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1.
Front Cell Infect Microbiol ; 12: 926699, 2022.
Article in English | MEDLINE | ID: mdl-35967878

ABSTRACT

Chagas disease (CD) affects at least 6 million people in 21 South American countries besides several thousand in other nations all over the world. It is estimated that at least 14,000 people die every year of CD. Since vaccines are not available, chemotherapy remains of pivotal relevance. About 30% of the treated patients cannot complete the therapy because of severe adverse reactions. Thus, the search for novel drugs is required. Here we tested the benznidazole (BZ) combination with the repositioned drug disulfiram (DSF) and its derivative diethyldithiocarbamate (DETC) upon Trypanosoma cruzi in vitro and in vivo. DETC-BZ combination was synergistic diminishing epimastigote proliferation and enhancing selective indexes up to over 10-fold. DETC was effective upon amastigotes of the BZ- partially resistant Y and the BZ-resistant Colombiana strains. The combination reduced proliferation even using low concentrations (e.g., 2.5 µM). Scanning electron microscopy revealed membrane discontinuities and cell body volume reduction. Transmission electron microscopy revealed remarkable enlargement of endoplasmic reticulum cisternae besides, dilated mitochondria with decreased electron density and disorganized kinetoplast DNA. At advanced stages, the cytoplasm vacuolation apparently impaired compartmentation. The fluorescent probe H2-DCFDA indicates the increased production of reactive oxygen species associated with enhanced lipid peroxidation in parasites incubated with DETC. The biochemical measurement indicates the downmodulation of thiol expression. DETC inhibited superoxide dismutase activity on parasites was more pronounced than in infected mice. In order to approach the DETC effects on intracellular infection, peritoneal macrophages were infected with Colombiana trypomastigotes. DETC addition diminished parasite numbers and the DETC-BZ combination was effective, despite the low concentrations used. In the murine infection, the combination significantly enhanced animal survival, decreasing parasitemia over BZ. Histopathology revealed that low doses of BZ-treated animals presented myocardial amastigote, not observed in combination-treated animals. The picrosirius collagen staining showed reduced myocardial fibrosis. Aminotransferase de aspartate, Aminotransferase de alanine, Creatine kinase, and urea plasma levels demonstrated that the combination was non-toxic. As DSF and DETC can reduce the toxicity of other drugs and resistance phenotypes, such a combination may be safe and effective.


Subject(s)
Chagas Disease , Trypanocidal Agents , Animals , Chagas Disease/parasitology , Disulfiram/pharmacology , Disulfiram/therapeutic use , Drug Resistance , Humans , Mice , Nitroimidazoles , Transaminases/therapeutic use , Trypanocidal Agents/pharmacology
2.
Molecules ; 26(11)2021 Jun 02.
Article in English | MEDLINE | ID: mdl-34199336

ABSTRACT

The natural compound ravenelin was isolated from the biomass extracts of Exserohilum rostratum fungus, and its antimicrobial, antiplasmodial, and trypanocidal activities were evaluated. Ravenelin was isolated by column chromatography and HPLC and identified by NMR and MS. The susceptibility of Gram-positive and Gram-negative bacteria strains to ravenelin was determined by microbroth dilution assay. Cytotoxicity was evaluated in hepatocarcinoma cells (HepG2) and BALB/c peritoneal macrophages by using MTT. SYBR Green I-based assay was used in the asexual stages of Plasmodium falciparum. Trypanocidal activity was tested against the epimastigote and intracellular amastigote forms of Trypanosoma cruzi. Ravenelin was active against Gram-positive bacteria strains, with emphasis on Bacillus subtilis (MIC value of 7.5 µM). Ravenelin's antiparasitic activities were assessed against both the epimastigote (IC50 value of 5 ± 1 µM) and the intracellular amastigote forms of T. cruzi (IC50 value of 9 ± 2 µM), as well as against P. falciparum (IC50 value of 3.4 ± 0.4 µM). Ravenelin showed low cytotoxic effects on both HepG2 (CC50 > 50 µM) and peritoneal macrophage (CC50 = 185 ± 1 µM) cells with attractive selectivity for the parasites (SI values > 15). These findings indicate that ravenelin is a natural compound with both antibacterial and antiparasitic activities, and considerable selectivity indexes. Therefore, ravenelin is an attractive candidate for hit-to-lead development.


Subject(s)
Anti-Bacterial Agents/pharmacology , Antiprotozoal Agents/pharmacology , Ascomycota/chemistry , Macrophages, Peritoneal/cytology , Xanthones/pharmacology , Animals , Anti-Bacterial Agents/chemistry , Antiprotozoal Agents/chemistry , Biological Products/chemistry , Biological Products/pharmacology , Biomass , Cell Proliferation/drug effects , Cell Survival/drug effects , Cells, Cultured , Chromatography, High Pressure Liquid , Gram-Negative Bacteria/drug effects , Gram-Positive Bacteria/drug effects , Hep G2 Cells , Humans , Macrophages, Peritoneal/drug effects , Macrophages, Peritoneal/parasitology , Magnetic Resonance Spectroscopy , Mice , Mice, Inbred BALB C , Microbial Sensitivity Tests , Molecular Structure , Plasmodium falciparum/drug effects , Trypanosoma cruzi/drug effects , Xanthones/chemistry
3.
Article in English | MEDLINE | ID: mdl-33688364

ABSTRACT

Syzygium aromaticum has a diversity of biological activities due to the chemical compounds found in its plant products such as total phenolic compounds and flavonoids. The present work describes the chemical analysis and antimicrobial, antioxidant, and antitrypanosomal activity of the essential oil of S. aromaticum. Eugenol (53.23%) as the major compound was verified by gas chromatography-mass spectrometry. S. aromaticum essential oil was more effective against S. aureus (MIC 50 µg/mL) than eugenol (MIC 250 µg/mL). Eugenol presented higher antioxidant activity than S. aromaticum essential oil, with an EC50 of 12.66 and 78.98 µg/mL, respectively. S. aromaticum essential oil and eugenol exhibited Trypanosoma cruzi inhibitory activity, with IC50 of 28.68 ± 1.073 and 31.97 ± 1.061 µg/mL against epimastigotes and IC50 of 64.51 ± 1.658 and 45.73 ± 1.252 µg/mL against intracellular amastigotes, respectively. Both compounds presented low cytotoxicity, with S. aromaticum essential oil displaying 15.5-fold greater selectivity for the parasite than the cells. Nitrite levels in T. cruzi-stimulated cells were reduced by essential oil (47.01%; p = 0.002) and eugenol (48.05%; p = 0.003) treatment. The trypanocidal activity of S. aromaticum essential oil showed that it is reasonable to use it in future research in the search for new therapeutic alternatives for trypanosomiasis.

4.
Antibiotics (Basel) ; 10(1)2020 Dec 30.
Article in English | MEDLINE | ID: mdl-33396612

ABSTRACT

Aniba rosaeodora is one of the most widely used plants in the perfumery industry, being used as medicinal plant in the Brazilian Amazon. This work aimed to evaluate the chemical composition of A. rosaeodora essential oil and its biological activities. A. rosaeodora essential oil presented linalool (93.60%) as its major compound. The A. rosaeodora essential oil and linalool showed activity against all the bacteria strains tested, standard strains and marine environment bacteria, with the lower minimum inhibitory concentration being observed for S. aureus. An efficient antioxidant activity of A. rosaeodora essential oil and linalool (EC50: 15.46 and 6.78 µg/mL, respectively) was evidenced by the inhibition of the 2,2-azinobis- (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical. The antitrypanosomal activity of A. rosaeodora essential oil and linalool was observed at high concentrations against epimatigote forms (inhibitory concentration for 50% of parasites (IC50): 150.5 ± 1.08 and 198.6 ± 1.12 µg/mL, respectively), and even higher against intracellular amastigotes of T. cruzi (IC50: 911.6 ± 1.15 and 249.6 ± 1.18 µg/mL, respectively). Both A. rosaeodora essential oil and linalool did not exhibit a cytotoxic effect in BALB/c peritoneal macrophages, and both reduced nitrite levels in unstimulated cells revealing a potential effect in NO production. These data revealed the pharmacological potential of A. rosaeodora essential oil and linalool, encouraging further studies.

5.
São Paulo; Aderaldo & Rothschild; 2008. 149 p. ilus, tab.
Monography in Portuguese | LILACS | ID: lil-558206

ABSTRACT

Descreve o processo de implementação do Programa Juventude Cidadã no município de Osasco. Caracteristicas do programa, dos jovens atendidos. São apresentados os referenciais teóricos e metodológicos da pesquisa avaliativa. Apresentação do processo investigativo no que diz respeito às percepções dos jovens, tais como puderam sera apreendidas pelos pesquisadores. Discussão da lógica da centralidade versus centralidades. O resultado apresentado além de evidenciar a natureza desses processos segundo o referencial explicitado, convida à refelxão sobre a própria natureza dos programas voltados para a juventude e sobre a visão que parecem portar a respeito dos jovens. A gestão do programa é avaliada na perspectiva de avaliação da efetividade.


Subject(s)
Humans , Male , Female , Adolescent , Employment , Evaluation Study , Health Policy , Public Policy , Qualitative Research , Work
6.
São Paulo; Aderaldo & Rothschild; 2008. 149 p. ilus, tab, ilus, tab.
Monography in Portuguese | CidSaúde - Healthy cities | ID: cid-61520

ABSTRACT

Descreve o processo de implementação do Programa Juventude Cidadã no município de Osasco. Caracteristicas do programa, dos jovens atendidos. São apresentados os referenciais teóricos e metodológicos da pesquisa avaliativa. Apresentação do processo investigativo no que diz respeito às percepções dos jovens, tais como puderam sera apreendidas pelos pesquisadores. Discussão da lógica da centralidade versus centralidades. O resultado apresentado além de evidenciar a natureza desses processos segundo o referencial explicitado, convida à refelxão sobre a própria natureza dos programas voltados para a juventude e sobre a visão que parecem portar a respeito dos jovens. A gestão do programa é avaliada na perspectiva de avaliação da efetividade


Subject(s)
Humans , Male , Female , Adolescent , Health Policy , Public Policy , Qualitative Research , Work , Employment , Evaluation Study
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