Maria Francesca Cometa
Istituto Superiore di Sanità
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Featured researches published by Maria Francesca Cometa.
Toxicology and Applied Pharmacology | 2003
Laura Ricceri; Nadja Markina; Angela Valanzano; Stefano Fortuna; Maria Francesca Cometa; Annarita Meneguz; Gemma Calamandrei
Neonatal mice were treated daily on postnatal days (pnds) 1 through 4 or 11 through 14 with the organophosphate pesticide chlorpyrifos (CPF), at doses (1 or 3 mg/kg) that do not evoke systemic toxicity. Brain acetylcholinesterase (AChE) activity was evaluated within 24 h from termination of treatments. Pups treated on pnds 1-4 underwent ultrasonic vocalization tests (pnds 5, 8, and 11) and a homing test (orientation to home nest material, pnd 10). Pups in both treatment schedules were then assessed for locomotor activity (pnd 25), novelty-seeking response (pnd 35), social interactions with an unfamiliar conspecific (pnd 45), and passive avoidance learning (pnd 60). AChE activity was reduced by 25% after CPF 1-4 but not after CPF 11-14 treatment. CPF selectively affected only the G(4) (tetramer) molecular isoform of AChE. Behavioral analysis showed that early CPF treatment failed to affect neonatal behaviors. Locomotor activity on pnd 25 was increased in 11-14 CPF-treated mice at both doses, and CPF-treated animals in both treatment schedules were more active when exposed to environmental novelty in the novelty-seeking test. All CPF-treated mice displayed more agonistic responses, and such effect was more marked in male mice exposed to the low CPF dose on pnds 11-14. Passive avoidance learning was not affected by CPF. These data indicate that developmental exposure to CPF induces long-term behavioral alterations in the mouse species and support the involvement of neural systems in addition to the cholinergic system in the delayed behavioral toxicity of CPF.
Natural Product Research | 2018
Lamberto Tomassini; Antonio Ventrone; Claudio Frezza; Ilaria Serafini; Armandodoriano Bianco; Maria Francesca Cometa
Abstract This paper reports on the first phytochemical analysis ever performed on Jasminum tortuosum Willd. This analysis, mainly carried out by means of column chromatography separation, NMR spectroscopy and mass spectrometry, led to the isolation and the identification of four compounds, namely the lignans ginkgool (1) and olivil-4′-O-β-glucopyranoside (2) and the secoiridoids oleoside dimethyl ester (3) and oleoside 11-methyl ester (4). The presence of these compounds is significant from a chemotaxonomic point of view, confirming the correct botanical classification of the species and, from a phytochemical standpoint, may suggest its possible use in the ethno-medicinal field.
Natural Product Research | 2017
Lamberto Tomassini; Mauro Serafini; Antonio Ventrone; Marcello Nicoletti; Maria Francesca Cometa; S. Ragusa
Abstract A new iridoid diglucoside has been isolated from an ethanolic extract of Antirrhinum siculum, together with five-known compounds. Its structure has been assigned as 5-O-glucopyranosyl-7α-hydroxyharpagide by spectroscopic means.
Annali dell'Istituto Superiore di Sanità | 2011
Patrizia Popoli; Maria Francesca Cometa; Fulvia Fabi; Annarita Meneguz
Advanced therapy medicinal products (ATMP) can offer new, effective therapeutic options for the treatment of severe illnesses, including cancer, neurodegenerative and cardiovascular diseases. Translation of advanced therapies to the clinic has been slow despite significant academic research from academia and foundations. The implementation of 2001/20 Directive in Italy established that the development of an ATMP should follow the GXP rules - good manufacturing practice (GMP) for production, good laboratory practice (GLP) for non clinical safety studies and good clinical practice (GCP) for clinical trials. The high costs of GCP application and the needs for GMP facilities are perceived as the most important bottlenecks for the development of ATMP. Here it is pointed out that a strategic cooperation between different actors (academia, industry and experts in regulatory issues) is strongly needed. In particular, it is highlighted that the Istituto Superiore di Sanità, as the competent authority for the authorization of Phase I clinical trials, has a specific responsibility in fostering the translation of safe and effective therapies for human diseases.
Toxicological Sciences | 2006
Laura Ricceri; Aldina Venerosi; Francesca Capone; Maria Francesca Cometa; Paola Lorenzini; Stefano Fortuna; Gemma Calamandrei
Planta Medica | 2001
F. Scazzocchio; Maria Francesca Cometa; L. Tomassini; M. Palmery
Toxicology | 2007
Maria Francesca Cometa; Franca M. Buratti; Stefano Fortuna; Paola Lorenzini; Maria Teresa Volpe; L. Parisi; Emanuela Testai; Annarita Meneguz
Toxicology | 2005
Maria Francesca Cometa; Paola Lorenzini; Stefano Fortuna; Maria Teresa Volpe; Annarita Meneguz; Maura Palmery
Environmental Health | 2015
Aldina Venerosi; Sabrina Tait; Laura Stecca; Flavia Chiarotti; Alessia De Felice; Maria Francesca Cometa; Maria Teresa Volpe; Gemma Calamandrei; Laura Ricceri
Fitoterapia | 2012
Maria Francesca Cometa; Stefano Fortuna; Giovanna Palazzino; Maria Teresa Volpe; Elsa Rengifo Salgado; Marcello Nicoletti; Lamberto Tomassini