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Dive into the research topics where Simone Cristina Baggio Gnoatto is active.

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Featured researches published by Simone Cristina Baggio Gnoatto.


European Journal of Medicinal Chemistry | 2008

Evaluation of ursolic acid isolated from Ilex paraguariensis and derivatives on aromatase inhibition

Simone Cristina Baggio Gnoatto; Alexandra Dassonville-Klimpt; Sophie Da Nascimento; Philippe Galéra; Karim Boumediene; Grace Gosmann; Pascal Sonnet; Safa Moslemi

The inhibitory potency of ursolic acid extracted from Ilex paraguariensis, a plant used in South American population for a tea preparation known as maté, and its derivatives to inhibit aromatase activity was assessed and compared to a phytoestrogen apigenin and a steroidal aromatase inhibitor 4-hyroxyandrostenedione (4-OHA). Among all compounds tested only ursolic acid 1 showed an efficient and dose-dependent aromatase inhibition with IC50 value of 32 microM as did apigenin (IC50=10 microM), whereas IC50 value of 4-OHA was 0.8 microM. Our results show that the incorporation of a metallocene moiety into the ursolic acid derivatives decreases the aromatase inhibition. Moreover, comparison of the structure/inhibitory potency relationship of compounds indicates that the presence of cycle A and the configuration of C3-OH and C17-COOH seems to be more favourable to recognize the active site of aromatase and to block its activity.


Journal of the Brazilian Chemical Society | 2005

HPLC method to assay total saponins in Ilex paraguariensis aqueous extract

Simone Cristina Baggio Gnoatto; Eloir Paulo Schenkel; Valquiria Linck Bassani

Ilex paraguariensis St. Hilaire is a South American tree from which leaves and twigs are used to prepare a commonly consumed tea in several South American countries. The plant is known as “erva-mate” in Portuguese or “yerba mate” in Spanish. Considering the potential use of the saponins as surfactant as well as its therapeutic potential, the present work was designed to propose extraction and quantitation methods for the saponins present in Ilex paraguariensis. The saponins were extracted by decoction, hydrolyzed and quantified by a HPLC method with UV detection. The saponins concentration was expressed in ursolic acid (total saponins). The method showed linearity for ursolic acid in the range of 13.5 to 135 µg mL -1 . The aqueous extract presented total saponins concentration of 352 µg mL -1 . The results also suggest the possibility of use of similar method for assaying triterpenoid saponins in other plants.


Molecules | 2012

Synthesis and antiplasmodial activity of betulinic acid and ursolic acid analogues.

Adrine Maria Innocente; Gloria Narjara Santos da Silva; Laura N. Cruz; Miriam S. Moraes; Myna Nakabashi; Pascal Sonnet; Grace Gosmann; Célia R.S. Garcia; Simone Cristina Baggio Gnoatto

More than 40% of the World population is at risk of contracting malaria, which affects primarily poor populations in tropical and subtropical areas. Antimalarial pharmacotherapy has utilised plant-derived products such as quinine and artemisinin as well as their derivatives. However, worldwide use of these antimalarials has caused the spread of resistant parasites, resulting in increased malaria morbidity and mortality. Considering that the literature has demonstrated the antimalarial potential of triterpenes, specially betulinic acid (1) and ursolic acid (2), this study investigated the antimalarial activity against P. falciparum chloroquine-sensitive 3D7 strain of some new derivatives of 1 and 2 with modifications at C-3 and C-28. The antiplasmodial study employed flow cytometry and spectrofluorimetric analyses using YOYO-1, dihydroethidium and Fluo4/AM for staining. Among the six analogues obtained, compounds 1c and 2c showed excellent activity (IC50 = 220 and 175 nM, respectively) while 1a and b demonstrated good activity (IC50 = 4 and 5 μM, respectively). After cytotoxicity evaluation against HEK293T cells, 1a was not toxic, while 1c and 2c showed IC50 of 4 μM and a selectivity index (SI) value of 18 and 23, respectively. Moreover, compound 2c, which presents the best antiplasmodial activity, is involved in the calcium-regulated pathway(s).


Molecules | 2012

Phenolic Enriched Extract of Baccharis trimera Presents Anti-inflammatory and Antioxidant Activities

Cristiane Oliveira; Lucimara Nardi Comunello; Adroaldo Lunardelli; Robson Henrich Amaral; Melissa Guerra Simões Pires; Gabriela Lucas da Silva; Vanusa Manfredini; Carmen Regla Vargas; Simone Cristina Baggio Gnoatto; Jarbas R. de Oliveira; Grace Gosmann

Baccharis trimera is a plant popularly used as a tea and to treat gastrointestinal diseases and inflammatory processes as well. The total phenolic content was determined and the antioxidant and anti-inflammatory activities of six extracts (dichloromethane, ethyl acetate, butanol, aqueous, saponin and phenolic) from B. trimera were evaluated. Using carrageenan-induced pleurisy as a model of acute inflammation, the phenolic extract at 15 mg/kg decreased significantly the analyzed parameters when compared to the carrageenan group (p < 0.05), thus showing potential anti-inflammatory activity. The total phenolic content and antioxidant activity were evaluated by the Folin-Ciocalteau and DPPH methods, respectively. Phenolic and ethyl acetate extracts presented higher antioxidant activity (p < 0.05) than ascorbic acid. The phenolic extract also showed the highest antioxidant potential in relation to the other extracts, thus suggesting that the antioxidant and anti-inflammatory activities were due to the presence of phenolic compounds.


Food Chemistry | 2017

Ursolic acid from apple pomace and traditional plants: A valuable triterpenoid with functional properties

Simone Tasca Cargnin; Simone Cristina Baggio Gnoatto

Apple juice production generates a large amount of residue comprising mainly peels, seeds, and pulp, known as apple pomace. In the global context, Brazil ranks 11th in apple production and thousands of tons of apple pomace are produced every year. This by-product is little explored, since it is a rich and heterogeneous mixture, containing interesting phytochemical groups. Among them, ursolic acid (UA) has attracted attention because of its therapeutic potential. UA is a pentacyclic triterpene found too in several traditional plants, and has shown several functional properties such as antibacterial, antiprotozoal, anti-inflammatory and antitumor. Therefore, this review attempts to shed some light on the economical viability of apple and apple pomace as sources of bioactive compounds, highlighting the UA extraction, and its main functional properties published in the last 5years (2010-2015).


Parasitology Research | 2012

Anti-Trichomonas vaginalis activity of saponins from Quillaja, Passiflora, and Ilex species

Tábitha Dahmer Rocha; Patrícia de Brum Vieira; Simone Cristina Baggio Gnoatto; Tiana Tasca; Grace Gosmann

Trichomonas vaginalis is a flagellated protozoan that causes trichomonosis, the most prevalent non-viral STD worldwide. The pathogen has been associated with serious health consequences including predisposition to cervical cancer and adverse pregnancy outcomes and infertility. It also acts as a co-factor in HIV transmission and acquisition. The 5-nitroimidazole drugs are used in the treatment, however, treatment noncompliance is observed, and a growing number of T. vaginalis isolates resistant to the drugs have been related. Saponins are natural products possessing many biological activities such as antiprotozoan activity. The aim of this study was to evaluate the anti-T. vaginalis activity of saponins from Quillaja, Passiflora, and Ilex species. Saponins from Passiflora alata and Quillaja saponaria presented the best anti-T. vaginalis activity (MIC = 0.025%). In addition, all samples induced erythrocyte lysis and LDH release. As far as we know, this is the first report demonstrating the potential anti-T. vaginalis activity of these saponins.


Journal of Enzyme Inhibition and Medicinal Chemistry | 2008

Synthesis and preliminary evaluation of new ursolic and oleanolic acids derivatives as antileishmanial agents.

Simone Cristina Baggio Gnoatto; Luciana Dalla Vechia; Claiton Leoneti Lencina; Alexandra Dassonville-Klimpt; Sophie Da Nascimento; Djavad Mossalayi; Jean Guillon; Grace Gosmann; Pascal Sonnet

A series of new ursolic and oleanolic acids derivatives was synthesized via ursolic or oleanolic acids, previously extracted from South American Ilex species. These new compounds were tested for in vitro antiparasitic activity on Leishmania amazonensis and Leishmania infantum strains. Some of these compounds showed activity against the promastigote forms of L. amazonensis or L. infantum, with IC50 ranging from 5 to 12 μM. As expected, most of the compounds showed a significant level of cytotoxicity against monocytes (IC50 = 2-50 μM). From a structure-activity relationships point of view, these pharmacological results enlightened mainly the importance of an acetylation at position 3 of the oleanolic acid skeleton in the activity against the L. amazonensis strain, and of a bis-(3-aminopropyl)piperazine moiety on the carboxylic function of ursolic acid against the L. infantum strain.


Química Nova | 2007

Influência do método de extração nos teores de metilxantinas em erva-mate (Ilex paraguariensis a. St.-Hil., aquifoliaceae)

Simone Cristina Baggio Gnoatto; Valquiria Linck Bassani; Geraldo Ceni Coelho; Eloir Paulo Schenkel

Ilex paraguariensis A. St. -Hil. is a native species of southern South America. The caffeine content in Ilex paraguariensis leaves has been considered an important quality parameter for mate-derived products. In this work different extraction methods for the determination of these methylxantines are compared. The influence of the extraction conditions on the methylxanthine yields was evaluated. Extraction by decoction with acidic aqueous solution (H2SO4 4N) presented the higher efficiency in the theobromine extraction. The extraction in a Soxhlet with acidic aqueous solution and decoction with acidic aqueous solution showed the highest caffeine yield. For the concomitant theobromine and caffeine quantification, the decoction with acidic aqueous solution is suggested.Ilex paraguariensis A. St. -Hil. is a native species of southern South America. The caffeine content in Ilex paraguariensis leaves has been considered an important quality parameter for mate-derived products. In this work different extraction methods for the determination of these methylxantines are compared. The influence of the extraction conditions on the methylxanthine yields was evaluated. Extraction by decoction with acidic aqueous solution (H2SO4 4N) presented the higher efficiency in the theobromine extraction. The extraction in a Soxhlet with acidic aqueous solution and decoction with acidic aqueous solution showed the highest caffeine yield. For the concomitant theobromine and caffeine quantification, the decoction with acidic aqueous solution is suggested.


Journal of Medicinal Food | 2010

Quantification of saponins in extractive solution of mate leaves (Ilex paraguariensis A. St. Hil.).

Geraldo Ceni Coelho; Simone Cristina Baggio Gnoatto; Valquiria Linck Bassani; Eloir Paulo Schenkel

Mate (Ilex paraguariensis A. St. Hil.) is a raw material used to prepare popular beverages in South America, whose healthy effects have been pointed out. The leaves and stems of mate contain a complex assemblage of saponins, mainly ursolic acid and oleanolic acid glycosides, and their quantification presents difficulties such as weak cromophorous sites and interference of other compounds. On the other hand, the sugar moieties are a chief character that distinguishes them. We developed and validated a high-performance liquid chromatography method using a refractometer detector for quantifying the major saponins in extractive solution of mate leaves. The validation indicates the suitability of the method, presenting linearity in the concentration range between 102.5 to 854.0 microg/mL to matesaponin 1 and between 103.0 to 515.0 microg/mL to matesaponin 3. The repeatability coefficient of variation was 4.70% and 6.61% for matesaponin 1 and matesaponin 3, respectively. The inter-day coefficient of variation was 6.77% and 7.79% for matesaponin 1 and matesaponin 3, respectively. The analysis of plants from Brazilian States Mato Grosso do Sul and Rio Grande do Sul showed the predominance of matesaponins 1, 2, and 3 in the corresponding extractive solution. The sum of these three saponins ranged between 3 and 10 mg/g for mature leaves in the majority of sampled plants.


Molecules | 2013

The Inhibitory Effects of Phenolic and Terpenoid Compounds from Baccharis trimera in Siha Cells: Differences in Their Activity and Mechanism of Action

Cristiane Oliveira; Lucimara Nardi Comunello; Érica S. Maciel; Scheron R. Giubel; Alessandra Nejar Bruno; Eduardo Cremonese Filippi Chiela; Guido Lenz; Simone Cristina Baggio Gnoatto; Andréia Buffon; Grace Gosmann

Baccharis trimera is used in folk medicine as a tea for digestive and liver diseases. It possesses anti-inflammatory and antioxidant properties that are related to the presence of phenolic compounds. The aim of this work was to investigate the anti-proliferative properties of phenolic (PHE) and terpenoid (SAP) compounds from B. trimera on human cervical cancer. The treatment of SiHa cells with PHE for 24 h suppressed colony formation in a dose-dependent manner, inhibited proliferation and inhibited cell motility. Although SAP inhibited the proliferation of SiHa cells in a dose-dependent manner, it increased colony formation and did not inhibit cell motility. PHE and SAP also promoted a significant increase in lactate dehydrogenase levels in the culture medium in a dose-dependent manner, indicating a loss of cell membrane integrity. Moreover, PHE promoted necrotic cell death, whereas SAP induced apoptosis. These compounds are new anticancer prototypes due their significant anticancer activity demonstrated herein.

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Grace Gosmann

Centre national de la recherche scientifique

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Gloria Narjara Santos da Silva

Universidade Federal do Rio Grande do Sul

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Pascal Sonnet

University of Picardie Jules Verne

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Tiana Tasca

Universidade Federal do Rio Grande do Sul

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Adrine Maria Innocente

Universidade Federal do Rio Grande do Sul

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Bruna Bento Casanova

Universidade Federal do Rio Grande do Sul

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Luciana Dalla Vechia

Universidade Federal do Rio Grande do Sul

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Patrícia de Brum Vieira

Universidade Federal do Rio Grande do Sul

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Alexandra Dassonville-Klimpt

University of Picardie Jules Verne

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Hugo Verli

Universidade Federal do Rio Grande do Sul

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