MEM INST OSWALDO CRUZ, RIO DE JANEIRO, 110(4) June 2015
PAGES: 566-568 DOI: 10.1590/0074-02760150007 Short communication
In vitro activity of 1,3-bisaryloxypropanamines against Trypanosoma cruzi-infected L929 cultures

Stefânia Neiva Lavorato1, Policarpo Ademar Sales Júnior2, Silvane Maria Fonseca Murta2, Alvaro José Romanha2,3, Ricardo José Alves1,+

1Departamento de Produtos Farmacêuticos, Faculdade de Farmácia, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brasil
2Laboratório de Parasitologia Celular e Molecular, Centro de Pesquisas René Rachou-Fiocruz, Belo Horizonte, MG, Brasil
3Departamento de Microbiologia, Imunologia e Parasitologia, Universidade Federal de Santa Catarina, Florianópolis, SC, Brasil

Abstract

We describe herein the antitrypanosomal activity of 20 novel 1,3-bis(aryloxy)propan-2-amine derivatives. Compounds 2, 4, 6, 12, 15, 16 and 19 were significantly active against amastigote and trypomastigote forms, with half maximal inhibitory concentration values in the range of 6-18 µM. In the cytotoxicity tests against L929 cells, only compound 4 presented selectivity index value above 10, indicating low toxicity.

Chagas disease, also referred to as American trypanosomiasis, is a neglected tropical disease caused by parasitic protozoa Trypanosoma cruzi. It is estimated that about seven-eight million people are infected by this parasite, mostly in Latin America, where the disease is endemic. The main mode of transmission to people is through faeces of infected triatomine bug left near the site of its bite wound. Due to population migration, an increase in the number of cases has been observed in some countries of North America, Europe and Western Pacific, associated with another ways of transmission, like transfusion of contaminated blood, congenital transmission and organ transplantation (WHO 2014).

There is no available vaccine to use in prevention of Chagas disease. The chemotherapy is restricted to two drugs, nifurtimox (NFX) and benznidazole (BZ), through generation of nitro-reduction intermediates that lead to oxidative stress for NFX or reductive stress for the latter drug (Urbina 2010). Besides, they are effective against acute infections, but show poor activity in the late chronic phase and the increase in cases of resistance and the toxicity associated with the use of these drugs limit the treatment efficacy and patient compliance (Le Loup et al. 2011). Thus, there is an urgent need for new safe and effective drugs that may act at all stages of illness.

Our research group has been interested in identifying the antitrypanosomal potential of several classes of new compounds synthesised in our laboratory (Oliveira et al. 2003, de Oliveira et al. 2006, Júnior et al. 2010). One chemical class that has been explored by our group is that of 1,3-bisaryloxypropanamines, prepared and evaluated initially as potential inhibitors of trypanothione reductase (Silva et al. 2010). A search in the literature revealed that there are only a few reports on these interesting compounds, that display several biological activities, like antifungal (Liu et al. 2000) and antibacterial (Heerding et al. 2003). They were also found to be DNA intercalating agents (Sánches et al. 2013) and sodium channels modulators (Choi et al. 2003). Due to our initial results on trypanothione reductase inhibition and the absence of reports in the literature about antitrypanosomal structurally-related compounds we decided to investigate the potential of this class as antitrypanosomal agents.

Thus, in this paper, we describe the antitrypanosomal activity and cytotoxicity profile of 20 novel 1,3-bis(aryloxy)propan-2-amine derivatives (SN Lavorato, unpublished observations) as new candidates for further development as potential antitrypanosomal agents.

Assays with T. cruzi amastigote and trypomastigote forms - For the experiments it was used the Tulahuen strain of the parasite expressing the Escherichia coli β-galactosidase as reporter gene as previously described (Buckner et al. 1996, Romanha et al. 2010). The compounds were dissolved in dimethyl sulfoxide (DMSO) with the final concentration of the solvent < 1%. Controls with uninfected cells, untreated infected cells, infected cells treated with 1 μg/mL BZ (positive control) and 1% DMSO were used. The results were expressed as the percentage of T. cruzi growth inhibition in compound-tested cells as compared to the infected cells and untreated cells. Quadruplicates were run in the same microplate and the experiments were repeated at least once. The half maximal inhibitory concentration (IC50) values were calculated by linear interpolation.

Cytotoxicity over vertebrate L929 cells and selectivity index (SI) - The potential toxicity of the compound to mammalian cells was assayed by the Alamar Blue® as previously described (Romanha et al. 2010). The 50% cytotoxic concentration (CC50) values were calculated by linear interpolation and the SI was determined by ratio CC50/ IC50.

1,3-bisaryloxypropanamines 1-20 (Table) were evaluated for their antitrypanosomal activity against T. cruzi amastigote and trypomastigote forms in just one system, using BZ as positive control. The results are expressed in the Table as IC50 values. Among tested compounds, only compound 20, bearing 2-naphthyl group as aromatic ring, was inactive. Several compounds displayed considerable activity, the most active being compounds 2 (m-CN) and 6 (p-NO2), which presented IC50 of 6 µM and 10 µM, respectively. Compounds 4 (o-NO2, IC50 = 18 µM), 12 (o-CH3, IC50 = 10 µM), 15 (o-Cl, IC50 = 12 µM), 16 (m-Cl, IC50 = 13 µM) and 19 (2,3-benzo, IC50 = 13 µM) were also significantly active. The less active compound was the unsubstituted 18, with IC50 of 100 µM.

Toxicity profiles of active compounds were determined against L929 cells. They are expressed as CC50 values in the Table. The ratio of IC50 and CC50 values is presented in the same Table as SI, indicating the selective toxicity of each compound. The most selective compound was 4 (o-NO2), with an SI above 11.

Twenty novel 1,3-bis(aryloxy)propan-2-amine derivatives with diverse substitution pattern at the aromatic ring were evaluated. The effect of substituent and its position to antitrypanosomal activity could not be clearly established, since the most active compounds, 2 (m-CN), 4 (o-NO2), 6 (p-NO2), 12 (o-CH3), 15 (o-Cl), 16 (m-Cl) and 19 (2,3-benzo), display different physicochemical characteristics. For comparison purposes, the electronic and steric effects of each substituent are represented in the Table by their phenyl substituent constants Hammet's electronic constant and molar refractivity (MRX), respectively, and the hydrophobic properties of each compound by their calculated partition coefficient (ClogP) values. The hydrophobicity influences the compound ability to cross biologic membranes, that is, to penetrate into the parasite. The electronic character of phenyl substituent affects the pKa of amino group, so the percentage of ionised and nonionised forms of each amine can vary according to the aryl substituent. This could interfere with the ability of crossing cell membranes and recognition of the compounds by their putative molecular targets and, consequently, on its activity. Besides, the molar refractivity is dependent on volume and polarisability, which can also influence the compound activity. No clear-cut structure-activity relationship can be inferred thus far, however, some observations could be done. For example, the less active compound was the unsubstituted 18, indicating that the introduction of ring substituent contributes to enhance the antitrypanosomal effect. Even though the two best antitrypanosomal compounds, 2 (m-CN, IC50 = 6 µM) and 6 (p-NO2, IC50 = 10 µM), are meta or para-substituted, we can notice a prevalence of ortho-substitution pattern among compounds with IC50 below 20 µM, suggesting that, due to "ortho effect" of substituent (Barreiro & Fraga 2008), those compounds could assume a particular conformation that improves their activity. Besides, when ortho substituent is introduced, the antitrypanosomal action increases as ClogP increases (Table). So, compounds bearing ortho-substituted aromatic rings with a group that contribute to increase molecular hydrophobicity, like CH3 and Cl, displayed higher activity than those substituted with a group that decrease hydrophobicity, like NO2, CN and OCH3. Regarding the meta-substituted compounds, a balance between molecular hydrophobicity and electronic effects of substituent could explain the high activity of compounds 2 (m-CN) and 16 (m-Cl). Moreover, analyses suggest that steric effects can also influence the activity of this series, since in general there is an increase in the antitrypanosomal activity as MRx value decreases. It was not possible to delineate the influence of physicochemical parameters on para-substituted compounds.

Cytotoxicity profiles of those compounds were also carried out to determine their toxicity on L929 cells. According to Pires et al. (2013), SI value above 10 is recommended to ensure the safety of a drug candidate. In this regard, our compounds, in general, did not present good SI. Among evaluated compounds, only compound 4 (o-NO2) presented SI value above 10 (SI > 11), fitting the safety requirement. All compounds bearing CN group (1, 2 and 3) and the nitro derivative 6 (p-NO2) exhibited SI values close to 10, presenting moderate selectivity.

In conclusion, we described herein the antitrypanosomal activity and cytotoxicity profile of 20 novel 1,3-bis(aryloxy)propan-2-amine derivatives. Six new 1,3-bisaryloxypropanamines, 2(m-CN), 4 (o-NO2), 6 (p-NO2), 12 (o-CH3), 15 (o-Cl), 16 (m-Cl) and 19 (2,3-benzo), were significantly active, with IC50 values in the range of 6-18 µM. To the best of our knowledge, this is the first report on the antitrypanosomal activity of this class of compounds. Finally, considering potency and selectivity, compounds 2 (m-CN), 4 (o-NO2) and 6 (p-NO2) appear to be good candidates for further structure modifications.

 

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Financial support: CAPES, CNPq, FAPEMIG, INCT-IF, PDTIS-FIOCRUZ
+ Corresponding author: This e-mail address is being protected from spambots. You need JavaScript enabled to view it.
Received 8 January 2015
Accepted 30 April 2015

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