Fernanda Barbisan

Prof. Fernanda Barbisan

Pathology, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

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

Representative Publications

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1 February 2018 in Chemico-Biological Interactions
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Journal Article
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IAIsabel Cristina da Costa Araldi
Isabel Cristina da Costa Araldi
FBFernando Primitivo Romero Bordin
Fernando Primitivo Romero Bordin
FCFrancine Carla Cadoná
Francine Carla Cadoná
FBFernanda Barbisan
Fernanda Barbisan
VAVerônica Farina Azzolin
Verônica Farina Azzolin
LBLiliane Bauermann
Liliane Bauermann

2 February 2019 in Lasers in Medical Science
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Journal Article
Closed access
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DMDaíse Raquel Maldaner
Daíse Raquel Maldaner
VAVerônica Farina Azzolin
Verônica Farina Azzolin
FBFernanda Barbisan
Fernanda Barbisan
MMMoisés Henrique Mastella
Moisés Henrique Mastella
CTCibele Ferreira Teixeira
Cibele Ferreira Teixeira
MDMarta Maria Medeiros Frescura Duarte
Marta Maria Medeiros Frescura Duarte

6 November 2019 in Journal of Cellular Biochemistry
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Journal Article
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RSRenata da Silva Pereira Saccol
Renata da Silva Pereira Saccol
KSKarine Lanes da Silveira
Karine Lanes da Silveira
AMAlessandra Guedes Manzoni
Alessandra Guedes Manzoni
FAFátima Husein Abdalla
Fátima Husein Abdalla
JOJuliana Oliveira
Juliana Oliveira
DLDaniela Bitencourt Rosa Leal
Daniela Bitencourt Rosa Leal

22 January 2021 in Journal of Food Biochemistry
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Journal Article
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JMJéssica Rosso Motta
Jéssica Rosso Motta
IJIvo Emilio da Cruz Jung
Ivo Emilio da Cruz Jung
VAVerônica Farina Azzolin
Verônica Farina Azzolin
CTCibele Ferreira Teixeira
Cibele Ferreira Teixeira
LBLuiza Elizabete Braun
Luiza Elizabete Braun
FBFernanda Barbisan
Fernanda Barbisan

1 December 2018 in Journal of Photochemistry and Photobiology B: Biology
Verified
Journal Article
Closed access
CCCamila Cuelho
Camila Cuelho
GAGeórgia de Assis Dias Alves
Geórgia de Assis Dias Alves
MLMarina Ortiz Lovatto
Marina Ortiz Lovatto
IBIuri França Bonilha
Iuri França Bonilha
FBFernanda Barbisan
Fernanda Barbisan
MMMelânia Palermo Manfron
Melânia Palermo Manfron

8 October 2018 in BioMed Research International
Verified
Journal Article
Open access
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NPNeida L. Pellenz
Neida L. Pellenz
FBFernanda Barbisan
Fernanda Barbisan
VAVeronica F. Azzolin
Veronica F. Azzolin
TDThiago Duarte
Thiago Duarte
ABAline Bolignon
Aline Bolignon
MDMarta M. M. F. Duarte
Marta M. M. F. Duarte
Barbatimão (Stryphnodendron adstringens, Mart.) is a native Brazilian species used in traditional medicine and some commercial preparations owing to its strong wound-healing activity. However, controversy regarding its use due to safety concerns over the potential genotoxic effect of this plant remains. In order to clarify this issue, the effect of hydroalcoholic extract of barbatimão in vitro on cell viability, DNA damage, and induction of apoptosis in two commercial cell lines of keratinocytes (HaCaT) and fibroblasts (HFF-1) was evaluated. Barbatimão stem bark hydroalcoholic extract (70% ethanol) was obtained and lyophilized for subsequent use in all experiments. The main bioactive molecules quantified by HPLC were gallic acid, caffeic acid, quercetin, catechin, and epigallocatechin gallate (EGCG). Barbatimão (0.024 to 1.99 mg/mL) was found to decrease cellular mortality as compared to the control group. GEMO assay, a noncellular DNA protocol that uses H2O2-exposed calf thymus DNA, revealed not only a genotoxic effect of barbatimão, but also a potential genoprotective action against H2O2-triggered DNA fragmentation. These results indicated that barbatimão at concentrations of 0.49 and 0.99 mg/mL, which are near to the levels found in commercial preparations, exerted an in vitro genoprotective effect on cells by decreasing the levels of DNA oxidation quantified by 8-hydroxy-2′-deoxyguanosine (8-OHdG) and reactive oxygen species (ROS) levels. Gene and protein apoptotic markers, quantified by qRT-PCR (BAX/Bcl-2 genes) and immunoassays (Caspases 3 and 8), respectively, also indicated a decrease in apoptotic events in comparison with control cells. Collectively, the results suggest that barbatimão could exert genoprotective and antiapoptotic effects on human keratinocytes and fibroblasts.