Maria Teresa Trevisan
University of Verona
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Featured researches published by Maria Teresa Trevisan.
Clinica Chimica Acta | 1994
Domenico Girelli; Anna Maria Stanzial; Patrizia Guarini; Maria Teresa Trevisan; Antonella Bassi; Roberto Corrocher
The relationship between formation of thiobarbituric acid reactive substances (TBARS) in red blood cells (RBC) after exposure to H2O2 and factors potentially able to modulate it was investigated by a multivariate analysis in 92 healthy volunteers. The independent covariates considered were: RBC membrane fatty acids and cholesterol, RBC antioxidant enzymes and zinc, plasma vitamins A and E and serum selenium, zinc and copper. The stepwise multiple-linear-regression analysis revealed RBC membrane fatty acids and cholesterol as predictors of a consistent proportion of the RBC-TBARS variability whereas none of the antioxidants entered the equation. The unsaturation index was the most important individual predictor; RBC-TBARS increased with increasing concentrations of total omega-3 polyunsaturated fatty acids, C 20:5 omega-3 and cholesterol, whereas they decreased with increasing concentrations of total monounsaturated fatty acids, saturated fatty acids, C 16:0 and C 18:0. It is suggested that formation of TBARS, at least in currently used conditions, reflects mainly the lipid composition of the tissue under investigation, without giving sufficient information about the status of the antioxidant defences.
Clinica Chimica Acta | 1990
Roberto Corrocher; Antonella Bassi; A. Gandini; Patrizia Guarini; Maria Teresa Trevisan; D. Schena; S. Ferrari
Cation transport systems and lipid composition of erythrocyte membrane were studied in 27 psoriatic patients and in 34 healthy individuals. Whereas intracellular Na and K content, Na- and K-passive permeability and Li-Na countertransport of psoriatics did not show any statistical difference from normals, the Na/K ATPase pump activity was significantly higher and Na-K cotransport was significantly lower. Membrane lipid composition of psoriatics was different from normals: an increase in arachidonic acid and in unsaturated (poly- and total unsaturated) fatty acid content was found. A positive correlation was demonstrated between unsaturated/saturated fatty acid ratio and Na/K ATPase pump activity. These results demonstrate an alteration of erythrocyte Na/K ATPase pump and Na-K cotransport in psoriasis. These alterations of cation transport are associated with a perturbation of membrane fatty acid composition which appears a widespread phenomenon in cells of psoriatic patients.
Journal of Endocrinological Investigation | 1991
Annamaria Stanzial; L. Bonomi; C. Cobbe; Domenico Girelli; Maria Teresa Trevisan; Antonella Bassi; S. Ferrari; Roberto Corrocher
The fatty acid composition and the glutathione-peroxidase activity (GSH-Px) of erythrocytes and platelets, the production of malondialdehyde (MDA) by platelets and the activity of the main systems of transmembrane cation transport in erythrocyte have been studied in 12 patients (5 males and 7 females) affected by retinitis pigmentosa (RP). A remarkable increase of saturated fatty acids (SFA), particularly of stearic acid (C18:0), has been noted in these patients. The reduced unsaturated/saturated fatty acids ratio (PUFA/SFA) observed in both erythrocytes and platelets and the decrease of arachidonic acid in platelets may depend by an active peroxidation process as documented by the increase of MDA. Platelet glutathione-peroxidase (PTL-GSH-PX) and plasma retinol were in the normal range, whereas erythrocyte glutathione-peroxidase (E-GSH-PX), MDA and plasma alfa-tocopherol were increased in patients with RP. The activities of Na+-K+ pump, cotransport and Na+-Li+countertransport were normal in RP erythrocytes.
Heart Asia | 2014
Alessandro Casartelli; Lisa Dacome; Michela Tessari; Jennifer P. Pascali; Federica Bortolotti; Maria Teresa Trevisan; Oliviero Bosco; Patrizia Cristofori; Franco Tagliaro
Objective Cocaine is known to produce life-threatening cardiovascular complications, and the investigation of the causes of death may be challenging in forensic medicine. The increasing knowledge of the cardiac function biomarkers and the increasing sensitivity of assays provide new tools in monitoring the cardiac life-threatening pathological conditions and in the sudden death investigation in chronic abusers. In this work, cardiac dysfunction was assessed in an animal model by measuring troponin I and natriuretic peptides as biomarkers, and considering other standard endpoints used in preclinical toxicology studies. Methods Lister Hooded rats were treated with cocaine in chronic self-administration studies. Troponin I (cTnI) and atrial natriuretic peptide (ANP) were evaluated at different time points and heart weight and histopathology were assessed at the end of the treatment period. Furthermore, cocaine and its main metabolites were measured in the rat fur to assess rats’ cocaine exposure. All the procedures and endpoints considered were designed to allow an easy and complete translation from the laboratory animals to human beings, and the same approach was also adopted with a group of 10 healthy cocaine abuse volunteers with no cardiac pathologies. Results Cardiac troponin I values were unaffected, and ANP showed an increasing trend with time in all cocaine-treated animals considered. Similarly, in the healthy volunteers, no changes were observed in troponin serum levels, whereas the N-terminal brain natriuretic pro-peptide (NT proBNP) showed variations comparable with the changes observed in rats. Conclusions In conclusion, natriuretic peptides could represent an early indicator of heart dysfunction liability in chronic cocaine abusers.
The American Journal of Clinical Nutrition | 1994
Anna Maria Stanzial; Domenico Girelli; Maria Teresa Trevisan; Patrizia Guarini; Marta Terzi; Sandro Caffi; Fabrizio Fontana; Massimo Casaril; S. Ferrari
Clinical Chemistry | 2005
Federica Bortolotti; Giorgia De Paoli; Jennifer P. Pascali; Maria Teresa Trevisan; Mirella Floreani; Franco Tagliaro
Clinica Chimica Acta | 1992
Domenico Girelli; Margherita Azzini; Patrizia Guarini; Maria Teresa Trevisan; Antonio Lupo; Patrizia Bernich; Giovanni Panzetta; Roberto Corrocher
British Journal of Haematology | 1995
Paolo Bellavite; Patrizia Guarini; Domenico Biasi; A. Carletto; Maria Teresa Trevisan; Paola Caramaschi; Lisa Maria Bambara; Roberto Corrocher
Clinica Chimica Acta | 2013
Federica Bortolotti; Maria Teresa Trevisan; Rocco Micciolo; Luisa Canal; Anthula Vandoros; Timothy Palmbach; Franco Tagliaro
RIVISTA DI MEDICINA DI LABORATORIO | 2004
Giorgia De Paoli; Maristella Trettene; Jennifer P. Pascali; Maria Teresa Trevisan; Federica Bortolotti; Franco Tagliaro