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Dive into the research topics where Maria Gonçalves Pereira is active.

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Featured researches published by Maria Gonçalves Pereira.


Thrombosis and Haemostasis | 2008

Slight differences in sulfation of algal galactans account for differences in their anticoagulant and venous antithrombotic activities.

Roberto J. C. Fonseca; Stephan-Nicollas M. C. G. Oliveira; Fabio R. Melo; Maria Gonçalves Pereira; Norma Maria Barros Benevides; Paulo A.S. Mourão

We compared sulfated galactans (SGs) from two species of red algae using specific coagulation assays and experimental models of thrombosis. These polysaccharides have an identical saccharide structure and the same size chain, but with slight differences in their sulfation patterns. As a consequence of these differences, the two SGs differ in their anticoagulant and venous antithrombotic activities. SG from G. crinale exhibits procoagulant and prothrombotic effects in low doses (up to 1.0 mg/kg body weight), but in high doses (>1.0 mg/kg) this polysaccharide inhibits both venous and arterial thrombosis in rats and prolongs ex-vivo recalcification time. In contrast, SG from B. occidentalis is a very potent anticoagulant and antithrombotic compound in low doses (up to 0.5 mg/kg body weight), inhibiting venous experimental thrombosis and prolonging ex-vivo recalcification time, but these effects are reverted in high doses. Only at high doses (>1.0 mg/kg) the SG from B. occidentalis inhibits arterial thrombosis. As with heparin, SG from G. crinale does not activate factor XII, while the polysaccharide from B. occidentalis activates factor XII in high concentrations, which could account for its procoagulant effect at high doses on rats. Both SGs do not modify bleeding time in rats. These results indicate that slight differences in the proportions and/or distribution of sulfated residues along the galactan chain may be critical for the interaction between proteases, inhibitors and activators of the coagulation system, resulting in a distinct pattern in anti- and procoagulant activities and in the antithrombotic action.


Brazilian Journal of Medical and Biological Research | 2005

Differential activity of a lectin from Solieria filiformis against human pathogenic bacteria

Márjory Lima Holanda; Vânia Maria Maciel Melo; Luana Maria Castelo Melo Silva; Rodrigo César das Neves Amorim; Maria Gonçalves Pereira; Norma Maria Barros Benevides

A lectin isolated from the red alga Solieria filiformis was evaluated for its effect on the growth of 8 gram-negative and 3 gram-positive bacteria cultivated in liquid medium (three independent experiments/bacterium). The lectin (500 microg/mL) stimulated the growth of the gram-positive species Bacillus cereus and inhibited the growth of the gram-negative species Serratia marcescens, Salmonella typhi, Klebsiella pneumoniae, Enterobacter aerogenes, Proteus sp, and Pseudomonas aeruginosa at 1000 microg/mL but the lectin (10-1000 microg/mL) had no effect on the growth of the gram-positive bacteria Staphylococcus aureus and B. subtilis, or on the gram-negative bacteria Escherichia coli and Salmonella typhimurium. The purified lectin significantly reduced the cell density of gram-negative bacteria, although no changes in growth phases (log, exponential and of decline) were observed. It is possible that the interaction of S. filiformis lectin with the cell surface receptors of gram-negative bacteria promotes alterations in the flow of nutrients, which would explain the bacteriostatic effect. Growth stimulation of the gram-positive bacterium B. cereus was more marked in the presence of the lectin at a concentration of 1000 microg/mL. The stimulation of the growth of B. cereus was not observed when the lectin was previously incubated with mannan (125 microg/mL), its hapten. Thus, we suggest the involvement of the binding site of the lectin in this effect. The present study reports the first data on the inhibition and stimulation of pathogenic bacterial cells by marine alga lectins.


Fundamental & Clinical Pharmacology | 2013

A report of a galactan from marine alga Gelidium crinale with in vivo anti-inflammatory and antinociceptive effects.

Albertina Antonielly Sydney de Sousa; Norma Maria Barros Benevides; Alana de Freitas Pires; Felipe P. Fiúza; Maria G.R. Queiroz; Thamires Maria Fontenele Morais; Maria Gonçalves Pereira; Ana Maria Sampaio Assreuy

The sulfated galactan of the red marine alga Gelidium crinale (SG‐Gc) was purified by ion exchange chromatography and tested by intravenous (i.v.) route in rodent experimental models of inflammation and nociception. The anti‐inflammatory activity of SG‐Gc (0.01, 0.1 and 1u2003mg/kg) was evaluated in the model of rat paw edema induced by different inflammatory stimuli, while SG‐Gc (0.1, 1 and 10u2003mg/kg) antinociceptive effect was assessed in models of nociception/hyperalgesia elicited by chemical (formalin test), thermal (hot plate), and mechanical (von Frey) stimuli in mice. In addition, the toxicity was evaluated after rat treatment with SG‐Gc (1u2003mg/kg; i.v.) during 10u2003days, followed by analysis of the wet weight of animal’s body/organs and hematological/biochemical parameters. Sulfated galactan of G. crinale inhibited the time course of dextran‐induced paw edema, at all doses, showing maximal effect at 1u2003mg/kg (42%) and that induced by carrageenan at 0.01 (18%) and 1u2003mg/kg (20%), but was ineffective on the edema elicited by zymosan. At the highest dose, SG‐Gc also inhibited the paw edema induced by histamine (49%), compound 48/80 (32%), and phospholipase A2 (44%). Sulfated galactan of G. crinale inhibited both neurogenic and inflammatory phases of the formalin test, at all doses, and at 10u2003mg/kg, the animals flinch reaction in the von Frey test in the 1st and 3rdu2003h by 19 and 26%, respectively. Additionally, SG‐Gc treatment was well tolerated by animals. In conclusion, SG‐Gc presents anti‐inflammatory effect involving the inhibition of histamine and arachidonic acid metabolites and also antinociceptive activity, especially the inflammatory pain with participation of the opioid system.


Journal of Ethnopharmacology | 2016

Modulator effect of a polysaccharide-rich extract from Caesalpinia ferrea stem barks in rat cutaneous wound healing: Role of TNF-α, IL-1β, NO, TGF-β

Lívia de Paulo Pereira; Mário Rogério Lima Mota; Luiz André Cavalcante Brizeno; Francisca C. Nogueira; Elda G.M. Ferreira; Maria Gonçalves Pereira; Ana Maria Sampaio Assreuy

ETHNOPHARMACOLOGICAL RELEVANCEnIn folk medicine stem barks of Caesalpinia ferrea (Caesalpinioideae) are used to treat enterocolitis, rheumatism and wounds and in experimental procedures, its aqueous extracts demonstrated antiulcer, anti-inflammatory, analgesic, and healing effects.nnnAIM OF THE STUDYnThe healing mechanism of the polyssacharide-rich extract of C. ferrea stem barks (TPL-Cf) was investigated in a model of excisional cutaneous wound in Wistar rats.nnnMATERIALS AND METHODSnExcisional wounds received topical treatment with TPL-Cf (0.025-0.1%) during 21 days. Hypernociception, macroscopical, histological and immunohistochemical parameters were evaluated and analyzed by ANOVA, Bonferroni and Kruskal-Wallis tests, followed by Dunn and Chi-Square tests.nnnRESULTSnTPL-Cf (0.1%) reduced wound area and hypernociception, and increased wound contraction. TPL-Cf reduced leukocyte infiltration and vascular permeability, and stimulated fibroblasia, angiogenesis, well formed granulation tissue, collagen deposition and epithelial layer formation. TPL-Cf reduced TNF-α expression and the levels of PGE2 (73%-day 5), IL-1 (42%-day 2), MDA (38%-day 5), total protein (53%-day 2; 73%-day 5) and MPO activity (53%-day 2), but increased the expression of i-NOS (days 5 and 7), TGF-β (day 5) and the levels of NO (3.6 fold-day 5).nnnCONCLUSIONnThe polysaccharide-rich extract of C. ferra stem barks accelerates wound healing by the control of the inflammatory phase and attenuates hypernociception via modulation of inflammatory mediators (TNF-α, IL-1β, NO, TGF-β).


Brazilian Journal of Botany | 2004

Purification and partial characterisation of a lectin from the red marine alga Vidalia obtusiloba C. Agardh

Fábio R. Melo; Norma Maria Barros Benevides; Maria Gonçalves Pereira; Márjory Lima Holanda; Francisca Noélia Pereira Mendes; Stélio R.M. Oliveira; Ana Lúcia Ponte Freitas; Luana Maria Castelo Melo Silva

A lectina da alga marinha vermelha Vidalia obtusiloba foi purificada atraves da combinacao de precipitacao com sulfato de amonio, cromatografia de troca ionica em DEAE-celulose e cromatografia de afinidade em goma de guar reticulada. A lectina preferencialmente aglutinou eritrocitos do grupo humano O, nativos e tratados com bromelaina. A atividade hemaglutinante revelou que a lectina era dependente de cations divalentes (Ca++ ou Mn++) e inibida por N-acetil-galactosamina, D-galactosamina, a-lactose and D-galactose e pela glicoproteina mucina de estomago de porco. A massa molecular da lectina, estimada por filtracao em gel, foi de 78,9 kDa, enquanto por SDS-PAGE, em presenca de b-mercaptoetanol, a lectina exibiu duas subunidades proteicas diferentes com Mr de 59,6 e 15,2 kDa, sugerindo que a lectina e uma proteina dimerica. Focalizacao isoeletrica revelou a presenca de uma proteina acida simples, com um ponto isoeletrico entre 4 e 5. A lectina purificada exibiu um conteudo de carboidrato de 43,2% e uma predominância dos aminoacidos Asp/Asn, Glu/Gln e Leu. A energia de ativacao (DG) para a desnaturacao da lectina foi calculada como sendo 25,4 kcalm.mol-1 a 90 oC. Ensaios imunoquimicos usando um anti-soro de coelho produzido contra a lectina purificada de V. obtusiloba mostraram que foi possivel detectar a presenca da lectina em diferentes etapas do processo de purificacao. Western blotting de geis de SDS-PAGE mostraram imunocoramento apenas da maior das subunidades da lectina.


Carbohydrate Polymers | 2015

Purified polysaccharides of Geoffroea spinosa barks have anticoagulant and antithrombotic activities devoid of hemorrhagic risks.

Racquel Oliveira da Silva Souza; Ana Maria Sampaio Assreuy; Juliana C. Madeira; Francisco D.S. Chagas; Luane A. Parreiras; Gustavo R.C. Santos; Paulo A.S. Mourão; Maria Gonçalves Pereira

Polysaccharides were extracted from the barks of Geoffroea spinosa, purified using anion exchange chromatography and characterized by chemical and methylation analysis, complemented by infrared and NMR spectroscopies. These polysaccharides were tested for their anticoagulant, antithrombotic and antiplatelet activities and also for their effects on bleeding. Unfractionated polysaccharide contains low levels of protein and high levels of carbohydrate (including hexuronic acid). The purified polysaccharides (fractions FII and FIII) are composed of arabinose (Ara), rhamnose (Rha), hexuronic acid, small amounts of galactose, but no sulfate ester. They have highly complex structure, which was partially characterized. NMR and methylation analysis indicate that the polysaccharides have a core of α-Rhap and branches of 5-linked α-Araf. Residues of 4-linked α-GalpA are also found in the structure. The unfractionated (TPL) and fraction FIII, but not fractions FI and FII, prolonged the activated partial thromboplastin time (aPTT). TPL, FII and FIII inhibited the platelet aggregation induced by ADP. More significantly, both unfractionated and purified fractions exhibited potent antithrombotic effect (31-60%) and the fractions did not modify the bleeding tendency. These plant polysaccharides could be alternative source of new anticoagulant, antiplatelet and antithrombotic compounds devoid of the undesirable risk of hemorrhage.


Archives of Biochemistry and Biophysics | 2014

Vasorelaxant activity of Canavalia grandiflora seed lectin: A structural analysis.

Ito L. Barroso-Neto; Rafael da Conceição Simões; Bruno Anderson Matias Rocha; Maria Júlia Barbosa Bezerra; Francisco Nascimento Pereira-Junior; Vinicius Jose Silva Osterne; Kyria S. Nascimento; Celso Shiniti Nagano; Plínio Delatorre; Maria Gonçalves Pereira; Alana de Freitas Pires; Alexandre Holanda Sampaio; Ana Maria Sampaio Assreuy; Benildo Sousa Cavada

Lectins are comprised of a large family of proteins capable of the specific and reversible recognition of carbohydrates. Legume lectins, the most studied plant lectins, show high structural similarity, but with modifications that imply a variation in the intensity of some biological activities. In this work, the primary and tertiary structures of Canavalia grandiflora (ConGF) were determined. ConGF, a lectin isolated from C. grandiflora seeds, is able to induce relaxant activity in rat aortic rings. The complete sequence of ConGF comprises 237 amino acids. This particular protein has primary sequence variations commonly found in lectins from Dioclea and Canavalia genera. The protein structure was solved at 2.3 Å resolution by X-ray crystallography. An X-Man molecule was modeled into the carbohydrate recognition domain. Still, ConGF (30 and 100 μg mL(-1)) elicited 25% of vasorelaxation (IC50=34.48 ± 5.07 μg mL(-1)) in endothelialized aortic rings. A nonselective inhibitor of nitric oxide blocked ConGF relaxant effect, showing mediation by nitric oxide. Key distances between ConGF carbohydrate recognition domain residues were determined in order to explain this effect, in turn revealing some structural aspects that could differentiate lectins from the Canavalia genera with respect to different efficacy in vasorelaxant effect.


International Journal of Biological Macromolecules | 2017

Structural studies of a vasorelaxant lectin from Dioclea reflexa Hook seeds: Crystal structure, molecular docking and dynamics

Vanir Reis Pinto-Junior; Vinicius Jose Silva Osterne; Mayara Queiroz Santiago; Jorge Luis Almeida Correia; Francisco Nascimento Pereira-Junior; Rodrigo Bainy Leal; Maria Gonçalves Pereira; Larissa da Silva Chicas; Celso Shiniti Nagano; Bruno Anderson Matias Rocha; José Caetano Silva-Filho; Wandemberg Paiva Ferreira; Cíntia Renata Costa Rocha; Kyria S. Nascimento; Ana Maria Sampaio Assreuy; Benildo Sousa Cavada

The three-dimensional structure of Dioclea reflexa seed lectin (DrfL) was studied in detail by a combination of X-ray crystallography, molecular docking and molecular dynamics. DrfL was purified by affinity chromatography using Sephadex G-50 matrix. Its primary structure was obtained by mass spectrometry, and crystals belonging to orthorhombic space group P212121 were grown by the vapor diffusion method at 293K. The crystal structure was solved at 1.765Å and was very similar to that of other lectins from the same subtribe. The structure presented Rfactor and Rfree of 21.69% and 24.89%, respectively, with no residues in nonallowed regions of Ramachandran plot. Similar to other Diocleinae lectins, DrfL was capable of relaxing aortic rings via NO induction, with CRD participation, albeit with low intensity (32%). In silico analysis results demonstrated that DrfL could strongly interact with complex N-glycans, components of blood vessel glycoconjugates. Despite the high similarity among Diocleinae lectins, it was also reported that each lectin has unique CRD properties that influence carbohydrate binding, resulting in different biological effects presented by these molecules.


Journal of Ethnopharmacology | 2018

Trypanocidal activity of polysaccharide extract from Genipa americana leaves

Racquel Oliveira da Silva Souza; Paloma Leão Sousa; Ramon Róseo Paula Pessoa Bezerra de Menezes; Tiago Lima Sampaio; Louise Donadello Tessarolo; Francisca Crislandia Oliveira Silva; Maria Gonçalves Pereira; Alice Maria Costa Martins

ETHNOPHARMACOLOGICAL RELEVANCEnThe parts of the Genipa americana (Rubiaceae) tree, also known as jenipapo or jenipapeiro, has been used in traditional Medicine in parasitic and bacterial infections. Thus, the experimental evolution of the antiparasitic activity of polysaccharide extracts from Genipa americana leaves, and correlation with antiparasitic and popular use is important.nnnAIM OF THE STUDYnTo evaluate the effect of polysaccharide extract obtained from Genipa americana leaves on all Trypanosoma cruzi (Y strain: benznidazole-resistant) developmental forms, a protozoan that causes Chagas disease.nnnMATERIALS AND METHODSnAn extract rich in polysaccharides was obtained from the leaves of Genipa americana (GaEPL) by associating depigmentation in methanol followed by extraction of polysaccharides in NaOH and precipitation with ethanol. Cytotoxicity to mammalian cells (LLC-MK2) was determined using an MTT assay. Antiparasitic activity was evaluated against epimastigote, trypomastigote and amastigote forms of T. cruzi. Cell-death mechanism was determined in epimastigote forms by flow cytometry analysis after FITC-annexin V (Ax), 7-AAD, and H2DCFDA staining. Striking morphological changes were observed by scanning electron microscope.nnnRESULTSnGaEPL (6.5% yield; 54.6% total carbohydrate; 21.1% uronic acid and 12% protein), inhibited all T. cruzi developmental forms, epimastigotes after periods of 24h (IC50 = 740 ± 0.075µg/mL), 48h (IC50 = 710 ± 0.053µg/mL) and 72h (IC50 = 870 ± 0.052µg/mL) of incubation; trypomastigotes (IC50 = 470 ± 0.082µg/mL) after periods of 24h and intracellular amastigotes (IC50/2 = 235 or IC50 = 470µg/mL) after periods of 24 and 48h of incubation, with no toxicity on LLC-MK2 cells at the used concentrations. Analysis of the possible action mechanism in the parasites suggested cell death by necrosis with the involvement of reactive oxygen species (ROS). The scanning electron microscopy (SEM) confirmed T. cruzi death by necrosis.nnnCONCLUSIONSnGaEPL showed significant activity against the epimastigote, trypomastigote and amastigote forms of T. cruzi, strain Y, suggesting cell death by necrosis with involvement of reactive oxygen species.


Journal of Ethnopharmacology | 2018

The polysaccharide-rich tea of Ximenia americana barks prevents indomethacin-induced gastrointestinal damage via neutrophil inhibition

Patrícia da Silva Pantoja; Ana Maria Sampaio Assreuy; Renan O. Silva; Samara Rodrigues Bonfim Damasceno; Vanessa Azevedo Mendonça; Tiago Santos Mendes; José Athayde Vasconcelos Morais; Samira Lopes de Almeida; António Teixeira; Marcellus H.L.P. Souza; Maria Gonçalves Pereira; Pedro Marcos Gomes Soares

ETHNOPHARMACOLOGICAL RELEVANCEnBarks of Ximenia americana are used by the population to treat gastrointestinal inflammatory disorders. Indomethacin is a non-selective non-steroidal anti-inflammatory drug that induces marked gastrointestinal damage.nnnAIMS OF THE STUDIESnTo evaluate the gastroprotective activity of total polysaccharides contained in the extract (TPL-Xa) or tea (Tea-Xa) of Ximenia americana barks in the mice gastric damage induced by indomethacin.nnnMATERIALS AND METHODSnTPL-Xa was obtained by a combination of NaOH extraction and ethanol precipitation. Tea-Xa was prepared in distilled water boiled during 5u202fmin. Animals received p.o. 0.9% NaCl (saline - control group), TPL-Xa (1-90u202fmg/kg) or Tea-Xa 1u202fh before gastritis induction by indomethacin (20u202fmg/kg). Mice were sacrificed 7u202fh after gastritis induction and analyzed for the following parameters: stomach lesions measurement; histological evaluation; myeloperoxidase (MPO) activity; nitrate/nitrite and cytokine levels; leukocyte adhesion and rolling by intravital microscopy.nnnRESULTSnTPL-Xa reduced macroscopic and microscopic damage, MPO activity (59%), leukocyte rolling (86%) and adhesion (84%), nitrite/nitrate ratio (100%) and IL-8 (69%), but increased IL-4 (50%). Tea-Xa (12.8 yield; 39.3% carbohydrate, including 25.8% uronic acid; 4% protein) reduced macroscopic damage (62%) and MPO activity (50%).nnnCONCLUSIONnTPL and Tea of Ximenia americana barks ameliorate the gastric injury induced by indomethacin in mice, an effect that was dependent on the reduction of neutrophil infiltration.

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Paulo A.S. Mourão

Federal University of Rio de Janeiro

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Benildo Sousa Cavada

Federal University of Ceará

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Celso Shiniti Nagano

Federal University of Ceará

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