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Analia Bortolozzi

4 papers in the library · 49 citations · publishing 2016-2024

Papers

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ER stress in mouse serotonin neurons triggers a depressive phenotype alleviated by ketamine targeting eIF2α signaling.

iScience May 17, 2024 Lluis Miquel-Rio, Unai Sarriés-Serrano, María Sancho-Alonso et al. 16 citations

Depression is a devastating mood disorder that causes significant disability worldwide. Current knowledge of its pathophysiology remains modest and clear biological markers are lacking. Emerging evidence from human and animal models reveals persistent alterations in endoplasmic reticulum (ER) homeostasis, suggesting that ER stress-related signaling pathways may be targets for prevention and...

DOI: 10.1016/j.isci.2024.109787 (opens in new tab) Full text (opens in new tab) Behavioral neuroscience Molecular biology Molecular neuroscience Depression research +2

Ketamine triggers rapid antidepressant effects by modulating synaptic plasticity in a new depressive-like mouse model based on astrocyte glutamate transporter GLT-1 knockdown in infralimbic cortex.

Revista de Psiquiatría y Salud Mental October 1, 2021 M. N. Fullana, Verónica Paz, Francesc Artigas et al.

OBJECTIVE Recently, we reported on a new MDD-like mouse model based on a regionally selective knockdown of astroglial glutamate transporters, GLAST/GLT-1, in infralimbic cortex (IL) which evokes widespread changes in mouse brain associated with the typical alterations found in MDD patients. To further characterize this new MDD-like mouse model, here we examine some transcriptional elements of...

Can we increase the speed and efficacy of antidepressant treatments? Part II. Glutamatergic and RNA interference strategies.

European Neuropsychopharmacology April 2018 Francesc Artigas, Pau Celada, Analia Bortolozzi

In the second part we focus on two treatment strategies that may overcome the main limitations of current antidepressant drugs. First, we review the experimental and clinical evidence supporting the use of glutamatergic drugs as fast-acting antidepressants. Secondly, we review the involvement of microRNAs (miRNAs) in the pathophysiology of major depressive disorder (MDD) and the use of small...

DOI: 10.1016/j.euroneuro.2018.01.005 (opens in new tab) Full text (opens in new tab) Ketamine Prefrontal cortex Rna interference Small interfering rna +1

The serotonergic hallucinogen 5-methoxy-N,N-dimethyltryptamine disrupts cortical activity in a regionally-selective manner via 5-HT(1A) and 5-HT(2A) receptors.

Neuropharmacology February 1, 2016 Maurizio S Riga, Analia Bortolozzi, Letizia Campa et al. 33 citations

5-Methoxy-N,N-dimethyltryptamine (5-MeO-DMT) is a natural hallucinogen, acting as a non-selective serotonin 5-HT(1A)/5-HT(2A)-R agonist. Psychotomimetic agents such as the non-competitive NMDA-R antagonist phencyclidine and serotonergic hallucinogens (DOI and 5-MeO-DMT) disrupt cortical synchrony in the low frequency range (<4 Hz) in rat prefrontal cortex (PFC), an effect reversed by...

DOI: 10.1016/j.neuropharm.2015.10.016 (opens in new tab) Full text (opens in new tab) 5-HT Receptors Oscillatory activity Prefrontal cortex Sensorial cortical areas +10