Skip to main content

Terminalia albida treatment improves survival in experimental cerebral malaria through reactive oxygen species scavenging and anti-inflammatory properties

Abstract

Background

The development of Plasmodium resistance to the last effective anti-malarial drugs necessitates the urgent development of new anti-malarial therapeutic strategies. To this end, plants are an important source of new molecules. The objective of this study was to evaluate the anti-malarial effects of Terminalia albida, a plant used in Guinean traditional medicine, as well as its anti-inflammatory and antioxidant properties, which may be useful in treating cases of severe malaria.

Methods

In vitro antiplasmodial activity was evaluated on a chloroquine-resistant strain of Plasmodium falciparum (K-1). In vivo efficacy of the plant extract was measured in the experimental cerebral malaria model based on Plasmodium berghei (strain ANKA) infection. Mice brains were harvested on Day 7–8 post-infection, and T cells recruitment to the brain, expression levels of pro- and anti-inflammatory markers were measured by flow cytometry, RT-qPCR and ELISA. Non-malarial in vitro models of inflammation and oxidative response were used to confirm Terminalia albida effects. Constituents of Terminalia albida extract were characterized by ultra‐high performance liquid chromatography coupled with high resolution mass spectrometry. Top ranked compounds were putatively identified using plant databases and in silico fragmentation patterns.

Results

In vitro antiplasmodial activity of Terminalia albida was confirmed with an IC50 of 1.5 μg/mL. In vivo, Terminalia albida treatment greatly increased survival rates in P. berghei-infected mice. Treated mice were all alive until Day 12, and the survival rate was 50% on Day 20. Terminalia albida treatment also significantly decreased parasitaemia by 100% on Day 4 and 89% on Day 7 post-infection. In vivo anti-malarial activity was related to anti-inflammatory properties, as Terminalia albida treatment decreased T lymphocyte recruitment and expression of pro-inflammatory markers in brains of treated mice. These properties were confirmed in vitro in the non-malarial model. In vitro, Terminalia albida also demonstrated a remarkable dose-dependent neutralization activity of reactive oxygen species. Twelve compounds were putatively identified in Terminalia albida stem bark. Among them, several molecules already identified may be responsible for the different biological activities observed, especially tannins and triterpenoids.

Conclusion

The traditional use of Terminalia albida in the treatment of malaria was validated through the combination of in vitro and in vivo studies.

Background

Malaria continues to be one of the primary medical concerns in many countries worldwide in terms of number of cases and deaths. In 2017, there were approximately 219 million malaria cases and 435,000 deaths worldwide, 91% of these in sub-Saharan Africa [1]. Today, there are few efficient anti-malarial treatments, and all are derived from artemisinin. However, Plasmodium falciparum has developed mechanisms of resistance to artemisinin and its derivatives, particularly in Southeast Asia [2]. Recent studies report increasing time for parasite clearance after treatment in a few parasite isolates originating from West Africa [3, 4]. The development of new treatments based on effective molecules using mechanisms of action, which are different to artemisinin and its derivatives, is thus urgently needed.

Malaria occurs in different forms; it can be uncomplicated, or it may lead to more severe pathologies, particularly cerebral malaria (CM). This is the deadliest form of malaria, with a mortality rate of approximately 15–25% [5]. The cerebral complications are related to a preferential localization of infected erythrocytes (iEs) in the brain through interactions between parasite proteins expressed on the surface of infected red blood cells and brain endothelium [6]. The mechanical obstruction of brain blood flow due to accumulation of iEs and rosetting leads to ischemia, hypoxia and activation of cerebral endothelium [7]. Activated endothelium produces pro-inflammatory cytokines and chemokines involved in the recruitment of immune cells. While the role of monocytes, macrophages and dendritic cells is to remove iEs by phagocytosis, they also produce pro-inflammatory cytokines that activate cytotoxic T cells involved in blood–brain barrier damage [8]. Degradation of haemoglobin by the parasite generates large quantities of toxic free haem and reactive oxygen species (ROS), causing cell damage to the host [9]. In addition, ROS production by monocytes/macrophages is an efficient host defence mechanism, although these oxidative processes lead to an imbalance between pro- and anti-oxidant responses, resulting in oxidative stress [10].

Plants are a significant source of molecules for the development of new drugs. Many plants from traditional medicine have provided opportunities for the identification of anti-malarial molecules. Artemisia annua (Asteraceae), a plant used in traditional Chinese medicine, is currently the basis of the last effective treatment strategy [11]. However, specific research of active natural products against severe malaria is scarce. Among the biologically active plant species, Terminalia albida, a member of the Combretaceae family traditionally used in Guinea to treat malaria, has shown promising anti-malarial effects against P. falciparum (clone Pf-K1, IC50 = 0.6 µg/mL) [12]. It was previously demonstrated that treatment with Terminalia macroptera, another species of the same genus, facilitated increased survival in experimental cerebral malaria (ECM) [13]. Therefore, this study was designed to assess the potential anti-malarial and antiplasmodial effects of Terminalia albida in the murine model of ECM. Anti-inflammatory and anti-oxidant mechanisms of Terminalia albida treatment, which may resolve neuro-inflammation, were also investigated both in vitro and in the murine model of ECM. The phytochemical content of the crude extract was then explored by a dereplication approach in order to understand the origin of the bioactivity.

Methods

Plant collection

The stem bark of Terminalia albida was collected in Danaya, Préfecture of Dubréka, Guinea. The plant was collected at maturity in a forest area. Authorization for collection of plant materials was obtained prior to collection at the Institut de Recherche et de Développement des Plantes Médicinales et Alimentaires de Guinée (IRDPMAG), Dubréka, Guinea. The identification and authentication was previously carried out by the Department of Botany of IRDPMAG where a voucher specimen (38HK457) was deposited [14].

Preparation of Terminalia albida extract

The stem barks of the plant were shade dried for 2 weeks and ground into powder. The powdered material (600 g) was macerated with 2 L of pure methanol (> 99%) for 72 h. The macerate was then filtered and evaporated under reduced pressure (Buchi® rotary evaporator, model R-200). The dried extracts were stored at − 20 °C until use. Before in vitro and in vivo experiments, stock solutions were dissolved in distilled water to provide working concentrations.

In vitro antiplasmodial activity

The in vitro antiplasmodial activity of Terminalia albida was investigated using the SYBR Green I-based fluorescence assay with P. falciparum chloroquine-resistant sensitive strain K1, as described before [15]. Chloroquine was used as the positive control. Briefly, K1 cultures were maintained at 2% haematocrit in RPMI 1640 containing 10% human serum, 3 g/L of glucose, 45 µg/L of hypoxanthine, and 50 µg/L of gentamicin, and incubated at 37 °C under a gas mixture of 5% O2, 5% CO2, and 90% N2. A suspension of sorbitol-synchronized, infected red blood cells was adjusted to 0.5% parasitaemia and 4% haematocrit in complete medium and added to the wells in a 96-well plate. Several wells containing non-parasitized erythrocytes at 4% haematocrit served as reference controls. Stock solutions (at 10 mM in ethanol for plant extracts and in water for chloroquine) were diluted serially in complete medium to test final concentrations ranging from 0 to 10−5 M in triplicates in the 96-well plate. Test plates were incubated at 37 °C for 48 h and 100 µL of SYBR Green I in lysis buffer was added to the wells. After 1 h of incubation in the dark at room temperature, fluorescence data were acquired on a Cytofluor II fluorescence multiwell plate reader (PerSeptive Biosystems, Framingham, USA) with excitation and emission wavelength bands at 485 and 530 nm, respectively, and a gain setting equal to 50. After subtraction of background values, the counts were plotted against the logarithm of the drug concentration and curve fitting by nonlinear regression (sigmoidal dose–response/variable slope equation) to yield the 50% inhibitory concentration (IC50) that served as a measure of the anti-malarial activity.

Animal studies

Female healthy C57BL/6 mice aged 12 weeks and weighing 20–22 g were obtained from Janvier Laboratories (Toulouse, France). For all in vivo experiments described below, the mice were kept in standard and constant laboratory conditions (23–25 °C, relative humidity around 60%, and light/dark cycles, i.e., 12/12 h) with unlimited access to food and tap water. Animal welfare requirements were strictly followed during the experiments as required by the Midi-Pyrénées ethics committee for animal experiments in Toulouse, France. The study was authorized with permit number APAFIS#5921-2016070118008477v3.

Acute oral toxicity assessment

Acute oral tests were performed as described before with slight modifications [13]. Mice were randomly divided in 2 groups of 3 mice and treated by oral route with a single dose of Terminalia albida (2000 mg/kg) or water (20 mL/kg) to follow the limit test proposed by the Organization for Economic Cooperation and Development (OECD) [16]. Animals were observed for the first 4 h after treatment to record immediate deaths, and once daily for 20 days to record deaths and behavioural changes. To evaluate the effect of Terminalia albida treatment on body weight, the weight was taken at Days 7, 14 and 20 and compared to Day 0 for both groups (Terminalia albida and water).

In vivo antiplasmodial and anti-malarial effects of Terminalia albida in ECM

The rodent malaria parasite, P. berghei (strain ANKA) (kindly given by A. Berry, CPTP research unit, Toulouse) was used throughout the study. Mice were infected by intraperitoneal injection with 200 µL of infected blood containing 1 × 106 parasitized erythrocytes on Day 0 (D0). The infected mice were randomly divided into 3 groups of 6 mice and treated by oral gavage for 4 consecutive days with 100 mg/kg of Terminalia albida crude extract. The positive control group received chloroquine (5 mg/kg) and the negative control group received distilled water (25 mL/kg). The extracts were administered orally once a day. Weight, parasitaemia, survival and neurological symptoms were followed daily. To evaluate the ability of treatments to prevent weight loss due to infection, the percentages of weight loss as compared to D0 were calculated. Parasitaemia was followed daily through thin blood smears from tail blood from the D3. Blood smears were fixed and stained with a fast-acting variation of May-Grünwald Giemsa staining (RAL 555 kit, RAL Diagnostics). Parasitaemia was determined by light microscopy using a 100 × objective lens as follows:  % parasitaemia = 100 × (number of parasitized RBC/total number of RBC counted). Average percentage of antiparasite activity was calculated at D4, D6, D7 and D8 as [(A − B)/A] × 100 where A is the average percentage parasitaemia in the negative control group (H2O) and B is the average percentage parasitaemia in the test group. To monitor the onset of neurological symptoms, 10 parameters were assessed daily between D3 and D7 to determine a rapid murine cerebral behaviour scale (RMCBS) as described by Caroll et al. [17]. The parameters measured were: gait, balance, exploratory behaviour, grooming, body position, limb strength, tactile escape reflex, ear pavilion reflex, toe reflex and aggressiveness. Each parameter was scored 0 to 2, with a 2 score correlating with the highest function. Survival was monitored twice daily. The percentage of survival was determined over a period of 20 days post-infection and compared between groups.

Brain cell analysis by flow cytometry

After 7 days of infection, mice brains were removed and crushed in PBS−/− (3 mice per group), centrifuged, filtered (100 μM) and mononuclear cells were separated over a Lymphoprep gradient (Alere Technologies AS, Oslo, Norway), and total leucocytes per brain counted. Isolated brain leucocytes were labelled with antibodies coupled to fluorochromes (all from Miltenyi Biotec, France) to distinguish the different T cell populations: CD3-PE (lymphocytes), CD4-VioBright FITC (CD4 T Lymphocytes), CD8-VioGreen (CD8 T Lymphocytes) and Live dead-Violet (dead cells). Cells were collected on a LSR Fortessa cytometer (BD Biosciences) using FACSDiva™ software.

Gene expression of pro- and anti-inflammatory markers in mice brains

To measure the effect of Terminalia albida treatment on the inflammatory response in P. berghei-infected mice, the mice were divided into 3 groups of 6 mice, infected and treated with Terminalia albida crude extract, chloroquine or distilled water, as before. Mice were sacrificed 7 or 8 days after infection (D7 or D8). Mice brains were dissected and divided longitudinally into two equal parts to be used for RT-qPCR and ELISA experiments. Half of the brain was placed in lysing matrix tubes (MP Biomedicals) containing 650 μL of RLT lysis buffer (from the EZ-10 Spin Column Total RNA Minipreps Super Kit, Bio Basic). The brains were crushed in a FastPrep®-24 (MP) and centrifuged for 10 min. mRNA was prepared with the EZ-10 Spin Column Total RNA Minipreps Super Kit (Bio Basic) using the manufacturer’s protocol. Synthesis of cDNA was performed according to the manufacturer’s recommendations (Verso kit, Thermo Scientific). RT–qPCR was performed on a LightCycler 480 system using LightCycler SYBR Green I Master Mix (Roche Diagnostics). The primers (Eurogentec) were designed with the software Primer 3. GAPDH mRNA was used as the invariant control. Serially diluted samples of pooled cDNA were used as external standards in each run for the quantification. The primers used are listed in Table 1.

Table 1 Sequences of murine primers used in quantitative RT-PCR experiments

Levels of cytokines in mice brains

The remaining half of the brain was crushed in PBS between two glass slides and filtered through a 100 µM sterile filter. After centrifugation (1 min at 10,000g and room temperature), the remaining pellet was homogenized in 5 mL IGEPAL, a protease inhibitor solution, and stored at − 80 °C until use. The levels of IL-6, TNF, IL-1β, and IL-10 were determined by enzyme-linked immunosorbent assay (ELISA) using commercially available OptiEIA murine kits (BD Biosciences) according to the manufacturers’ instructions.

Gene expression of pro- and anti-inflammatory markers by murine macrophages after LPS/IFNγ activation and Terminalia albida treatment

Peritoneal macrophages were harvested from 6 healthy mice. The peritoneal cavity of each mouse was washed with 5 mL of sterile NaCl 0.9% before harvesting resident peritoneal cells. Collected cells were centrifuged at 1500 rpm for 10 min and the cell pellet was suspended in Dulbecco’s modified Eagle’s medium (Invitrogen) supplemented with glutamine (Invitrogen), penicillin, streptomycin (Invitrogen) and 5% heat-inactivated fetal calf serum. Cells (5.105/well) were left to adhere for 2 h at 37 °C and 5% CO2, and non-adherent cells were removed by washing with PBS. After washing, adherent macrophages were immediately stimulated with 10 ng/mL lipopolysaccharide (LPS) and 40 UI/mL IFNγ (Clinisciences) during 2 h. After stimulation, cells were washed and treated with 10 µg/mL Terminalia albida crude extract diluted in medium or with medium alone for 4 h at 37 °C and 5% CO2. The dose of 10 µg/mL was previously determined by an LDH test showing that this concentration is not toxic to mouse peritoneal macrophages (Additional file 1: Fig. S1). Each condition was tested in triplicate. mRNA extraction, cDNA synthesis and RT–qPCR were performed as described above. The primers used are listed in Table 1.

Levels of cytokines produced by murine macrophages after LPS/IFNγ activation and Terminalia albida treatment

After LPS/IFNγ stimulation (10 ng/mL LPS and 40 UI/mL IFNγ) during 2 h, murine peritoneal macrophages were treated with Terminalia albida (10 µg/mL) or medium alone for 24 h at 37 °C and 5% CO2. Each condition was tested in triplicate. The supernatants were then assayed to quantify cytokines (TNF, IL-1β, IL-6, IL-10) by ELISA using commercially available OptiEIA murine kits (BD Biosciences) according to the manufacturers’ instructions.

In vitro ROS production model and Terminalia albida scavenging activity

The Light-Up Cell System (LUCS) was used to evaluate the ability of Terminalia albida to inhibit the production of ROS by HepG2 cells, as previously described [18]. Briefly, Terminalia albida methanolic extract was solubilized in DMSO and 9 serial dilutions were prepared from 1.92 mg/mL to 0.0075 mg/mL. Since DMSO 4% was used to dilute the highest concentration of extract, DMSO 4% was used as negative control. No toxic effect was observed on HEpG2 cells at this concentration. HepG2 cells (75,000/well) were cultured for 24 h in DMEM complemented with 10% FBS and 1% penicillin–streptomycin solution at 37 °C and 5% CO2. The experiments were carried out in DMEM without SVF. At least two independent experiments were performed on 96-well plates, each in triplicate. Cells were then incubated for 4 h in the presence or not of increased concentrations of Terminalia albida extract. Extract dilutions were added by replacing the media. Cells were then treated with the fluorescent marker thiazole orange at 4 µM for 1 h and fluorescence was measured at 535 nm (emission) during 20 recurrent irradiations at 480 nm (excitation). Antioxidant index (AI) was calculated from the kinetics using the formula AI = 100 – 100 (0∫12 RFUn sample/0∫12 RFUn control). Dose/response curves were obtained by combining AI as a function of the logarithm (10) of the sample concentration and processed by fit sigmoid according to the equation AI = AImin + (AImax − AImin)/(1 + 10(Log(EC50−CE)*HS)) to determine EC50value.

UHPLC-HRMS profiling

Acquisition of metabolite profiles of Terminalia albida methanol extract (1 mg/mL), data processing and statistical analysis were performed as previously described [19].

Statistical analysis

Results were expressed as mean ± SEM (standard error of mean) and analysed using Graph Pad Prism software version 6. Comparisons were performed by a one-way analysis of variance (ANOVA) followed by the means multiple comparison method of Bonferroni–Dunnett. Mann–Whitney U-test was used for two-by-two comparisons. Differences were considered significant if P < 0.05.

Results

Acute oral toxicity assessment and determination of the test dose

Terminalia albida administration to C57BL/6 mice at a dose of 2000 mg/kg did not cause mortality or major behavioural changes among experimental animals during the 20 days of follow-up. Mice body weight was not modified by the administration of Terminalia albida (Additional file 2: Fig. S2). Thus, LD50 of Terminalia albida is greater than 2000 mg/kg in C57BL/6 mice. Terminalia albida crude extract, as prepared in this work, can therefore be classified as category 5 and considered non-toxic orally, according to the OECD’s Globally Harmonized System of Classification [16]. Based on these results, anti-malarial activity in ECM was assessed at 100 mg/kg.

In vitro and in vivo antiplasmodial activity

Terminalia albida crude extract presented an IC50 of 1.5 μg/ml and IC50 for chloroquine was 0.08 µM on the chloroquine-resistant K1 strain of P. falciparum. In vivo, mice that received water were parasitized from D4, while mice treated with Terminalia albida were positive from D7. Mice that received water were all dead at D8. At D4, parasite chemosuppression by Terminalia albida was 100% and this complete inhibition lasted until D6. At D7, Terminalia albida treatment resulted in parasite suppression of 89% compared to water (Fig. 1a, b, P < 0.0001). However, Terminalia albida treatment did not limit parasite multiplication since parasitaemia increased until 7% at D20. Conversely, chloroquine treatment abolished parasite multiplication (Fig. 1a, b).

Fig. 1
figure1

Antiplasmodial activity of Terminalia albida treatment in ECM model. C57BL/6 mice were infected with P. berghei ANKA and treated 2 h later with chloroquine (5 mg/kg), Terminalia albida crude extract (100 mg/kg) or water (25 mL/kg) from Day 0 to Day 3. a Mean parasite densities during infection. b Percentages of parasite suppression according to the treatment, calculated by comparison to H2O treated mice. **P < 0.005, ***P < 0.0005 compared Terminalia albida to H2O group

Effect of Terminalia albida treatment on survival, weight and neurologic symptoms in ECM

Terminalia albida treatment greatly improved survival as chloroquine and Terminalia albida treatments were statistically similar until D20 although Fig. 2a suggests that Terminalia albida treatment was less effective than chloroquine from D12 onwards. At D20, chloroquine was statistically more effective than Terminalia albida treatment (Fig. 2a, P = 0.045). Terminalia albida treatment prevented death up to D12 and maintained a 50% survival rate at D20 (Fig. 2a. P = 0.003 at D8, P = 0.0005 from D9 to D13, and P < 0.05 until D20 for the comparison between Terminalia albida and water). Terminalia albida treatment improved the overall condition of the mice since the treated group lost less weight than the water group (the groups were compared up to D7 only because the group that received water had only one living mouse left on D8. P = 0.037 at D7. Figure 2b). The comparison of RMCBS between groups showed a rapid deterioration of cerebral functions in untreated mice from D5 (Fig. 2c). Although mice treated with Terminalia albida had slightly impaired brain functions at D6 and D7, there was no statistical difference between the scores of the CQ and Terminalia-treated mice at D6 and D7 (Fig. 2c).

Fig. 2
figure2

Effect of Terminalia albida treatment on survival, weight and cerebral symptoms in ECM model. C57BL/6 mice were infected with P. berghei ANKA and treated 2 h later with chloroquine (5 mg/kg), Terminalia albida crude extract (100 mg/kg) or water (25 mL/kg) from Day 0 to Day 4. a Percentage of survival. b Percentage of weight loss at each day compared to Day 0. c Rapid murine cerebral behavior scale (RMCBS) between D3 and D7. *P < 0.05 compared Terminalia albida to H2O groups at D7. *P < 0.05 and **P < 0.005 compared Terminalia albida to H2O groups. §P < 0.05 compared Terminalia albida to chloroquine groups

Effect of Terminalia albida on T cell infiltration in the brain of Plasmodium berghei-infected mice

Leucocyte recruitment and activation in the brain is one of the key mechanisms of ECM, particularly CD8 effector T cells [20]. To assess such mechanism of P. berghei-infected mice according to the treatment received (chloroquine or Terminalia albida or H2O), the percentages of the different T cell populations were compared in brains after 7 days of infection by flow cytometry. Interestingly, the percentages of CD3 T and CD3 CD8 T cells in brain was lower in mice treated with chloroquine or Terminalia albida extract, compared to mice that received water (Fig. 3a, b). Conversely, the percentage of CD4 T cells was higher in chloroquine and Terminalia albida-treated mice, compared to water-treated mice (Fig. 3c, P = 0.04 for both comparisons).

Fig. 3
figure3

Effect of Terminalia albida on cell infiltration in the brain of Plasmodium berghei-infected mice. C57BL/6 mice were infected with P. berghei and treated 2 h later with chloroquine (5 mg/kg), Terminalia albida crude extract (100 mg/kg) or water (25 mL/kg) from Day 0 to Day 4. Brains were analysed by flow cytometry at D7 post-infection. Percentages of cell populations were compared between groups for CD3+ (a), CD8+ (b) and CD4+ T lymphocytes (c). *P < 0.05, **P < 0.005, ***P < 0.0005

Absence of pro-inflammatory response in brains of Terminalia albida-treated mice during ECM

To assess the immunological state of brains from Terminalia albida-treated mice during ECM, mRNA levels of pro- and anti-inflammatory markers were measured in the 3 groups of mice (Terminalia albida, chloroquine and H2O). Plasmodium berghei mRNA was undetectable at D7 in brains of chloroquine and Terminalia albida-treated mice (Fig. 4a). The expression of VEGF, a marker of vascular permeability and endothelial activation, was lowered in the chloroquine group compared to the water group (Fig. 4a). Conversely, the expression of ICAM-1, another marker of endothelial activation was diminished in brains of mice treated with Terminalia albida (Fig. 4a, P = 0.002). Among the pro-inflammatory cytokines tested, IFNγ expression was completely abolished in mice treated with Terminalia albida similarly to the chloroquine group, in comparison to untreated mice (Fig. 4b. P = 0.006 and P = 0.005 for Terminalia albida versus H2O and chloroquine versus H2O, respectively). Interestingly, Terminalia albida treatment also significantly limited the expression of granzyme B similarly to chloroquine (Fig. 4a. P = 0.003 and 0.002 for H2O versus Terminalia albida and versus chloroquine). For TNF, IL-1β and IL-12 expression, the effect of Terminalia albida treatment compared to chloroquine or H2O was not significant (Fig. 4b). Among the other pro-inflammatory markers tested, Terminalia albida treatment also diminished CD11b expression similarly to chloroquine (Fig. 4b, P = 0.006). Finally, for TLR2, NFκB, PGES and anti-inflammatory markers (TGFβ, CD36 and haem oxygenase 1 named HO-1), Terminalia albida treatment had no significant effect (Fig. 4c, d). Cytokine levels were also measured in brains on D8. However, cytokine levels were similar regardless of the treatment received by the mice (Fig. 4e).

Fig. 4
figure4

Effect of Terminalia albida treatment on the expression of pro- and anti-inflammatory markers in brains of Plasmodium berghei-infected mice. C57BL/6 mice were infected with P. berghei and treated with chloroquine (5 mg/kg), Terminalia albida (100 mg/kg) or water. Brains were harvested at D7 (for P. berghei and VEGF) or D8 post-infection (for the other markers). Gene expression was measured by RT-qPCR and cytokine levels were measured by ELISA. Gene expression levels of (a) P. berghei, VEGF, ICAM and Granzyme B; b pro-inflammatory cytokines, c other pro-inflammatory markers, and d anti-inflammatory markers. e Cytokine levels in pg/mL. *P < 0.05, **P < 0.005, ***P < 0.0005. Data presented are mean ± standard deviation

Anti-inflammatory properties of Terminalia albida in a non-malarial context

To further confirm the anti-inflammatory properties of Terminalia albida assessed in the ECM model, additional experiments were performed by stimulating the peritoneal macrophages of C57BL/6 healthy mice with LPS and IFN and treating them with the methanolic extract of Terminalia albida. The expression of several pro-inflammatory markers was decreased following treatment of the cells with Terminalia albida compared to untreated cells: TNF (P = 0.04), IL12 (P = 0.003), NFkB (P = 0.005) and inducible nitric oxide synthase (iNOS) (P = 0.001) (Fig. 5a, c). Notably, CD36 and HO-1, two anti-inflammatory markers, were more expressed by Terminalia albida-treated cells (Fig. 5d, P = 0.001 and P = 0.01, respectively). In addition, a significant decrease was also obtained in the enzymatic quantification of TNF, IL-6 and IL-1β for Terminalia albida treated-cells (Fig. 5e, P = 0.001, P = 0.02 and P = 0.03, respectively).

Fig. 5
figure5

Assessment of in vitro anti-inflammatory properties of Terminalia albida. Murine macrophages were activated by LPS and IFNγ in the presence or not of 10 µg/mL of Terminalia albida. Gene expression levels of a pro-inflammatory cytokines, b other pro-inflammatory markers, c pro-inflammatory signalling pathways, and d anti-inflammatory markers. e Cytokine levels measured in supernatants, in pg/mL. *P < 0.05, **P < 0.005, ***P < 0.0005. Data are presented as mean ± SD

Anti-oxidative properties of Terminalia albida

The evaluation of Terminalia albida’s ability to neutralize intracellular radical species of the human HepG2 cells showed a remarkable dose-dependent antioxidant activity (Fig. 6a). The antioxidant index (AI) calculated from the area under curves was 997 at concentrations greater than or equal to 60 μg/mL (Fig. 6b). The EC50 of the extract was 10.2 μg/mL. Finally, the absence of a fluorescent signal higher than the control at time 0 indicates an absence of cytotoxicity at 4 h of treatment.

Fig. 6
figure6

LUCS anti-oxidant assay. a Kinetics of fluorescence emission recorded under illumination for different concentrations of extract (7.5 10−3 mg/mL–1.92 mg/mL) using the LUCS assay. b Corresponding antioxidant index calculated from RFU values as follows: AI = 1000–1000 (0∫12 RFUn sample/0∫12 RFUn control)

Phytochemical characterization of the Terminalia albida crude extract

After maceration with methanol for 72 h, 253.5 g of crude extracts were obtained. The extracts were qualitatively analysed by UHPLC-HRMS. Metabolite profiling of Terminalia albida was acquired in positive and negative ionization mode. Qualitative analysis by UHPLC-HRMS of Terminalia albida stem bark enabled the putative identification of 16 known compounds through HRMS and MS/MS fragmentation patterns using MzMine, MS-DIAL and MS-FINDER software (Table 2). Among the top 12 annotated compounds, 6 are tannins (flavogallonic acid, flavogallonic acid-Me ester, ellagic acid, ellagic acid 3,8-di-Me ether, corilagin, ellagic acid; 2,3,7-tri-me ether), 4 are triterpenoids (23-O-galloylarjunolic acid 28-O-β-d-glucopyranosyl ester, 23-galloylarjunolic acid, 23-galloylterminolic acid, 7-beta-hydroxy-23-deoxojessic acid), 1 is phenol glucoside gallate (vanillic acid 4-(6-galloylglucoside)) and 1 is cycloartanols and derivatives (ouadrangularic acid F).

Table 2 Putative identified features (m/z × RT pairs) using HRMS and MS/MS fragmentation patterns using MzMine, MS-finder and DNP database

Discussion

In this study, the anti-malarial and antiparasite activity of Terminalia albida found respectively in ECM and in vitro was high. In vivo, mice survived until D12, the limit for neurological symptoms in this model, and there was a 50% rate after 20 days of infection, while untreated mice were all dead by D8. Such a result obtained with a crude plant extract is quite remarkable when compared to many other similar studies (performed with crude plant extracts at doses ≤ 300 mg/Kg) in which mean mice survival often did not exceed 9 days [21,22,23]. Antiparasite activity was also very high in vivo, 100% at D4 and until D6, 89% at D7, and 61% at D8. Interestingly, mice treated with Terminalia albida have developed a parasitaemia that remained below 8% until D20, while the average parasitaemia of untreated mice reached 10%. This result may be explained by the pharmacokinetics of the active principle(s) responsible for the antiparasite activity. Further bio-guided fractionation is needed to decipher the reasons of such activity.

In addition, antiparasite activity found in vitro was also interesting with an IC50 of 1.5 µg/ml. This value is slightly higher than that of 0.6 µg/mL, previously found by Traore et al. in 2014 [12]. This difference may be due to the disparity of harvesting locations, harvest time, and extraction methods that influence plant biological active compounds [24]. In addition, Traore et al. used the lactate dehydrogenase assay to measure antiplasmodial activity whereas a Sybr green assay was used in the present study. These different methods may also explain the small disparities between the two studies.

In this research, the aim was to elucidate whether, in addition to its antiparasitic properties, Terminalia albida presents anti-inflammatory and anti-oxidant activities useful for the resolution of cerebral malaria. During malaria, the first immune responses (oxidative and inflammatory) induced by monocytes are essential to control parasite multiplication. However, excessive and inappropriate activation of the immune system is detrimental to the host and contributes to the severe form that can lead to death [25]. Mechanisms leading to ECM involve the recruitment of T lymphocytes to the brain, particularly CD8 T cells known to be responsible for lethal neuropathology [8]. In the ECM model, treatment with Terminalia albida, similarly to chloroquine, greatly restrained the recruitment of T cells and more specifically of CD8 T cells in mice brains after 7 days of infection. It seems logical since at D7, the parasitaemia of the treated mice was very low and the parasite mRNA undetectable.

Here, brains from infected mice treated with the methanolic extract of Terminalia albida showed reduced expression of IFNγ, CD11b, ICAM-1 and granzyme B. The secretion of IFNγ by NK cells contributes to the CM pathogenesis by increasing the expression of endothelial receptors including ICAM-1 and VCAM involved in the sequestration of parasitized red blood cells in the murine model [26]. This phenomenon induces the activation of endothelial cells by excessive production of pro-inflammatory cytokines such as TNF, IL-6, IL-1β, IL-12 and the recruitment of inflammatory leukocytes in the cerebral micro-vessels that damage the blood–brain barrier [25]. CD11b constitutes a marker of brain endothelium disruption, as described before [27]. In addition, CD8 + T cells have been identified as a major mediator in death during ECM by their capacity to produce granzyme B able to kill P. berghei antigen-presenting endothelial cells and to damage neuronal cells [8]. Thus, during ECM, Terminalia albida treatment not only limits parasitaemia but also reduces the expression of mediators involved in pathogenesis. Such anti-inflammatory properties were confirmed in vitro in a non-malarial context. After LPS/IFNγ stimulation in murine peritoneal macrophages, Terminalia albida treatment led to a significant inhibition of the expression of TNF, IL-1β, IL-6 and IL12, four pro-inflammatory cytokines. NFkB, the transcription factor regulating the inflammatory response has been suggested as therapeutic target to treat severe malaria [28]. In the present study, NFkB was also less expressed by cells treated with the plant compared to untreated cells. Similarly, CD36, an important marker for malaria, was higher in treated cells compared to untreated ones (Fig. 4). Through PPARγ activation, the scavenger receptor CD36 is known for its implication in P. berghei elimination through non-opsonic phagocytosis [29].

Terminalia albida also presented highly interesting antioxidant properties in vitro. LPS/IFNγ-activated cells treated with Terminalia albida showed a lower expression of iNOS and higher HO-1. In addition, Terminalia albida neutralized intracellular radical species of the human HepG2 cells in a dose-dependent antioxidant activity. It is largely accepted that oxidative stress is involved in the pathogenesis of severe malaria [30]. Nitric oxide is produced via the enzyme NOS and the substrate l-arginine. However, its beneficial or unfavourable effect is controversial in the experimental model [31, 32]. In the present study, Terminalia albida limits iNOS expression in vitro and increases survival in ECM. HO-1 is a key protective gene in the host infected by Plasmodium, able to catabolize toxic free haem into iron, biliverdin and carbon monoxide. HO-1 induction has been shown to prevent blood–brain barrier disruption, brain microvasculature congestion and neuro-inflammation in the murine model [33]. Thus, Terminalia albida presents antiplasmodial, anti-inflammatory and anti-oxidant properties. However, these activities are not sufficient to limit parasitic multiplication as chloroquine does. These results suggest that the anti-inflammatory and anti-oxidant activities of the extract limit neuro-inflammation secondary to infection, but that the antiplasmodial activity is not sufficient to cancel the multiplication of the parasite in this model.

Terminalia species are rich sources of secondary metabolites including cyclic triterpenes and their derivatives, and polyphenols (flavonoids, phenolic acids and tannins). Several Terminalia extracts or fractions have been tested for their anti-Plasmodium activities [34,35,36,37,38,39,40,41,42] but most of these studies lack chemical characterization of the studied extracts, except Muganga et al. [36] who isolated the active compounds, through a bioguided fractionation [36]. Among all the compounds isolated, ellagic acid, already know to have a strong anti-malarial activity (IC50 between 90 and 175 ng/mL) [43], was found to be the main antiplasmodial compound (IC50 = 0.175 μg/mL) in Terminalia mollins, while ellagic acid derivatives were inactive, suggesting the crucial role of the free hydroxyl groups in antiplasmodial activity. In addition, gallic acid and some condensed tannins, such as catechin, gallocatechin and epigallocatechin, have been isolated and found to have a lower antiplasmodial activity (IC50 > 25 μg/mL) than the one found for ellagic acid, and a mixture of punicalagin A and B (anomeric isomers) did not present any interesting antiplasmodial activity. Akanbi et al. [44] evaluated the anti-malarial activity of total saponins extracted from Terminalia avicennioides and concluded that the Terminalia’s saponins may be able to increase the level of immunity against malaria infection, responsible for the antiplasmodial activity displayed by the extract [44]. However, saponin isolation was based on a phytochemical extraction followed by TLC analysis and a non-specific colorimetric test. No complementary analyses such as IR, UV, LC–MS/MS dereplication or NMR, were carried out to confirm the composition of this extract, which makes these results questionable. In addition, saponins are characterized by a strong haemolytic activity and may be toxic [45]. Finally, 23-galloylarjunolic acid, a triterpene of the galloyl group type, has shown interesting antiplasmodial activity against the chloroquine-sensitive (D6) and chloroquine-resistant (W2) strains with respective IC50s of 4.5 µg/mL and 2.8 µg/mL and selectivity index greater than 1 [46]. Thus, in Terminalia albida extract, ellagic acid and 23-galloylarjunolic acid may be responsible, at least in part, for the antiplasmodial activity.

Phenolic compounds are widely described in the literature for their potential biological activity such as anti-inflammatory and immunomodulatory effects [47, 48]. They are excellent anti-oxidants due to the presence of a hydroxyl group capable of capturing oxygen free radicals [49]. In addition to anti-Plasmodium activity, ellagic acid has known anti-oxidant and anti-inflammatory activity that could explain the higher survival rate obtained after Terminalia albida treatment in ECM [47, 50]. In a model of carrageenan-induced inflammation, ellagic acid prevented the production of pro-inflammatory mediators and promoted the production of anti-inflammatory IL-10 and antioxidant glutathione [51]. Eschweilenol C has also been reported for anti-inflammatory activity in the aqueous extract of Terminalia fagifolia by inhibition of NFkB pathway in LPS-activated microglial cells [48]. Corilagin has also been studied for its anti-inflammatory activity based on the inhibition of the NFkB signaling pathway and even tested as a treatment in a model of sepsis [52,53,54]. Anti-inflammatory and anti-oxidant effects of a derivative of vanillic acid, vanillic acid 4-(6-galloylglucoside), were also reported both in vitro and in vivo in the carrageenan-based inflammation murine model [55, 56]. Finally, cyclic triterpenes are also a phytochemical group with various biological activities, particularly in inflammatory and oxidative diseases [57]. Nevertheless, further bioassay-guided fractionation will be necessary to confirm the origin of the antiplasmodial, anti-inflammatory and anti-oxidant activities of Terminalia albida, including synergistic potential between tannins, lignans and terpenoids found in this plant.

Conclusion

Terminalia albida displays highly interesting anti-malarial, anti-inflammatory and anti-oxidant properties. UHPLC-HRMS analysis showed that 12 compounds are found in Terminalia albida and may be implicated in its biological activities. However, further investigations into the long-term toxicity, prophylactic effects and antiparasite mechanisms are necessary before recommending the use of Terminalia albida or its constituents for malaria treatment or prevention.

Availability of data and materials

The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CD:

cluster of differentiation

CPTP:

Centre de Physiopathologie de Toulouse Purpan

ECM:

experimental cerebral malaria

HepG2:

liver hepatocellular cells G2

HO-1:

haem oxygenase-1

IC50:

50% inhibitory concentration

ICAM-1:

intercellular adhesion protein 1

iEs:

infected erythrocytes

IFNγ:

interferon gamma

IL:

interleukin

iNOS :

nitric oxide synthase

LC/MS:

liquid chromatography–mass spectrometry

LD50:

50% lethal dose

LPS :

lipopolysaccharide

NFkB:

nuclear factor-kappa B

NK:

natural killer

OECD:

Organization for Economic Cooperation and Development

PPARγ:

peroxisome proliferator-activated receptor

ROS:

reactive oxygen species

TNF:

tumor necrosis factor

VCAM-1:

vascular cell adhesion protein 1

References

  1. 1.

    WHO. World malaria report. Geneva: World Health Organization; 2017.

    Google Scholar 

  2. 2.

    Ashley EA, Dhorda M, Fairhurst RM, Amaratunga C, Lim P, Suon S, et al. Spread of artemisinin resistance in Plasmodium falciparum malaria. N Engl J Med. 2014;371:411–23.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  3. 3.

    Ikeda M, Kaneko M, Tachibana S-I, Balikagala B, Sakurai-Yatsushiro M, Yatsushiro S, et al. Artemisinin-resistant Plasmodium falciparum with high survival rates, Uganda, 2014–2016. Emerg Infect Dis. 2018;24:718–26.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  4. 4.

    Lu F, Culleton R, Zhang M, Ramaprasad A, von Seidlein L, Zhou H, et al. Emergence of indigenous artemisinin-resistant Plasmodium falciparum in Africa. N Engl J Med. 2017;376:991–3.

    PubMed  Article  PubMed Central  Google Scholar 

  5. 5.

    Dondorp AM, Fanello CI, Hendriksen ICE, Gomes E, Seni A, Chhaganlal KD, et al. Artesunate versus quinine in the treatment of severe falciparum malaria in African children (AQUAMAT): an open-label, randomised trial. Lancet. 2010;376:1647–57.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  6. 6.

    Storm J, Craig AG. Pathogenesis of cerebral malaria-inflammation and cytoadherence. Front Cell Infect Microbiol. 2014;4:100.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  7. 7.

    White NJ, Turner GDH, Day NPJ, Dondorp AM. Lethal malaria: Marchiafava and Bignami were right. J Infect Dis. 2013;208:192–8.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  8. 8.

    Howland SW, Poh CM, Rénia L. Activated brain endothelial cells cross-present malaria antigen. PLoS Pathog. 2015;11:e1004963.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  9. 9.

    Becker K, Tilley L, Vennerstrom JL, Roberts D, Rogerson S, Ginsburg H. Oxidative stress in malaria parasite-infected erythrocytes: host-parasite interactions. Int J Parasitol. 2004;34:163–89.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  10. 10.

    Aguilar R, Marrocco T, Skorokhod OA, Barbosa A, Nhabomba A, Manaca MN, et al. Blood oxidative stress markers and Plasmodium falciparum malaria in non-immune African children. Br J Haematol. 2014;164:438–50.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  11. 11.

    Ouji M, Augereau J-M, Paloque L, Benoit-Vical F. Plasmodium falciparum resistance to artemisinin-based combination therapies: a sword of Damocles in the path toward malaria elimination. Parasite. 2018;25:24.

    PubMed  PubMed Central  Article  Google Scholar 

  12. 12.

    Traore MS, Diane S, Diallo MST, Balde ES, Balde MA, Camara A, et al. In Vitro antiprotozoal and cytotoxic activity of ethnopharmacologically selected Guinean plants. Planta Med. 2014;80:1340–4.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  13. 13.

    Haidara M, Haddad M, Denou A, Marti G, Bourgeade-Delmas S, Sanogo R, et al. In vivo validation of anti-malarial activity of crude extracts of Terminalia macroptera, a Malian medicinal plant. Malar J. 2018;17:68.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  14. 14.

    Traore MS, Baldé MA, Diallo MST, Baldé ES, Diané S, Camara A, et al. Ethnobotanical survey on medicinal plants used by Guinean traditional healers in the treatment of malaria. J Ethnopharmacol. 2013;150:1145–53.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  15. 15.

    Smilkstein M, Sriwilaijaroen N, Kelly JX, Wilairat P, Riscoe M. Simple and inexpensive fluorescence-based technique for high-throughput antimalarial drug screening. Antimicrob Agents Chemother. 2004;48:1803–6.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  16. 16.

    OECD, et al. OECD guidelines for the testing of chemicals, Section 4: health effects. Test no. 425: acute oral toxicity: up-and-down procedure. Paris: OECD Publishing; 2008.

    Google Scholar 

  17. 17.

    Carroll RW, Wainwright MS, Kim K-Y, Kidambi T, Gómez ND, Taylor T, et al. A rapid murine coma and behavior scale for quantitative assessment of murine cerebral malaria. PLoS One. 2010;5(10):e13124.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  18. 18.

    Derick S, Gironde C, Perio P, Reybier K, Nepveu F, Jauneau A, et al. LUCS (Light-Up Cell System), a universal high throughput assay for homeostasis evaluation in live cells. Sci Rep. 2017;7:18069.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  19. 19.

    Chassagne F, Haddad M, Amiel A, Phakeovilay C, Manithip C, Bourdy G, et al. A metabolomic approach to identify anti-hepatocarcinogenic compounds from plants used traditionally in the treatment of liver diseases. Fitoterapia. 2018;127:226–36.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  20. 20.

    Howland SW, Claser C, Poh CM, Gun SY, Rénia L. Pathogenic CD8 + T cells in experimental cerebral malaria. Semin Immunopathol. 2015;37:221–31.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  21. 21.

    Hintsa G, Sibhat GG, Karim A. Evaluation of antimalarial activity of the leaf latex and TLC isolates from Aloe megalacantha Baker in Plasmodium berghei infected mice. Evid-Based Complement Altern Med. 2019;2019:6459498.

    Article  Google Scholar 

  22. 22.

    Mzena T, Swai H, Chacha M. Antimalarial activity of Cucumis metuliferus and Lippia kituiensis against Plasmodium berghei infection in mice. Res Rep Trop Med. 2018;9:81–8.

    PubMed  PubMed Central  Google Scholar 

  23. 23.

    Nureye D, Assefa S, Nedi T, Engidawork E. In vivo antimalarial activity of the 80% methanolic root bark extract and solvent fractions of Gardenia ternifolia Schumach. & Thonn. (Rubiaceae) against Plasmodium berghei. Evid-Based Complement Altern Med. 2018;2018:9217835.

    Article  Google Scholar 

  24. 24.

    Conforti F, Marcotullio MC, Menichini F, Statti GA, Vannutelli L, Burini G, et al. The influence of collection zone on glucosinolates, polyphenols and flavonoids contents and biological profiles of Capparis sicula ssp. sicula. Food Sci Technol Int. 2011;17:87–97.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  25. 25.

    Dunst J, Kamena F, Matuschewski K. Cytokines and chemokines in cerebral malaria pathogenesis. Front Cell Infect Microbiol. 2017;7:324.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  26. 26.

    Amante FH, Haque A, Stanley AC, de Rivera F, Randall LM, Wilson YA, et al. Immune-mediated mechanisms of parasite tissue sequestration during experimental cerebral malaria. J Immunol. 2010;185:3632–42.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  27. 27.

    Cahayani WA, Norahmawati E, Budiarti N, Fitri LE. Increased CD11b and hypoxia-inducible factors-1 alpha expressions in the lung tissue and surfactant protein-D levels in serum are related with acute lung injury in severe malaria of C57BL/6 mice. Iran J Parasitol. 2016;11:303–15.

    PubMed  PubMed Central  Google Scholar 

  28. 28.

    Tripathi AK, Sha W, Shulaev V, Stins MF, Sullivan DJ. Plasmodium falciparum-infected erythrocytes induce NF-kappaB regulated inflammatory pathways in human cerebral endothelium. Blood. 2009;114:4243–52.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  29. 29.

    McGilvray ID, Serghides L, Kapus A, Rotstein OD, Kain KC. Nonopsonic monocyte/macrophage phagocytosis of Plasmodium falciparum-parasitized erythrocytes: a role for CD36 in malarial clearance. Blood. 2000;96:3231–40.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  30. 30.

    Percário S, Moreira DR, Gomes BAQ, Ferreira MES, Gonçalves ACM, Laurindo PSOC, et al. Oxidative stress in malaria. Int J Mol Sci. 2012;13:16346–72.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  31. 31.

    Serghides L, Kim H, Lu Z, Kain DC, Miller C, Francis RC, et al. Inhaled nitric oxide reduces endothelial activation and parasite accumulation in the brain, and enhances survival in experimental cerebral malaria. PLoS One. 2011;6:e27714.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  32. 32.

    Xu H, Feng Y, Chen G, Zhu X, Pang W, Du Y, et al. L-arginine exacerbates experimental cerebral malaria by enhancing pro-inflammatory responses. Tohoku J Exp Med. 2015;236:21–31.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  33. 33.

    Pamplona A, Ferreira A, Balla J, Jeney V, Balla G, Epiphanio S, et al. Heme oxygenase-1 and carbon monoxide suppress the pathogenesis of experimental cerebral malaria. Nat Med. 2007;13:703–10.

    CAS  PubMed  Article  Google Scholar 

  34. 34.

    Ohashi M, Amoa-Bosompem M, Kwofie KD, Agyapong J, Adegle R, Sakyiamah MM, et al. In vitro antiprotozoan activity and mechanisms of action of selected Ghanaian medicinal plants against Trypanosoma, Leishmania, and Plasmodium parasites. Phytother Res. 2018;32:1617–30.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  35. 35.

    Mbouna CDJ, Kouipou RMT, Keumoe R, Tchokouaha LRY, Fokou PVT, Tali BMT, et al. Potent antiplasmodial extracts and fractions from Terminalia mantaly and Terminalia superba. Malar J. 2018;17:142.

    PubMed  PubMed Central  Article  Google Scholar 

  36. 36.

    Muganga R, Angenot L, Tits M, Frédérich M. In vitro and in vivo antiplasmodial activity of three Rwandan medicinal plants and identification of their active compounds. Planta Med. 2014;80:482–9.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  37. 37.

    Apel C, Bignon J, Garcia-Alvarez MC, Ciccone S, Clerc P, Grondin I, et al. N-myristoyltransferases inhibitory activity of ellagitannins from Terminalia bentzoë (L.) L. f. subsp. bentzoë. Fitoterapia. 2018;131:91–5.

    CAS  PubMed  Article  Google Scholar 

  38. 38.

    Razak MR, Afzan A, Ali R, Jalaluddin NF, Wasiman MI, Zahari SH, Abdullah NR, Ismail Z, et al. Effect of selected local medicinal plants on the asexual blood stage of chloroquine resistant Plasmodium falciparum. BMC Complement Altern Med. 2014;14:492.

    Article  Google Scholar 

  39. 39.

    Abiodun O, Gbotosho G, Ajaiyeoba E, Happi T, Falade M, Wittlin S, et al. In vitro antiplasmodial activity and toxicity assessment of some plants from Nigerian ethnomedicine. Pharm Biol. 2011;49:9–14.

    PubMed  Article  Google Scholar 

  40. 40.

    Sanon S, Gansane A, Ouattara LP, Traore A, Ouedraogo IN, Tiono A, et al. In vitro antiplasmodial and cytotoxic properties of some medicinal plants from western Burkina Faso. Afr J Lab Med. 2013;2:81.

    PubMed  PubMed Central  Article  Google Scholar 

  41. 41.

    Ouattara LP, Sanon S, Mahiou-Leddet V, Gansané A, Baghdikian B, Traoré A, et al. In vitro antiplasmodial activity of some medicinal plants of Burkina Faso. Parasitol Res. 2014;113:405–16.

    PubMed  Article  PubMed Central  Google Scholar 

  42. 42.

    Bagavan A, Rahuman AA, Kamaraj C, Kaushik NK, Mohanakrishnan D, Sahal D. Antiplasmodial activity of botanical extracts against Plasmodium falciparum. Parasitol Res. 2011;108:1099–109.

    PubMed  Article  PubMed Central  Google Scholar 

  43. 43.

    Soh PN, Witkowski B, Olagnier D, Nicolau M-L, Garcia-Alvarez M-C, Berry A, et al. In vitro and in vivo properties of ellagic acid in malaria treatment. Antimicrob Agents Chemother. 2009;53:1100–6.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  44. 44.

    Akanbi OM, Elekofehinti O, Olatokunbo A, Adejuyigbe A, Jegede A. Anti-malarial activity of total saponins from Terminalia avicennioides and its effect on liver and haematological of infected mice. Drug Des. 2018;7:2169.

    Google Scholar 

  45. 45.

    Haddad M, Laurens V, Lacaille-Dubois M-A. Induction of apoptosis in a leukemia cell line by triterpene saponins from Albizia adianthifolia. Bioorg Med Chem. 2004;12:4725–34.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  46. 46.

    Machumi F, Midiwo JO, Jacob MR, Khan SI, Tekwani BL, Zhang J, et al. Phytochemical, antimicrobial and antiplasmodial investigations of Terminalia brownii. Nat Prod Commun. 2013;8:761–4.

    CAS  PubMed  PubMed Central  Google Scholar 

  47. 47.

    Abiodun OO, Rodríguez-Nogales A, Algieri F, Gomez-Caravaca AM, Segura-Carretero A, Utrilla MP, et al. Antiinflammatory and immunomodulatory activity of an ethanolic extract from the stem bark of Terminalia catappa L. (Combretaceae): in vitro and in vivo evidences. J Ethnopharmacol. 2016;192:309–19.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  48. 48.

    de Araújo A, Iles B, de Nogueira K, Dias J, Plácido A, Rodrigues A, et al. Antifungal and anti-inflammatory potential of eschweilenol C-rich fraction derived from Terminalia fagifolia Mart. J Ethnopharmacol. 2019;240:111941.

    Article  CAS  Google Scholar 

  49. 49.

    Manosroi A, Jantrawut P, Ogihara E, Yamamoto A, Fukatsu M, Yasukawa K, et al. Biological activities of phenolic compounds and triterpenoids from the galls of Terminalia chebula. Chem Biodivers. 2013;10:1448–63.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  50. 50.

    Zeb A. Ellagic acid in suppressing in vivo and in vitro oxidative stresses. Mol Cell Biochem. 2018;448:27–41.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  51. 51.

    El-Shitany NA, El-Bastawissy EA, El-desoky K. Ellagic acid protects against carrageenan-induced acute inflammation through inhibition of nuclear factor kappa B, inducible cyclooxygenase and proinflammatory cytokines and enhancement of interleukin-10 via an antioxidant mechanism. Int Immunopharmacol. 2014;19:290–9.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  52. 52.

    Zhao L, Zhang SL, Tao JY, Pang R, Jin F, Guo YJ, et al. Preliminary exploration on anti-inflammatory mechanism of corilagin (beta-1-O-galloyl-3,6-(R)-hexahydroxydiphenoyl-d-glucose) in vitro. Int Immunopharmacol. 2008;8:1059–64.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  53. 53.

    Dong XR, Luo M, Fan L, Zhang T, Liu L, Dong JH, et al. Corilagin inhibits the double strand break-triggered NF-kappaB pathway in irradiated microglial cells. Int J Mol Med. 2010;25:531–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  54. 54.

    Li H-R, Liu J, Zhang S-L, Luo T, Wu F, Dong J-H, et al. Corilagin ameliorates the extreme inflammatory status in sepsis through TLR4 signaling pathways. BMC Complement Altern Med. 2017;17:18.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  55. 55.

    Kim M-C, Kim S-J, Kim D-S, Jeon Y-D, Park SJ, Lee HS, et al. Vanillic acid inhibits inflammatory mediators by suppressing NF-κB in lipopolysaccharide-stimulated mouse peritoneal macrophages. Immunopharmacol Immunotoxicol. 2011;33:525–32.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  56. 56.

    Calixto-Campos C, Carvalho TT, Hohmann MSN, Pinho-Ribeiro FA, Fattori V, Manchope MF, et al. Vanillic acid inhibits inflammatory pain by inhibiting neutrophil recruitment, oxidative stress, cytokine production, and NFκB activation in mice. J Nat Prod. 2015;78:1799–808.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  57. 57.

    Yadav VR, Prasad S, Sung B, Kannappan R, Aggarwal BB. Targeting inflammatory pathways by triterpenoids for prevention and treatment of cancer. Toxins. 2010;2:2428–66.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

Download references

Acknowledgements

we thank Melissa Parny who kindly provided us with ELISAs reagents.

Funding

A. Camara received funding for her PhD research from the French Embassy in Guinea (Grant No. 001) and from the Guinean Ministry of Higher Education and Scientific Research (Grant No. 001).

Author information

Affiliations

Authors

Contributions

AMB, AA and AiC designed the study and wrote the publication with the help of AC. MST, AOB and ESB performed the field work. AiC carried out most of the in vitro and in vivo lab experiments with the help of JR. MAB evaluated the in vitro anti-malarial activity of the extracts and analysed the results. PB and MaH helped for murine models. MoH managed the dereplication approach and KR the Light-Up Cell System to measure Terminalia albida scavenging activity. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Aissata Camara.

Ethics declarations

Ethics approval and consent to participate

Mice studies (oral toxicity tests and anti-malarial in vivo evaluation) were approved by the Midi-Pyrénées ethic committee for animal experimentation in Toulouse, France. The study was authorized with the permit number APAFIS#5921-2016070118008477 v3.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Additional file 1: Fig. S1. Terminalia albida cytotoxicity against healthy murine peritoneal macrophages by the lactate deshydrogenase (LDH) test. Cells (2.105/well) were left to adhere for 2 h at 37 °C and 5% CO2, and non-adherent cells were removed by washing with PBS. Adherent cells were treated with serial dilutions of Terminalia albida extract (100 μg/mL, 50 μg/mL, 25 μg/mL, 10 μg/mL, 5 μg/mL) and incubated at 37 °C and 5% CO2 for 24 h. LDH leakage from the cells was determined using a commercial LDH cytotoxicity detection kit according to the manufacturer’s protocols (Cytotoxicity detection Kit, Roche, France). Absorbance was measured at 490 nm with a Wallac Victor 2 1420 Multilabel Counter. Cell mortality was calculated as a percentage: (absorbance of wells treated with extract *100/absorbance of wells treated with triton).

Additional file 2: Fig. S2. Acute oral toxicity test in vivo: effect of Terminalia albida treatment on body weight. Mice were treated by oral route with a single dose of Terminalia albida (2000 mg/kg) or water (20 mL/kg). To evaluate the effect of Terminalia albida treatment on body weight, the weight was taken at D7, D14 and D20 and compared to D0 for both groups (Terminalia albida and water).

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Camara, A., Haddad, M., Reybier, K. et al. Terminalia albida treatment improves survival in experimental cerebral malaria through reactive oxygen species scavenging and anti-inflammatory properties. Malar J 18, 431 (2019). https://doi.org/10.1186/s12936-019-3071-9

Download citation

Keywords

  • Terminalia albida
  • Malaria
  • Experimental cerebral malaria
  • Inflammatory response
  • Oxidative stress
  • UHPLC-HRMS