Catia Scassellati

Dr. Catia Scassellati


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2002 in Experimental Cell Research
Verified
Journal Article
Closed access
ISIrina Solovei
Irina Solovei
ACAntonio Cavallo
Antonio Cavallo
LSLothar Schermelleh
Lothar Schermelleh
FJFrançoise Jaunin
Françoise Jaunin
CSCatia Scassellati
Catia Scassellati
TCThomas Cremer
Thomas Cremer

1 October 2012 in Journal of the American Academy of Child & Adolescent Psychiatry
Verified
Journal Article
Closed access
CSCatia Scassellati
Catia Scassellati
CBCristian Bonvicini
Cristian Bonvicini
SFStephen V. V Faraone
Stephen V. V Faraone
MGMassimo Gennarelli
Massimo Gennarelli

24 May 2016 in Molecular Psychiatry
Verified
Journal Article
Open access
CBCristian Bonvicini
Cristian Bonvicini
SFS V Faraone
S V Faraone
CSCatia Scassellati
Catia Scassellati
Molecular Psychiatry publishes work aimed at elucidating biological mechanisms underlying psychiatric disorders and their treatment

22 June 2022 in Antioxidants
Verified
Journal Article
Open access
PDF file
AVAngelica Varesi
Angelica Varesi
Salvatore ChirumboloSalvatore Chirumbolo
Salvatore Chirumbolo
LCLucrezia Irene Maria Campagnoli
Lucrezia Irene Maria Campagnoli
EPElisa Pierella
Elisa Pierella
GPGaia Bavestrello Piccini
Gaia Bavestrello Piccini
APAlessia Pascale
Alessia Pascale
Cellular senescence is an irreversible state of cell cycle arrest occurring in response to stressful stimuli, such as telomere attrition, DNA damage, reactive oxygen species, and oncogenic proteins. Although beneficial and protective in several physiological processes, an excessive senescent cell burden has been involved in various pathological conditions including aging, tissue dysfunction and chronic diseases. Oxidative stress (OS) can drive senescence due to a loss of balance between pro-oxidant stimuli and antioxidant defences. Therefore, the identification and characterization of antioxidant compounds capable of preventing or counteracting the senescent phenotype is of major interest. However, despite the considerable number of studies, a comprehensive overview of the main antioxidant molecules capable of counteracting OS-induced senescence is still lacking. Here, besides a brief description of the molecular mechanisms implicated in OS-mediated aging, we review and discuss the role of enzymes, mitochondria-targeting compounds, vitamins, carotenoids, organosulfur compounds, nitrogen non-protein molecules, minerals, flavonoids, and non-flavonoids as antioxidant compounds with an anti-aging potential, therefore offering insights into innovative lifespan-extending approaches.

10 October 2014 in Current Psychiatry Reports
Verified
Journal Article
Closed access
PDF file
SFStephen V. V Faraone
Stephen V. V Faraone
CBCristian Bonvicini
Cristian Bonvicini
CSCatia Scassellati
Catia Scassellati

1 November 2020 in Ageing Research Reviews
Verified
Journal Article
Open access
CSCatia Scassellati
Catia Scassellati
AGAntonio Carlo Galoforo
Antonio Carlo Galoforo
CBCristian Bonvicini
Cristian Bonvicini
CECiro Esposito
Ciro Esposito
GRGiovanni Ricevuti
Giovanni Ricevuti
• Aging and neurodegenerative diseases are characterized by complex and multifactorial aetiology and challenges regarding treatments efficacy and costs persist. • Oxygen-ozone (O2-O3) therapy is a non-invasive, non-pharmacological, low cost and no-side effect procedure based on antioxidant capacity of O3. • A plethora of scientific evidence supports other crucial properties of O3 in physiopathological processes. • Nrf2 is one of the principal molecular signalling on which O3 exercises its antioxidant/anti-apoptotic/pro-autophagy effects, involved in aging and in neurodegenerative disorders. • This review provides a consistent rationale to implement future clinical studies to apply the O2-O3 treatment along with other antioxidants (polyphenols, mushrooms) in aging and in neurodegeneration.