In vitro investigation of Brazilian Cerrado plant extract activity against Plasmodium falciparum, Trypanosoma cruzi and T-brucei gambiense

被引:15
|
作者
Charneau, Sebastien [1 ]
de Mesquita, Mariana Laundry [2 ]
Dourado Bastos, Izabela Marques [3 ]
Santana, Jaime Martins [3 ]
de Paula, Jose Elias [4 ]
Grellier, Philippe [5 ]
Espindola, Laila Salmen [2 ]
机构
[1] Univ Brasilia, Inst Ciencias Biol, Dept Biol Celular, Lab Bioquim Quim & Prot, Campus Univ Darcy Ribeiro, BR-70910900 Brasilia, DF, Brazil
[2] Univ Brasilia, Fac Ciencias Saude, Lab Farmacognosia, Campus Univ Darcy Ribeiro, BR-70910900 Brasilia, DF, Brazil
[3] Univ Brasilia, Inst Ciencias Biol, Dept Biol Celular, Lab Interacao Patogenohospedeiro, Campus Univ Darcy Ribeiro, BR-70910900 Brasilia, DF, Brazil
[4] Univ Brasilia, Inst Ciencias Biol, Lab Anat Vegetal, Campus Univ Darcy Ribeiro, BR-70910900 Brasilia, DF, Brazil
[5] Museum Natl Hist Nat, UMR CNRS 7245, Mol Commun & Adaptat Microorganismes, CP52,61 Rue Buffon, F-75231 Paris 05, France
关键词
anti-protozoal activity; malaria; Chagas disease; sleeping sickness; Brazilian Cerrado; Connarus suberosus; MEDICINAL-PLANTS; NATURAL-PRODUCTS; ESSENTIAL OIL; ANTIMALARIAL; DISCOVERY; LEAVES;
D O I
10.1080/14786419.2015.1055264
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The threatened Brazilian Cerrado biome is an important biodiversity hotspot but still few explored that constitutes a potential reservoir of molecules to treat infectious diseases. We selected eight Cerrado plant species for screening against the erythrocytic stages of Plasmodium falciparum, human intracellular stages of Trypanosoma cruzi and bloodstream forms of T. brucei gambiense, and for their cytotoxicity upon the rat L6-myoblast cell line. Bioassays were performed with 37 hexane, ethyl acetate and ethanol extracts prepared from different plant organs. Activities against parasites were observed for 24 extracts: 9 with anti-P. falciparum, 4 with anti-T. cruzi and 11 with anti-T. brucei gambiense activities. High anti-protozoal activity (IC50 values<10g/mL) without obvious cytotoxicity to L6 cells was observed for eight extracts from plants: Connarus suberosus, Blepharocalyx salicifolius, Psidium laruotteanum and Myrsine guianensis. Overall, studies of plant extracts will contribute to increase the biodiversity knowledge essential for Cerrado conservation and sustainable development.
引用
收藏
页码:1320 / 1326
页数:7
相关论文
共 31 条
  • [1] Glutathione derivatives active against Trypanosoma brucei rhodesiense and T-brucei brucei in vitro
    Daunes, S
    D'Silva, C
    ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (02) : 434 - 437
  • [2] In vitro activity of diospyrin and derivatives against Leishmania donovani, Trypanosoma cruzi and Trypanosoma brucei brucei
    Yardley, V
    Snowdon, D
    Croft, S
    Hazra, B
    PHYTOTHERAPY RESEARCH, 1996, 10 (07) : 559 - 562
  • [3] In vitro Screening of Traditional South African Malaria Remedies against Trypanosoma brucei rhodesiense, Trypanosoma cruzi, Leishmania donovani, and Plasmodium falciparum
    Mokoka, Tsholofelo A.
    Zimmermann, Stefanie
    Julianti, Tasqiah
    Hata, Yoshie
    Moodley, Nivan
    Cal, Monica
    Adams, Michael
    Kaiser, Marcel
    Brun, Reto
    Koorbanally, Neil
    Hamburger, Matthias
    PLANTA MEDICA, 2011, 77 (14) : 1663 - 1667
  • [4] Novel Purine Chemotypes with Activity against Plasmodium falciparum and Trypanosoma cruzi
    Martinez-Peinado, Nieves
    Lorente-Macias, Alvaro
    Garcia-Salguero, Alejandro
    Cortes-Serra, Nuria
    Fenollar-Collado, Angel
    Ros-Lucas, Albert
    Gascon, Joaquim
    Pinazo, Maria-Jesus
    Molina, Ignacio J.
    Unciti-Broceta, Asier
    Diaz-Mochon, Juan J.
    de las Infantas y Villatoro, Maria J. Pineda
    Izquierdo, Luis
    Alonso-Padilla, Julio
    PHARMACEUTICALS, 2021, 14 (07)
  • [5] Synthesis and structure-activity relationships of parasiticidal thiosemicarbazone cysteine protease inhibitors against Plasmodium falciparum, Trypanosoma brucei, and Trypanosoma cruzi
    Greenbaum, DC
    Mackey, Z
    Hansell, E
    Doyle, P
    Gut, J
    Caffrey, CR
    Lehrman, J
    Rosenthal, PJ
    McKerrow, JH
    Chibale, K
    JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (12) : 3212 - 3219
  • [6] Activities of Pt(II) and Ru(III) triazole-pyrimidine complexes against Trypanosoma cruzi and T-brucei brucei
    Magán, R
    Marín, C
    Rosales, MJ
    Barrera, MA
    Salas, JM
    Sánchez-Moreno, M
    PHARMACOLOGY, 2004, 70 (02) : 83 - 90
  • [7] Synthesis and activity of azaterphenyl diamidines against Trypanosoma brucei rhodesiense and Plasmodium falciparum
    Hu, Laixing
    Arafa, Reem K.
    Ismail, Mohamed A.
    Patel, Alpa
    Munde, Manoj
    Wilson, W. David
    Wenzler, Tanja
    Brun, Reto
    Boykin, David W.
    BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (18) : 6651 - 6658
  • [8] Eugenol carbonate activity against Plasmodium falciparum, Leishmania braziliensis, and Trypanosoma cruzi
    Clemente, Camila M.
    Pineda, Tatiana
    Yepes, Lina M.
    Upegui, Yulieth
    Allemandi, Daniel A.
    Robledo, Sara M.
    Ravetti, Soledad
    ARCHIV DER PHARMAZIE, 2022, 355 (03)
  • [9] In vitro antitrypanosomal activity of plant terpenes against Trypanosoma brucei
    Otoguro, Kazuhiko
    Iwatsuki, Masato
    Ishiyama, Aki
    Namatame, Miyuki
    Nishihara-Tukashima, Aki
    Kiyohara, Hiroaki
    Hashimoto, Toshihiro
    Asakawa, Yoshinori
    Omura, Satoshi
    Yamada, Haruki
    PHYTOCHEMISTRY, 2011, 72 (16) : 2024 - 2030
  • [10] Chemical constituents from Waltheria indica exert in vitro activity against Trypanosoma brucei and T. cruzi
    Cretton, Sylvian
    Breant, Lise
    Pourrez, Lucie
    Ambuehl, Chiara
    Perozzo, Remo
    Marcourt, Laurence
    Kaiser, Marcel
    Cuendet, Muriel
    Christen, Philippe
    FITOTERAPIA, 2015, 105 : 55 - 60