Sabrina Somacal

Dr. Sabrina Somacal

Biochemistry and Molecular Biology, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil
orcid
Federal University of Santa Maria

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

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

Representative Publications

View All Publications
1 January 2012 in Journal of Clinical Biochemistry and Nutrition
Verified
Journal Article
Open access
PAPaula R Augusti
Paula R Augusti
AQAndrÉIa Quatrin
AndrÉIa Quatrin
Sabrina SomacalSabrina Somacal
Sabrina Somacal
GCGreicy Mm Conterato
Greicy Mm Conterato
RSRocheli Sobieski
Rocheli Sobieski
Tatiana EmanuelliTatiana Emanuelli
Tatiana Emanuelli
This study explored the effects of the antioxidant astaxanthin on paraoxonase and thioredoxin reductase activities as well as on other oxidative stress parameters and on the lipid profile in hypercholesterolemic rabbits. Rabbits were fed a standard or a hypercholesterolemic diet alone or supplemented with 50, 100 and 500 mg/100 g of astaxanthin for 60 days. Antioxidant enzymes activities, lipid profile and oxidative stress markers were evaluated in the serum. The hypercholesterolemic diet increased lipids, including unsaturated fatty acids level, whereas it decreased saturated fatty acids level. These changes were accompanied by increased levels of oxidized low-density lipoprotein and oxidized low-density lipoprotein antibodies, as well as lipid and protein oxidation. Astaxanthin (100 and 500 mg/100 g) prevented hypercholesterolemia-induced protein oxidation, whereas 500 mg/100 g of astaxanthin decreased protein oxidation per se. The activities of superoxide dismutase and thioredoxin reductase were enhanced, whereas paraoxonase activity was inhibited in hypercholesterolemic rabbits. All astaxanthin doses prevented changes in thioredoxin reductase and paraoxonase activities. This effect was not related to a direct effect of astaxanthin on these enzymes, because in vitro astaxanthin enhanced thioredoxin reductase and had no effect on paraoxonase activity. Astaxanthin could be helpful in cardiovascular diseases by restoring thioredoxin reductase and paraoxonase activities.

1 January 2008 in Food and Chemical Toxicology
Verified
Journal Article
Closed access
PAP.R. Augusti
P.R. Augusti
GCG.M.M. Conterato
G.M.M. Conterato
Sabrina SomacalSabrina Somacal
Sabrina Somacal
RSR. Sobieski
R. Sobieski
PSP.R. Spohr
P.R. Spohr
Tatiana EmanuelliTatiana Emanuelli
Tatiana Emanuelli

22 February 2015 in Molecular and Cellular Biochemistry
Verified
Journal Article
Closed access
PDF file
Sabrina SomacalSabrina Somacal
Sabrina Somacal
CFCassieli G. Figueiredo
Cassieli G. Figueiredo
AQAndréia Quatrin
Andréia Quatrin
ARAmanda R. Ruviaro
Amanda R. Ruviaro
LCLisiane Conte
Lisiane Conte
Tatiana EmanuelliTatiana Emanuelli
Tatiana Emanuelli

1 November 2020 in Food Research International
Verified
Journal Article
Closed access
JGJulheli R. Girardelo
Julheli R. Girardelo
EMEduarda L. Munari
Eduarda L. Munari
JDJulio C.S. Dallorsoleta
Julio C.S. Dallorsoleta
GCGustavo Cechinel
Gustavo Cechinel
AGAndré L.F. Goetten
André L.F. Goetten
GCGreicy Michelle Marafiga Conterato
Greicy Michelle Marafiga Conterato

17 April 2007 in Basic & Clinical Pharmacology & Toxicology
Verified
Journal Article
Open access
PDF file
PAPaula R. Augusti
Paula R. Augusti
GCGreicy M. M. Conterato
Greicy M. M. Conterato
Sabrina SomacalSabrina Somacal
Sabrina Somacal
LELídia Einsfeld
Lídia Einsfeld
ARAdriano T. Ramos
Adriano T. Ramos
Tatiana EmanuelliTatiana Emanuelli
Tatiana Emanuelli
Abstract: Oxidative stress is an important molecular mechanism for kidney injury in mercury poisoning. We studied lycopene, a potent carotenoid found in tomatoes due to its large antioxidant properties, and also evaluated the ability of lycopene to prevent HgCl2nephrotoxicity. Rats were injected with HgCl2(0 or 5 mg/kg body weight, subcutaneously) 6 hr after lycopene administration (0, 10, 25 or 50 mg/kg by gavage) and were killed 12 hr after HgCl2exposure. HgCl2‐induced inhibition of δ‐aminolevulinate dehydratase activity (∼35%) and increase of lipid peroxidation in kidney (∼37%) were prevented by lycopene. However, lycopene did not prevent the increase of plasma creatinine levels (∼123%) and renal tubular necrosis induced by HgCl2. Glutathione peroxidase and catalase activities were enhanced (∼71% and ∼41%), while superoxide dismutase activity was depressed (∼44%) in HgCl2‐treated rats when compared to control and these effects were prevented by lycopene. Our results indicate that although lycopene did not prevent HgCl2‐induced renal failure, it could play a beneficial role against HgCl2toxicity by preventing lipid peroxidation and changes in the activity of δ‐aminolevulinate dehydratase and antioxidant enzymes.

12 September 2014 in Nutrients
Verified
Journal Article
Open access
PDF file
MBMarília Baierle
Marília Baierle
PVPatrícia H. Vencato
Patrícia H. Vencato
LOLuiza Oldenburg
Luiza Oldenburg
SBSuelen Bordignon
Suelen Bordignon
MZMurilo Ricardo Zibetti
Murilo Ricardo Zibetti
SGSolange Cristina Garcia
Solange Cristina Garcia
Polyunsaturated fatty acids (PUFAs), especially the n-3 series, are known for their protective effects. Considering that cardiovascular diseases are risk factors for dementia, which is common at aging, the aim of this study was to evaluate whether fatty acid status in the elderly was associated with cognitive function and cardiovascular risk. Forty-five elderly persons (age ≥60 years) were included and divided into two groups based on their Mini-Mental Status Examination score adjusted for educational level: the case group (n = 12) and the control group (n = 33). Serum fatty acid composition, homocysteine (Hcy), hs-CRP, lipid profile and different cognitive domains were evaluated. The case group, characterized by reduced cognitive performance, showed higher levels of 14:0, 16:0, 16:1n-7 fatty acids and lower levels of 22:0, 24:1n-9, 22:6n-3 (DHA) and total PUFAs compared to the control group (p < 0.05). The n-6/n-3 ratio was elevated in both study groups, whereas alterations in Hcy, hs-CRP and lipid profile were observed in the case group. Cognitive function was positively associated with the 24:1n-9, DHA and total n-3 PUFAs, while 14:0, 16:0 and 16:1n-7 fatty acids, the n-6/n-3 ratio and Hcy were inversely associated. In addition, n-3 PUFAs, particularly DHA, were inversely associated with cardiovascular risk, assessed by Hcy levels in the elderly.