Acute and 4-Week Repeated-Dose Oral Toxicity Studies of Cirsium setidens in Rats
1
Department of Food Science and Biotechnology, Kangwon National University, Chuncheon 200-701, Korea
2
Department of Food and Nutrition, Yeungnam University, Gyeongsan, Gyeongbuk 712-749, Korea
*
Authors to whom correspondence should be addressed.
Molecules 2014, 19(6), 7138-7151; https://doi.org/10.3390/molecules19067138
Submission received: 10 April 2014
/
Revised: 26 May 2014
/
Accepted: 28 May 2014
/
Published: 30 May 2014
(This article belongs to the Section Natural Products Chemistry)
Abstract
:Cirsium setidens is a wild perennial plant species found in Korea that may have anti-oxidative, anti-adipogenic, and hepatoprotective activities. However, details of the toxicology of C. setidens remain unknown. This study was performed to evaluate the toxicological effects of an acute administration and 4-week repeated dosing of a C. setidens extract in Sprague-Dawley rats to ensure the safe use of this extract. C. setidens (1250, 2500, and 5000 mg/kg body weight/day) did not induce significant toxicological changes in groups matched by gender with respect to mortality, clinical signs, body weight, urinalysis, ophthalmoscopy, necropsy findings, hematology, and histopathology. Therefore, this study demonstrates that acute administration and 4-week repeated dosing of C. setidens extract orally using this administration protocol is safe.
1. Introduction
Plants have the ability to synthesize a wide variety of chemical compounds with important biological effects [1]. Many of these plant-derived compounds have beneficial effects on long-term health when consumed by humans and are commonly employed in developing countries for the treatment of various human diseases [2]. Many studies have shown that plant-derived compounds have a number of health benefits [3,4,5,6,7]. Epigallocatechin gallate has been extensively studied for insight into its beneficial health effects as a nutriceutical agent [8,9]. Morin hydrate, a member of flavonoid family, is shown to be an effective hepatoprotector in vitro and in vivo via modulation oxidative stress [10,11]. In particular, bioactive ingredients of C. setidens may exhibit hepatoprotective activity mainly via an SOD antioxidant mechanism [12]. However, herbs are composed of numerous bioactive chemicals, some of which may be toxic, and a number of studies have reported the toxic effects of herbal medicines [13].
Cirsium setidens, a wild perennial herb, has been used in Korean medicine for treating hemostasis, hematemesis, hematuria and hypertension [14]. Previous studies have demonstrated that C. setidens contains several bioactive ingredients with various medicinal activities, including cytotoxicity against human cancer cell lines [15,16]. Some studies have also reported that C. setidens shows hepatoprotective activity against CCl4- or D-galactosamine-induced liver damage via an antioxidant mechanism [12,17]. In a recent study, C. setidens inhibited hepatic fat accumulation by up-regulating the expression of fatty acid β-oxidation genes [18]. In our previous study, we found that C. setidens had an anti-adipogenic effect during the adipogenesis of 3T3-L1 cells [19]. However, despite several studies on the biological activity of C. setidens, there has been no toxicological study of C. setidens, to our knowledge.
Therefore, a systemic safety evaluation on the extract of C. setidens is necessary for the development of new foods or drugs. In this study, an aqueous extract from the dried C. setidens was prepared and its safety was evaluated in Sprague-Dawley (SD) rats by using an oral acute toxicity and a 4-week repeated-dose oral toxicity study, in compliance with the guidelines for testing the toxicity of pharmaceuticals from the Korea Food and Drug Administration (KFDA), using the Good Laboratory Practice regulations for Nonclinical Laboratory Studies.
2. Results and Discussion
2.1. Acute Oral Toxicity
Various bioactive compounds in herbal plants possess the capacity to significantly modulate the complex mechanisms involved in the pathology of chronic diseases such as cardiovascular disease, cancer, aging, and diabetes [20,21]. In addition, some ingredients have been reported to help improve psychiatric disorders such as depression [22,23,24]. In the search for new sources of health-promoting constituents in herbal plants, we focused on the C. setidens extract, which has recently shown hepatoprotective activities against CCl4- or D-galactosamine-induced liver damage and an anti-adipogenic effect during adipogenesis of 3T3-L1 cells via an antioxidant mechanism [12,17,19]. However, safety data are needed to assess potential toxicological concerns regarding the C. setidens extract. We therefore evaluated, for the first time, the acute oral safety/toxicity of C. setidens (Table 1). Thus, C. setidens was orally administered once at doses of 1,250, 2,500 and 5,000 mg/kg BW in SD rats. Mortality, clinical signs, and body weight changes were observed for 14 days after administration. In addition, necropsy was performed to examine any abnormalities in the main organs. This study complied with the test guidelines from the Korea Food and Drug Administration (KFDA). No animal deaths or abnormal clinical signs related to the administration of C. setidens were observed during the experimental period. In addition, there were no significant changes in body weight in the C. setidens-treated groups compared with the control group. In addition, no abnormalities related to the administration of C. setidens were found during necropsy. These results suggest that the C. setidens extract is essentially non-toxic after acute exposure. We conclude that the no-observed-adverse-effect-level (NOAEL) of C. setidens is 5000 mg/kg.
| Group a | Dose (mg/kg) | Sex | Body Weights (g) | Clinical Signs | No Gross Finding | Mortality (Dead/Total) | ||
|---|---|---|---|---|---|---|---|---|
| Day 0 | Day 7 | Day 14 | ||||||
| G1 | 0 | M b | 153.8 ± 9.8 | 242.8 ± 10.6 | 304.7 ± 13.7 | N d | 5 | 0% (0/5) |
| F c | 123.7 ± 7.3 | 173.7 ± 12.0 | 197.7 ± 11.0 | N | 5 | 0% (0/5) | ||
| G2 | 1250 | M | 153.9 ± 4.5 | 238.5 ± 10.5 | 307.4 ± 18.8 | N | 5 | 0% (0/5) |
| F | 125.1 ± 5.1 | 173.5 ± 11.6 | 198.2 ± 11.4 | N | 5 | 0% (0/5) | ||
| G3 | 2500 | M | 155.3 ± 4.5 | 242.4 ± 16.7 | 297.8 ± 19.6 | N | 5 | 0% (0/5) |
| F | 123.8 ± 3.7 | 168.8 ± 5.3 | 191.2 ± 8.5 | N | 5 | 0% (0/5) | ||
| G4 | 5000 | M | 157.8 ± 8.0 | 237.6 ± 15.0 | 293.0 ± 18.2 | N | 5 | 0% (0/5) |
| F | 124.4 ± 4.7 | 170.8 ± 11.7 | 191.7 ± 13.7 | N | 5 | 0% (0/5) | ||
a G1, Control; G2, Group 2 (1250 mg/kg body weight); G3, Group 3 (2500 mg/kg body weight); G4, Group 4 (5000 mg/kg body weight); b M: Male; c F: Female; d N: Normal.
2.2. Four-Week Repeated-Dose Oral Toxicity
2.2.1. General Appearance, Body Weight, Food Intake and Water Consumption
Changes in general behavior and body weight are critical parameters for the objective evaluation of the effect of a compound on test animals because such changes are often the first signs of toxicity [25]. In a 4-week repeated-dose oral toxicity study, no animal deaths or abnormal clinical signs related to the administration of C. setidens were observed throughout the duration of the experiment at any dose used. The animals in the treatment groups did not appear seriously diseased at the end of the treatment period (data not shown). During the experimental period, a decrease in food consumption was observed in the 1250 and 2500 mg/kg female groups on week 4 (Table 2). As a result of water consumption, an increase was observed in the C. setidens-treated male groups administered 1,250 and 5000 mg/kg in week 1 and in the C. setidens-treated male groups in weeks 3 and 4 (all doses) compared to the control group (Table 3). In the female group, an increase in water consumption was observed in the group administered 5000 mg/kg in week 1 and in the groups administered 1250 and 5000 mg/kg in week 3 compared with the control group (Table 3). However, there were no significant changes in body weight in the C. setidens-treated groups compared with the control group throughout the study (Figure 1). Therefore, these changes were transient and appeared to be unrelated to the doses or to the treatment with C. setidens.
| Dose (mg/kg) | Mean Food Intake (g/rat/day) During Week | |||
|---|---|---|---|---|
| 1 | 2 | 3 | 4 | |
| Male | ||||
| 0 | 27.3 ± 0.2 | 27.8 ± 1.0 | 31.8 ± 0.4 | 31.0 ± 0.9 |
| 1250 | 26.9 ± 0.1 | 26.2 ± 0.2 | 31.6 ± 0.3 | 31.8 ± 0.1 |
| 2500 | 27.7 ± 0.7 | 26.3 ± 0.5 | 29.8 ± 2.8 | 30.8 ± 2.4 |
| 5000 | 27.5 ± 0.9 | 26.0 ± 0.4 | 30.0 ± 1.0 | 31.0 ± 1.1 |
| Female | ||||
| 0 | 19.8 ± 1.2 | 19.6 ± 1.6 | 20.8 ± 0.9 | 22.9 ± 3.0 |
| 1250 | 20.1 ± 0.5 | 17.4 ± 1.4 | 22.3 ± 0.7 | 18.6 ± 0.2 * |
| 2500 | 19.5 ± 0.4 | 19.4 ± 1.1 | 20.8 ± 1.0 | 18.3 ± 0.0 * |
| 5000 | 18.1 ± 0.3 | 18.2 ± 1.3 | 21.1 ± 0.9 | 21.1 ± 0.5 |
* Significant differences were compared with the control at p < 0.05.
| Dose (mg/kg) | Mean Water Consumption (g/rat/day) During Week | |||
|---|---|---|---|---|
| 1 | 2 | 3 | 4 | |
| Male | ||||
| 0 | 38.5 ± 2.2 | 40.7 ± 1.2 | 39.2 ± 2.3 | 34.9 ± 3.3 |
| 1250 | 43.5 ± 1.2 * | 39.3 ± 6.4 | 47.6 ± 3.6 * | 43.4 ± 2.2 * |
| 2500 | 41.2 ± 3.2 | 38.9 ± 3.3 | 47.0 ± 1.9 * | 48.5 ± 1.9 * |
| 5000 | 45.7 ± 0.3 * | 38.0 ± 2.0 | 58.6 ± 4.5 * | 57.0 ± 0.2 * |
| Female | ||||
| 0 | 29.9 ± 2.8 | 31.2 ± 4.9 | 27.1 ± 0.7 | 31.8 ± 1.3 |
| 1250 | 33.1 ± 1.8 | 26.2 ± 2.7 | 31.2 ± 1.8 * | 27.0 ± 2.6 |
| 2500 | 31.7 ± 0.2 | 31.3 ± 1.4 | 32.8 ± 3.4 | 32.7 ± 2.4 |
| 5000 | 36.3 ± 0.9 * | 33.0 ± 2.8 | 38.2 ± 1.4 * | 32.5 ± 1.4 |
* Significant differences were compared with the control at p < 0.05.
Figure 1.
Growth curves for SD rats treated with C. setidens for 4 weeks. (● ○) Group 1 (control); (■ □) Group 2 (1250 mg/kg body weight per day); (▼ ▽) Group 3 (2500 mg/kg body weight per day); (◆ ◇) Group 4 (5000 mg/kg body weight per day).
Figure 1.
Growth curves for SD rats treated with C. setidens for 4 weeks. (● ○) Group 1 (control); (■ □) Group 2 (1250 mg/kg body weight per day); (▼ ▽) Group 3 (2500 mg/kg body weight per day); (◆ ◇) Group 4 (5000 mg/kg body weight per day).
2.2.2. Urinary, Hematological and Biochemical Findings
In terms of urinary parameters such as specific gravity, pH, and the levels of leukocytes, nitrites, protein, glucose, ketones, blood, urobilinogen, and bilirubin, no treatment-related adverse effects were observed in male and female rats following the administration of C. setidens at doses of 1250, 2500, and 5000 mg/kg/day (Table 4). Bilirubin, a breakdown product of hemoglobin, is associated with hepatic diseases such as jaundice and ineffective erythropoiesis. Increased bilirubin levels reflect the extent of jaundice [26]. In the present study, no significant changes were observed in the levels of bilirubin in the C. setidens-treated and control rats, suggesting that C. setidens has no toxic effects on the erythropoietic system. In the 5000 mg/kg male group, although a high increase in protein excretion was noted, the other parameters exhibited no significant differences compared with the control group (Table 4).
Hematopoietic parameters are some of the most sensitive to assess the toxicity of drugs in humans and animals, and a blood profile usually gives vital information on the response of the body to injury or stress [27,28]. The hematological results for the male and female rats administered C. setidens are shown in Table 5. Hb concentration in female rats was increased at doses of 1,250 and 2,500 mg/kg C. setidens. Despite an increase in Hb concentration, this group of animals appeared normal, and the level stayed within the physiological range and appeared to be unrelated to the dose. This change was not observed in male C. setidens-treated rats. There were no consistent, statistically significant, dose-dependent adverse effects on any of the hematological parameters in the rats after 4 weeks of C. setidens treatment. In addition, there were no significant alterations in the biochemical parameters in all the groups treated with a 4-week repeated dose of C. setidens (Table 5). Symptoms of disorder in the liver and kidneys, which are the major internal organs in the body and have several important functions, appear only in serious disease [25]. The liver is the main site of the synthesis of plasma proteins, especially ALB. Changes in total serum proteins or the A/G ratio may indicate hepatic dysfunction [29]. In this study, the daily administration of C. setidens in feed for 4 weeks did not produce any significant changes in the TP, ALB, and A/G ratio of the treated rats from all the doses used compared with the control group (Table 5). The levels of serum biomarker enzymes such as ALP, AST, and ALT are usually assayed to evaluate any toxic effects on the liver [30]. In the present study, no significant increases in the levels of serum ALP, AST, and ALT in male and female rats were observed, although a few changes were noted (Table 5). These changes were not considered to be treatment related, as the changes were slight and the values were within the normal physiological range. CREA and BUN are known as important markers of kidney dysfunction [27]. No significant differences in CREA and BUN were found in treated rats compared with the control group. Changes in the BUN value were very slight and not dose-dependent (Table 5). These results suggest that C. setidens does not have a toxic effect on the liver and kidneys.
2.2.3. Organ Weights and Histopathology
The absolute and relative organ weight data for males and females are summarized in Table 6. No significant treatment-related changes were observed in the absolute and relative organ weights of male and female rats following the administration of C. setidens at dosages of 1250, 2500, and 5000 mg/kg/day for 4 weeks.
| Sex | Dose (mg/kg) | No. of Animals | Urinary Analysis on Week 4 | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| SG a | Glu b | Bili c | Ketone d | Blood e | pH | Protein f | Urobilinogen | Nitrite g | Leukocyte h | |||||||||||||
| − | − | − | T | 1+ | − | 6.5 | 7.0 | 7.5 | 8.0 | 8.5 | − | T | 1+ | 0.2 | 1.0 | − | − | T | ||||
| Male | 0 | 5 | 1.014 ± 0.002 | 5 | 5 | 1 | 4 | 0 | 5 | 0 | 0 | 0 | 1 | 4 | 4 | 1 | 0 | 5 | 0 | 5 | 5 | 0 |
| 1250 | 5 | 1.014 ± 0.002 | 5 | 5 | 5 | 0 | 0 | 5 | 0 | 0 | 0 | 0 | 5 | 5 | 0 | 0 | 5 | 0 | 5 | 5 | 0 | |
| 2500 | 5 | 1.010 ± 0.000 | 5 | 5 | 5 | 0 | 0 | 5 | 0 | 0 | 0 | 0 | 5 | 5 | 0 | 0 | 5 | 0 | 5 | 5 | 0 | |
| 5000 | 5 | 1.010 ± 0.000 | 5 | 5 | 3 | 1 | 1 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | 3 | 2 | 5 | 0 | 5 | 5 | 0 | |
| Female | 0 | 5 | 1.014 ± 0.002 | 5 | 5 | 5 | 0 | 0 | 5 | 0 | 0 | 0 | 0 | 5 | 0 | 5 | 0 | 2 | 3 | 5 | 5 | 0 |
| 1250 | 5 | 1.010 ± 0.000 | 5 | 5 | 5 | 0 | 0 | 5 | 0 | 0 | 0 | 2 | 3 | 3 | 2 | 0 | 5 | 0 | 5 | 5 | 0 | |
| 2500 | 5 | 1.010 ± 0.000 | 5 | 5 | 5 | 0 | 0 | 5 | 0 | 0 | 0 | 0 | 5 | 2 | 3 | 0 | 5 | 0 | 5 | 5 | 0 | |
| 5000 | 5 | 1.011 ± 0.002 | 5 | 5 | 4 | 1 | 0 | 5 | 0 | 0 | 0 | 0 | 5 | 1 | 3 | 1 | 5 | 0 | 5 | 5 | 0 | |
a SG: specific gravity; b Glucose, −: negative; c Bilirubin, −: negative; d Ketone, −: negative; T: 5 mg/dL; 1+: 15 mg/dL; e Blood, −: negative; f Protein, −: negative; T: <30 mg/dL; 1+: 30 mg/dL; g Nitrite: −: negative; h Leukocyte: −: negative; T: 15 Leu/μL.
Table 5.
Hematological results and serum biochemical data of male and female SD rats treated orally with C. setidens for 4 weeks.
| Sex | Male | Female | ||||||
|---|---|---|---|---|---|---|---|---|
| Dose (mg/kg) | 0 | 1250 | 2500 | 5000 | 0 | 1250 | 2500 | 5000 |
| WBC (K/μL) | 5.9 ± 1.1 | 7.1 ± 1.6 | 6.3 ± 1.4 | 5.9 ± 1.0 | 3.4 ± 0.1 | 5.1 ± 0.6 | 5.0 ± 0.9 | 5.2 ± 2.1 |
| RBC (M/μL) | 7.2 ± 0.3 | 7.2 ± 0.4 | 7.0 ± 0.2 | 7.0 ± 0.2 | 7.0 ± 0.1 | 7.7 ± 0.4 | 7.2 ± 0.2 | 7.1 ± 0.1 |
| Hb (g/dL) | 14.6 ± 0.4 | 14.4 ± 0.7 | 14.4 ± 0.4 | 14.2 ± 0.3 | 13.9 ± 0.5 | 15.3 ± 0.4 | 14.7 ± 0.3 | 14.4 ± 0.1 |
| PLT (K/μL) | 1319 ± 136 | 1374 ± 74 | 1369 ± 79 | 1391 ± 131 | 1364 ± 102 | 1340 ± 90 | 1342 ± 109 | 1251 ± 90 |
| PT (s) | 12.1 ± 2.0 | 11.0 ± 0.4 | 10.6 ± 1.3 | 9.6 ± 0.9 | 8.9 ± 0.8 | 9.8 ± 0.7 | 9.6 ± 2.2 | 8.8 ± 1.1 |
| APTT (s) | 20.7 ± 1.3 | 19.1 ± 2.2 | 19.8 ± 2.4 | 17.6 ± 1.6 | 18.2 ± 1.7 | 20.6 ± 4.2 | 17.9 ± 1.9 | 15.7 ± 1.4 |
| TP (g/dL) | 5.3 ± 0.2 | 5.5 ± 0.3 | 5.3 ± 0.3 | 5.5 ± 0.2 | 5.8 ± 0.5 | 5.7 ± 0.5 | 5.7 ± 0.3 | 5.6 ± 0.1 |
| ALB (g/dL) | 2.2 ± 0.1 | 2.3 ± 0.1 | 2.3 ± 0.1 | 2.3 ± 0.1 | 2.5 ± 0.2 | 2.5 ± 0.2 | 2.6 ± 0.1 | 2.6 ± 0.1 |
| T-BIL (mg/dL) | 0.02 ± 0.03 | 0.02 ± 0.03 | 0.00 ± 0.01 | 0.00 ± 0.00 | 0.00 ± 0.00 | 0.02 ± 0.02 | 0.02 ± 0.01 | 0.02 ± 0.01 |
| ALP (U/L) | 588 ± 138 | 644 ± 174 | 616 ± 96 | 587 ± 147 | 478 ± 74 | 450 ± 111 | 437 ± 159 | 421 ± 134 |
| AST (U/L) | 154 ± 22 | 154 ± 43 | 149 ± 27 | 146 ± 27 | 126 ± 39 | 136 ± 30 | 108 ± 31 | 125 ± 22 |
| ALT (U/L) | 29 ± 4 | 33 ± 6 | 34 ± 7 | 32 ± 6 | 24 ± 1 | 30 ± 8 | 24 ± 2 | 25 ± 4 |
| CREA (mg/dL) | 0.5 ± 0.0 | 0.5 ± 0.0 | 0.5 ± 0.0 | 0.5 ± 0.0 | 0.5 ± 0.1 | 0.5 ± 0.1 | 0.5±0.1 | 0.6 ± 0.0 |
| BUN (mg/dL) | 12.2 ± 0.6 | 12.0 ± 1.8 | 14.1 ± 0.6 | 13.5 ± 0.9 | 15.2 ± 1.4 | 18.0 ± 1.2 | 17.3 ± 1.6 | 17.5 ± 1.6 |
| TC (mg/dL) | 56 ± 13 | 64 ± 13 | 56 ± 10 | 55 ± 12 | 85 ± 16 | 66 ± 10 | 76 ± 6 | 71 ± 6 |
| TG (mg/dL) | 85 ± 15 | 115 ± 51 | 77 ± 44 | 81 ± 30 | 31 ± 11 | 18 ± 8 | 32 ± 8 | 18 ± 4 |
| GLU (mg/dL) | 116 ± 13 | 140 ± 42 | 131 ± 30 | 92 ± 13 | 126 ± 25 | 110 ± 12 | 111 ± 13 | 92 ± 13 |
| Ca (mg/dL) | 9.9 ± 0.3 | 10.0 ± 0.3 | 9.9 ± 0.2 | 10.2 ± 0.2 | 10.0 ± 0.2 | 10.2 ± 0.5 | 10.3 ± 0.2 | 10.2 ± 0.3 |
| Na (mmol/L) | 141.3 ± 1.1 | 140.4 ± 0.6 | 139.4 ± 0.9 | 139.6 ± 1.0 | 140.0 ± 0.8 | 140.0 ± 0.8 | 139.3 ± 0.5 | 138.0 ± 0.4 |
| K (mmol/L) | 4.5 ± 0.3 | 4.4 ± 0.2 | 4.8 ± 0.2 | 4.7 ± 0.2 | 4.2 ± 0.2 | 4.3 ± 0.4 | 4.3 ± 0.2 | 4.6 ± 0.5 |
| Cl (mmol/L) | 107.5 ± 2.0 | 105.4 ± 1.5 | 105.8 ± 1.2 | 105.5 ± 0.8 | 108.0 ± 1.6 | 106.4 ± 1.9 | 104.8 ± 1.0 | 104.8 ± 0.5 |
Table 6.
Absolute and relative organ weights of male and female rats treated orally with C. setidens for 4 weeks.
| Sex | Male | Female | ||||||
|---|---|---|---|---|---|---|---|---|
| Dose (mg/kg) | 0 | 1250 | 2500 | 5000 | 0 | 1250 | 2500 | 5000 |
| Absolute Body Weight | ||||||||
| Liver (g) | 11.05 ± 1.60 | 11.04 ± 0.99 | 11.39 ± 1.60 | 11.34 ± 0.58 | 6.66 ± 0.46 | 6.15 ± 0.58 | 6.70 ± 0.52 | 6.65 ± 0.75 |
| Kidneys (g) | 3.01 ± 0.31 | 2.97 ± 0.18 | 3.01 ± 0.32 | 2.94 ± 0.13 | 1.82 ± 0.11 | 1.78 ± 0.09 | 1.92 ± 0.16 | 1.84 ± 0.17 |
| Spleen (g) | 0.85 ± 0.09 | 0.88 ± 0.32 | 0.80 ± 0.09 | 0.82 ± 0.11 | 0.53 ± 0.08 | 0.52 ± 0.09 | 0.52 ± 0.09 | 0.53 ± 0.10 |
| Lungs (g) | 1.71 ± 0.41 | 1.61 ± 0.08 | 1.64 ± 0.11 | 1.64 ± 0.15 | 1.25 ± 0.04 | 1.19 ± 0.09 | 1.25 ± 0.09 | 1.15 ± 0.08 |
| Heart (g) | 1.49 ± 0.18 | 1.50 ± 0.12 | 1.5 1± 0.16 | 1.60 ± 0.20 | 1.01 ± 0.10 | 0.96 ± 0.18 | 0.98 ± 0.07 | 0.93 ± 0.05 |
| Relative Body Weight | ||||||||
| Body Weight (g) | 379.4 ± 32.4 | 379.4 ± 14.1 | 386.9 ± 37.7 | 378.4 ± 18.0 | 231.7 ± 12.5 | 226.4 ± 4.3 | 220.8 ± 23.6 | 226.6 ± 12.7 |
| Liver (%) | 2.90 ± 0.20 | 2.91 ± 0.19 | 2.94 ± 0.21 | 3.00 ± 0.08 | 2.88 ± 0.21 | 2.72 ± 0.29 | 3.05 ± 0.29 | 2.93 ± 0.24 |
| Kidneys (%) | 0.40 ± 0.02 | 0.40 ± 0.02 | 0.40 ± 0.03 | 0.39 ± 0.02 | 0.39 ± 0.04 | 0.39 ± 0.02 | 0.43 ± 0.05 | 0.40 ± 0.03 |
| Spleen (%) | 0.23 ± 0.03 | 0.23 ± 0.09 | 0.21 ± 0.03 | 0.22 ± 0.02 | 0.23 ± 0.03 | 0.23 ± 0.04 | 0.24 ± 0.02 | 0.23 ± 0.05 |
| Lungs (%) | 0.46 ± 0.13 | 0.43 ± 0.03 | 0.43 ± 0.04 | 0.43 ± 0.03 | 0.54 ± 0.02 | 0.52 ± 0.05 | 0.57 ± 0.04 | 0.51 ± 0.02 |
| Heart (%) | 0.39 ± 0.06 | 0.40 ± 0.04 | 0.39 ± 0.04 | 0.42 ± 0.04 | 0.44 ± 0.04 | 0.42 ± 0.08 | 0.44 ± 0.05 | 0.41 ± 0.03 |
Gross examination of internal organs, including the brain, pituitary gland, thymus, lungs, heart, spleen, liver, adrenals, kidneys, thyroids, testis (males), prostate gland (males), uterus (females), and ovaries (females), of the control and C. setidens-treated rats and histopathological examination in the main organs (liver, spleen, heart, kidneys, and lungs) did not show any abnormal findings (data not shown). Therefore, these results indicate that the oral administration of C. setidens for 4 weeks did not show toxic effects in rats.
3. Experimental Section
3.1. Animal Husbandry and Maintenance
A total of 80 specific pathogen-free, 6-week-old SD rats, which included 40 males weighing between 139.8 g and 201.9 g and 40 females weighing between 115.6 g and 167.7 g, were purchased from Orient Bio Co. (Kapyong, Korea) and used after a week of quarantine and acclimatization. The animal facility is maintained at 22 ± 3 °C, relative humidity of 50% ± 20%, air ventilation of 10-15 times/h, and a 12 h light/dark cycle (light 08:00-20:00) at 150-300 Lux (Korea Testing and Research Institute, Seoul, Korea). The animals were fed sterilized tap water and commercial rodent chow (Cargill Co. Gunsan, Korea) ad libitum. This experiment was conducted in facilities approved by the Association for Assessment and Accreditation of Laboratory Animal Care (AAALAC) International. All procedures were approved by the Institutional Animal Care and Use Committee (IACUC).
3.2. Test Substance
C. setidens (10 kg) was extracted with distilled water (200 L) at 90 °C for 4 h and then allowed to cool at room temperature. The extractive solution was filtered with Whatman filter paper (0.2 µm), concentrated to 15 brix using a vacuum evaporator (Eyela, Tokyo, Japan) at 80 °C, and then freeze-dried for 96 h using a freeze dryer (Ilshin, Seoul, Korea). The extract of C. setidens was dissolved in distilled water for oral administration. The phenolic compounds in the samples were analyzed using an HPLC-DAD analyses were performed on an Agilent series 1100 HPLC instrument allowing the determination at different wavelengths (280, 320, and 370 nm) of single molecules belonging to different subclasses [31]. In detail, the Nucleosil 100-5 C-18 column (Macherey-Nagel, Diiren, Germany; 250 mm × 4.0 mm i.d., 5 μm particle size) which was protected by a 10 mm guard column was used. The eluents were water at pH 3.29 by formic acid (0.035%, v/v) (A) and acetonitrile (B). The analyses were performed by a multistep linear solvent gradient as follows: 0%-15% B (45 min): 15%-30% B (15 min): 30%-50% B (5 min), 50%-100% B (5 min) and 100%-0% B (10 min). The diode array detector monitored at 270 nm, and the injection volume of the samples was 10 µL.
The standards used for the analysis were 4-hydroxyl benzohydrazide, gallic acid, vanillic acid, p-anisic acid, alizarin, chlorogenic acid, caffeic acid, syringic acid, p-coumaric acid, trans-ferulic acid, catechin, epigallocatechin gallate, quercetin hydrate, myricetin, morin hydrate, 3-hydroxyflavone, rutin, and naringin which were purchase from Sigma (St. Louis, MO, USA). The results are shown in Table 7.
| Compounds | Contents (mg/100 g Extract) |
|---|---|
| Phenolic acid | |
| Phloroglucinol | ND |
| 4-Hydroxybenzhydrazide derivative | 72.77 |
| Gallic acid | 15.39 |
| Vanillic acid | 48.90 |
| Protocatechuic acid ethyl ester | 19.98 |
| 2-Amino-3,4-dimethylbenzoic acid | ND |
| p-Anisic acid | 23.24 |
| Chlorogenic acid | 53.04 |
| Caffeic acid | 36.30 |
| Syringic acid | 0.87 |
| p-Coumaric acid | 8.20 |
| Chlorogenic derivative | ND |
| trans-Ferulic acid | 18.24 |
| Total of phenolic acid | 296.93 |
| Flavonoids | |
| (+)-Catechin hydrate | 93.04 |
| Gallocatechin | 264.05 |
| (−)-Epigallocatechin | 2376.00 |
| Epicatechin | 18.96 |
| Epigallocatechin gallate | 52.25 |
| Quercetin hydrate | 20.31 |
| Myricetin | 167.69 |
| Morin hydrate | 610.07 |
| Quercetin dihydrate | 8.81 |
| 3-Hydroxyflavone | 13.07 |
| Rutin hydrate | 63.14 |
| Naringin | 74.51 |
| Total of flavonoids | 3761.90 |
ND, not detected.
3.3. Acute Oral Toxicity
C. setidens (0, 1250, 2500, and 5000 mg/kg) was administered by oral gavage to age-matched male and female SD rats. Forty SD rats were randomly divided into a control (Group 1, n = 10 [5 males and 5 females]) and three dosages (Groups 2, 3, and 4 with 1250, 2500, and 5000 mg/kg/day, respectively) with equal numbers of males and females. Samples were administered once by oral gavage at 10 mL/kg of body weight (BW). The control animals were treated with the same volume of distilled water. Rats were anesthetized with diethyl ether followed by cervical decapitation. During the experimental period, all animals were observed one or more times per day. However, after administration, all animals were observed every half hour for 4 h. Observation was performed for 14 days post-administration. Body weights were measured at the initiation of treatment, and 7 and 14 days post-administration. On day 14 after administration, the animals were sacrificed and the external surface, thoracic organs, abdominal organs and their contents were macroscopically examined.
3.4. Four-Week Repeated-Dose Oral Toxicity
3.4.1. Study Design
C. setidens (0, 1250, 2500, and 5000 mg/kg) was administered by oral gavage to male and female SD rats. Forty SD rats were randomly divided into a control (Group 1, n = 10 [five males and five females]) and three dosages (Groups 2, 3, and 4 with 1250, 2500, and 5000 mg/kg/day, respectively) with equal numbers of males and females. Samples were administered by oral gavage at 10 mL/kg of BW on a daily basis 7 days a week for 4 weeks. The control animals were treated with the same volume of distilled water. During the administration period, the animals were observed for general appearance twice daily, and body weight, food intake, and water consumption were recorded once a week.
3.4.2. Urinalysis
On the last week of the administration period, a urine test was performed with fresh urine to determine specific gravity, pH, and levels of leukocytes, nitrites, protein, glucose, ketones, blood, urobilinogen, and bilirubin using a Clinitek 500 urine chemistry analyzer (Bayer Health Care, Cambridge, MA, USA) and a Multistix 10SG (Bayer, IN, USA). The microscopic examination of urinary sediments and urinary color was conducted with fresh urine from the control and highest dose groups after collecting for 3 h. The urine volume was checked after collecting for 24 h.
3.4.3. Ophthalmoscopy
External eye examinations were performed shortly before the start of the experiment and before the termination of treatment. The ocular fundus was examined before the termination of treatment using an indirect binocular ophthalmoscope on the negative control group and the highest dose group.
3.4.4. Hematology and Serum Biochemistry
Hematological and biochemical studies of liver function, plasma constituents, and electrolyte concentrations were determined using standard clinical procedures. The animals were fasted overnight prior to necropsy and blood collection. Blood samples were taken from the abdominal aorta using a syringe under isoflurane anesthesia. Blood samples were collected into CBC bottles containing EDTA-3K (Sewon Medical, Seoul, Korea) and analyzed within 20 min. Hematological parameters were determined using an ADVIA 120 hematology analyzer (Siemens Medical Solutions Diagnostics, Tarrytown, NY, USA), including total leucocyte count (WBC), red blood cell (RBC) count, hemoglobin (Hb) concentration, platelet (PLT) count, prothrombin time (PT), and activated partial thrombo-plastin time (APTT).
Serum biochemical parameters, measured with a Daiichi diagnostics reagent kit and an automated serum analyzer (Hitachi 7060 chemistry analyzer, Tokyo, Japan) and electolyte analyzer (Bayer 644 Na/K/Cl analyzer, PA, USA), were total serum protein (TP), albumin (ALB), total bilirubin (T-BIL), alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), creatinine (CREA), blood urea nitrogen (BUN), total cholesterol (TC), triglycerides (TG), glucose (GLU), and electrolytes such as calcium (Ca), sodium (Na), potassium (K), and chloride (Cl).
3.4.5. Necropsy
At the end of the treatment period, all male and female SD rats were anesthetized by isoflurane and then sacrificed by exsanguination from the carotid artery. Complete gross postmortem examinations were performed on all animals. All organs were carefully examined macroscopically and the brain, pituitary gland, thymus, lungs, heart, spleen, liver, adrenals, kidneys, thyroids, testis (males), prostate gland (males), uterus (females), and ovaries (females), were weighed relative to the total body weight.
3.4.6. Histopathology
Organs were fixed and preserved in 10% phosphate-buffered formalin. Fixed tissues were routinely processed for embedding in paraffin, sectioned, and stained with hematoxylin and eosin. Collected tissues were grossly and microscopically examined.
3.5. Statistical Analysis
Data are expressed as the means ± SEM and analyzed by a one-way analysis of variance (ANOVA) followed by Fisher’s Least Significant Difference test using SPSS software version 10 [32]. p < 0.05 was considered a significant difference as compared with control.
4. Conclusions
In summary, our toxicological studies revealed no toxic effects of oral administration of C. setidens during acute administration and 4-week repeated doses in male or female rats. A chronic toxicity study should be further performed to assess the long-term safety of the C. setidens extract.
Acknowledgments
This research was supported by the Yeungnam University Research Grant in 212-A-380-089.
Author Contributions
J.S. Lee, Y.-H. Kim, and D.-B. Kim performed research and analyzed data. J.S. Lee, W.-S. Bang, O.-H. Lee designed research and wrote the paper.
Conflicts of Interest
The authors declare no conflict of interest.
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Lee, J.S.; Kim, Y.-H.; Kim, D.-B.; Bang, W.-S.; Lee, O.-H. Acute and 4-Week Repeated-Dose Oral Toxicity Studies of Cirsium setidens in Rats. Molecules 2014, 19, 7138-7151. https://doi.org/10.3390/molecules19067138
AMA Style
Lee JS, Kim Y-H, Kim D-B, Bang W-S, Lee O-H. Acute and 4-Week Repeated-Dose Oral Toxicity Studies of Cirsium setidens in Rats. Molecules. 2014; 19(6):7138-7151. https://doi.org/10.3390/molecules19067138
Chicago/Turabian StyleLee, Jong Seok, Young-Hyun Kim, Dan-Bi Kim, Woo-Suk Bang, and Ok-Hwan Lee. 2014. "Acute and 4-Week Repeated-Dose Oral Toxicity Studies of Cirsium setidens in Rats" Molecules 19, no. 6: 7138-7151. https://doi.org/10.3390/molecules19067138
APA StyleLee, J. S., Kim, Y. -H., Kim, D. -B., Bang, W. -S., & Lee, O. -H. (2014). Acute and 4-Week Repeated-Dose Oral Toxicity Studies of Cirsium setidens in Rats. Molecules, 19(6), 7138-7151. https://doi.org/10.3390/molecules19067138
