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Rizzi, L.

Publications and source records attributed to Rizzi, L..

2 recordsLinked to original sources

Distinct cortical patches for syntactic and semantic composition in the human brain

Although the brain areas for language processing are well delimited, whether lexical-semantic and syntactic processes are spatially segregated remains debated. To clarify this issue, we conducted two experiments using 7-Tesla functional MRI in 20 participants performing: a functional localizer involving reading sequences of words of increasing linguistic complexity; and a presentation of short, semantically impoverished three-word mini-sentences, flashed in a single glance (e.g., "he does it"), whose grammaticality and syntactic complexity was manipulated through syntactic movement. Our results reveal two functionally dissociable sets of cortical patches within the language system: one sensitive to syntactic structure even in the absence of meaning, and the other involved in semantic composition. This dual-network architecture was consistently observed in the majority of participants, although its precise anatomical localization varied. The two types of voxels coexisted even within a given brain region of the Glasser atlas. Results were confirmed using subject-specific analyses and region-by-condition interactions, as voxels in those two systems displayed markedly different responses to mini-sentences. Thus, high-resolution functional imaging reveals a division of labor between syntactic and semantic composition within the classical language network.

neuroscience↗

Hexarelin exerts neuroprotective and antioxidant effects against hydrogen peroxide-induced toxicity through the modulation of MAPK and PI3K/Akt patways in Neuro-2A cells.

Hexarelin, a synthetic hexapeptide, protects cardiac and skeletal muscles by inhibiting apoptosis, both in vitro and in vivo. Moreover, evidence suggests that hexarelin could have important neuroprotective bioactivity. Oxidative stress and the generation of free radicals has been implicated in the etiologies of several neurodegenerative diseases, including amyotrophic lateral sclerosis, Parkinsons disease, Alzheimers disease, Huntingtons disease and multiple sclerosis. In addition to direct oxidative stress, exogenous hydrogen peroxide (H2O2) can penetrate biological membranes and enhance the formation of other reactive oxygen species. The aim of this study was to examine the inhibitory influence of hexarelin on H2O2-induced apoptosis in Neuro-2A cells, a mouse neuroblastoma cell line. Our results indicate that H2O2 reduced the viability of Neuro-2A cells in a dose-related fashion. Furthermore, H2O2 induced significant changes in the morphology of Neuro-2A cells, reflected in the formation of apoptotic cell bodies, and an increase of nitric oxide (NO) production. Hexarelin effectively antagonized H2O2 oxidative damage to Neuro-2A cells as indicated by improved cell viability, normal morphology and reduced nitrite (NO2-) release. Hexarelin treatment of Neuro-2A cells also reduced mRNA levels of caspases-3 and -7 and those of the pro-apoptotic molecule Bax; by contrast, hexarelin treatment increased anti-apoptotic Bcl-2 mRNA levels. Hexarelin also reduced MAPKs phosphorylation induced by H2O2 and concurrently increased p-Akt protein expression. In conclusion, our results identify several neuroprotective and anti-apoptotic effects of hexarelin. These properties suggest that further investigation of hexarelin as a neuroprotective agent in an investigational and therapeutic context are merited.

pharmacology and toxicology↗