Evidence-Based Complementary and Alternative Medicine

Evidence-Based Complementary and Alternative Medicine / 2013 / Article

Research Article | Open Access

Volume 2013 |Article ID 102987 | https://doi.org/10.1155/2013/102987

Ching-Hao Li, Jiunn-Wang Liao, Po-Lin Liao, Wei-Kuang Huang, Ling-Shan Tse, Cheng-Hui Lin, Jaw-Jou Kang, Yu-Wen Cheng, "Evaluation of Acute 13-Week Subchronic Toxicity and Genotoxicity of the Powdered Root of Tongkat Ali (Eurycoma longifolia Jack)", Evidence-Based Complementary and Alternative Medicine, vol. 2013, Article ID 102987, 11 pages, 2013. https://doi.org/10.1155/2013/102987

Evaluation of Acute 13-Week Subchronic Toxicity and Genotoxicity of the Powdered Root of Tongkat Ali (Eurycoma longifolia Jack)

Academic Editor: Pradeep Visen
Received30 Apr 2013
Revised23 Jul 2013
Accepted24 Jul 2013
Published25 Aug 2013

Abstract

Tongkat Ali (Eurycoma longifolia) is an indigenous traditional herb in Southern Asia. Its powdered root has been processed to produce health supplements, but no detailed toxicology report is available. In this study, neither mutagenicity nor clastogenicity was noted, and acute oral LD50 was more than 6 g/kg b.w. After 4-week subacute and 13-week subchronic exposure paradigms (0, 0.6, 1.2, and 2 g/kg b.w./day), adverse effects attributable to test compound were not observed with respect to body weight, hematology, serum biochemistry, urinalysis, macropathology, or histopathology. However, the treatment significantly reduced prothrombin time, partial thromboplastin time, blood urea nitrogen, creatinine, aspartate aminotransferase, creatine phosphate kinase, lactate dehydrogenase, and cholesterol levels, especially in males ( ). These changes were judged as pharmacological effects, and they are beneficial to health. The calculated acceptable daily intake (ADI) was up to 1.2 g/adult/day. This information will be useful for product development and safety management.

1. Introduction

Herbal medicines, originating in China, Europe, and India, have a rich history. Over the last 30 years, the use of herbal medicines as complementary/alternative therapies has become increasingly popular throughout the world. A study in the Journal of the American Medical Association demonstrated that 40% of US residents regularly use these therapies. These people are well educated and are not dissatisfied with conventional medicines [1].

Eurycoma longifolia Jack (genus: Eurycoma; family: Simaroubaceae) is one of the most popular tropical herbal plants in Southeast Asia countries. In these countries, E. longifolia is identified locally as “Tongkat Ali” or “Malaysia ginseng” (Malaysia), “Pasak Bumi” or “Bedara Pahit” (Indonesia), “Ian-don” (Thailand), and “Cay ba binh” (Vietnam). It is an evergreen, slow-growing shrub with maximum height of 15–18 m, and it is commonly found in tropical forests. After 2-3 years of cultivation, this dioecious plant, with male and female flowers produced in large panicles on different trees, becomes mature and bears fruit. For commercial uses, their roots are harvested after 4 years of cultivation [2, 3]. Their roots, stems, and bark are used as folk medicines in different ways for the alleviation of various illnesses, including aches, intermittent fever, sexual insufficiency, dysentery, glandular swelling, and fatigue. Traditionally, the water decoction of E. longifolia root is consumed. Nowadays, more convenient formulas are available, primarily additives mixed with teas and coffees, and over 200 products are available either in the form of raw crude root powder or as capsules mixed with other herbs in the health food market [3]. Some of these products, such as Libidus and Maxidus (which claim to use E. longifolia as the principal ingredient), have been issued with warnings or even banned in the USA, Canada, and Singapore, because of the lack of science-based safety information, the presence of undeclared prescription drugs, and the use of fake ingredients.

Tongkat Ali, the local name for E. longifolia (in which “Tongkat” meaning “walking stick” refers to the presence of long twisted roots), is known to be enriched with many valuable phytochemicals. More than 65 bioactive compounds have been isolated and characterized, including -carboline and canthine-6-one alkaloids, quassinoids (laurycomalactone, eurycomalactone, longilactone, eurylactone, and eurycomanone), squalene derivatives, tirucallane triterpenes, mucopolysaccharides, biphenylneolignans, and eurypeptides [35]. Alkaloids and quassinoids comprise majority of the chemical composition and exhibit antimalarial [4], antioxidant [5], antiosteoporotic [6], antidiabetic [7], anticancer [8], antipyretic, and antianxiety activities, some of which have been demonstrated by pharmacological studies. As a health supplement ingredient, the efficacy of E. longifolia in restoring energy, improving muscle strength, alleviating aging males’ symptoms [9], and acting as an aphrodisiac on late-onset hypogonadism management [10], has been highlighted. Water-soluble E. longifolia extract was reported to be able to enhance male fertility (with regards to higher semen volumes, spermatozoa count, and motility) in rodents [11, 12] and in human trials [1315]. Scientific evidence proved these efficacies that resulted from the increase in testosterone levels via hypothalamic-pituitary-gonadal axis stimulation [12]. Eurycomanone, the major quassinoids in E. longifolia, enhances testosterone steroidogenesis at the leydig cells by inhibiting aromatase conversion of testosterone to oestrogen [16]. Besides, eurypeptides have been shown to activate the 17α-hydroxylase (CYP17 enzyme), triggering the biosynthesis of dehydroepiandrosterone which can act on androgen receptors to initiate the conversion of androstenedione to testosterone [10, 13, 17]. Therefore, E. longifolia supplementation may be an alternative for testosterone replacement therapy and the bone volume restoration from androgen deficient osteoporosis [1821], or it may be able to improve certain mood state parameters in elders [22].

Although herbal medicines rely on remedies of natural origin and have fewer side effects than allopathic medicines, the use of herbal remedies is not always safe. Hence, concerns about their safety and toxicity are increasing, especially within the context of chronic or cumulative dosing [23]. Numerous commercial E. longifolia supplements do not provide their information about bioactive constituents, extraction methodology, and purity. In general, alcohol extracts (usually enriched eurycomalactone) are more toxic than water extracts [24, 25]. Although oral toxicity studies show that the lethal dose 50 (LD50) of E. longifolia water extract is at the dosage of 2 g/kg b.w. (acute), and that the no observed adverse effect level (NOAEL) is greater than 1 g/kg b.w. (28-day subacute feeding) [26] however, to our knowledge, these toxicological reports are incomplete and insufficient for demonstrating either long-term safety or prediction of acceptable daily intake (ADI). To establish evidence-based data, acute, subacute, and subchronic toxicity studies were conducted after single, 4-week, and 13-week repeated oral dosing in Wistar rats, and genotoxic parameters were also evaluated in vitro and in vivo. This study was performed in compliance with the testing guidelines of the Organization for Economic Cooperation and Development (OECD) and the Taiwan Food and Drug Administration.

2. Materials and Methods

2.1. E. longifolia Powdered Root Preparation

The powder of E. longifolia roots used in this study was supplied by Exclusive Mark (M) Sdn Bhd, Malaysia. Roots, at least 3 inches in diameter, were harvested, washed to remove stones and soil, and sliced by hand. The slices were dried in an oven at 110°C for 2 h and then crushed and ground to a fine powder. The powdered root was vibrated through a 150-grade mesh and submitted for quality control. The dry powder was stored at room temperature and resuspended in sterile water at the time of use.

2.2. Salmonella/Microsome Reversion Assay: Ames Test

The Salmonella typhimurium histidine auxotrophs TA98, TA100, TA1537, TA1535, and TA102 were purchased from Moltox (TM, USA). Mutagenicity was determined by incorporation method in the presence and absence of S9 metabolic activation [27]. One hundred microliters of each test bacterial culture (109 cells/mL), 2 mL soft agar (0.6% agar, 0.5% NaCl, 5 mM histidine, and 50 mM biotin, pH 7.4, 40–50°C), 0.5 mL S9 mixture (if necessary), and test compounds were mixed well in a test tube. Immediately after mixing, the sample was poured into a minimal agar plate (1.5% agar, Vogel-Bonner E medium containing 2% glucose). Plates were incubated for 48 h at 37°C in the dark. The revertant colonies were counted macroscopically. A compound was considered positive for mutagenicity only when (i) the number of revertants was at least double the spontaneous yield, (ii) a statistical significance was found, and (iii) a reproducible positive dose response was present.

2.3. Chromosomal Aberration

Chinese hamster ovary epithelial cells (CHO-K1, ATCC: CCL-61) were plated in 6 cm dishes at 5 × 105 cells/plate for the 24 h treatment group. After overnight incubation, cells were treated with vehicle, mitomycin C (1 μg/mL), benzo(a)pyrene (5 μg/mL), or test compounds (1.25, 2.5, or 5 mg/mL) for 3–24 h, with or without S9. Then, 3 h after the end of the treatment time, 0.1 μg/mL colcemid was administered, and metaphase chromosomes were prepared as previously described [27]. After trypsinization, cells were treated with 0.9% sodium citrate at 37°C for 10 min, fixed in Carnoy’s solution (methanol : acetic acid, 3 : 1), and spread on glass slides. Specimens were stained with 3% Giemsa solution in 0.07 M phosphate buffer (pH 6.8) for 30 min. For determination of chromosome aberrations (e.g., chromosome-type gap (G), break (B), and dicentric (D); chromatid-type gap (g), break (b), and exchange (e)), a total of 100 well-spread diploid M1 metaphase cells per treatment were classified and scored. Data were expressed as the total mean number of chromosomal aberrations per treatment ± SEM from 300 cells scored in 3 independent experiments.

2.4. Animal Husbandry

Adult 4–6-week-old male and female Wistar rats, weighing 170–200 g, were obtained from BioLASCO Ltd. (Taipei, Taiwan). Male 6-week-old ICR mice were obtained from the Animal Center of National Taiwan University (Taipei, Taiwan). Animals were separated by sex, housed 3-4 per cage, quarantined, and acclimated for 1 week in the housing room under a 12 h light/dark cycle at °C and 39–43% relative humidity. Water and food (Rodent LabDiet 5001; PMI Nutrition International, LLC, Richmond, IN, USA) were available ad libitum. All procedures involving the use of animals were in compliance with the “Guide for the Care and Use of Laboratory Animals” (National Academy of Sciences Press, 1996) and approved by the Institutional Animal Care and Use Committee at our institution (Approval no. LAC-97-0146).

2.5. Micronucleus Assay

Male ICR mice ( ) were administered test compounds orally by gavage at doses of 0.6, 1.2, and 2.0 g/kg body weight. Negative controls received the vehicle, and positive controls were administered an intraperitoneal injection of 200 mg/kg body weight cyclophosphamide. Peripheral blood (10–20 μL) was sampled from the tail vein at 24, 48, and 72 h after-dosing, smeared on a glass microscope slide, and stained with acridine orange (40 μg/mL). The prepared slides were immediately examined by fluorescence microscopy. The ratio (%) of polychromatic erythrocytes (PCEs) to total erythrocytes and the frequency of micronucleated polychromatic erythrocytes (MNPCEs; ) were calculated by counting a total of 1000 erythrocytes or PCEs per animal, respectively.

2.6. Single-Dose Acute Toxicity Study

Forty healthy Wistar rats were divided into 5 groups (4 males and 4 females per group). The first group (control) received sterile water, given orally. Groups 2–5 were orally treated with test compounds in doses of 1, 2, 4, and 6 g/kg, respectively. Animals were observed for general behavioral and body weight changes, hazardous symptoms, and mortality for a 14-day period after treatment. At the end of the study (on day 14), rats were anesthetized with isoflurane, blood (for serum biochemistry analysis) was collected from the abdominal aorta, and gross necropsies were conducted.

2.7. 4-Week Subacute and 13-Week Subchronic Toxicity Studies

Healthy Wistar rats were randomly divided into 4 groups. Group 1 (control) animals received vehicle treatment by oral gavage throughout the course of the study. Animals in groups 2–4 were orally administered test compound at doses of 0.6, 1.2, and 2 g/kg body weight/day for 4 weeks (10 males per group) or 13 weeks (10 males + 10 females per group). Body weight, food consumption, and water intake (by subtracting the weight of the remaining food/water from the weight of the supplied food/water) were recorded weekly. Mortality and signs of abnormalities were observed twice daily. At the end of the study, rats were fasted overnight (with water still supplied ad libitum) and anesthetized with isoflurane. Blood samples were obtained from the abdominal aorta using capillary tubes for hematological, clotting, and serum biochemical studies.

2.8. Hematological, Clotting, and Serum Biochemical Analysis

Hematological profiles were obtained using an automatic analyzer (Sysmex K-4500, TOA Medical Electronics Co., Kobe, Japan). Before serum biochemistry (Express Plus automatic clinical chemistry analyzer, Siemens Medical Diagnostics) and clotting (AMAX 200, Trinity Biotec Plc., Ireland) analysis, serum and plasma samples were obtained by centrifugation at 1500 ×g for 10 min. Hematological and serum biochemical analyses were conducted according to the OECD Guidelines for the Testing of Chemicals no. 407 and no. 408.

2.9. Urinalysis

Urinalyses were conducted during the last 4 days of the testing period. Changes in pH, protein and glucose content, specific gravity, uric acid composition, and the presence of occult blood or ketones were assessed (Miditron Junior, Roche, Diagnostics Gmbh, Mannheim, German). Samples were also examined microscopically for the presence of urinary sediments.

2.10. Gross Necropsy

Gross necropsies were performed to analyze macroscopic external and internal features (OECD Guidelines for the Testing of Chemicals no. 407 and no. 408). Vital organs were carefully removed, defatted, and individually weighed and then fixed in 10% neutral buffered formalin. Organ wet weights were expressed in absolute and relative terms (g and g/100 g body weight or brain weight, resp.).

2.11. Histopathology

The biopsy sections were prepared as described in Supplementary Materials available online at http://dx.doi.org/10.1155/2013/102987 histopathological report and examined by an experienced pathologist. Microscopic features of the organs of male and female rats were compared in the control and 2 g/kg body weight-treated groups.

2.12. Statistical Analysis

All values are expressed as the mean ± SD. Comparisons between groups were performed using one-way analysis of variance (ANOVA) followed by Dunnett multiple comparison tests using SPSS statistical software (DrMarketing Co. Ltd., New Taipei City, Taiwan). A value of <0.05 was considered significant.

3. Results

3.1. Neither Mutagenicity nor Clastogenicity Was Caused by E. longifolia Powdered Root Treatment In Vitro and In Vivo

In the Ames test, on increase in the number of revertants was observed in the positive control group ( ). After treatment with various concentrations of E. longifolia powdered root, none of the testing concentrations (5, 2.5, 1.25, 0.625, or 0.3125 mg/plate) resulted in a clear growth in the number of colonies with or without S9 metabolic activation in all 5 test strains (TA97, TA98, TA100, TA102, and TA1535; Table 1).


TA98TA100TA102TA1535TA1537

Without S9 metabolic activation
Negative1
Positive2
E. longifolia powdered root (mg/plate)
 0.3125
 0.625
 1.25
 2.5
 5

With S9 metabolic activation
Negative1
Positive2
E. longifolia powdered root (mg/plate)
 0.3125
 0.625
 1.25
 2.5
 5

The values were presented as Mean ± S.D. . No significant changes of revertants were observed at any concentrations of test compound treatments in five tester strains. Statistical analysis: indicates a statistical difference with the control group by one-way ANOVA when the number of revertants was twice than control at TA98, TA100, and TA102 and triple than control at TA1537 and TA1535.
Solvent (sterile water) was used as negative control.
Positive control in w/o S9 plate: TA98 (4-nitro-o-phenylenediamine 2.5 μg/plate); TA100 and TA1535 (sodium azide 5 μg/plate); TA102 (mitomycin C 0.5 μg/plate); TA1537 (9-aminoacridine 50 μg/plate); in w/w S9 plate: TA100/TA102/TA1535/TA1537 (2-aminoanthrene 5 μg/plate); TA98 (benzo(a)pyrene 5 μg/plate).

According to the cell viability assay, the selected testing concentrations (1.25, 2.5, and 5 mg/mL) were less than the LC50 (Supplementary Table 1). Compared to positive control treatments with mitomycin C (1 μg/mL, without S9 activation) or benzo(a)pyrene (5 μg/mL; with S9 activation), which showed abnormal increases in the number of damaged chromosomes ( ), no increases or irregularities in chromosome aberrations were recorded in all test treatment groups (Table 2).


Aberrant cells (%)Number of aberrations/100 cells3-4
GBDgbe

3 h treatment/without S9 metabolic activation
Negative1 0 0
Positive2
E. longifolia powdered root (mg/mL)
 1.25 000 0
 2.5 000 0
 5 000 0

3 h treatment/with S9 metabolic activation
Negative1 0 000
Positive2 0
E. longifolia powdered root (mg/mL)
 1.25 000 0
 2.5 000 0
 5 000 0

24 h treatment/without S9 metabolic activation
Negative1 0000 0
Positive2 0
E. longifolia powdered root (mg/mL)
 1.25 000 0
 2.5 000 0
 5 000 0

Solvent (sterile water) was used as negative control.
Positive control in w/o S9 condition: mitomycin C 1 μg/mL; in w/w S9 condition: benzo(a)pyrene 5 μg/mL.
The chromosomal aberrations were counted by 100 independent cells. For each treatment, at least 300 cells were examined as described in Section 2. The data are expressed as the Mean ± SEM . Significant difference between control treated group at * versus control by one-way ANOVA.
G: chromosome gap; B: chromosome break; D: dicentric; g: gap; b: chromatid break; e: exchange.

A reduction in the ratio of PCEs to total erythrocytes (%) and an increase in the frequency of MNPCEs (‰) were found in the positive control group ( ). The proportion of PCEs and the frequency of MNPCEs in treated (0.6, 1.2, and 2 g/kg b.w.) groups were not statistically different from those of the negative control animals (Table 3). These data indicated that neither mutagenicity nor clastogenicity was caused by E. longifolia powdered root treatments.


TreatmentDose Frequency of micronucleated polychromatic erythrocyte (‰) Ratio of polychromatic erythrocyte (PCE) to total erythrocytes (%)
Day 1Day 2Day 3Day 1Day 2Day 3

Negative10
Positive cyclophosphamide (mg/kg b.w.)200
E. longifolia powdered root (g/kg b.w.)0.6
1.2
2.0

Both the ratios of polychromatic erythrocyte (PCE) to total erythrocytes (%) and the frequency of micronucleated polychromatic erythrocyte (%) in treated group were not statistically different from those of the negative control animals, suggesting that the treatment with E. longifolia powdered root did not cause erythropoietic cell toxicity and genotoxicity in vivo. Data were expressed as Mean ± S.D. . Statistical analysis: , and indicate a statistical difference with the control group by one-way ANOVA.
Mice in negative control group received single gavage of vehicle (sterile water).
3.2. No Deaths or Abnormalities Were Observed in the Single-Dose Acute Toxicity Study

No deaths or hazardous signs were recorded in rats during the 14-day observation period for rats orally treated with E. longifolia powdered root (1, 2, 4, and 6 g/kg b.w.). Hematological and serum biochemical profiles of both sexes, as shown in Supplementary Table 2, remained unaffected.

3.3. E. longifolia Powdered Root Treatment Was Nontoxic but Induced Pharmacological Effects in Subacute and Subchronic Toxicity Studies

No treatment-related mortality or clinical signs of toxicity were observed throughout the 4- or 13-week consecutive testing period (at 0, 0.6, 1.2, and 2 g/kg b.w.). No statistically significant changes were found in body weight (Supplementary Table 3), food consumption, or water intake (data not shown), regardless of sex or treatment. Most hematology measures (WBC, RBC, Hb, HCT, PLT, MPV, RDW, and Fbg) in treated rats were not significantly different from controls, with the exception of marginal variations in certain parameters (MCHC and MCV; Table 4). The PT and APTT of treated males (in both the 4-week and 13-week treatment groups) were significantly decreased compared to control male rats ( ), whereas the PT and APTT were not different in control versus treated female rats (Table 4 and Supplementary Table 4). Serum biochemistry profiles are shown in Table 5. E. longifolia powdered root had no effects on serum electrolytes, such as calcium, potassium, sodium, and chloride, but did cause marginal variations in phosphate and magnesium. No statistically significant differences in liver function parameters (ALT, ALP, and GGT) were noted. However, the activities of AST, CPK, and LDH were reduced in a dose-dependent manner in both 4-week and 13-week treated males ( ). Dose-dependent reductions in kidney function parameters, creatinine, and BUN were noted in male rats treated for 13 weeks (the reduction in BUN was also noted in male rats in the 4-week treatment group) ( ). No similar changes in AST, CPK, LDH, BUN, or creatinine were found in the female groups. Serum cholesterol was significantly decreased in both male and female rats after 4 and 13 weeks of administration ( ). No significant changes in total protein, globulin, albumin, glucose, triglycerides, or amylase were noted.


Item (abbreviation)UnitTreatment (g/kg b.w.)
MaleFemale
00.61.2200.61.22

Red blood cell count (RBC)106/μL
Hematocrit (HCT)%
Hemoglobin (Hb)g/dL
Mean corpuscular hemoglobin (MCH)pg
MCH concentration (MCHC)g/dL
Mean corpuscular volume (MCV)fL
Red cell distribution width (RDW)fL
Mean platelet volume (MPV)fL
Platelet distribution width (PDW)fL
White blood cell count (WBC)103/μL
Lymphocytes103/mm3
Neutrophils103/mm3
Monocytes103/mm3
Eosinophil103/mm3
Basophils103/mm3
Platelets count (PLT)103/μL
Prothrombin time (PT)Sec
Partial thromboplastin time (APTT)Sec