Antiplasmodial activity of chloroquine analogs against chloroquine-resistant parasites, docking studies and mechanisms of drug action
© de Souza et al.; licensee BioMed Central Ltd. 2014
Received: 3 July 2014
Accepted: 4 November 2014
Published: 2 December 2014
Given the threat of resistance of human malaria parasites, including to artemisinin derivatives, new agents are needed. Chloroquine (CQ) has been the most widely used anti-malarial, and new analogs (CQAns) presenting alkynes and side chain variations with high antiplasmodial activity were evaluated.
Six diaminealkyne and diaminedialkyne CQAns were evaluated against CQ-resistant (CQ-R) (W2) and CQ-sensitive (CQ-S) (3D7) Plasmodium falciparum parasites in culture. Drug cytotoxicity to a human hepatoma cell line (HepG2) evaluated, allowed to calculate the drug selectivity index (SI), a ratio of drug toxicity to activity in vitro. The CQAns were re-evaluated against CQ-resistant and -sensitive P. berghei parasites in mice using the suppressive test. Docking studies with the CQAns and the human (Hss LDH) or plasmodial lactate dehydrogenase (Pf LDH) enzymes, and, a β-haematin formation assay were performed using a lipid as a catalyst to promote crystallization in vitro.
All tested CQAns were highly active against CQ-R P. falciparum parasites, exhibiting half-maximal inhibitory concentration (IC50) values below 1 μΜ. CQAn33 and CQAn37 had the highest SIs. Docking studies revealed the best conformation of CQAn33 inside the binding pocket of Pf LDH; specificity between the residues involved in H-bonds of the Pf LDH with CQAn37. CQAn33 and CQAn37 were also shown to be weak inhibitors of Pf LDH. CQAn33 and CQAn37 inhibited β-haematin formation with either a similar or a 2-fold higher IC50 value, respectively, compared with CQ. CQAn37 was active in mice with P. berghei, reducing parasitaemia by 100%. CQAn33, -39 and -45 also inhibited CQ-resistant P. berghei parasites in mice, whereas high doses of CQ were inactive.
The presence of an alkyne group and the size of the side chain affected anti-P. falciparum activity in vitro. Docking studies suggested a mechanism of action other than Pf LDH inhibition. The β-haematin assay suggested the presence of an additional mechanism of action of CQAn33 and CQAn37. Tests with CQAn34, CQAn37, CQAn39 and CQAn45 confirmed previous results against P. berghei malaria in mice, and CQAn33, 39 and 45 were active against CQ-resistant parasites, but CQAn28 and CQAn34 were not. The result likely reflects structure-activity relationships related to the resistant phenotype.
KeywordsMalaria Chloroquine analogs Diaminealkyne Diaminedialkyne P. falciparum Lactate-dehydrogenase enzyme Docking
Malaria remains a major public health problem, resulting in 207 million cases and 627,000 deaths worldwide in 2012 . There is no available vaccine, and the control of the disease relies on the use of bed nets, other individual protection against mosquito bites, and the successful drug treatment of infected patients . Presently, chemotherapy has been hampered by the low sensitivity of the parasite to most available anti-malarial drugs , including artemisinin derivatives [4–6]. Resistance to chloroquine, in the case of P. falciparum, is linked to mutations in the P. falciparum chloroquine resistance transporter (pfcrt) gene, which alters the transport and accumulation of the drug in the digestive vacuole (DV) of the parasite [7, 8]. Plasmodium vivax resistance to CQ has been described [9, 10] and seems related to the intense malaria morbidity in the Amazon region . However, neither CQ-R nor mutation markers were detected among P. vivax in recent studies of 47 isolates from the West Amazon, all from patients with non-severe malaria .
Chemical modifications of CQ have been used as a powerful strategy to find new anti-P. falciparum agents effective against drug-resistant parasites [13, 14]. Structural modifications of the alkyldiamine side chains have provided rather active compounds with decreased cross-resistance to CQ  and with different structure-activity relationships [16–18]. In the present work, six CQ analogs (CQAns) that reduced parasitaemia in P. berghei-infected mice , comprising diaminealkynes and diaminedialkynes, were evaluated in vitro against CQ-R (W2 clone) and CQ-S (3D7 strain) forms of P. falciparum parasites in cultures. These CQAns were then reevaluated in mice with CQ-sensitive or CQ-resistant P. berghei parasites. The compounds with the best selectivity index, based on drug cytotoxicity and activity in vitro, were evaluated for the inhibition of β-hematin formation. To clarify the possible mechanism of action of the CQAns evaluated herein, docking studies were also performed based on interactions between the CQAns and the plasmodial lactate dehydrogenase (Pf LDH) enzyme, a known target of 4-aminoquinolines [20, 21].
Synthesis of the molecules
Cytotoxicity tests in vitro
A human hepatoma cell line (HepG2), originally received from the University of Lisbon as a kind gift, was cultured as described . The cells were maintained in RPMI 1640 medium (Sigma-Aldrich, ref 6504) supplemented with 40 mg/L gentamicin and 10% heat-inactivated foetal calf serum (FCS), and they were maintained in a 5% CO2 atmosphere at 37°C. When confluent, the cell monolayer was trypsinized, washed with culture medium supplemented with 10% FCS, counted, diluted (5 × 103 cells/well), placed in flat-bottom 96-well plates (Corning, Santa Clara, CA, USA), and incubated for 18 h at 37°C to allow cell adhesion. The compounds were added to the plates at concentrations up to 1,700 μM, followed by incubation for an additional 24 h, after which 20 μL (5 μg/mL) of 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide (MTT) solution was added per well to evaluate drug cytotoxicity. After 3 h, the supernatant was discarded, 100 μL of dimethyl sulphoxide (DMSO) was added per well, and the optical density was measured (SpectraMax340PC384, Molecular Devices) at 570 nm (test) and 630 nm (background). Cell viability was expressed as the percentage of the absorbance compared to the absorbance of the untreated cells and subtracted from the appropriate background measurement. The lethal drug dose for 50% of the cells (MLD50) was determined as described  and was used to calculate the SI of the active compounds, a ratio of the in vitro cell toxicity and activity against P. falciparum (MLD50/IC50).
Continuous cultures of P. falciparum
CQ-R P. falciparum parasites (W2 clone)  and CQ-S (3D7 strain), originally received from New York University Medical School, were maintained in continuous culture at 37°C in human erythrocytes (A+) using complete medium (RPMI 1640 supplemented with 10% blood group A+ human serum) changed daily . Before tests with the molecules were performed, ring stage parasites were synchronized using sorbitol  and the parasitaemia and haematocrit were adjusted; 180 μL/well was added to 96-well microtiter plates (Corning, Santa Clara, CA, USA) containing the diluted compounds tested in triplicate. Drug activity was evaluated in relation to control cultures with no drugs  and was measured using the anti-histidine-rich protein II (HRPII) test as described . CQ was used in each test as a control, and two to four experiments were performed for each parasite strain.
In vitro tests of drug activity
The anti-HRPII test was performed using P. falciparum cultures adjusted for 0.05% parasitaemia and 1.5% haematocrit. The cultures were added to plates containing the diluted drugs, followed by incubation for 24 h under standard culture conditions . The contents of six wells with no drugs were harvested in each test plate, pooled in microtubes, and frozen for later use to measure the background parasite growth as described . After a 48 h incubation, the plates were frozen and thawed twice, and 100 μL of lysed cells from each well was added to a plate that had been precoated overnight at 4°C with a primary anti-HRPII monoclonal antibody (MPFM-55A ICLLAB®, USA) for an immunoassay. Phosphate-buffered saline (PBS) containing 0.05% Tween and 4% bovine serum albumin was used for plate blocking (3 h at room temperature) to avoid nonspecific antibody binding. After 1 h at room temperature, the plate was washed, and 100 μL/well of a secondary antibody solution (MPFG-55P ICLLAB®, USA) was added, followed by incubation with 3,3′,5,5′-tetramethylbenzidine (TMB) chromogen (KPL, Gaithersburg, MD, USA) in the dark. The reaction was stopped using 1 M sulfuric acid, and the absorbance was read (450 nm) in a spectrophotometer (SpectraMax340PC384, Molecular Devices). The anti-P. falciparum drug activity was evaluated by comparing the parasite growth in the drug-free control cultures, considered 100% growth, with that in the drug test cultures. Using curve-fitting software (Microcal Origin Software 5.0, Inc.), a sigmoidal dose–response curve was generated, enabling the determination of drug IC50 values. CQAns presenting IC50 ≤ 1 μM were considered active; between 1–5 μM as partially active; and above 5 μM as inactive.
Protocol for animal use in the anti-malarial tests
The protocol for animal use was approved by the Ethics Committee for Animal Use (CEUA LW-23/13) of the Oswaldo Cruz Foundation (Fiocruz). Only Swiss adult female mice (20 ± 2 g weight) were used; they were raised at the animal facilities at FIOCRUZ-Minas.
Anti-malarial tests against P. berghei in mice
The suppressive test was performed as described  using the P. berghei NK65 blood parasites, with some modifications . Briefly, the blood parasites were maintained through weekly blood passages in mice. For the experiments, groups of 20–30 mice were inoculated with 1 × 105 infected erythrocytes. Approximately three hours later, they were randomly distributed into groups of five to six mice per cage, which were treated daily by gavage for four consecutive days. All the compounds were freshly diluted in 3% DMSO (Sigma-Aldrich) in RPMI medium and were administered orally at doses of 25 mg/kg or 50 mg/kg. The control mice received the drug vehicle. On days 5 and 7 after parasite inoculation, blood was taken from the tail of each mouse and used to prepare thin smears, which were methanol-fixed, Giemsa-stained and examined microscopically to determine parasitaemia. The inhibition of parasite growth was evaluated in relation to parasitaemia in the untreated mice, which were considered to have 100% parasite growth.
A P. berghei NK65 CQ-resistant strain maintained at -70°C, selected by increasing doses of CQ, maintained in mice under constant drug pressure (CQ 150 mg/kg)  and stored at -70°C was also defrosted and used to inoculate mice. When parasitaemic, the drug-resistant parasites were subjected to serial blood passages maintained under CQ treatment with increasingly higher doses, up to 150 mg/kg, then used for the experiments. The mice were inoculated with 107 parasitized RBCs using blood parasites from a donor with parasites resistant to 150 mg/kg of CQ. Groups of five mice each were separated 24 h after the parasite inoculation, then treated orally with the test CQAn at doses of 25 or 50 mg/kg for three consecutive days. Two control groups were used in each experiment; one received CQ at 150 mg/kg and the other was infected but treated with vehicle only (no drugs). The inhibition of parasitaemia was evaluated as described for the mice inoculated with the CQ-sensitive parasites. A compound was considered active when it inhibited parasitaemia more than 40% in relation to the infected but vehicle-treated (no drugs) group.
Inhibition of β-haematin formation assay
The assay was performed using a lipid as a catalyst to promote crystallization . Briefly, drug stock solutions were prepared in DMSO and were used at a final concentration of up to 30 mM. A haem stock (10 mM) was made in DMSO and was diluted to 50 μM with 100 mM sodium acetate (pH 4.8). A 10 mM 1-monooleoyl-rac-glycerol (MOG) stock was made in ethanol and was sonicated before being added to a 50 μM haem stock to make 25 μM MOG–50 μM haem in 100 mM sodium acetate (pH 4.8). The 25 μM MOG–50 μM haem solution was sonicated and added to the assay plate at 100 μL/well. The plates were incubated at 37°C for 2 h to allow crystallization, followed by the addition of 100 μl of 200 mM sodium bicarbonate (pH 9.1) to solubilize any remaining monomeric haem. After incubation for 30 min at room temperature, the amount of solubilized monomeric haem was determined by measuring the absorbance at 405 nm. Finally, 20 μl of 1 M sodium hydroxide was added to the plates to dissolve any crystals that had been formed, and the absorbance was read at 405 nm to determine the total amount of haem present in each well. The inhibition of haem crystallization was determined as a function of the amount of monomeric haem that was not crystallized divided by the total amount of haem present in the assay mixture. The results are expressed as IC50 values based on the percentage inhibition of β-haematin formation by the CQAn.
The structures of the inhibitors studied were constructed and optimized with the program Spartan 08  using the Merck Molecular Force Field (MMFF) method . In addition, the partial charges were calculated by single-point energy calculations using the RM1 method . The crystallographic structures of Pf LDH and Hss LDH were downloaded from the Protein Data Bank  under the codes 1LDG (resolution 1.74 Å and R factor = 0.197) and 1IOZ (resolution 2.10 Å and R factor = 0.179), respectively.
The program Molegro Virtual Docker® (MVD)  was used for the docking studies, and the methodology used was validated by re-docking. To observe possible interactions of the ligands with the solvent present in the crystal, 35 water molecules from a cavity approximately 10 Å in size were considered for the calculations with Pf LDH, whereas 54 molecules were considered for the calculations with Hss LDH. The docking region was restricted to a radius of 15 Å from the centre of the cavity inside each enzyme. The best ligand conformations inside the enzymes were chosen based on 100 runs for each ligand, and considering the superposition to the structure of NADH molecules present in the crystallographic structures combined with the best values for interaction energy, and for the H-bonds with water molecules and the residues of the active sites.
The volumes of the cavities of the NADH-binding sites inside Pf LDH and Hss LDH were determined using MVD® .
Anti-P. falciparum activity and selectivity indexes of CQAns
Activity of CQ and CQAn against P . falciparum (IC 50 ) CQ-R (W2) or CQ-S (3D7) parasites
Anti- P. falciparum activity (IC50in μM)*
W2( CQ- R)
3D7l( CQ- S)
0.71 ± 0.03
14.87 ± 3.58
0.02 ± 0.001
1.17 ± 0.10
0.23 ± 0.15
0.3 ± 0.01
0.07 ± 0.03
0.57 ± 0.24
0.64 ± 0.29
2.39 ± 0.11
0.77 ± 0.21
1.17 ± 0.00
0.081 ± 0.019
Cytotoxicity of CQ and CQAn and SI on P . falciparum parasites and therapeutic activity or selectivity index (SI), a ratio between toxicity and activity
Cytotoxicity* MLD 50 (μM)
SI(MLD 50 /IC 50 )
1508.56 ± 344.50
152.89 ± 12.86
943.29 ± 73.15
1699.24 ± 10.07
1015.84 ± 42.97
Anti-P. berghei malaria activity of the CQAns
Anti-malarial activity of chloroquine (CQ) and its analogs (CQAn) against P . berghei evaluated as percentage reduction of parasitaemia on days after inoculation with either a CQ sensitive or resistant strain of the parasite*
CQ-Sensitive 25 mg/Kg
CQ-Resistant 50 mg/Kg
The CQAns were evaluated against a CQ-resistant P. berghei strain (maintained by constant drug pressure at a dose of 150 mg/kg daily until the last passage before the test). The dose of 50 mg/kg was active for all the CQAns on day 5. CQAn45 caused the highest parasitaemia reduction (63%), followed by CQAn39, CQAn33 and CQAn37, which reduced parasitaemia by 62%, 53% and 47%, respectively. CQAn28 and CQAn34 were inactive at 25 mg/kg. As expected, CQ at the highest tolerated dose of 150 mg/kg was inactive against the CQ-resistant P. berghei parasites in mice (Table 3).
Inhibition of β-haematin formation by CQAn
Inhibitory concentrations of β-haematin formation by chloroquine (CQ) and two analogs (CQAn)*
Mean ± SD
4.3 ± 1.3
8.9 ± 3.8
3.5 ± 2.2
Docking studies and the mechanism of activity of the CQAns
Docking results of NADH, CQ and CQAn inside Pf LDH
Intermolecular energy (kcal mol-1)
H-bond energy (kcal mol-1)
Residues and water molecules involved in H-bonds
H-bond energy (kcal mol-1)
NADH RMSD 1.437
Docking results of NADH, CQ and CQAn inside Hss LDH
Intermolecular energy (kcal mol-1)
H-bond energy (kcal mol-1)
Residues and water molecules involved in H-bonds
H-bond energy (kcal mol-1)
NADH RMSD 0.956
Inside Pf LDH, all the compounds (except CQAn45) H-bonded to Asp53 and/or Thr97 plus water molecules and displayed good (negative) H-bond energy values. The intermolecular energies were ranked as follows: CQ > CQAn39 > CQAn37 > CQAn33 > CQAn28 > CQAn45 > CQAn34, with lower values than NADH. The highest H-bond energy was observed for CQAn33 and the lowest for CQAn45.
Most of the active-site residues of Pf LDH involved in H-bonds differed from those of Hss LDH. Thus, the residues of Pf LDH involved in H-bonds with CQAn33 and CQAn37 were Thr97, Val138 and H20; and Asp53 and H20, respectively. The residues of Hss LDH for the same molecules were Lys147, Ala146 and Asn116; and Gly15, Asn116, Ala146 and Lys147, respectively.
Although CQ-R is widespread, CQAns may help to overcome the drug resistance, especially considering that it is believed to be stage specific  and/or related to the compound structure . Indeed, various CQAns have shown potent antiplasmodial activity against CQ-R P. falciparum blood parasites [40–42]. Among the six CQAns tested against P. falciparum in the present work, all exhibited high activity against CQ-R parasites. CQAn28, 33, 37 and 39 were more potent against the CQ-R W2 clone than against the 3D7 CQ-S parasites.
Variation in side chains seems to be a promising strategy concerning the anti-malarial activity of CQAns, and small changes in the spacer length can dramatically affect the activity exhibited against CQ-S and CQ-R parasites . Moreover, the presence of a terminal alkyne seems important: CQAn33, which has a terminal alkyne, showed an IC50 more than 10-fold higher than that of CQ, which has no terminal alkyne.
The activity of 4-aminoquinolines involves their binding to haematin in the monomeric and dimeric forms, inhibiting haemozoin formation and resulting in parasite death . The activity of CQ against P. falciparum also involves interactions with the parasite enzyme Pf LDH , as shown by in silico studies with docking and molecular dynamics in the present work. The complex formed between the dimeric haematin and the quinolinic drugs inhibited Pf LDH, as shown with other quinoline derivatives .
In previous studies, RMSD values below 2.00 Å were obtained for the plasmodial and human enzymes in re-docking studies, which validates this methodology [45–47]. The intermolecular energy values for the CQAns were higher than for CQ and NADH, showing that the molecules studied here are weak inhibitors of Pf LDH and suggesting that they have a different mechanism of action.
CQAn33 and CQAn37, the molecules with the highest SI in vitro, were also evaluated for their ability to inhibit β-haematin formation. The results showed that CQAn33 inhibited β-haematin formation with an IC50 similar to that of CQ, whereas CQAn37 exhibited an IC50 more than 2-fold higher than CQ, which is in accordance with this molecule being less active than CQAn33 against P. falciparum. The results obtained for anti-P. falciparum activity through the HRPII test showed a rather higher activity of these CQAns in relation to CQ, suggesting another mechanism of action than that related to haemozoin formation, such as apoptosis, autophagy or the inhibition of P-glycoprotein-mediated transport. Metacaspase-like proteins, which are related to caspases , have previously been shown to be inducers of apoptosis in P. falciparum parasites exposed to CQ, with more intense DNA fragmentation in CQ-R parasites than in CQ-S . Autophagy-related proteins have been identified in P. falciparum[50, 51]. Indeed, after CQ pressure, P. falciparum parasites exhibited cytoplasmic vacuolization , a sign of autophagic cell death  rather than of apoptosis. A recent study showed that CQ significantly inhibited P-glycoprotein-mediated transport , which is involved in drug evasion in P. falciparum.
The highest and lowest H-bond energies were observed for CQAn33 and CQAn45, respectively, a result that corroborates the in vitro data showing that CQAn33 was the most active molecule and CQAn45 the least active against P. falciparum. Another difference is the residues of the plasmodial and human enzymes involved in the H-bonds, specific for CQAn33 and CQAn37; this result is consistent with them having the highest SIs.
The differences in the binding pockets of the studied compounds’ tails inside Pf LDH and Hss LDH could be explained by a large concentration of negative charges due to the presence of the alkyne groups. This finding suggests a better stabilization inside the more positive pocket of Pf LDH, which is caused by the size of the cavity and increases drug specificity. Indeed, the smaller cavity of Pf LDH allows for better accommodation of the ligands than inside Hss LDH.
The most active CQAn in vitro also inhibited P. berghei parasitaemia in mice, as shown in the present work and in our previous studies with the same compounds . An increase in mouse survival resulting from treatment with CQAn37 may well be a consequence of the alkyl side chain altering the structure-activity relationship in the terminal nitrogen , which may favor drug lipophilicity. All the CQAns inhibited CQ-R P. berghei parasitaemia in mice, translating the in vitro data, with the exception of CQAn28 and 34, which is likely a result of metabolism  or of the structure-activity relationships inherent to the resistance phenotype, e.g., those related to pfcrt[7, 56], also in vivo.
The data reported herein highlight the use of CQAns in malaria-endemic areas where drug resistance has been reverted, i.e., sensitivity to CQ has reappeared . CQ is the most widely used anti-malarial drug worldwide  due to its low cost, high efficacy and lack of toxicity. In addition, the cost of a treatment course is rather low at US$0.21 per patient . The CQAns evaluated in this study are generated in two steps using readily available, inexpensive starting materials and can be produced in good yields  at a cost expected to be as low as that of CQ. Thus, the CQAns studied in the present work may be produced at large scale to proceed in drug development for anti-malarials, since they are promising alternatives for malaria control.
Among the six CQAns tested in vitro, three were more active than CQ, inhibiting 50% of P. falciparum growth at low doses: CQAn33 (IC50 0.02 ± 0.001 μM), CQAn34 (IC50 0.23 ± 0.15 μM), and CQAn37 (IC50 0.07 ± 0.03 μM). All were more active against the CQ-R (W2) parasites than against the CQ-S (3D7) parasites, which suggests the absence of cross-CQ-R. In addition, the therapeutic indexes (or SI) of all CQAns, with the exception of CQAn45, were higher than that of CQ. Docking studies with CQAn33 and CQAn37 corroborated the outstanding anti-P. falciparum activity observed herein and showed that CQAn33 had the highest H-bond energy with the plasmodial enzyme, indicating specificity for Pf LDH. Additionally, they showed that the CQAns are weak inhibitors of Pf LDH, suggesting a different mechanism of action. The inhibition of β-haematin formation by CQAn33 and CQAn37 also suggested mechanisms of action other than those related to haemozoin formation. The in vivo results with CQAn34, CQAn37, CQAn39, and CQAn45 confirm previous data showing their high anti-malarial activity. Furthermore, the CQAns also inhibited the parasitaemia caused by CQ-R P. berghei but CQ did not, translating in vitro to in vivo data. However, CQAn28 and CQAn34 did not inhibit CQ-R P. berghei parasitaemia, what may be a result of metabolism issues or structure-activity relationships related to the resistant phenotype. Altogether, the present results highlight the CQAns studied here as promising anti-malarial agents due to their SI and in vivo activity against malaria in mice.
We thank the financial support from the Brazilian funding agencies MCT/CNPq/CT-Saúde/MS/SCTIE/DECIT (Edital PRONEX-55675/2009-2 and Edital Doenças Negligenciadas-404455/2012-3); to FAPEMIG (PRONEX-Project 16712); FIOCRUZ for providing facilities and mice, and to CNPq for the fellowships to the authors (AUK; NBS).
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