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Methods Activities of nutritional supplements were screened in vitro against bloodstream forms of T. To evaluate selectivity, we used two mammalian cells, Jurkat cells and Vero cells. The IC 50 values and selectivity index values were calculated, and supplements with promising efficacy in vitro were selected for further testing in vivo. Mice were infected intraperitoneally with 1 × 10 3 T. We observed parameters for disease progression such as parasitemia, red blood cell count, white blood cell count, survivability, and splenomegaly. Morphological profiles after the treatment were analyzed by scanning electron microscopy. Results Vitamin D 3 showed anti-trypanosome efficacies both in vitro and in vivo.

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It seemed to have suppressive effects on parasitemia, and spleen weight was also significantly lower in vitamin D 3-treated mice when compared to non-treated control mice. There was, however, no significant prolonged survivability of infected mice treated with vitamin D 3. Among green tea extracts, polyphenon-60 and epigallocatechin gallate had suppressive effects against T. Brucei in vitro, but in vivo efficacies were marginal. Background African trypanosomiasis consisting of human African trypanosomiasis (HAT) and animal African trypanosomiasis (AAT/Nagana) are listed as neglected tropical diseases endemic in sub-Saharan Africa ,. It is caused by parasitic protist of the order Kinetoplastida and genus Trypanosoma. HAT is primarily caused by two subspecies of the protozoan parasite, i.e., Trypanosoma brucei gambiense and Trypanosoma brucei rhodesiense.

In Western and Central African subregions, T. Gambiense is the major causative parasite of the disease, while in Eastern Africa, T. Rhodesiense predominates. A third closely related subspecies, Trypanosoma brucei brucei, cannot survive in the human host due to the human serum lytic factor but is responsible for many cases of nagana in cattle in East Africa ,.

Trypanosomes are transmitted by insect vector, tsetse flies ( Glossina spp.). At the onset of infection, the parasites proliferate in the bloodstream and lymphatic system and after a few weeks, they are able to cross the blood-brain barrier and enter the central nervous system. Once this occurs, patients show a variety of neurological symptoms becoming fatal without proper treatment resulting in coma and ultimately death –. Therefore, effective treatment at the early stage is crucial. The current drugs available for treatment of trypanosomiasis are less effective with severe side effects.

Furthermore, the route of administration of these drugs and their optimal doses should be re-considered to achieve better treatment efficacy. The host immune response system is known to play an important role in the disease progression and is considered to be highly essential for the control of the early phase of parasite replication which may be associated with host resistance to the parasite proliferation.

The use of nutritional supplements to aid in host response against protozoan parasites has been studied, some of which revealed anti-trypanosome effects. Ascorbic acid (vitamin C) has been shown to aid in combating the oxidative stress injuries in vital organs of mice infected with Trypanosoma cruzi. Epigallocatechin gallate (an analog of green tea extract) administration to mice showed significant levels of decreased parasitism and increased survival rates suggesting that epigallocatechin gallate may be potentially useful for the protection against T. Zinc supplementation has also shown beneficial activity in the reduction of parasitemia in T. Brucei-infected mice. Considering the situation that no safe and effective drugs are available, treatment regimens using drugs and supplements might be a challenge for the trypanosomiasis control strategy.

In view of these, we postulated that nutritional supplements may have some inhibitory/protective activity against T. Thus, we screened various nutritional supplements from different functional groups for their inhibitory effects in vitro and compounds that showed promising results were further assessed in vivo for their protective abilities.

Parasite strains T. Brucei bloodstream forms of strain GUTat 3.1 and TC221 maintained at Tokyo Medical and Dental University were used for all in vitro and in vivo experimental procedures. Parasites were cultured in Iscove’s modified Dulbecco’s medium (IMDM) (Sigma-Aldrich, St. Louis, MO, USA) supplemented with two mixtures; mixture 1 consisted of 0.1 M HCl, 100 μM hypoxanthine (Sigma-Aldrich), 30 μM thymidine (Sigma-Aldrich), and 40 μM adenosine (WAKO, Osaka, Japan) and mixture 2 consisted of a mixture of 1 mM sodium pyruvate (WAKO), 200 μM l-alanine (WAKO), 100 μM glycine (WAKO), 20 μM l-ornithine monohydrochloride (Tokyo Kasei, Tokyo, Japan), 10 μM l-citrullin (Sigma-Aldrich) and 100 μM 2-mercaptoethanol (WAKO), and 200 ml of distilled water.

The adjusted IMDM had a further 10% fetal bovine serum (FBS), 2 mM l-glutamine (WAKO), and 100 U/ml penicillin-100 μg/ml streptomycin added to it. Parasites were cultured at 37 °C and 5% CO 2 humid atmosphere as described previously. Supplements tested in this study All supplements used in the experimental protocol are listed in Table. Vitamin D 3 (Cayman Chemical, Ann Arbor, MI, USA), Vitamin C (WAKO), catechin hydrate (Sigma-Aldrich), polyphenon-60 (Sigma-Aldrich), Vitamin E (WAKO), epigallocatechin gallate (Sigma-Aldrich), coenzyme Q 10 (WAKO), and 5-aminolevulinic acid (WAKO) were tested for their activities against T. Vitamin D 3 was dissolved in 100% ethanol; the other supplements were dissolved in 100% dimethyl sulfoxide (DMSO) before use. Suramin (WAKO) and curcumin (WAKO) were used as positive controls.

Efficacy of supplements against T. Brucei in vitro Effects of the nine supplements against the bloodstream form of T. Brucei GUTat 3.1 were determined using the alamarBlue method (Sigma-Aldrich) as was shown elsewhere. Each well contained 1 × 10 5 cells in 100 μl medium with supplement concentrations in 1:2 serial dilutions (1001.5 μM) except for vitamin D 3. Vitamin D 3 had a starting concentration of 13 μM and also dissolved in a 1:2 serial dilution. To check the viability of trypanosomes at 24 and 48 h, 10 μl of alamarBlue solution was added to each well at 23 and 47 h of incubation, respectively, followed by further 1 h incubation.

Fluorescence was read in FLUOstar OPTIMA (BMG Labtech, Aylesbury, UK; λ excitation = 540 nm; λ emission = 590 nm) and absorbance measured by TriStar LB941 (Belthold, Oak Ridge, TN, USA). We determined selectivity index of tested supplements against trypanosome cells by comparing the efficacies against two mammalian cells, Jurkat cells and Vero cells. Cells were cultured in conditioned medium of Roswell Park Memorial Institute medium-1640 (RPMI-1640) with 10% FBS or Dulbecco’s modified Eagle’s medium (D-MEM) (WAKO) for 24 h and were exposed to various concentrations of supplements for 48 h. Sensitivity of the mammalian cells was measured using alamarBlue assay, as described previously.

Testing in experimental murine infection model Female BALB/c mice aged 6 weeks were purchased from CLEA (Tokyo, Japan). Mice were randomly assigned into five mice/group and treated with three test supplements, vitamin D 3, polyphenon-60, catechin hydrate, positive control (suramin), and a healthy control (infection-free). Sample size for mice was chosen by referring to a previous report. Catechin hydrate and polyphenon-60 dissolved in DMSO were administered at a dose of 50 mg/kg via intraperitoneal route every 2 days in experimental period. Vitamin D 3 was dissolved in ethanol and administered at a dose of 250 ng/kg by subcutaneous injection. After that, mice were infected with 1 × 10 3 T.

Brucei TC221 via the peritoneum. Suramin was used at a dose of 30 mg/kg, while phosphate-buffered saline (PBS) (pH 7.4) was used as a positive control. The parameters used to assess the disease progression were body weight, level of parasitemia, total red blood cell count (RBC count), total white blood cell count (WBC count), survivability, and splenomegaly. All parameters were measured independently by two researchers to reduce bias and for comparison. In cases of discordant results, the parameters were measured again for confirmation and consistency. Animal study was done in strict accordance with the guidelines approved by the Committee of Animal Ethics of Tokyo Medical and Dental University (0160295A, 2015, and 0170274A, 2016).

Scanning electron microscopy T. Brucei GUTat 3.1 treated with supplements in vitro were fixed in 3.5% glutaraldehyde placed in a fridge at 4 °C for overnight fixation. The next day, it was washed with PBS. Small droplets containing parasites were put on poly-lysine coated slides. Samples on slide glass were then stained in 1% osmium tetraoxide (OsO 4) and dehydrated in a series of graded ethanol concentrations for 10 min each. They were dried in a critical point dryer (Hitachi, Tokyo, Japan) using liquid carbon dioxide. The samples were then sputter coated with platinum in an ion sputter coater (Hitachi).

Digital images were collected using a scanning electron microscope (S-4500, Hitachi) operating at 10 kV at 500 to 40,000 times magnification. In vitro effects of the supplements against T.

Brucei Nutritional supplements with possible anti-trypanosome efficacy were assayed for inhibitory activity against T. In the in vitro assay, polyphenon-60, vitamin D 3, and epigallocatechin gallate showed relatively low IC 50 values of 16.9, 4.58, and 8.40 μM, respectively, which were, however, less effective than that of suramin (1.18 μM) (Table ).

From the results obtained by testing those supplements against mammalian cells, the selectivity index of vitamin D 3 was good enough, but other supplements had medium or low selectivity index values (Table ). Based on these in vitro results, we selected vitamin D 3 and polyphenon-60 to observe the effects in vivo. In vivo observation of anti-trypanosome activity of supplements Selected nutritional supplements were assessed for five parameters in vivo. During the 10 days before trypanosome infection, treatments with polyphenon-60 made no significant changes in body weight and RBC and WBC count, suggesting no apparent negative effects for mice. After trypanosome infection, efficacies of supplement treatment on three parameters assessed are summarized in Table.

In brief, there was no detectable difference in body weight but continuous administration of vitamin D 3 may cause statistically significant differences in body weight. When we compared results of parameters of RBC count and WBC count with infection-free control mice, RBC count recovered by vitamin D 3 treatment, polyphenon-60, and suramin, indicated that treated mice recovered from anemic conditions induced by infection with T. On the other hand, WBC count significantly reduced in infected groups ( p. Discussion Human African trypanosomiasis is still a disease of tremendous public health and economic importance, but the major challenge in the control is the development of safe and effective drugs available for treatment. In parallel with therapeutic drugs, various nutritional supplements have been tested for inhibitory effects, if not therapeutic, against African trypanosomiasis ,. In our study, we examined the possible efficacy of available nutritional supplements in enhancing host defense response to suppress parasite growth and disease progression.

Results obtained here suggested that vitamin D 3 and polyphenon-60 showed anti-trypanosome activity both in vitro and in vivo, while catechin hydrate showed only a faint effect in vivo (data not shown). Vitamin D 3 showed a parasite growth inhibition in vitro with a good selectivity index. Although vitamin D 3 failed to show curable effects in vivo, significant parasite growth inhibition was observed in vivo, and also splenomegaly during the disease course was suppressed. In this sense, vitamin D 3 cannot be a therapeutic drug for African trypanosomiasis in the protocol tested here which is severely dose dependent, but it might be expected to enhance efficacy of therapeutic drugs. Previous researchers have postulated that vitamin D reduced the risk of certain infections through multiple mechanisms ,. It has been shown that vitamin D boosts innate immunity by modulating production of anti-microbial peptides (AMPs) and cytokine response ,. For an experimental T.

Cruzi infection, vitamin D treatment favored the hosts be able to overcome acute phase of the disease and to prolong survivability in the chronic phase. When efficacy of vitamin D was discussed, vitamin D was likely to have an effect indirectly to the pathogen. For instance, vitamin D exerts an immunomodulatory effect through complex interactions with vitamin D receptors (VDR). VDR is a member of the superfamily of nuclear hormone receptors expressed on immune cells in humans ,.

Circulating vitamin D levels has a direct influence on macrophages, increasing their oxidative potential. There was a report showing that vitamin D 3 facilitates neutrophil motility and phagocytic function. All those seem to show that the efficacy of vitamin D was indirect to the pathogen, but rather immune cells were activated and subsequently suppressed parasite growth in vivo. In this sense, our observation suggests that vitamin D 3 could have direct effect(s) against T. Brucei, since treatment of vitamin D 3 in vitro in the absence of host immune cells also has detectable inhibitory effects. Polyphenon-60 is a derivative of green tea extracts.

It has been suggested that green tea extracts including catechin seem to have inhibitory effects against T. B brucei in vitro. Polyphenon-60 also showed significant inhibitory effect against parasite proliferation in vitro. Furthermore, slight prolongation of survivability was observed in infected mice treated with polyphenon-60, although it was not statistically significant.

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Administration of tea extracts has also been previously shown to prevent reduction in albumin concentration during T. Brucei infection in mice, thereby suggesting decreased inflammation due to the trypanosome parasite. Polyphenon-60 has extensive protein-denaturing characteristics as shown against influenza virus. Alternatively, polyphenon-60 is a supplement with anti-oxidative effects and immune-enhancing effects as has been already reported.

It is possible to speculate that those functions contributed to anti-trypanosome activities of polyphenon-60 in our study. It is again likely that polyphenon-60 could support and/or enhance the efficacy of anti-trypanosome drugs.

Nutritional supplements are not necessarily safe in daily use. Previous research had shown that vitamin D 3 treatment produced calcinosis lesions in the myocardium, coronary and kidney arteries, and may have induced mice death. In our study, several mice died during the treatment of vitamin D 3 even in the situation of relatively low parasitemia level (Fig. ) while using high dose of vitamin D 3 (500 ng/kg). Although we did not study the possible histopathological changes due to vitamin D 3 treatment, similar phenomena were observed by one of the authors in the murine experimental malaria (KY, manuscript in preparation).

Brucei infection could produce acute and chronic fatal conditions just like splenomegaly to the host. On the other hand, polyphenon-60 has been shown to have toxic effects when administered in high doses to mice, where they induce reactive oxygen species formation, and affect mitochondrial membrane potential thereby causing death. In the murine experimental malaria, high doses of polyphenon-60 administration caused significant toxicity and mortality in the infected mice (KY, unpublished data). Such information strongly suggests that supplement treatment should be under strict control to avoid negative effects. More detailed studies are needed to establish the optimal protocol for safe and effective treatment of supplements with anti-trypanosome activities. Conclusions We observed inhibitory effects of vitamin D 3 against T.

Brucei in vitro and possibly in vivo. We were not able to observe curable effects for this supplement in vivo; several parameters of disease progression were improved by the treatment with this supplement. Orihime and ulquiorra.

The results obtained suggest that treatment with nutritional supplements may possibly have protective/prophylactic roles; we therefore recommend that vitamin D 3 and green tea extracts could be included in the treatment protocols. In addition, further test should be conducted to confirm the efficacy of dietary supplements as treatment regimens in trypanosome infections. Abbreviations AAT, animal African trypanosomiasis; D-MEM, Dulbecco’s modified Eagle’s medium; DMSO, dimethyl sulfoxide; FBS, fetal bovine serum; HAT, human African trypanosomiasis; IC 50, half maximal (50%) inhibitory concentration (growth rate); IMDM, Iscove’s modified Dulbecco’s medium; PBS, phosphate-buffered saline; RBC, red blood cell; RPMI-1640, Roswell Park Memorial Institute medium-1640; SEM, scanning electron microscopy; T. Cruzi, Trypanosoma cruzi; T. Brucei, Trypanosoma brucei brucei; VDR, vitamin D receptors; WBC, white blood cell.