Effects of Dendropanax morbifera Léveille extracts on cadmium and mercury secretion as well as oxidative capacity: A randomized, double-blind, placebo-controlled trial

Introduction

Heavy metal intoxication and/or oxidative stress are implicated in numerous chronic diseases, including metabolic and neurological disorders. Environmental contamination by heavy metals such as cadmium (Cd) and mercury (Hg) is a serious international concern as these heavy metals can enter the food chain, accumulate in fishes and animals, and thus, endanger human health (1–5). According to the World Health Organization, the limit of tolerable intake for Cd, methylmercury and inorganic Hg in an adult human is 7, 1.6 and 4 µg/kg of body weight per week, respectively (6).

One of the possible mechanisms underlying the effects of Cd and Hg is oxidative cytotoxicity. Cd and Hg interaction with the carboxyl and sulfhydryl group of proteins results in free radical generation (7–10). In addition, Cd and Hg can deplete antioxidant levels, resulting in an imbalance between oxidant and antioxidant ability. An increase in reactive oxygen species levels results in oxidation of polyunsaturated fatty acids, causing neuronal damage due to high acid content in the nervous system. In addition, our previous study demonstrated that Cd administration significantly increased lipid peroxidation and reduced levels of antioxidant enzymes such as Cu, Zn-superoxide dismutase (SOD1), catalase and glutathione peroxidase (11).

Dendropanax morbifera Léveille (DML), which belongs to the family Araliaceae, is an endemic species found in the southwestern region of South Korea (12). Recently, studies have investigated the effects of DML on various conditions, including their antioxidant and antidotal capacities (11,13). For example, a methanol extract of the debarked stem of DML contains abundant phenolic and flavonoid compounds, which show strong antioxidant activities (13). In addition, our previous study demonstrated that DML extracts facilitate Cd excretion and suppress Cd-induced lipid peroxidation in hippocampal homogenates (11). However, to the best of our knowledge, no clinical study has examined the possible health benefits of a DML extract on heavy metal and antioxidant levels in human subjects.

The aim of the present randomized, double-blind, placebo-controlled cross-over study was to examine the effects of repeated application of DML extract on the antioxidant status and oxidative damage in healthy adults.

Subjects and methods

Preparation of the test product from the leaf extract of DML

The DML extract used was manufactured by a good manufacturing practices-certified company (Natural F&P Corp., Cheonwon, Korea). Fresh leaves from DML were obtained from Hambakjae Biopharm Co., Ltd. (Jeju, Korea). The plant was authenticated by two practitioners of traditional Asian medicine. Leaves from the plant samples (15 kg) were chopped, blended and soaked in 2 liters of 80% ethanol, and refluxed three times at 20°C for 2 h. The insoluble materials were removed by centrifugation at 10,000 × g for 30 min, and the resulting supernatant was concentrated and freeze-dried to obtain a powder. For the test product preparation, DML, stearin magnesium and silicon dioxide were mixed. For the placebo, microcrystalline cellulose 102 was mixed with lactose powder, and dextrin was added to obtain a tablet form. Food colors (red, yellow and blue) were also added to produce the same color as the test product (Table I). The raw materials used in the test product and placebo were placed in a mixer and blended sufficiently to ensure homogeneity; subsequently, these were made into tablet at 300 mg/tablet.

Table I. Composition of Dendropanax morbifera Léveille (DML) extracts and placebo tablets.

Table I.

Composition of Dendropanax morbifera Léveille (DML) extracts and placebo tablets.

Composition	DML	Placebo (%)
Dendropanax extracts	98.000
Cellulose 102		59.852
Lactose powder		39.600
Stearin magnesium	1.000
Dextrin		0.400
Silicon dioxide	1.000
Food color (red/yellow/blue)		0.148
Total	100.000	100.000

Stability testing for the test product and placebo

The test product and placebo were assessed for stability; moisture content (%); coliform group; lead (mg/kg), arsenic (mg/kg) and sodium (mg/100 g) levels; and disintegration by outsourcing to ‘Korea Health Supplements Association’ (Seongnam, South Korea). All test results were acceptable as per the requirements set by the Food Sanitation Act. No preservative was added to the test product.

Study approval and sample target group selection

In accordance with the Functional Foods for Health Act (http://www.mfds.go.kr/files/upload/eng/FOOD_SANITATION_ACT.pdf), all issues associated with human trials were approved by the Institutional Review Board for Human Trials of Hallym University (Hwaseong, Korea) (IRB approval no. 2014-074); the study was conducted in agreement with the Declaration of Helsinki and performed in accordance with International Conference on Harmonization guidelines. In addition, the study was retrospectively registered at the WHO Primary Registries in Republic of Korea (Clinical Research Information Service) (registration no. KCT0001472, May 8, 2015).

Subjects were male and female volunteers aged 23–65 years (n=61). The subjects were informed of the details of the trial, and only those who fully understood the purpose of trial participation and gave consent for participation were selected as subjects. All the subjects were considered suitable for the trial as they had normal liver functions, as assessed by measuring glutamate-oxaloacetate transaminase (AST) and glutamate-pyruvate transaminase (ALT) levels in the blood. Exclusion criteria consisted of intestinal absorption abnormalities and liver functions. Subjects with ALT or AST >60 U/T were also excluded. One subject was excluded due to high levels of ALT and AST. The others (n=60) (Fig. 1) were randomly assigned to treatment groups, minimizing any intentional elements of group assignment, in a double-blind procedure to ensure that the subjects did not know which group they were assigned to (test group or comparative control group) (Fig. 1). The sample size of a minimum 9 per treatment group would provide ≥95% power to detect a difference of Cd values in the serum based on the previous animal study (11).

Figure 1. Consort flow diagram of the patients enrolled, allocated, followed up and analyzed during the study.

Analytical procedures

For heavy metal, lipid peroxidation and antioxidant analysis, the assay was performed prior and subsequent to administration of the test product and the placebo (Fig. 2). All the subjects were instructed to ingest the tablets after breakfast over a 60-day period. The placebo group was comparable in all characteristics to the DML group. Food and water intake was not limited.

Figure 2. Experimental design and baseline characteristics (gender, number and age) of the subjects in the present study.

Measurement of Cd, Hg and malondialdehyde (MDA) levels and SOD1 activity in the serum

By vein puncture with a syringe, blood samples were collected in tubes containing ethylenediaminetetraacetic acid. The tubes were immediately centrifuged at 4°C and 500 × g for 10 min to obtain serum and plasma for measuring Cd, Hg and MDA levels and SOD1 activity. These parameters were measured using routine automated methods. Adverse experiences were rated by the investigators for intensity and their association to the DML extract. Efficacy and safety measurements were conducted at a Hallym University Dongtan Sacred Heart Hospital (Dongtan, South Korea) laboratory and at a Seoul National University College of Veterinary Medicine (Seoul, South Korea) by technicians or graduate students blinded to the placebo and treatment groups.

Statistical analysis

The measured Hg and Cd levels were calculated into excretion ratio (delta% value), as shown in Fig. 2. The MDA levels and SOD1 activities 60 days after placebo or DML consumption are shown. All the data are expressed as mean ± standard error of the mean. To determine the effects of the DML tablet, differences between the means of the two groups were statistically analyzed using two-way analysis of variance with repeated measures and Bonferroni's post hoc test using GraphPad Prism 5.01 (GraphPad Software, La Jolla, CA, USA) software.

Results

Patient characteristics

The baseline characteristics and biochemical values of the subjects did not significantly differ between the placebo and DML groups (data not shown). In addition, no significant differences between male and female participants were identified.

Cd and Hg excretion

Serum Cd levels were increased in the male and female subjects in the placebo group and decreased in the DML group; however, no significant difference between the two groups was identified (P=0.3008) (Fig. 3). Serum Hg levels decreased in all the groups, but serum levels were more prominently decreased in the DML-male and DML-female groups compared to the placebo-male and placebo-female groups, respectively (P=0.1336 and P=0.1937, respectively) (Fig. 3).

Figure 3. Effects of Dendropanax morbifera Léveille (DML) extract on cadmium (Cd) and mercury (Hg) concentration in the blood of subjects who consumed placebo and DML. The data represent the mean ± standard error of the mean.

Oxidative stress biomarkers

Serum MDA levels were increased in the DML-male group compared to the placebo-male group (P=0.3125), while these were decreased in the DML-female group compared to the placebo-female group (P=0.0842) (Fig. 4); however, no significant differences were identified.

Figure 4. Malondialdehyde (MDA) levels and superoxide dismutase 1 (SOD1) activity in the serum of subjects who consumed placebo and Dendropanax morbifera Léveille (DML) extract. Significant difference between the placebo and DML groups (*P<0.05). The data represent means ± standard error of the mean.

Serum SOD1 activity was increased in DML-treated groups, but the SOD1 activity was significantly increased in the DML-female group compared to the placebo-female group (P=0.02031). However, no significant difference in SOD1 activity was observed between the placebo-male and DML-male group (P=0.2031) (Fig. 4).

Discussion

Several lines of evidence demonstrate that DML and its components reduce reactive oxygen species generation and have antioxidant effects (13,14). In addition, our previous study demonstrated that DML facilitates Cd excretion and exerts antioxidant effects against Cd-induced oxidative damage (11). The present study attempted to use DML to facilitate Cd and Hg excretion in humans and to increase the antioxidant capacity in the serum, as Cd and Hg have been shown to inhibit antioxidant enzymes (15–17).

No significant decrease in serum Cd or Hg levels was observed. However, the consumption of the DML tablet for 2 months facilitated excretion of Cd to 4.6% in male subjects and Hg to 23.0 and 17.3% in male and female subjects, respectively. This result suggests that consumption of DML tablet facilitates Cd and Hg excretion from the serum. The facilitated excretion rate is relatively low for Cd; however, the facilitation is extremely important as cadmium is tightly bound to metallothionein, which is almost completely reabsorbed in the renal tubules and accumulates in the body over the lifetime with a biological half-life of ≤38 years (6).

Heavy metals contribute to oxidative processes (18,19), and the levels of reactive oxygen species are important factors associated with the development of chronic disease (20,21). In the present study, the levels of MDA, a well-known product of lipid peroxidation (22,23), were measured in human subjects. MDA levels were decreased in the DML group compared to the placebo group. This result was consistent with our previous study showing that supplementation with the DML suppressed Cd-induced increase of MDA levels, as well as protein carbonylation due to modified proteins in the rat hippocampus (11). In the present study, the DML significantly increased SOD levels in the female treatment group compared to the female placebo group; this suggests that treatment with the extract for 2 months increases the antioxidant capacity in the blood. This is consistent with our previous study showing that administration of DML increased SOD1 activity in normal healthy rats (11).

In conclusion, administration of DML has positive effects on excretion of Cd and Hg from the blood and increases antioxidant capacity by decreasing MDA levels and increasing SOD activity in the serum.

Acknowledgements

The present study was supported by the High Value-added Food Technology Development Program, Ministry for Agriculture, Food and Rural Affairs, Republic of Korea (grant no. 112106-022-HD020).

References