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Guadalupe Soria

2 papers in the library · 75 citations · publishing 2014-2025

Papers

The natural hallucinogen 5-MeO-DMT, component of Ayahuasca, disrupts cortical function in rats: reversal by antipsychotic drugs.

The International Journal of Neuropsychopharmacology August 1, 2014 Maurizio S Riga, Guadalupe Soria, Raúl Tudela et al. 75 citations

5-MeO-DMT, a natural hallucinogen found in ayahuasca, disrupts brain activity in the medial prefrontal cortex (mPFC) of rodents, increasing firing in 51% and decreasing it in 35% of pyramidal neurons, while reducing the power of low-frequency cortical oscillations (<4 Hz) by 31%. This effect, which depends on 5-HT1A and 5-HT2A receptor activation, resembles disruptions caused by other psychotomimetic agents like phencyclidine and DOI. Antipsychotic drugs (haloperidol, clozapine, risperidone) and an mGlu2/3 agonist reversed the oscillation reduction. 5-MeO-DMT also decreased blood-oxygen level dependent (BOLD) responses in visual cortex and mPFC. The findings suggest these cortical alterations underlie hallucinogenic effects and may aid antipsychotic drug development.

Long-lasting behavioral, molecular and functional connectivity alterations after chronic THC exposure during adolescence in mice.

Progress in neuro-psychopharmacology & biological psychiatry July 13, 2025 Laura Gómez-Acero, Federico Varriano, Nuria Sánchez-Fernández et al.

Adolescent mice treated with THC, the main psychoactive compound in cannabis, later showed impaired social interaction and sensorimotor gating deficits similar to those seen in heavy human cannabis users. The exposure caused long-term disruption of connectivity between the cortex and striatum, which correlated with social problems in adulthood. Molecular changes in the striatum altered the balance among dopamine D2, adenosine A2A, and cannabinoid CB1 receptors, key regulators of the brain's reward system. These results help explain how heavy adolescent cannabis use may increase the risk of psychosis.