Mohamed Attya

Dr. Mohamed Attya


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

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

Representative Publications

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4 February 2011 in British Journal of Nutrition
Verified
Journal Article
Open access
PDF file
JMJocelijn Meijerink
Jocelijn Meijerink
Pierluigi PlastinaPierluigi Plastina
Pierluigi Plastina
JVJean-Paul Vincken
Jean-Paul Vincken
MPMieke Poland
Mieke Poland
MAMohamed Attya
Mohamed Attya
RWRenger Witkamp
Renger Witkamp
Several mechanisms have been proposed for the positive health effects associated with dietary consumption of long-chainn-3 PUFA (n-3 LC-PUFA) including DHA (22 : 6n-3) and EPA (20 : 5n-3). After dietary intake, LC-PUFA are incorporated into membranes and can be converted to their correspondingN-acylethanolamines (NAE). However, little is known on the biological role of these metabolites. In the present study, we tested a series of unsaturated NAE on the lipopolysaccharide (LPS)-induced NO production in RAW264.7 macrophages. Among the compounds tested, docosahexaenoylethanolamine (DHEA), the ethanolamide of DHA, was found to be the most potent inhibitor, inducing a dose-dependent inhibition of NO release. Immune-modulating properties of DHEA were further studied in the same cell line, demonstrating that DHEA significantly suppressed the production of monocyte chemotactic protein-1 (MCP-1), a cytokine playing a pivotal role in chronic inflammation. In LPS-stimulated mouse peritoneal macrophages, DHEA also reduced MCP-1 and NO production. Furthermore, inhibition was also found to take place at a transcriptional level, as gene expression of MCP-1 and inducible NO synthase was inhibited by DHEA. To summarise, in the present study, we showed that DHEA, a DHA-derived NAE metabolite, modulates inflammation by reducing MCP-1 and NO production and expression. These results provide new leads in molecular mechanisms by which DHA can modulate inflammatory processes.

1 December 2013 in Food Chemistry
Verified
Journal Article
Closed access
LDLeonardo Di Donna
Leonardo Di Donna
DTDomenico Taverna
Domenico Taverna
FMFabio Mazzotti
Fabio Mazzotti
HBHicham Benabdelkamel
Hicham Benabdelkamel
MAMohamed Attya
Mohamed Attya
GSGiovanni Sindona
Giovanni Sindona

1 December 2010 in Molecules
Verified
Journal Article
Open access
PDF file
MAMohamed Attya
Mohamed Attya
HBHicham Benabdelkamel
Hicham Benabdelkamel
EPEnzo Perri
Enzo Perri
ARAnna Russo
Anna Russo
GSGiovanni Sindona
Giovanni Sindona
The quality of olive oils is sensorially tested by accurate and well established methods. It enables the classification of the pressed oils into the classes of extra virgin oil, virgin oil and lampant oil. Nonetheless, it would be convenient to have analytical methods for screening oils or supporting sensorial analysis using a reliable independent approach based on exploitation of mass spectrometric methodologies. A number of methods have been proposed to evaluate deficiencies of extra virgin olive oils resulting from inappropriate technological treatments, such as high or low temperature deodoration, and home cooking processes. The quality and nutraceutical value of extra virgin olive oil (EVOO) can be related to the antioxidant property of its phenolic compounds. Olive oil is a source of at least 30 phenolic compounds, such as oleuropein, oleocanthal, hydroxytyrosol, and tyrosol, all acting as strong antioxidants, radical scavengers and NSAI-like drugs. We now report the efficacy of MRM tandem mass spectrometry, assisted by the isotope dilution assay, in the evaluation of the thermal stability of selected active principles of extra virgin olive oil.

27 April 2009 in Synthesis
Verified
Journal Article
Closed access
PDF file
Bartolo GabrieleBartolo Gabriele
Bartolo Gabriele
MAMohamed Attya
Mohamed Attya
AFAlessia Fazio
Alessia Fazio
LDLeonardo Di Donna
Leonardo Di Donna
Pierluigi PlastinaPierluigi Plastina
Pierluigi Plastina
GSGiovanni Sindona
Giovanni Sindona
A new total synthesis of the mycotoxin ochratoxin A (OTA) is presented, in which it is prepared in 9% overall yield from commercially available substrates. The key step consists of the condensation reaction between protected l-phenylalanine and 5-chloro­-8-hydroxy-3-methyl-1-oxoisochromane-7-carboxylic acid (ochratoxin α, OTα). The same strategy could be successfully applied to l-d 5-phenylalanine, leading to the first total synthesis of d 5-OTA, a molecular tracer for the detection and analytical quantification of the natural mycotoxin in food samples by means of stable isotope dilution assay (SIDA).

11 November 2009 in Rapid Communications in Mass Spectrometry
Verified
Journal Article
Closed access
PDF file
FMFabio Mazzotti
Fabio Mazzotti
LDLeonardo Di Donna
Leonardo Di Donna
MAMohamed Attya
Mohamed Attya
Bartolo GabrieleBartolo Gabriele
Bartolo Gabriele
AFAlessia Fazio
Alessia Fazio
GSGiovanni Sindona
Giovanni Sindona

20 October 2011 in Journal of Cellular Biochemistry
Verified
Journal Article
Closed access
PDF file
HZHylde Zirpoli
Hylde Zirpoli
MCMariella Caputo
Mariella Caputo
ACAntonio Carraturo
Antonio Carraturo
GTGaetano Torino
Gaetano Torino
AFAlessia Fazio
Alessia Fazio
Mario Felice TecceMario Felice Tecce
Mario Felice Tecce