RESUMO
Chagas disease is a major health problem not only in Latin America but also in Europe and North America due to the spread of this disease into nonendemic areas. In terms of global burden, this major tropical infection is considered to be one of the most neglected diseases, and there are currently only two available chemotherapies: benznidazole and nifurtimox. Unfortunately, although these chemotherapies are beneficial in the acute phase of the disease, benznidazole and nifurtimox lead to significant side effects, including hepatitis and neurotoxicity. Therefore, the search for and development of more effective, safe and inexpensive anti-Trypanosoma cruzi drugs are required. In this work, a series of 10 nitroaromatic Schiff bases bearing different (nitro) aromatic rings-was synthesized. Subsequently, the in vitro and in vivo anti-T. cruzi activities of the Schiff bases were investigated, as well as the in vivo toxicity and the biological effects. The basic structure of the most promising in vivo Schiff base, 10 would be useful in the synthesis of new compounds for Chagas disease treatment.
Assuntos
Hidrocarbonetos Aromáticos/farmacologia , Bases de Schiff/síntese química , Bases de Schiff/farmacologia , Testes de Toxicidade , Tripanossomicidas/síntese química , Tripanossomicidas/farmacologia , Trypanosoma cruzi/efeitos dos fármacos , Administração Oral , Animais , Feminino , Hidrocarbonetos Aromáticos/síntese química , Hidrocarbonetos Aromáticos/química , Hidrocarbonetos Aromáticos/toxicidade , Fígado/efeitos dos fármacos , Fígado/patologia , Camundongos , Parasitemia/tratamento farmacológico , Bases de Schiff/química , Bases de Schiff/toxicidade , Tripanossomicidas/química , Tripanossomicidas/toxicidadeRESUMO
Fifteen quantitative structure-activity relationship (QSAR) models developed by various authors for the prediction of mutagenicity of aromatic and heteroaromatic amines were analyzed and thirteen of them, based on 95 amines, were compared using their respective statistics and order theory (Hasse Diagram Technique, HDT) to obtain an ordering of QSAR models. The technique of Formal Concept Analysis (FCA) was applied to the set of 95 amines to extract concepts and, in general, knowledge about the relationship between structural attributes and mutagenicity. HDT may be useful as a general tool for the comparison of different classes of QSAR models. FCA turns out to be a novel mathematical technique for seeking for relationships between molecular structure and activity.
Assuntos
Aminas/química , Aminas/farmacologia , Hidrocarbonetos Aromáticos/química , Hidrocarbonetos Aromáticos/farmacologia , Mutagênicos/química , Mutagênicos/farmacologia , Relação Quantitativa Estrutura-Atividade , Aminas/toxicidade , Animais , Humanos , Hidrocarbonetos Aromáticos/toxicidade , Modelos Genéticos , Modelos Estatísticos , Testes de Mutagenicidade , Mutagênicos/toxicidadeRESUMO
Excessive release of proinflammatory cytokines by innate immune cells is an important component of the pathogenic basis of malaria. Proinflammatory cytokines are a direct output of Toll-like receptor (TLR) activation during microbial infection. Thus, interference with TLR function is likely to render a better clinical outcome by preventing their aberrant activation and the excessive release of inflammatory mediators. Herein, we describe the protective effect and mechanism of action of E6446, a synthetic antagonist of nucleic acid-sensing TLRs, on experimental cerebral malaria (ECM) induced by Plasmodium berghei ANKA. We show that in vitro, low doses of E6446 specifically inhibited the activation of human and mouse TLR9. Tenfold higher concentrations of this compound also inhibited the human TLR8 response to single-stranded RNA. In vivo, therapy with E6446 diminished the activation of TLR9 and prevented the exacerbated cytokine response observed during acute Plasmodium infection. Furthermore, severe signs of ECM, such as limb paralysis, brain vascular leak, and death, were all prevented by oral treatment with E6446. Hence, we provide evidence that supports the involvement of nucleic acid-sensing TLRs in malaria pathogenesis and that interference with the activation of these receptors is a promising strategy to prevent deleterious inflammatory responses that mediate pathogenesis and severity of malaria.
Assuntos
Hidrocarbonetos Aromáticos/farmacologia , Malária Cerebral/prevenção & controle , Malária Cerebral/terapia , Ácidos Nucleicos/metabolismo , Receptores Toll-Like/antagonistas & inibidores , Animais , Barreira Hematoencefálica/efeitos dos fármacos , Barreira Hematoencefálica/patologia , Humanos , Hidrocarbonetos Aromáticos/química , Inflamação/complicações , Inflamação/patologia , Lipopolissacarídeos/farmacologia , Malária Cerebral/induzido quimicamente , Malária Cerebral/parasitologia , Camundongos , Camundongos Endogâmicos C57BL , Plasmodium chabaudi/efeitos dos fármacos , Plasmodium chabaudi/fisiologia , Choque Séptico/induzido quimicamente , Choque Séptico/complicações , Receptores Toll-Like/metabolismoRESUMO
Sixteen aromatic Morita-Baylis-Hillman adducts (MBHA) 1-16 were efficiently synthesized in a one step Morita-Baylis-Hillman reaction (MBHR) involving commercial aldehydes with methyl acrylate or acrylonitrile (81-100% yields) without the formation of side products on DABCO catalysis and at low temperature (0°C). The toxicities of these compounds were assessed against promastigote form of Leishmania amazonensis and Leishmania chagasi. The low synthetic cost of these MBHA, green synthetic protocols, easy one-step synthesis from commercially available and cheap reagents as well as the very good antileishmanial activity obtained for 14 and 16 (IC50 values of 6.88µgmL⻹ and 11.06µgmL⻹ respectively on L. amazonensis; 9.58µgmL⻹ and 14.34µgmL⻹ respectively on L. chagasi) indicates that these MBHA can be a novel and promising class of anti-parasitic compounds.
Assuntos
Antiparasitários/síntese química , Antiparasitários/farmacologia , Química Verde/métodos , Hidrocarbonetos Aromáticos/síntese química , Hidrocarbonetos Aromáticos/farmacologia , Leishmania/efeitos dos fármacos , Acrilatos/química , Aldeídos/química , Antiparasitários/química , Catálise , Química Verde/economia , Humanos , Hidrocarbonetos Aromáticos/química , Leishmaniose/tratamento farmacológico , Piperazinas/químicaRESUMO
N-alquil nitrones 1c and 3-6 were prepared from aromatic aldehydes and N-tert-butylhydroxylamine or N-methylhydroxylamine in good yields and soft conditions. Their protective effect against microvascular damages caused by ischemia/reperfusion in 'hamster cheek pouch' assay was investigated and compare with that observed for nitrones 1a,b and 2, previously studied. Nitrones 3b, 4b and 4c were the most active ones in inhibiting macromolecular permeability increase induced by ischemia/reperfusion when administered by gavage and intravenous, while 3a and 4a were active only after intravenous administration. N-tert-butylhydroxylamine and Nt-methylhydroxylamine, products of the hydrolysis of these nitrones, were weakly active when administered by gavage or intravenous. Nitrone (4a) was the most potent in inhibiting macromolecular permeability increase induced by histamine. In this case, N-tert-butylhydroxylamine was as active as 4a. The lypophylicity in nitrones, specially in N-methyl nitrones, play an important role on the protective action when compounds were administered by gavage.
Assuntos
Permeabilidade Capilar/efeitos dos fármacos , Hidrocarbonetos Aromáticos/farmacologia , Isquemia , Óxidos de Nitrogênio/química , Reperfusão , Animais , Cricetinae , Hidrocarbonetos Aromáticos/química , Hidrocarbonetos Aromáticos/farmacocinética , Masculino , Camundongos , Estrutura Molecular , Óxidos de Nitrogênio/farmacologiaRESUMO
A new 3D descriptor, the local intersection volume (LIV), was developed by our group and applied to the construction of 3D-QSAR models for ligands of the PGI(2) receptor (IP). The target compounds are a set of 42 aromatic heterocyclic derivatives [Meanwell et al., J. Med. Chem. 36 (1993), 3884], which show agonist activities in the IP receptor and are inhibitors of platelet aggregation. The LIV-3D-QSAR models were obtained through the analysis of 30% of the generated conformations for each compound, using a combined Genetic Algorithm (GA) and Partial Least Square (PLS) approach [Rogers and Hopfinger, J. Inf. Comput. Sci. 34 (1994) 854]. Statistically, Model 3 is the best as well as the most comprehensive in a mechanistic sense. Furthermore, it can be applied to design new IP ligands.