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Determination of chemical structure and anti-Trypanosoma cruzi activity of extracts from the roots of Lonchocarpus cultratus (Vell.) A.M.G. Azevedo & H.C. Lima
Authors:Aline Antunes Maciel Bortoluzzi  Izabela Virginia Staffen  Fernanda Weyand Banhuk  Aline Griebler  Patricia Karoline Matos  Thaís Soprani Ayala  Edson Antonio Alves da Silva  Maria Helena Sarragiotto  Ivânia Teresinha Albrecht Schuquel  Tereza Cristina Marinho Jorge  Rafael Andrade Menolli
Institution:1. Center of Medical and Pharmaceutical Sciences, Western Parana State University (UNIOESTE), 2069 Universitaria St., Cascavel, PR, Brazil;2. Center of Exact Sciences and Technology, Western Parana State University (UNIOESTE), 2069 Universitaria St., Cascavel, PR, Brazil;3. Center of Exact Sciences, Department of Chemistry, State University of Maringa (UEM), 5790 Colombo Av., Maringa, PR, Brazil
Abstract:Trypanosoma cruzi is the agent of Chagas disease, an infection that affects around 8 million people worldwide. The search for new anti-T. cruzi drugs are relevant, mainly because the treatment of this disease is limited to two drugs. The objective of this study was to investigate the trypanocidal and cytotoxic activity and elucidate the chemical profile of extracts from the roots of the Lonchocarpus cultratus. Roots from L. cultratus were submitted to successive extractions with hexane, dichloromethane, and methanol, resulting in LCH, LCD, and LCM extracts, respectively. Characterization of extracts was done using 1H-RMN, 13C-RMN, CC and TLC. Treatment of T. cruzi forms (epimastigotes, trypomastigotes, and amastigotes) with crescent concentrations of LCH, LCD, and LCM was done for 72, 48, and 48 h, respectively. After this, the percentage of inhibition and IC50/LC50 were calculated. Benznidazole was used as a positive control. Murine macrophages were treated with different concentrations of both extracts for 48 h, and after, the cellular viability was determined by the MTT method and CC50 was calculated. The chalcones derricin and lonchocarpine were identified in the hexane extract, and for the first time in the genus Lonchocarpus, the presence of a dihydrolonchocarpine derivative was observed. Other chalcones such as isocordoin and erioschalcone B were detected in the dichloromethane extract. The dichloromethane extract showed higher activity against all tested forms of T. cruzi than the other two extracts, with IC50 values of 10.98, 2.42, and 0.83 µg/mL, respectively; these values are very close to those of benznidazole. Although the dichloromethane extract presented a cytotoxic effect against mammalian cells, it showed selectivity against amastigotes. The methanolic extract showed the lowest anti-T. cruzi activity but was non-toxic to peritoneal murine macrophages. Thus, the genus Lonchocarpus had demonstrated in the past action against epimastigotes forms of T. cruzi but is the first time that the activity against infective forms is showed, which leading to further studies with in vivo tests.
Keywords:Chalcones  Chagas disease  Trypanosomiasis  Plant extract  ANOVA"}  {"#name":"keyword"  "$":{"id":"k0035"}  "$$":[{"#name":"text"  "_":"Analysis of Variance  BZN"}  {"#name":"keyword"  "$":{"id":"k0045"}  "$$":[{"#name":"text"  "_":"Benznidazole  CC"}  {"#name":"keyword"  "$":{"id":"k0055"}  "$$":[{"#name":"text"  "_":"column chromatography  Cytotoxic Concentration 50%  Deuterate chloroform  Carbon dioxide  DC"}  {"#name":"keyword"  "$":{"id":"k0095"}  "$$":[{"#name":"text"  "_":"DMSO Control  DMSO"}  {"#name":"keyword"  "$":{"id":"k0105"}  "$$":[{"#name":"text"  "_":"Dimethyl Sulfoxide  FBS"}  {"#name":"keyword"  "$":{"id":"k0115"}  "$$":[{"#name":"text"  "_":"Fetal Bovine Serum  Inhibitory Concentration 50%  Lafepe"}  {"#name":"keyword"  "$":{"id":"k0135"}  "$$":[{"#name":"text"  "_":"Pharmaceutical Laboratory of Pernambuco State  LC-1"}  {"#name":"keyword"  "$":{"id":"k0145"}  "$$":[{"#name":"text"  "_":"2 and 3: Fractions obtained from LCH extract  LC-4 and 5"}  {"#name":"keyword"  "$":{"id":"k0155"}  "$$":[{"#name":"text"  "_":"fractions obtained from LCD extract  Lethal Concentration 50%  LCD"}  {"#name":"keyword"  "$":{"id":"k0175"}  "$$":[{"#name":"text"  "$$":[{"#name":"__text__"  "_":"Extract from "}  {"#name":"italic"  "_":"L  cultratus"}  {"#name":"__text__"  "_":" obtained by extraction with dichloromethane  LCH"}  {"#name":"keyword"  "$":{"id":"k0185"}  "$$":[{"#name":"text"  "$$":[{"#name":"__text__"  "_":"Extract from "}  {"#name":"italic"  "_":"L  cultratus"}  {"#name":"__text__"  "_":" obtained by extraction with hexane  LCM"}  {"#name":"keyword"  "$":{"id":"k0195"}  "$$":[{"#name":"text"  "$$":[{"#name":"__text__"  "_":"Extract from "}  {"#name":"italic"  "_":"L  cultratus"}  {"#name":"__text__"  "_":" obtained by extraction with methanol  LIT"}  {"#name":"keyword"  "$":{"id":"k0205"}  "$$":[{"#name":"text"  "_":"Liver Infusion Tryptose  MTT"}  {"#name":"keyword"  "$":{"id":"k0215"}  "$$":[{"#name":"text"  "_":"3-(4  5-dimethylthiazol-2-yl)-2  5-diphenyltetrazolium bromide  NMR"}  {"#name":"keyword"  "$":{"id":"k0225"}  "$$":[{"#name":"text"  "_":"Nuclear Magnetic Resonance  NO"}  {"#name":"keyword"  "$":{"id":"k0235"}  "$$":[{"#name":"text"  "_":"Nitric Oxide  PBS"}  {"#name":"keyword"  "$":{"id":"k0245"}  "$$":[{"#name":"text"  "_":"Phosphate-Buffered Saline  RPMI"}  {"#name":"keyword"  "$":{"id":"k0255"}  "$$":[{"#name":"text"  "_":"Roswell Park Memorial Institute  SI"}  {"#name":"keyword"  "$":{"id":"k0265"}  "$$":[{"#name":"text"  "_":"Selectivity Index  TLC"}  {"#name":"keyword"  "$":{"id":"k0275"}  "$$":[{"#name":"text"  "_":"Thin Layer column  TMS"}  {"#name":"keyword"  "$":{"id":"k0285"}  "$$":[{"#name":"text"  "_":"Tetramethylsilane  UC"}  {"#name":"keyword"  "$":{"id":"k0295"}  "$$":[{"#name":"text"  "_":"Untreated Control  UEM"}  {"#name":"keyword"  "$":{"id":"k0305"}  "$$":[{"#name":"text"  "_":"State University of Maringa/PR
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