested in Psychedelics, Synthetic Cathinones and other NPS. 👩🏻‍🔬🔬🐭

A fantastic day discussing the latest advances in psychoactive substance research at our symposium! Thanks to all the speakers, attendees, and the Càtedra UB – Dr. Antoni Esteve i Subirana de Recerca en Farmacologia for making it possible. Looking forward to the next edition!

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Join us on July 9 at the Faculty of Pharmacy and Food Sciences (UB, Barcelona) for the symposium "From Classical to Novel Psychoactive Substances: Toxicological Risks and Therapeutic Opportunities". Featuring researchers from across Europe sharing the latest advances in NPS and psychedelic research.

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🎓 Congratulations to our PhD candidate Martalu D. Pazos, who will represent the University of Barcelona in the international 3 Minute Thesis competition (Coimbra Group)! A fantastic achievement and a great opportunity to share her research with a broad audience 👏

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Excited to share our new paper in ACS Chemical Neuroscience! 🎉 In this work, we study MDMA analogues, exploring their pharmacological properties and potiential for safer therapeutic use. A great collaboration we’re very happy about! Read it here: pubs.acs.org/doi/10.1021/...

Next-Generation MDMA Analogue SDMA: Pharmacological and Metabolic Insights

3,4-Methylenedioxymethamphetamine (MDMA), commonly known as ecstasy, shows promise in treating depression and post-traumatic stress disorder (PTSD), resulting in breakthrough status. However, concerns regarding MDMA’s abuse potential and cytotoxicity have sparked interest in developing safer analogues with similar therapeutic benefits. This study investigated the pharmacological properties of MDMA analogues in which the 1,3-benzodioxole group is replaced by a 1,3-benzoxathiole, termed SDA and SDMA, compared to MDA and MDMA through in silico, in vitro, and in vivo assays. In vitro experiments using human embryonic kidney (HEK293) cells examined the interactions with monoamine transporters. SDA and SDMA showed similar profiles to MDMA at the serotonin transporter (SERT), while both inhibited dopamine (DAT) and norepinephrine (NET) transporters more potently, in line with in silico molecular docking fitness scores of binding. SDA and SDMA also showed increased potency in evoking efflux through SERT and DAT acting as partial releasers. SDA and SDMA exhibited a similar interaction profile with 5-HT2 receptors compared with their respective analogues. Metabolism studies revealed faster clearance rates for SDA and SDMA, in contrast to MDA and MDMA, which exhibited only weak degradation. In contrast to MDMA’s rewarding effects, SDMA did not induce significant effects in mice, while SDA only produced a significant preference for the drug-paired compartment at the lowest dose tested. Moreover, while SDMA shares similar locomotor and hyperthermic profiles as MDMA in mice, SDA induced increased hyperlocomotion and more sustained hyperthermia. In conclusion, these findings suggest that SDMA, with enhanced metabolic profiles and reduced abuse potential, is a promising candidate for further studies.

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Hello Bluesky! 👋 We are a research group from @ub.edu focused on the neuropsychopharmacology of emerging psychostimulants and psychedelics. Our work bridges neuroscience and toxicology to better understand how these compounds affect the brain🧠.