PMID- 20645716 OWN - NLM STAT- MEDLINE DCOM- 20101130 LR - 20100721 IS - 1744-5116 (Electronic) IS - 1388-0209 (Linking) VI - 48 IP - 4 DP - 2010 Apr TI - Antifungal activity of extracts of some plants used in Brazilian traditional medicine against the pathogenic fungus Paracoccidioides brasiliensis. PG - 388-96 LID - 10.3109/13880200903150385 [doi] AB - Paracoccidioidomycosis (PCM) is a systemic granulomatous disease caused by Paracoccidioides brasiliensis Almeida (Onygenales) that requires 1-2 years of treatment. In the absence of drug therapy, the disease is usually fatal, highlighting the need for the identification of safer, novel, and more effective antifungal compounds. With this need in mind, several plants employed in Brazilian traditional medicine were assayed on P. brasiliensis and murine macrophages. Extracts were prepared from 10 plant species: Inga spp. Mill. (Leguminosae), Schinus terebinthifolius Raddi (Anacardiaceae), Punica granatum L. (Punicaceae), Alternanthera brasiliana Kuntze (Amaranthaceae), Piper regnellii CDC. (Piperaceae), P. abutiloides Kunth (Piperaceae), Herissantia crispa L. Briz. (Malvaceae), Rubus urticaefolius Poir (Rosaceae), Rumex acetosa L. (Polygonaceae), and Baccharis dracunculifolia DC. (Asteraceae). Hexane fractions from hydroalcoholic extracts of Piper regnellii and Baccharis dracunculifolia were the most active against the fungus, displaying minimum inhibitory concentration (MIC) values of 7.8 microg/mL and 7.8-30 mug/mL, respectively. Additionally, neither of the extracts exhibited any apparent cytotoxic effects on murine macrophages at 20 microg/mL. Analyses of these fractions using gas chromatography-mass spectrometry (GC-MS) showed that the major components of B. dracunculifolia were ethyl hydrocinnamate (14.35%) and spathulenol (16.02%), while the major components of the hexane fraction of Piper regnellii were 1-methoxy-4-(1-propenyl) benzene (21.94%) and apiol (21.29%). The activities of these fractions against P. brasiliensis without evidence of cytotoxicity to macrophages justify their investigation as a potential source of new chemical agents for the treatment of PCM. FAU - Johann, Susana AU - Johann S AD - Laboratorio de Quimica dos Produtos Naturais, Centro de Pesquisas Rene Rachou, Fiocruz, Belo Horizonte, MG, Brazil. sjohann@cpqrr.fiocruz.br FAU - Cisalpino, Patricia Silva AU - Cisalpino PS FAU - Watanabe, Gisele Almeida AU - Watanabe GA FAU - Cota, Betania Barros AU - Cota BB FAU - de Siqueira, Ezequias Pessoa AU - de Siqueira EP FAU - Pizzolatti, Moacir Geraldo AU - Pizzolatti MG FAU - Zani, Carlos Leomar AU - Zani CL FAU - de Resende, Maria Aparecida AU - de Resende MA LA - eng PT - Journal Article PL - England TA - Pharm Biol JT - Pharmaceutical biology JID - 9812552 RN - 0 (Antifungal Agents) RN - 0 (Plant Extracts) SB - IM MH - Animals MH - *Antifungal Agents/adverse effects/isolation & purification/pharmacology MH - Brazil MH - Cell Survival/drug effects MH - Cells, Cultured MH - Macrophages/drug effects MH - Medicine, Traditional/*methods MH - Mice MH - Microbial Sensitivity Tests MH - Paracoccidioides/*drug effects/growth & development MH - *Plant Extracts/adverse effects/isolation & purification/pharmacology MH - Plants, Medicinal/*chemistry EDAT- 2010/07/22 06:00 MHDA- 2010/12/14 06:00 CRDT- 2010/07/22 06:00 PHST- 2010/07/22 06:00 [entrez] PHST- 2010/07/22 06:00 [pubmed] PHST- 2010/12/14 06:00 [medline] AID - 10.3109/13880200903150385 [doi] PST - ppublish SO - Pharm Biol. 2010 Apr;48(4):388-96. doi: 10.3109/13880200903150385.