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Dive into the research topics where Paula Acosta Maldonado is active.

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Featured researches published by Paula Acosta Maldonado.


Clinical Biochemistry | 2008

Measurement of oxidative stress and antioxidant status in acute lymphoblastic leukemia patients

Vanessa Battisti; Liési D.K. Maders; Margarete Dulce Bagatini; Karen F. Santos; Roselia Spanevello; Paula Acosta Maldonado; Alice Odete Brülê; Maria do Carmo Araújo; Maria Rosa Chitolina Schetinger; Vera Maria Morsch

OBJECTIVES To evaluate the oxidative status and antioxidant defense in patients with acute lymphoblastic leukemia (ALL). DESIGN AND METHODS We measured concentrations of plasmatic thiobarbituric acid reactive substances (TBARS), serum protein carbonylation, whole blood catalase (CAT) and superoxide dismutase (SOD) activities, as well as the plasmatic and erythrocyte thiol levels and serum vitamin E concentration. This study was performed on 80 children with ALL divided into 4 groups: just diagnosed, remission induction, remission maintenance and out-of-treatment. RESULTS TBARS levels and serum protein carbonylation were higher in ALL patients than in controls and reduced levels of antioxidants were found in these patients. CONCLUSION These findings may indicate a possible link between decreased antioxidants and increased levels of cells alterations due to oxidative damage, supporting the idea that there is a persistence of oxidative stress in acute lymphoblastic leukemia.


Clinical Biochemistry | 2008

Ectonucleotide Pyrophosphatase/Phosphodiesterase (E-NPP) and Adenosine Deaminase (ADA) activities in patients with uterine cervix neoplasia

Paula Acosta Maldonado; Maísa de Carvalho Corrêa; Lara Vargas Becker; Clóvis Flores; Maria Beatriz Moretto; Vera Maria Morsch; Maria Rosa Chitolina Schetinger

OBJECTIVE Ectonucleotide pyrophosphatase/phosphodiesterase (E-NPP) and adenosine deaminase (ADA) activities, in the platelets and serum, were examined in patients with uterine cervix neoplasia without treatment as well as in patients treated by conization or radiotherapy (RTX). DESIGN AND METHODS The patients were divided based on the amount of time from the end of the treatments until the day of the blood sampling. Groups I (n=19) (conization) and III (n=11) (radiotherapy) (treated from one to five years earlier), groups II (n=19) (conization) and IV (n=16) (radiotherapy) (treated recently; up to three months earlier) and the non-treated group (cancer) (n=7). RESULTS E-NPP and ADA in the platelets and E-NPP in the serum were decreased in all the treated groups in relation to the control and non-treated groups, while ADA in the serum was decreased only in the conization groups in relation to them. In group II, E-NPP and ADA, in the platelets, were increased in relation to group IV. CONCLUSION The tendency of reduction for E-NPP and ADA indicates that they may act together to control nucleotide levels and it may also be speculated that surgery causes greater platelet activation contributing to the changes seen in the conization groups. In this sense, platelets seem to be more sensitive than serum.


International Journal of Developmental Neuroscience | 2007

The effect of aluminium on NTPDase and 5′-nucleotidase activities from rat synaptosomes and platelets

Rosilene Rodrigues Kaizer; Paula Acosta Maldonado; Roselia Maria Spanevello; Maísa de Carvalho Corrêa; Jamile F. Gonçalves; Lara Vargas Becker; Vera Maria Morsch; Maria Rosa Chitolina Schetinger

Aluminium (Al), a neurotoxic compound, has been investigated in a large number of studies both in vivo and in vitro. In this study, we investigated the effect in vivo of long‐term exposure to Al on NTPDase (nucleoside triphosphate diphosphohydrolase) and 5′‐nucleotidase activities in the synaptosomes (obtained from the cerebral cortex and hippocampus) and platelets of rats. Here, we investigated a possible role of platelets as peripheral markers in rats. Rats were loaded by gavage with AlCl3 50 mg/(kg day), 5 days per week, totalizing 60 administrations. The animals were divided into four groups: (1) control (C), (2) 50 mg/kg of citrate solution (Ci), (3) 50 mg/kg of Al plus citrate (Al + Ci) solution and (4) 50 mg/kg of Al (Al). ATP hydrolysis was increased in the synaptosomes from the cerebral cortex by 42.9% for Al + Ci and 39.39% for Al, when compared to their respective control (p < 0.05). ADP hydrolysis was increased by 13.15% for both Al and Al + Ci, and AMP hydrolysis increased by 32.7% for Al and 27.25% for Al + Ci (p < 0.05). In hippocampal synaptosomes, the hydrolysis of ATP, ADP and AMP, was increased by 58.5%, 28.5% and 25.92%, respectively, for Al (p < 0.05) and 36.7%, 22.5% and 37.64% for Al + Ci, both when compared to their respective controls. ATP, ADP and AMP hydrolysis, in platelets, was increased by 172.3%, 188.52% and 92.1%, respectively in Al + Ci, and 317.9%, 342.8% and 177.9%, respectively, for Al, when compared to their respective controls (p < 0.05). Together, these results indicate that Al increases NTPDase and 5′‐nucleotidase activities, in synaptosomal fractions and platelets. Thus, we suggest that platelets could be sensitive peripheral markers of Al toxicity of the central nervous system.


Biomedicine & Pharmacotherapy | 2013

Ectonucleotide pyrophosphatase/phosphodiesterase (E-NPP) and adenosine deaminase (ADA) activities in prostate cancer patients: influence of Gleason score, treatment and bone metastasis.

Vanessa Battisti; Liési D.K. Maders; Margarete Dulce Bagatini; Iara E. Battisti; Luziane Potrich Bellé; Karen F. Santos; Paula Acosta Maldonado; Gustavo R. Thomé; Maria Rosa Chitolina Schetinger; Vera Maria Morsch

The relation between adenine nucleotides and cancer has already been described in literature. Considering that the enzymes ectonucleotide pyrophosphatase/phosphodiesterase (E-NPP) and adenosine deaminase (ADA) act together to control nucleotide levels, we aimed to investigate the role of these enzymes in prostate cancer (PCa). E-NPP and ADA activities were determined in serum and platelets of PCa patients and controls. We also verified the influence of the Gleason score, bone metastasis and treatment in the enzyme activities. Platelets and serum E-NPP activity increased, whereas ADA activity in serum decreased in PCa patients. In addition, Gleason score, metastasis and treatment influenced E-NPP and ADA activities. We may propose that E-NPP and ADA are involved in the development of PCa. Moreover, E-NPP and ADA activities are modified in PCa patients with distinct Gleason score, with bone metastasis, as well as in patients under treatment.


Ciência e Natura | 2012

ORAL ADMINISTRATION OF N-ACETYLCYSTEINE IMPROVES BIOCHEMICAL PARAMETERS IN DIABETIC RATS

Jamile F. Gonçalves; Cinthia M. Mazzanti; Alexssandro Geferson Becker; Rosilene Rodriguez Kaizer; Vanessa Battisti; Maísa de Carvalho Corrêa; Paula Acosta Maldonado; Roberta Schmatz; Gustavo R. Thomé; Vera Maria Morsch; Maria Rosa Chitolina Schetinger

To evaluate the effect of N-acetylcysteine (NAC), a potent ROS scavenger and thiol group supplier, on normoglycemic and diabetic rats, the animals received 50 or 200 mg/kg NAC by gavage daily for 45 days. The results showed a lack of uniformity in acetylcholinesterase activity among the four cerebral structures. While neither dose of NAC produced significant hypoglycemic activity, 50 mg/kg NAC partially reverted the weight loss of diabetics and was effective in restoring aminolevulinate dehydratase activity and non-protein thiol content in liver, and in diminishing serum protein carbonylation. The dose of 200 mg/kg NAC presented some negative effects per se in both the antioxidant and cholinergic systems. In conclusion, 50 mg/kg NAC produced an improvement in some parameters suggesting NAC as a possible drug in antioxidant therapies against diabetic state. However, future studies are necessary to investigate the better dose of this compound to counteract its undesirable effects.


Life Sciences | 2009

Effects of resveratrol on nucleotide degrading enzymes in streptozotocin-induced diabetic rats

Roberta Schmatz; Maria Rosa Chitolina Schetinger; Roselia Maria Spanevello; Cinthia M. Mazzanti; Naiara Stefanello; Paula Acosta Maldonado; Jessié M. Gutierres; Maísa de Carvalho Corrêa; Eduardo Girotto; Maria Beatriz Moretto; Vera Maria Morsch


Brain Research Bulletin | 2009

Ectonucleotidase and acetylcholinesterase activities in synaptosomes from the cerebral cortex of streptozotocin-induced diabetic rats and treated with resveratrol

Roberta Schmatz; Cinthia M. Mazzanti; Roselia Maria Spanevello; Naiara Stefanello; Jessié M. Gutierres; Paula Acosta Maldonado; Maísa Corrêa; Cíntia Saydelles da Rosa; Lara Vargas Becker; Margarete Dulce Bagatini; Jamile F. Gonçalves; Jeandre Dos Santos Jaques; Maria Rosa Chitolina Schetinger; Vera Maria Morsch


Biomedicine & Pharmacotherapy | 2007

Oxidative stress and δ-ALA-D activity in chronic renal failure patients

Adriane Cismoski da Silva; João Batista Teixeira da Rocha; André Morsch; Rafael Fernandes Zanin; Rosilene Rodrigues Kaizer; Paula Acosta Maldonado; Luís C. Arantes; Luís A. Lima Silva; Vera Maria Morsch; Maria Rosa Chitolina Schetinger


Brain Research Bulletin | 2009

Effect of vitamin E on ectonucleotidase activities in synaptosomes and platelets and parameters of oxidative stress in rats experimentally demyelinated

Roselia Spanevello; Cinthia M. Mazzanti; Roberta Schmatz; Margarete Dulce Bagatini; Naiara Stefanello; Maísa Corrêa; Rosilene Rodrigues Kaizer; Paula Acosta Maldonado; Alexandre Mazzanti; Dominguita Lühers Graça; Tessie Beck Martins; Cristiane Cademartori Danesi; Vera Maria Morsch; Maria Rosa Chitolina Schetinger


Biomedicine & Pharmacotherapy | 2008

Oxidative stress and erythrocyte acetylcholinesterase (AChE) in hypertensive and ischemic patients of both acute and chronic stages.

Maísa de Carvalho Corrêa; Paula Acosta Maldonado; Cíntia Saydelles da Rosa; Gilberto Lunkes; Daniéle Sausen Lunkes; Rosilene Rodrigues Kaizer; Mushtaq Ahmed; Vera Maria Morsch; Maria Ester Pereira; Maria Rosa Chitolina Schetinger

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Vera Maria Morsch

Universidade Federal de Santa Maria

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Maísa de Carvalho Corrêa

Universidade Federal de Santa Maria

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Roberta Schmatz

Universidade Federal de Santa Maria

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Cinthia M. Mazzanti

Universidade Federal de Santa Maria

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Rosilene Rodrigues Kaizer

Universidade Federal de Santa Maria

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Vanessa Battisti

Universidade Federal de Santa Maria

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Margarete Dulce Bagatini

Universidade Federal de Santa Maria

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Naiara Stefanello

Universidade Federal de Santa Maria

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Roselia Maria Spanevello

Universidade Federal de Pelotas

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