Evaluation of Anti-Trypanosoma cruzi Activity of Chemical Constituents from Baccharis sphenophylla Isolated Using High-Performance Countercurrent Chromatography

被引:0
作者
Silva, Matheus L. [1 ]
Sales, Felipe S. [1 ]
Levatti, Erica V. C. [2 ]
Antar, Guilherme M. [3 ]
Tempone, Andre G. [2 ]
Lago, Joao Henrique G. [1 ]
Jerz, Gerold [4 ]
机构
[1] Fed Univ ABC, Ctr Nat Sci & Humanities, BR-09210580 Santo Andre, Brazil
[2] Butantan Inst, Lab Pathophysiol, BR-05508040 Sao Paulo, Brazil
[3] Univ Fed Espirito Santo, Dept Agr & Biol Sci, BR-29932540 Sao Mateus, Brazil
[4] Tech Univ Carolo Wilhelmina Braunschweig, Inst Food Chem, D-38106 Braunschweig, Germany
来源
MOLECULES | 2024年 / 29卷 / 01期
基金
巴西圣保罗研究基金会;
关键词
Baccharis sphenophylla; Asteraceae; diterpenes; flavonoids; Trypanosoma cruzi; high-performance countercurrent chromatography; CHAGAS-DISEASE; DERIVATIVES;
D O I
10.3390/molecules29010212
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endemic in 21 countries, Chagas disease, also known as American Trypanosomiasis, is a neglected tropical disease (NTD) caused by the protozoan parasite Trypanosoma cruzi. The available drugs for the treatment of this disease, benznidazole and nifurtimox, are outdated and display severe side effects. Thus, the discovery of new drugs is crucial. Based on our continuous studies aiming towards the discovery of natural products with anti-T. cruzi potential, the MeOH extract from aerial parts of Baccharis sphenophylla Dus & eacute;n ex. Malme (Asteraceae) displayed activity against this parasite and was subjected to high-performance countercurrent chromatography (HPCCC), to obtain one unreported syn-labdane diterpene - sphenophyllol (1) - as well as the known compounds gaudichaudol C (2), ent-kaurenoic acid (3), hispidulin (4), eupafolin (5), and one mixture of di-O-caffeoylquinic acids (6-8). Compounds 1-8 were characterized by analysis of nuclear magnetic resonance (NMR) and mass spectrometry (MS) data. When tested against trypomastigote forms, isolated labdane diterpenes 1 and 2 displayed potent activity, with EC50 values of 20.1 mu M and 2.9 mu M, respectively. The mixture of chlorogenic acids 6-8, as well as the isolated flavones 4 and 5, showed significant activity against the clinically relevant amastigotes, with EC50 values of 24.9, 12.8, and 2.7 mu M, respectively. Nonetheless, tested compounds 1-8 displayed no cytotoxicity against mammalian cells (CC50 > 200 mu M). These results demonstrate the application of HPCCC as an important tool to isolate bioactive compounds from natural sources, including the antitrypanosomal extract from B. sphenophylla, allowing for the development of novel strategic molecular prototypes against tropical neglected diseases.
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页数:13
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共 40 条
  • [1] Population movements, borders, and Chagas disease
    Avaria, Andrea
    Ventura-Garcia, Laia
    Sanmartino, Mariana
    Van der Laat, Carlos
    [J]. MEMORIAS DO INSTITUTO OSWALDO CRUZ, 2022, 117
  • [2] Chagas Disease in the United States: a Public Health Approach
    Bern, Caryn
    Messenger, Louisa A.
    Whitman, Jeffrey D.
    Maguire, James H.
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2020, 33 (01)
  • [3] Phytochemical Study and Evaluation of the Cytotoxic Properties of Methanolic Extract from Baccharis obtusifolia
    Carlos Romero-Benavides, Juan
    Ortega-Torres, Gina C.
    Villacis, Javier
    Vivanco-Jaramillo, Sara L.
    Galarza-Urgiles, Karla I.
    Bailon-Moscoso, Natalia
    [J]. INTERNATIONAL JOURNAL OF MEDICINAL CHEMISTRY, 2018, 2018
  • [4] Total Synthesis of Hispidulin and the Structural Basis for Its Inhibition of Proto-oncogene Kinase Pim-1
    Chao, Shi-Wei
    Su, Ming-Yuan
    Chiou, Lih-Chu
    Chen, Liang-Chieh
    Chang, Chung-I
    Huang, Wei-Jan
    [J]. JOURNAL OF NATURAL PRODUCTS, 2015, 78 (08): : 1969 - 1976
  • [5] Chagas disease research and development: Is there light at the end of the tunnel?
    Chatelain, Eric
    [J]. COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL, 2017, 15 : 98 - 103
  • [6] Counter-current chromatography: Simple process and confusing terminology
    Conway, Walter D.
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2011, 1218 (36) : 6015 - 6023
  • [7] A modular approach for facile biosynthesis of labdane-related diterpenes
    Cyr, Anthony
    Wilderman, P. Ross
    Determan, Mara
    Peters, Reuben J.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (21) : 6684 - +
  • [8] Ent-kaurane diterpenes isolated from n-hexane extract of Baccharis sphenophylla by bioactivity-guided fractionation target the acidocalcisomes in Trypanosoma cruzi
    da Costa-Silva, Thais A.
    Silva, Matheus L.
    Antar, Guilherme M.
    Tempone, Andre G.
    Lago, Joao Henrique G.
    [J]. PHYTOMEDICINE, 2021, 93
  • [9] CLERODANE DITERPENOIDS FROM BACCHARIS-ARTICULATA
    DAI, J
    SUTTISRI, R
    BORDAS, E
    SOEJARTO, DD
    KINGHORN, AD
    [J]. PHYTOCHEMISTRY, 1993, 34 (04) : 1087 - 1090
  • [10] Chagas Disease: From Discovery to a Worldwide Health Problem
    Freitas Lidani, Karita Claudia
    Andrade, Fabiana Antunes
    Bavia, Lorena
    Damasceno, Flavia Silva
    Beltrame, Marcia Holsbach
    Messias-Reason, Iara J.
    Sandri, Thaisa Lucas
    [J]. FRONTIERS IN PUBLIC HEALTH, 2019, 7