Pre-infection administration of asiatic acid retards parasitaemia induction in Plasmodium berghei murine malaria infected Sprague-Dawley rats

Background Malaria prevention has remained a critical area in the absence of efficacious vaccines against malaria. Drugs currently used as chemotherapeutics are also used in chemoprophylaxis increasing possible drug resistance. Asiatic acid is a natural phytochemical with oxidant, antioxidant and anti-inflammatory properties with emerging anti-malarial potential. The influence of asiatic acid administration prior to Plasmodium berghei infection of Sprague-Dawley rats on parasitaemia induction is here reported. Methods Sprague-Dawley rats (90–120 g) were administered with asiatic acid (10 mg/kg) 48 h before intraperitoneal infection with P. berghei. Parasitaemia induction and progression, food and water intake as well as weight were compared to 30 mg/kg chloroquine-treated and infected control rats during sub-chronic studies (21 days). Results Asiatic acid pre-infection administration preserved food and water intake as well as increase in percentage weight gain of infected animals. In pre-infection treated animals, the pre-patent period was extended to day 6 from 72 h. Asiatic acid suppressed parasitaemia while oral chloroquine (30 mg/kg) did not influence malaria induction. Conclusions Per-oral, pre-infection, asiatic acid administration influenced parasitaemia patency and parasitaemia progression, food, water, and weight gain percentage. This may suggest possible chemoprophylaxis effects of asiatic acid in malaria.


Background
Chemoprophylaxis can either be causal prophylaxis (absolutely prevents patent malaria development by eradicating liver stage parasites) or parasitaemia and malaria symptom suppression, referred to as suppressive or clinical prophylaxis, where blood stage parasites are destroyed from circulation [1]. Drugs used as prophylaxis need to be long acting or have longer half-lives as frequent dosing may lead to non-compliance [2,3]. The drug also needs to be palatable and tolerable, facets absent in most prophylaxis drugs with phytochemical origins [4,5]. In Uganda, an infusion of Artemisia annua consumed once weekly reduced risk of Plasmodium falciparum infection episodes due to as yet an unidentified constituent [6] with a longer half-life than artemisinin. However, its only drawback is the bitterness [7]. Fascinating results have also started to emerge where triterpenes oleanolic acid (OA) [8] and maslinic acid (MA) [9] have shown amelioration of metabolic dysfunction in malaria. These triterpenes have been reported to have anti-inflammatory activities as well [10,11]. These findings suggest that other triterpenes may also have anti-malarial activity giving rise to this current investigation of asiatic acid (AA) as a potential anti-malarial. Asiatic acid is an intriguing molecule with antioxidant and pro-oxidant [12], anti-inflammatory [13] and immunomodulatory [14] activities. Chemically known as (4α)-2α, 3β, 23-trihydroxy-urs-12-en-28-oic acid, having redox reaction capability, amphiphilic with a hydrogen bond donor/acceptor ratio of 7.1/4.172 [15], AA has potential for anti-disease properties in malaria. Indeed, ongoing (unpublished) anti-malarial work with the triterpene AA has shown that the phytochemical has an abrupt or sudden parasite killing effect during the post-dosing period in infected Sprague-Dawley (SD) male rats. In those experiments high percentage parasitaemia seemed to just 'disappear' from subsequent peripheral slides without a predictable gradual decline seen with other anti-malarial drugs. With this in mind, the aim of the study was to establish whether the amphiphilic triterpenoid could have cumulative long-acting pharmacodynamics potentially useful for malaria chemoprevention. Findings on the influence of pre-infection administration of AA on the retardation of malaria development in Plasmodium berghei-infected SD male rats by monitoring malaria infection, percentage parasitaemia, as well as food and water intake are here reported.

Drugs and chemicals
The initial AA (500 mg) of 97 % purity used in the preliminary studies was a kind donation from Prof Van Heerden (University of KwaZulu Natal). Further quantities of AA (97 % purity) were purchased together with Giemsa stain, dimethyl sulfoxide (DMSO), chloroquine diphosphate (CHQ) from Sigma-Aldrich (St. Louis, MI, USA). All other chemicals and reagents were of analytical grade.

Animals
Male SD rats weighing 90-120 g were obtained from the Biomedical Research Animal Unit (BRU) of the University of KwaZulu where they were bred and housed for the entire experiment period. The animals were kept under maintained laboratory conditions of constant temperature (22 ± 1 °C); Co 2 (<5000 ppm), humidity of 55 ± 5 % and illumination (12 h light/dark cycles). Food, standard rat chow (Meadows Feeds, Pietermaritzburg, South Africa) and water were supplied ad libitum. All animals were sacrificed by day 21 through exposure to halothane for 3 min via an anaesthetic gas chamber (100 mg/kg). All experiments and protocols were reviewed and approved by the animal ethics committee of the University of KwaZulu Natal (UKZN) with ethical clearance numbers 079/14/Animal and 013/15/Animal issued.

Murine malaria model
Chloroquine-susceptible strain of P. berghei ANKA, was a kind donation from Prof Peter Smith (University of Cape Town, Division of Clinical Pharmacology, South Africa). The parasite was sub-cultured in SD rats and harvested into Na 2 EDTA whole blood. The blood was washed and stored in freeze media containing 30 % glycerol at −80 °C until used.

Experimental design
Animal groups (n = 6) were divided according to whether they were infected or received treatment. Animals treated with CHQ (30 mg/kg) served as the positive control. The groups were as follows: Non-infected treated control (NIC) Infected non-treated control (IC) Infection groups treated with CHQ 30 mg/kg (30CHQ) Infected groups treated with AA 10 mg/kg (10AA).

Monitoring of physicochemical properties
Six animals per group were housed individually in Makrolon polycarbonate metabolic cages (Techniplast, Labotec, South Africa) with food and water availed to them ad libitum. Food, water intake and weight gain were determined gravimetrically every other day at 09.00 h.

Pre-infection oral administration
AA (10 mg/kg) and CHQ (30 mg/kg) were administered on successive days (days 0-5). AA was administered once daily (09.00) according to the posology developed for triterpenes [11,[16][17][18] and what doses others have advocated for treatment of other conditions [12,19,20]. CHQ was administered twice daily (09.00 and 16.00) for the same duration as AA. CHQ dose is a standard regimen for malaria prophylaxis in combination with doxycycline or proguanil [1]. A ball-tipped, 18-gauge gavage needle (Kyron Laboratories (Pty) Ltd, Benrose, South Africa) attached to a 1-ml syringe was used intragastric (ig) to deliver AA and CHQ.

Induction of parasitaemia
Plasmodium berghei (10 5 parasitized red blood cells (pRBCs) suspension in saline) was inoculated intraperitoneal (ip) [21]. Control animals received equivalent amounts of saline. Animals were inoculated 48 h after AA or CHQ administration. Administration of AA and CHQ was continued up to day 5 giving a total of 5 days administration inclusive of the pre-infection period.

Evaluation of parasitaemia
Appearance of parasites in blood after ip inoculation takes 2 to 3 days [22]. Pre-patent period was expected at 72 h post-infection and a stable parasitaemia at 15-20 % on day 7 [23]. After inoculation, parasitaemia was monitored at 72 h (pre-patent period) and every third day during the patent period [24] thereafter, until day 21. A 15-20 % parasitaemia was considered as stable state severe malaria (SM) capable of inducing severe malaria anaemia (SMA). Stable state malaria was expected at day 7.

Influence of AA on percentage parasitaemia
Giemsa staining: peripheral blood obtained through a tail prick was made into thin blood smears and stained with Giemsa stain for monitoring of percentage parasitaemia by examination under a light microscope (Olympus Cooperation, Tokyo, Japan). The actual number of pRBCs relative to 2 × 10 4 RBCs was used to calculate parasitaemia [22].
Full blood count: To further explore the influence of AA on malaria and its co-morbidities of inflammation and SMA, white cell count (WBC) and haemoglobin estimations were made from blood obtained through cardiac puncture at days 0, 3, 9, 12, and 21 after administration of lethal anaesthesia with halothane. All IC animals were sacrificed by day 12 on ethical grounds to reduce pain and suffering using a humane method of halothane anaesthetic inhalation in gas chamber (100 mg/kg) and blood collected by cardiac puncture.

Statistical analysis
Unless otherwise stated, data were presented as mean plus standard error of the mean (M ± SEM). Statistical comparisons was performed by one-way analysis of variance (ANOVA), followed by Tukey-Kramer multiple comparison post hoc test using Graph-pad Prism Software (version 5, GraphPad Software, San Diego, CA USA). P < 0.05 was considered statistically significant. Table 1 shows the influence of AA administration on food and water as well as percentage weight gain. IC animals had significantly decreased water and food intake as well as body weight at day 12 compared to animals administered with AA (10 mg/kg) (*p < 0.05). CHQ treatment decreased food and water intake together with percentage weight gain when compared to AA (10 mg/ kg) administration at relevant time points (**p < 0.05). Animals treated with 30CHQ had lower food and water intake as well as percentage weight gain when compared to NIC (γp < 0.05). Table 2 shows the influence of AA (10 mg/kg) on prepatent period, percentage parasitaemia. AA (10 mg/ kg) administration significantly influenced prolongation of the pre-patent period, parasitaemia inhibition by day 3 while reducing percentage parasitaemia at day 7 in comparison to the IC (*p < 0.05). AA (10 mg/kg), in comparison to 30CHQ (**p < 0.05) influenced prolongation of pre-patent period, parasitaemia inhibition at day 3 and reduction of percentage parasitaemia by day 7. In comparison to the IC, the positive control 30CHQ reduced percentage parasitaemia at day 3 (*p < 0.05). Animals administered AA (10 mg/kg) did not reach stable state malaria by day 7 in comparison to IC and 30CHQ (* , **p < 0.05, respectively). AA (10 mg/kg) had lower peak percentage parasitaemia compared to both the IC and 30CHQ controls (* , **p < 0.05, respectively). AA (10 mg/kg) peak period (day) was statistical different compared to that of 30CHQ (**p < 0.05).

Validation of asiatic acid influence on cellular morphology
As seen on Fig. 1, patent parasitaemia showed differential staining with Giemsa stain (×100 objective) where pRBCs showed as purple cells with or without parasites in them. By day 12 npRBCs in IC and CHQ groups were pail pick and reduced in number showing anaemia. There was minimum anisocytosis with slight polychromasia. Slides [C] and [D] from IC and CHQ-treated groups at days 12 and 9, respectively showed increased parasitaemia. Most cells were parasitized with visible parasite ring forms chromatin evident. Slides [E] was from AA (10 mg/ kg)-administered group showing parasitaemia suppression at day 21. No pRBCs could be demonstrated in all AA-administered animals by day 21. Micrograph [E] from 30CHQ-treated animals showed that parasitaemia was still evident although significantly reduced compared to day 9. Figure 2 shows changes in percentage parasitaemia over time. AA (10 mg/kg) administration displayed significantly lower percentage parasitaemia compared to the IC (*p < 0.05) on days 3-12. Compared to 30CHQ, AA (10 mg/kg) had lower percentage parasitaemia (***p < 0.05) throughout the 21 days of the sub-chronic study. 30CHQ treatment lowered percentage parasitaemia significantly at day 12 in comparison to the IC (***p < 0.05). Figure 3 shows the influence of AA (10 mg/kg) on percentage parasitaemia-time area under the curve (AUC 0-21days ). AA (10 mg/kg) decreased the percentage parasitaemia-time curve significantly compared to the IC AUC 0-12days (*p < 0.05). Compared to 30CHQ treatment, AA (10 mg/kg) administration reduced the AUC 0-21days significantly (**p < 0.05) at the same time points. Compared to IC AUC 0-12days , 30CHQ treatment reduced AUC 0-21days significantly (***p < 0.05). Overall, the percentage parasitaemia-time IC AUC 0-12 days was significantly higher than either AA (10 mg/kg) or 30CHQ AUC 0-21 days (* , ***p < 0.05, respectively), regardless of the shorter time period. Figure 4 shows the effect of AA (10 mg/kg) on WBC count over time. AA (10 mg/kg) administration lowered WBC count significantly compared to IC (*p < 0.05). Compared to 30CHQ, AA (10 mg/kg) decreased WBC significantly (**p < 0.05). At peak percentage parasitaemia AA (10 mg/kg) administered animal had a significantly higher WBC count compared to the NIC (α p < 0.05). Treatment with 30CHQ had higher WBC counts compared to the NIC (***p < 0.05) throughout the 21-day period. Figure 5 shows changes in haemoglobin (Hb) with administration of AA (10 mg/kg) over time. Administration of AA (10 mg/kg) had significantly higher Hb levels compared to the IC (**p < 0.05). Compared to 30CHQ, AA (10 mg/kg) had significantly higher Hb levels (***p < 0.05) throughout the 21-day study.

Discussion
Anecdotal information ascribes anti-malarial activity to Centella asiatica (CA) [25,26] but there are no reports of chemoprophylaxis or chemotherapeutic effects of AA on malaria. There is a close resemblance in malaria pathophysiology between P. berghei and P. falciparum, the virulent species of human malaria parasites, warranting the former to be used as a safer analogue in experimental malaria. Studies have indicated, also proven by earlier  AA10 mg/kg 6* , ** 0.00 ± 0.0* , ** 0.13 ± 2.03* , ** 7.51 ± , ** 12** research, that P. berghei causes SM proceeding to cerebral malaria (CM) in younger animals [23,[27][28][29][30]. Here, demonstrated is the novel influence of pre-infection po administration of AA on malaria in young, six weeks old SD rats (90-120 g) displaying hyperparasitaemia, SM and SMA. Both murine malaria parasite (P. berghei) and SD rat malaria animal models conformed to a high predictive validity at days 3 and 7 in the IC and 30CHQ controls but not in the AA-administered group. Infection induction by an ip inoculation of 10 5 of pRBCs saline suspension invariably results in SM within 2 weeks, however this did not seem to happen in animals administered with AA (10 mg/kg) during the pre-infection period of 48 h. The pre-patent duration (the time it takes for parasites to Fig. 1 Giemsa staining showing asiatic acid (10 mg/kg) influence on cellular morphology. Micrographs were before (day 0), during (day 7) and after malarial infection (day 21) and were compared to IC (day 12) and CHQ (days 9 and 21) controls. Slide are from: a AA 10 adminisitered animals on day 7; b day 0; c IC day 12; d CHQ day 9; e AA 10 day 21; f CHQ day 21. Parasitized red blood cells (pRBCs) are indicated by black arrows in slide a, red arrows in slides c, d and f. Non-parasitized red blood cells (npRBCs) are shown in slides b and e. ×500 magnification used in all slides be detected in peripheral blood from the day of inoculation) is usually 72 h. This period was, however, prolonged by a further 3 days to a period beyond day 6 when AA (10 mg/kg) was administered 48 h before the animals were infected. The prevention of malaria could only be ascribed to the influence of AA as animal groups treated with CHQ (30 mg/kg) showed a malaria progression pattern as predicted [22]. Furthermore, subdued patent percentage parasitaemia, which failed to reach stable state malaria in AA (10 mg/kg) ( Table 2)-administered groups, shows a possible cumulative concentration or effect of AA which continued to interact with the parasite well after administration of AA had ceased. This phenomenon was supported by observations of the percentage parasitaemia-time curve in this study (Fig. 2) which clearly showed AA10 administration causing a diminutive infection-time course compared to that of the IC and the CHQ controls. Notably, the IC percentage parasitaemia-time area under the curve covered only a maximum of 12 days, yet it was several times higher than that of AA10. Although others factors may be at play, the most probable cause of this difference may be attributable to the influence of AA10 on parasitaemia development. The CHQ-positive control also showed a similar, albeit higher AUC 0-21 days than AA10, trend which effect may also be attributable to the influence of the drug on the percentage parasitaemia. The elongation of the bioavailability of AA in plasma, after oral administration, depends on a number of factors of which the amphiphilic nature of the triterpenoid is a major one [31,32]. Indeed, AA percentage human intestinal absorption (% HIA) was predicted as 91.23 %, Caco-2 cell permeability as 20.97 nm sec −1 and plasma protein distribution as 96.45 %, suggesting well absorptivity, middle permeability and strong binding, respectively [33], which could account for possible AA accumulation in plasma relative to the albumin concentration [34][35][36]. Indeed, AA bioavailability and accumulation in circulation and tissues has been reported to increase with the duration of AA intake and with possible local and systemic protective effects [37]. This may explain how the parasitaemia was suppressed even when high erythrocytic-phase parasite inoculum (0.6-0.7 mL pRBC suspension), several-fold higher than human infection dose (50-100 μL), was used to establish malaria. An efficient chemoprophylaxis is expected to inhibit establishment of patent malaria. While this did not happen, the later clearance of parasitaemia may indicate that AA has suppressive or clinical prophylaxis and will require certain levels to be reached for efficacy to be achieved. In the experiment by Yin et al. (2012) the recovery of intact AA from tissues and plasma after dietary intake which reached peak plasma concentrations quickly (0.5 h) after oral intake [37], the rapid metabolic rate of AA in rat liver microsomes and primary hepatocytes (t 1/2 = 9.493 min) and accompanying low AA bioavailability (16.25 % or 394.2 ng/mL) [38] further indicate that the phytochemical needs time to reach certain lethal levels against malaria. In the current study there was no indication of low bioavailability as the phytochemical managed to retard parasitaemia patency. Oral absorption of AA occurs throughout the small intestines with the highest absorption occurring in the jejunum [38]. Absorption is characterized by two peaks from a single dose inter-spaced by 8 hours, which could be attributable to the enterohepatic circulation [39] and avid binding by albumin [40].
Animals administered with AA (10 mg/kg AA) preinfection besides suppressing parasitaemia, also preserved food and water intake as well as increased weight gain (Table 1). This may mean that po administration of AA is optimum at 10 mg/kg. Unlike some bitter tasting anti-malarials used for prophylaxis, AA is tasteless having most likely no effect on the brain-gut axis that senses the bitterness, inducing satiety, reduced food and water intake in treated animals [41][42][43]. Indeed, animals that received CHQ, which is bitter, posted reduced food and water intake as well as weight loss.
Infected animals that were not treated (IC) showed critically low food and water intake as well as negative weight gain. Prolonged reduced food intake results in increased breakdown of stored fat and proteins, production of keto acids with concurrent acidosis and increased oxidative stress (OS). These conditions weaken the animal, promoting parasitaemia, aspects which may have led to the spectacular percentage parasitaemia differences between the AA (10 mg/kg) and the IC. These same effects of hyperparasitaemia were also evident in the animals treated with 30CHQ showing lack of prophylaxis of the drug at this concentration. Furthermore, AA has been reported to have an anti-hyperglycaemic effect through attenuation of glycolytic enzymes and inhibition of glycogen phosphorylase [20]. Asiatic acid was administered in normoglycaemic animals. Consequently, AA inhibition of gluconeogenesis whilst increasing glucose oxidation (upregulation of glycolysis), resulted in energy deficits that could only be satisfied by exogenous sources. Animals administered with AA 10 mg/kg necessarily had to increase food and water intake, which resulted in an increase percentage weight gain, to avert hypoglycaemia. In other words, while the innate immune system combats the infection [44], continued food intake is paramount to alleviate parasitic effects [45] making AA's ability to increase feeding crucial in malaria [46]. Micronutrient malnutrition has been linked to malaria anaemia pathogenesis [47] and the three (malaria, malnutrition, anaemia) are the common face of childhood disease in many parts of the developing world [48].
To corroborate the reduced food intake was the retardation in RBC mass reduction, as shown by the SMA in thin blood smears (Fig. 1) as well as Hb measurements (Fig. 5), in animals administered with AA 10 mg/ kg in comparison to the IC on day 12. There is a contrast between the RBC morphology on day 7 when compared to day 21 for the AA 10 mg/kg administered animals that reflects the slight slump in Hb observed on the earlier time period. Compared to the NIC this change in Hb in AA 10 mg/kg shows that no chemoprophylaxis agent may be 100 % effective all the time [1]. However, the low Hb observed in the IC demonstrates SMA caused by npRBC destruction [49], dyserythropoesis and/or ineffective erythropoiesis [50] and the general cachexia of the inflammatory disease [51] in the absence of effective chemoprophylaxis (Fig. 1c). Driving the hypochromic morphology observed with both IC and CHQ-treated animals (Fig. 1c, d) is a synchronous release of parasite pyrogens such as tumour necrosis factor-α (TNF-α) and interleukin-1β (IL-1β) that are also associated with anaemia, various pathologies and death from malaria [52,53]. While haemolysis results in reduced RBC mass, the more devastating effect is the release of merozoites which will infect more RBCs, inflammatory chemokines that upregulate leucocytosis, free Hb that rapidly inactivates nitric oxide with concomitant endothelium insults that follow which leads to vasoconstriction and damage to critical organs [54,55]. Compared to the CHQ-treated and the IC groups, AA administration did avert anaemia showing also that npRBC haemolysis was inhibited and with it, deleterious inflammatory mediators were also suppressed. With malaria-induced anaemia being one of the major contributors to the 43 % anaemia prevalence in children between the age of six and 59 months [56], its inhibition by AA administration from developing in young rats, provides possible leads into preventive malarial disease management.
Elevated leucocytosis, a surrogate marker of inflammation, was observed in the IC and the CHQ-treated animals but not in the NIC or AA (10 mg/kg) administered animals (Fig. 4). In malaria, inflammation is initiated by the release of glycosylphosphatidylinositol (GPI) during or at the end of merogony or RBC death when the pRBCs rapture [51]. The parasite pleiotropic influence-exerting GPI induces high levels of cytokines (TNF-α, IL-1β, IL-6) release from macrophages, causing the pyrexia and cachexia of malaria when it substitutes for the host GPIbased signal transduction in regulating protein kinase C, calcium levels, cell adhesion and nitric oxide (NO) synthesis [57,58]. Macrophages and polyclonal lymphocyte activation, which was observed as leucocytosis in the IC and CHQ treated animals ( Fig. 4) but not in AA-administered animals, may be a reflection of the aberrant GPI hyperactivity and excitation of both pro-inflammatory and anti-inflammatory responses [59] involving the nuclear factor-Kβ (NF-Kβ) [60] in the malaria syndrome. With all this in perspective, it will be safe to infer that the prophylaxis administration of AA (10 mg/kg) did inhibit WBC count increase resulting from reduction in parasite infectivity, merogony abatement and subsequent insufficient GPI release as compared to the IC and CHQtreated animals.
The founding principles of malaria lie in the successful activation of the immune system, incitement of the inflammatory cascade, abrogation of the haematopoietic function, systemic and endothelial changes with end organ failure, invariably initiated and orchestrated by an obligate intracellular protozoa [61,62]. Therefore, it stands to reason that chemoprophylaxis approaches of malaria may of necessity focus on the prevention of these abnormalities from developing. While it might be impossible to have 100 % chemoprevention in malaria, infringement on the development of post-infection pathophysiology is crucial in keeping in check overt malaria disease occurrence [63]. Administered before infection or at the onset of the infection, AA10 may be able to avert the development of SM and the accompanying pathophysiology.

Conclusions
Presented here is data that demonstrate positive AA influence on food and water intake as well as percentage weight gain. Animals administered with AA (10 mg/kg) averted inflammation and severe malaria anaemia development. The anti-parasitic and anti-disease activities of AA in suppressing the parasite while inhibiting infectioninduced pathology was evident. Administration of AA (10 mg/kg) showed a suppressive or clinical chemoprophylaxis better than chloroquine at 30 mg/kg, suggesting that AA may be used successfully in the prevention of malaria infection.