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Candidacidal potential of licorice phenolic extract: emphasis on its mode of action

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5th

Portuguese Young

Chemists Meeting

(5th PYCheM)

&

1st

European Young

Chemists Meeting

{1st EYCheM)

Centro Cultural Vila Flor

Guimaraes, Portugal

(2)

COMMITTEES

ORGANIZING COMMITTEE

Catarina Cust6dio (3B's Research Group) Lufsa Rodrigues (3B's Research Group) Joi!o Borges (3B's Research Group) Ana Rita Araujo (3B 's Research Group) Sara Amorim (3B' s Research Group) lvo Aroso (3B's Research Group) Raquel Teixeira(3B's Research Group) Rarnon Novoa-Carballal (3B's Research Group)

Ana Soares (Chemistry Department of University ofMinho) Cristina Sousa (Chemistry Department of University ofMinho) Tiago Silva (3B's Research Group)

Lara Reys (3B 's Research Group) Sandra Silva (3B' s Research Group) Leonardo Mendes (SPQ)

SCIENTIFIC COMMITTEE

Joilo F. Mano (Univ. do Minho, Portugal) lva Pashkuleva (Univ. do Minho, Portugal) Femanda Proen~ (Univ. do Minho, Portugal) Artur Silva (Univ. de Aveiro, Portugal) Ant6nio Femando Silva (Univ. do Porto, Portugal) Maria Joa:o Moreno (Univ. de Coimbra, Portugal)

Ver6nica Bermudez (Univ. de Tn\s os Montes e Alto Douro, Portugal) Matilde Marques (Inst. Superior Tecnico, Portugal)

Isabel Ferreira (Inst.Politecino de Bragan~a, Portugal) Arrnando Silvestre (Univ. de Aveiro, Portugal) Jose Esperan~a (ITQB, Portugal)

Ant6nio Varandas (Univ. de Coimbra, Portugal) Fatima Bento (Univ. do Minho, Portugal) Aranzazu del Campo (MPIP Mainz, Germany) Radim Hrdina (Univ. ofPardubice, Czech Republic) Edward Matthijs (KU Leuven, Belgium)

SPQ SECRETARIAT

Leonardo Mendes Cristina Campos

5th PYCheM & 1st EYCheM- 2016 Guimaraes, Portugal

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·1111!

..

26 April 27 April 28 April

RegistratiOn and

Workshop of Organic

Inorganic, Physical,

9:00- Open Sc1ence and Chemistry and

13:20 European Open Medicinal Analytical and

Access Policies in Chemistry Electrochemistry

H2020

13:30 Operung Ceremony Lunch Lunch

CHEM2NATURE Symposmm Chelllical

strategies for modification of natural ongm matenals Biochemistry and 14:00. Green Chemistry + Medicinal 18:00 Chemistry of Chemistry Natural Products Assembleia GQJ (17h) 18:00 Walking Tour 19:00

J

Welcome Cocktail

21:30 Get-together mght Gala Dmner

29 April Materials Chemistry and Nanomaterials and Surface Chemistry Lunch Materials Chemistry and Nanomaterials and Surface Chemistry Closmg Ceremony 11

(4)

27th

April

PU • Nuno Maulide (50+ 10)

I

8h30 "'Oreanic synthesi' with rearrangemeDts: catalrsit ofunusual bond formino reaction:.!'t

OPIO· Novel Metal-Free Approach to Promising 09h30 COX-2 Inhibitors via Bronsted Acids-Catalyzed

Decomposition of Diazofuranones

Organic Chemistry Dmilrii Semeuok (10+5)

OPII· Luminescent Boranils and Boron-diketonates 09h45 +

Samuel Guieu (10+5) Medicinal Chemistry

OP12· Synthesis ofcopper(II) complexes of

!OhOO Chair: Dr. Fernanda Proen~a aJ)'lhydrazone and their application as catalysts in

oxidation of cycloalkanes in different media Young chair: Raquel Ribeiro Seixas Gon~alo

Antunes de Oliveira Tia2o 00+5) OP13-A novel strategy towards a regioselective

one-10hl5 pot synthesis of azaindoles

Marina Joana Dias Pires (lO+S) OP14· Functionalization oflnternal Alkynes: A New 10h30 Approach to 1,2-Disubstituted Cyclopentadienes

Nikola Topolovcan (10+5)

10h45 Coffee break+ Poster session

IL4. Artnr Siba (30+5)

llh!S "Greener heating methodJ in the oynthesis of biolotrlcally active heterocvclic compounds"

OP15 ·Application of Cinchona-alkaloids

llh50 Organocatalysts Pathway to in an Novel Rivastigmine and Efficient Synthetic SOvia Domin2os Fernandes (10+5) OP!6-Modular Oxindole Synthesis-a General an

Efficient Rhodiunt-Catalysed Addition of

12h05 Arylboronic Acids to !satin-Derived

N-Boc-Protected

··Carolina Silva Marques (10+5)

OP17-Iridium Catalyzed Asymmetric

12h20 Organic Chemistry Hydrogenation ofQninoline and Derivatives Quinoxaline

+ Tahar Ayad (10+5)

Medicina I Chemistry OP 18-Novel Fluorescent Organic Salts based on

12h35 Chair: Dr. Armando Silvestre Cationic or Anionic Dyes Andreia Sofia de Almeida Baptista Forte Young Chair: Silvia Domingos Fernandes (10+5)

OP 19-Candidacidal potential of licorice phenolic 12h50 extract: emphasis on its mode of action

Natalia Ana Pereira da Cruz Martins{lOill

OP20- Development oflntegrated S}stems for

Extraction and Purification ofMonoclonal 13h05 Antibodies directly from CHO Cell Cultures

Emanuel Auguato Vieira Capela (10+5)

42

(5)

14h20 15h20 15h35 15h50 16h05 Biochemistry 16h20 + Medicinal Chemistry

16h35 Chair: Vitor Gaspar Young chair: Filipa Joilo Femandes Gomes 16h50

17h05

17h35

!ShOO

PL3 - Helder Santos (Sll+ I 0) "Bridging between engineering and medidne

-Current applications of nanomedicines for cancer,

diabetes and cardiovascular diseases'' OP21- Development of new anti-bacterial agents

Carolina dos Santos Vina~:reiro (10+S) OP22- Synthesis of Anticancer Symmetric

Bis(N-alkylaniline)triruylmethanes via Friedel-Crafts-Catalyzed Reaction between

Secondary Anilines

Rafael Filine Teixeira Arbnez Goems (10+5} OP23- Identification oflnhibitors and Mechanisms

oflnhibition ofProtein Tyrosine Phosphatases -Potential Therapeutical Targets in Various

Pathological Disorders Knban-Jankowska Alicja (10+5) OP24- Anticancer activity and molecular signalling of potent chemotherapeutics- 2-methoxyestradiol and

fulvestrant in therapy of osteosarcoma Magdalena Gorska (111+5} OP25- Action of new porphyrin conjugates with

potential anti-malaria activity on membranes SofJa Ines Leal Dnarte (10+5} OP26- Self-assembled polymer-metal micelles: new

promising anticancer agentes Leonor de Sa No~:ueira Corte-Real (10+5}

PYCAAward (10+5)

IL5 - Moria Joiio Moreno (30 + 5) "Importance of passive processes in cholesterol

homeostasis- absorption at the intestine and distribution in the blood" Coffee Break + Poster Session

Walking Tour

(6)

OP19 • Candidacidal potential of licorice phenolic extract: emphasis on its mode of action

Natfllia Martins u Sofia Costa-Oliveira '·Jsabel C F R Ferreira 1 S6nia Sjlva 2' Mariana Heruiqyes 2 Corresponding Author: [email protected]

1 Mountain Research Centre (CIMO), ESA, Polytechnic Institute of Braganra, Campus de Santa Apol01tia, ]]72, 5301-855 Braganra. Portugal.

2CEB, Centre of Biological Engineering, UBRO-Laboratorio de Investigariio em Bioftlmes Rosdrio

0/iveira, University of Minho, 4710-057 Braga, Portugal.

3Departmenl of Microbiology, Faculty of Medicine, Porta University, Alameda Professor Hemani

Manteira, 4200-319 Porta, Portugal.

Medicinal plants bave gained a special attention in the last years, due to its renowned health benefits, such as antimicrobial effects [I]. In fact, several natural matrices bave been increasingly studied, namely for its antifungal activity against opportunistic fungi [2,3]. Candida species, although commensa! microorganisms, have caused severe organic dysfunctions to the host, once current antifungal agents have lost their recognized efficiency [2]. So, numerous studies have been carried out focusing the mechanisms of acquired drug-resistance by Candida species [<Hi]. However, apart from the discovery of an efficient multi-drug therapy (i.e. chemical drugs and also natural extracts combination), the discovery of the involved mechanisms of actions, morphological changes and related kinetic parameters are of major

importance. Glycyrrhiza glabra L. (licorice) hydromethanolic extract have evidenced promissory

candidacidal effects, and therefore, the involved mechanisms of action need to be clarified. Thus, in the present study these modes of action were assessed, by using flow cytometry.Overall, the licorice extract induced significant and irreversible primary damages on Candida cells, being membrane disruption and

consequent unviability one of the main targets. In fact, after membrane destabilization, cells lost their

proper homeostasis, their metabolic functions were blocked and, consequently cells lost functionality. The relevance and interest of the achieved results open new insights towards the upcorning use of the present phenolic matrix, being important to evaluate its in viva efficacy. Therefore, further studies are necessary to deepen knowledge on this field, aiming not only to establish therapeutic and prophylactic doses, but also to improve the clinical intervention in Candida infections.

References

[I] Sher, A., Gomal J. Med. Sci. 2009, 7, 72--78.

[2] Martins, N.; Ferreira, I. C. F. R; Barros, L.; Si!va, S.; Heruiques, M., Mycopathol2014, 177, 223-240. [3] Martins, N.; Barros, L.; I. C. F. R., Ind. Crops Prod. 2015, 74,648-670.

[4] Kanafani, Z. A.; Perfect, J. R, C!in. Infect. Dis.-Antirnicrob. Resist. 2008, 46, 120-128.

[5] Sang!ard, D.; Odds, F. C., Lancet Infect. Dis. 2002, 2, 73-85.

[6] White, T. C.; Holleman, S.; Dy, F.; Laurence, F.; Stevens, D. A.; Mirels, L. F., Antimicrob. Agents

Chemother. 2002, 46, 1704-1713.

Acknowledgments The authors acknowledge FCT (Portugal) for financial support to CIMO

(PEst-OE/AGUI0690/2014) and N. Martins grant (SFRHIBD/87658/2012).

54

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