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1.
Article in English | MEDLINE | ID: mdl-29888213

ABSTRACT

Chagas disease is a neglected tropical disease endemic to Latin America, though migratory movements have recently spread it to other regions. Here, we have applied a cascade virtual screening campaign combining ligand- and structure-based methods. In order to find novel inhibitors of putrescine uptake in Trypanosoma cruzi, an ensemble of linear ligand-based classifiers obtained by has been applied as initial screening filter, followed by docking into a homology model of the putrescine permease TcPAT12. 1,000 individual linear classifiers were inferred from a balanced dataset. Subsequently, different schemes were tested to combine the individual classifiers: MIN operator, average ranking, average score, average voting, with MIN operator leading to the best performance. The homology model was based on the arginine/agmatine antiporter (AdiC) from Escherichia coli as template. It showed 64% coverage of the entire query sequence and it was selected based on the normalized Discrete Optimized Protein Energy parameter and the GA341 score. The modeled structure had 96% in the allowed area of Ramachandran's plot, and none of the residues located in non-allowed regions were involved in the active site of the transporter. Positivity Predictive Value surfaces were applied to optimize the score thresholds to be used in the ligand-based virtual screening step: for that purpose Positivity Predictive Value was charted as a function of putative yields of active in the range 0.001-0.010 and the Se/Sp ratio. With a focus on drug repositioning opportunities, DrugBank and Sweetlead databases were subjected to screening. Among 8 hits, cinnarizine, a drug frequently prescribed for motion sickness and balance disorder, was tested against T. cruzi epimastigotes and amastigotes, confirming its trypanocidal effects and its inhibitory effects on putrescine uptake. Furthermore, clofazimine, an antibiotic with already proven trypanocidal effects, also displayed inhibitory effects on putrescine uptake. Two other hits, meclizine and butoconazole, also displayed trypanocidal effects (in the case of meclizine, against both epimastigotes and amastigotes), without inhibiting putrescine uptake.


Subject(s)
Biological Transport/drug effects , Putrescine/metabolism , Trypanocidal Agents/antagonists & inhibitors , Trypanocidal Agents/chemistry , Trypanocidal Agents/isolation & purification , Chagas Disease/diet therapy , Cinnarizine/antagonists & inhibitors , Clofazimine/antagonists & inhibitors , Drug Evaluation, Preclinical/methods , Drug Repositioning , Imidazoles/antagonists & inhibitors , Meclizine/antagonists & inhibitors , Membrane Transport Proteins , Molecular Docking Simulation , Molecular Dynamics Simulation , Trypanosoma cruzi/drug effects , Trypanosoma cruzi/metabolism
2.
Exp Parasitol ; 171: 23-32, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27729250

ABSTRACT

Benznidazole is the first-line drug used in treating Chagas disease, which is caused by the parasite Trypanosoma cruzi (T. cruzi). However, benznidazole has limited efficacy and several adverse reactions. Pentamidine is an antiprotozoal drug used in the treatment of leishmaniasis and African trypanosomiasis. In T. cruzi, pentamidine blocks the transport of putrescine, a precursor of trypanothione, which constitutes an essential molecule in the resistance of T. cruzi to benznidazole. In the present study, we describe the effect of the combination of benznidazole and pentamidine on isolated parasites, mammalian cells and in mice infected with T. cruzi. In isolated trypomastigotes, we performed a dose-matrix scheme of combinations, where pentamidine antagonized the effect of benznidazole, mainly at concentrations below the EC50 of pentamidine. In T. cruzi-infected mammalian cells, pentamidine reversed the effect of benznidazole (measured by qPCR). In comparison, in infected BALB/c mice, pentamidine failed to get synergy with benznidazole, measured on mice survival, parasitemia and amastigote nest quantification. To further explain the in vitro antagonism, we explored whether pentamidine affects intracellular trypanothione levels, however, pentamidine produced no change in trypanothione concentrations. Finally, the T. cruzi polyamine permease (TcPAT12) was overexpressed in epimastigotes, showing that pentamidine has the same trypanocidal effect, independently of transporter expression levels. These results suggest that, in spite of the high potency in the putrescine transport blockade, TcPAT12 permease is not the main target of pentamidine, and could explain the lack of synergism between pentamidine and benznidazole.


Subject(s)
Chagas Disease/drug therapy , Nitroimidazoles/antagonists & inhibitors , Pentamidine/pharmacology , Trypanocidal Agents/pharmacology , Trypanosoma cruzi/drug effects , Animals , Chagas Disease/pathology , Chlorocebus aethiops , DNA, Protozoan/analysis , DNA, Protozoan/isolation & purification , Dose-Response Relationship, Drug , Glutathione/analogs & derivatives , Glutathione/drug effects , Glutathione/metabolism , Macrophages/parasitology , Male , Mice , Mice, Inbred BALB C , Myocardium/pathology , Parasitemia/drug therapy , Parasitemia/parasitology , Putrescine/metabolism , Random Allocation , Spermidine/analogs & derivatives , Spermidine/metabolism , Thymidine/metabolism , Trypanocidal Agents/antagonists & inhibitors , Vero Cells
3.
Toxicol In Vitro ; 27(7): 2094-104, 2013 Oct.
Article in English | MEDLINE | ID: mdl-23933437

ABSTRACT

Novel ß-lapachone analogs 2-phenyl-3,4-dihydro-2H-benzo[h]chromene-5,6-dione (NQ1), 2-p-tolyl-3,4-dihydro-2H-benzo[h]chromene-5,6-dione (NQ3) and 2-methyl-2-phenyl-3,4-dihydro-2H-benzo[h]chromene-5,6-dione (NQ7), which have trypanocidal activity, were assayed for cytotoxic effects on murine EL-4 T lymphoma cells. The NQs inhibited the proliferation of EL-4 cells at concentrations above 1µM. Nuclear staining of the EL-4 cells revealed chromatin condensation and a nuclear morphology compatible with the induction of apoptosis. Flow cytometry assays with annexin V-FITC and propidium iodide confirmed the cell death by apoptosis. Using electron paramagnetic resonance (EPR), a semiquinone radical was detected in EL-4 cells treated with NQs. In addition, a decrease in the GSH level in parallel with reactive oxygen species (ROS) production was observed. Preincubation with n-acetyl-l-cysteine (NAC) was able to reverse the inhibitory effects of the NQs on cell proliferation, indicating that ROS generation is involved in NQ-induced apoptosis. In addition, the NQs induced a decrease in the mitochondrial membrane potential and increased the proteolytic activation of caspases 9 and 3 and the cleavage of Poly (ADP-Ribose) Polymerase (PARP). In conclusion, these results indicate that redox cycling is induced by the NQs in the EL-4 cell line, with the generation of ROS and other free radicals that could inhibit cellular proliferation as a result of the induction of the intrinsic apoptosis pathway.


Subject(s)
Antineoplastic Agents/pharmacology , Apoptosis/drug effects , Lymphoma, T-Cell/drug therapy , Naphthoquinones/pharmacology , Reactive Oxygen Species/metabolism , Up-Regulation/drug effects , Acetylcysteine/pharmacology , Animals , Antineoplastic Agents/antagonists & inhibitors , Benzopyrans/antagonists & inhibitors , Benzopyrans/pharmacology , Benzoquinones/metabolism , Cell Line, Tumor , Cell Nucleus Shape/drug effects , Cell Proliferation/drug effects , Cell Survival/drug effects , Chromatin Assembly and Disassembly/drug effects , Free Radical Scavengers/pharmacology , Glutathione/antagonists & inhibitors , Glutathione/metabolism , Kinetics , Lymphoma, T-Cell/metabolism , Lymphoma, T-Cell/pathology , Membrane Potential, Mitochondrial/drug effects , Mice , Naphthoquinones/antagonists & inhibitors , Reactive Oxygen Species/antagonists & inhibitors , Trypanocidal Agents/antagonists & inhibitors , Trypanocidal Agents/pharmacology
4.
Infect Immun ; 67(6): 2810-4, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10338485

ABSTRACT

Trypanosoma cruzi replicates in nucleated cells and is susceptible to being killed by gamma interferon-activated macrophages through a mechanism dependent upon NO biosynthesis. In the present study, the role of platelet-activating factor (PAF) in the induction of NO synthesis and in the activation of the trypanocidal activity of macrophages was investigated. In vitro, PAF induced NO secretion by T. cruzi-infected macrophages and the secreted NO inhibited intracellular parasite growth. The addition of a PAF antagonist, WEB 2170, inhibited both NO biosynthesis and trypanocidal activity. The inducible NO synthase/L-arginine pathway mediated trypanocidal activity, since it was inhibited by treatment with L-N-monomethyl arginine (L-NMMA), an L-arginine analog. PAF-mediated NO production in infected macrophages appears to be dependent on tumor necrosis alpha (TNF-alpha) production, since the addition of a neutralizing anti-TNF-alpha monoclonal antibody mAb inhibited NO synthesis. To test the role of PAF in mediating resistance or susceptibility to T. cruzi infection, infected mice were treated with WEB 2170, a PAF antagonist. These animals had higher parasitemia and earlier mortality than did vehicle-treated mice. Taken together, our results suggest that PAF belongs to a group of mediators that coordinate the mechanisms of resistance to infections with intracellular parasites.


Subject(s)
Macrophages/immunology , Nitric Oxide/biosynthesis , Platelet Activating Factor/immunology , Receptors, Cell Surface , Receptors, G-Protein-Coupled , Trypanocidal Agents/immunology , Trypanosoma cruzi/immunology , Animals , Cell Line , Cells, Cultured , Chagas Disease/immunology , Disease Models, Animal , Female , Immunity, Innate/immunology , Macaca mulatta , Macrophages/cytology , Macrophages/drug effects , Macrophages/parasitology , Mice , Mice, Inbred BALB C , Mice, Inbred C3H , Parasitemia , Platelet Activating Factor/antagonists & inhibitors , Platelet Activating Factor/pharmacology , Platelet Membrane Glycoproteins/immunology , Trypanocidal Agents/antagonists & inhibitors , Trypanocidal Agents/pharmacology , Trypanosoma cruzi/growth & development
5.
Proc Natl Acad Sci U S A ; 92(22): 10262-6, 1995 Oct 24.
Article in English | MEDLINE | ID: mdl-7479764

ABSTRACT

Trypanosomes are protozoan parasites of medical and veterinary importance. Trypanosoma brucei rhodesiense and Trypanosoma brucei gambiense infect humans, causing African sleeping sickness. However, Trypanosoma brucei brucei can only infect animals, causing the disease Nagana in cattle. Man is protected from this subspecies of trypanosomes by a toxic subtype of high density lipoproteins (HDLs) called the trypanosome lytic factor (TLF). The toxic molecule in TLF is believed to be the haptoglobin-related protein that when bound to hemoglobin kills the trypanosome via oxidative damage initiated by its peroxidase activity. The amount of lytic activity in serum varies widely between different individuals with up to a 60-fold difference in activity. In addition, an increase in the total amount of lytic activity occurs during the purification of TLF, suggesting that an inhibitor of TLF (ITLF) exists in human serum. We now show that the individual variation in trypanosome lytic activity in serum correlates to variations in the amount of ITLF. Immunoblots of ITLF probed with antiserum against haptoglobin recognize a 120-kDa protein, indicating that haptoglobin is present in partially purified ITLF. Haptoglobin involvement is further shown in that it inhibits TLF in a manner similar to ITLF. Using an anti-haptoglobin column to remove haptoglobin from ITLF, we show that the loss of haptoglobin coincides with the loss of inhibitor activity. Addition of purified haptoglobin restores inhibitor activity. This indicates that haptoglobin is the molecule responsible for inhibition and therefore causing the individual variation in serum lytic activity.


Subject(s)
Haptoglobins/pharmacology , Lipoproteins, HDL/blood , Trypanocidal Agents/blood , Trypanosoma brucei brucei/drug effects , Anemia, Hemolytic/blood , Animals , Cattle , Chromatography, Affinity , Haptoglobins/isolation & purification , Humans , Immunoblotting , Kinetics , Lipoproteins, HDL/antagonists & inhibitors , Lipoproteins, HDL/classification , Lipoproteins, HDL/isolation & purification , Lipoproteins, HDL/pharmacology , Trypanocidal Agents/antagonists & inhibitors , Trypanocidal Agents/isolation & purification
6.
Arzneimittelforschung ; 39(2): 254-6, 1989 Feb.
Article in English | MEDLINE | ID: mdl-2499341

ABSTRACT

The influence of the alpha-receptor agonist oxymetazoline, the antihistaminics mepyramine and cimetidine and of cromoglicic acid disodium salt (disodium cromoglycate, DSCG) on the hypotension produced by the trypanocidal diamidines pentamidine, diamidinophenylindole (DAPI) and diimidazolinophenylindole (DIPI) was investigated. 75-100 nmol/kg oxymetazoline were effective only in DAPI-treated animals and diminished the drop of the systolic blood pressure by 25-49%. Pretreatment with DSCG was ineffective in all groups under the conditions used. Preapplication of a combination of 5 mumol/kg mepyramine and 10 mumol/kg cimetidine was effective only in pentamidine-treated animals and reduced the drop of the systolic pressure by 57%.


Subject(s)
Amidines/toxicity , Hemodynamics/drug effects , Trypanocidal Agents/toxicity , Amidines/antagonists & inhibitors , Animals , Blood Pressure/drug effects , Cell Membrane/drug effects , Cimetidine/pharmacology , Cromolyn Sodium/pharmacology , Male , Pulse/drug effects , Pyrilamine/pharmacology , Rats , Rats, Inbred Strains , Regional Blood Flow/drug effects , Trypanocidal Agents/antagonists & inhibitors
11.
Science ; 201(4360): 1018-20, 1978 Sep 15.
Article in English | MEDLINE | ID: mdl-356267

ABSTRACT

The parasite Trypanosoma cruzi metabolizes allopurinol by a sequential conversion to allopurinol mononucleotide and aminopurinol mononucleotide. The latter is incorporated into RNA. This transformation of a widely used innocuous agent, allopurinol, into a toxic adenine analog appears to account for the antiprotozoan effect of allopurinol. These unique enzymatic activities appear to occur only in T. cruzi and the pathogenic lesihaminae. Allopurinol may serve as a model for the synthesis of similar antiprotozoan agents.


Subject(s)
Allopurinol/pharmacology , Pyrimidine Nucleotides/biosynthesis , Trypanocidal Agents/metabolism , Trypanosoma cruzi/metabolism , Adenine/pharmacology , Allopurinol/antagonists & inhibitors , Allopurinol/metabolism , Animals , Pyrimidine Nucleotides/antagonists & inhibitors , Pyrimidine Nucleotides/pharmacology , Ribonucleotides/antagonists & inhibitors , Ribonucleotides/biosynthesis , Ribonucleotides/pharmacology , Trypanocidal Agents/antagonists & inhibitors , Trypanocidal Agents/pharmacology , Trypanosoma cruzi/drug effects , Trypanosoma cruzi/growth & development
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