1. Background
Ecstasy or 3,4-methylenedioxymethamphetamine (MDMA), one of the amphetamine components, has been widely abused as a recreational drug. Researchers have shown that ecstasy is a neurotoxic agent for dopaminergic and serotonergic neurons, lowering 5-HT transporters (1, 2). Moreover, they have found that MDMA side effects include hyperthermia, rhabdomyolysis, and cardiac dysrhythmias (3, 4). Besides, its users have linked hepatitis and liver induced injuries to the presence or absence of MDMA systemic features. Ecstasy hepatotoxicity can be identified in various levels and seems to manifest with different intensities, ranging from mild hepatitis with spontaneous resolution to fulminate liver failure, requiring liver transplantation (5, 6). The MDMA induced dopamine consumption result in releasing 5-HT striatum so that its depletion has been assessed (7). Reports carried out have observed serotonin transport and serotonergic terminal loss among ecstasy users (8).
According to Passie et al. MDMA causes significant increase in the level of plasma cortical, dehydroepiandrosterone (DHEA), and protection. However, Ecstasy, in contrast to sensual enhancement and affection emotion, hinders adverse sexual drive and functioning (9), which is associated with the probable threat of life (10, 11). According to Ninkovic et al. super oxide dismutase (SOD) activity increased in the liver of animals after treatment using a single dose of MDMA, while chronically treated animals exhibited increase in SOD activity after receiving the optimum dose (12). Investigations by Connor et al. showed that MDMA administration induced rapid and persistent suppression of user’s immune system (13).
2. Objectives
Despite the status of worldwide ecstasy abuse, it is nontoxic for humans. The study was carried out to determine the effects of ecstasy tablet administration on blood sugar, lipid profile, and liver functionality tests using the male rat model.
3. Materials and Methods
3.1. Study Population
This experimental study was conducted on 50 adult (5-7 months old) male Wistar-Albino rats. All experimental rats (weighing 200-250 g) were separately caged (one rat per cage). Animals were maintained under a standard environment at a temperature of 22 ± 2˚C, 12 h:h light/dark cycle. Animals had a standard rat chow; food and water were provided ad-libitum. The rats were acclimatized for 5 days, then divided into five groups (n = 10).
3.2. Protocol of the Experiment
Ecstasy tablets were purchased from street narcotic vendors. The range of tablet weight was 200 ± 2 mg. Five ecstasy tablets were analyzed in Tehran laboratory doping by GC/MS and gas chromatography (Agilent GC5973 Agilent MS 6890 USA). After analysis, percentage of the purified ecstasy in a tablet was found to be 60 ± 2 mg. Other components of the tablets were filler, lubricant, sweetener, color blinder, and disintegrate agents. tablets had been dissolved in normal saline 0.9% before they were diluted in an appropriate dose.
Rats in sham control (A) received standard rat chow and tap water. Control (B) received saline 0.9% (200 µL) (gavages). Group C was supplied with a single dose of MDMA tablet solution (20 mg/kg) (gavages). Eight hours prior to sacrifice, their blood samples were collected (8 hours MDMA exposure) (14). Group D1 received repeated dose of MDMA tablet solution (20 mg/kg/d) for 14 days. Group D1 was sacrificed 8 hours after the end of their treatment. Group D2 received repeated dose of MDMA tablets solution (20 mg/kg/d gavages) for 14 days and was sacrificed 1 week after the last intake (14).
3.3. Blood and Data Collection
At the end of the trial, the rats were sacrificed by cervical decapitation under ether anesthesia, and blood samples were collected from the cervical vessels. Serum AST and ALT, fasting blood sugar (FBS), triglyceride (TG), and total cholesterol (TCH) levels were measured using the standard methods adapted for RA 1000 analyzer (Technicon, USA) after calibration by Pars Azmon kit Iran. Serum high density lipoprotein (HDL) was measured by precipitation of non-HDL lipoprotein with dextran/MgSO4, followed by enzymatic cholesterol assay. Low density lipoprotein (LDL) was calculated according to Friedewald equation (15).
3.4. Statistical Analysis
Data were analyzed using SPSS 11.0. Analysis of variance was used to compare the treatment groups while Tukey multiple comparison test was applied to compare treatment with control groups. P values less than 0.05 were considered significant.
4. Results
Our results indicated that blood glucose level, increased significantly in group C and group D1 compared with other groups (Table 1). Low density lipoprotein (LDL) in group C increased significantly compared with other groups (Table 2). Serum alanine transaminase (ALT) and serum aspartate transaminase (AST) in group D1 and D2 were significantly higher than other groups (Table 1).
| (A) | (B) | (C) | (D1) | (D2) | |
|---|---|---|---|---|---|
| BS, mg/dL | 135.9 ± 12.7 | 140 ± 18.8 | 193.8 ± 11.6 | 176 ± 12.3 | 152.1 ± 11.2 |
| ALT, U/L | 45.4 ± 9.8 | 49.8 ± 2.1 | 52.1 ± 7.6 | 91.1 ± 8.1 | 75.4 ± 7.8 |
| AST, U/L | 107.2 ± 8.1 | 79.8 ± 12.1 | 115.6 ± 17.5 | 145.8 ± 14.7 | 159.4 ± 13.8 |
| (A) | (B) | (C) | (D1) | (D2) | P Value | |
|---|---|---|---|---|---|---|
| LDL( mg/dL) | 9.1 ± 4.6 | 10.2 ± 3.7 | 19.2 ± 7.9 | 11.2 ± 4.3 | 8.3 ± 5.9 | < 0.01 |
| HDL(mg/l) | 37.6 ± 7.7 | 45.3 ± 13.9 | 42.8 ± 3 | 48.8± 12.8 | 46.9 ± 8.8 | > 0.05 |
| Chol (mg/l) | 59.1 ± 12.1 | 49.4 ± 10.61 | 61.6 ± 7.5 | 76.1 ±14.7 | 60.1. ± 5.6 | < 0.02 |
| TG ( mg/dL) | 59.1 ± 12.1 | 69.4 ± 10.7 | 71.6 ± 7.5 | 76.1 ± 16.6 | 66.5 ± 13.3 | > 0.05 |
5. Discussion
Our findings in this study pointed out that acute and repeated administration of ecstasy (MDMA), (20 mg/kg) caused a significant increase in blood sugar, serum alanine transaminase (ALT), aspartate transaminase (AST) in group D1. Our findings revealed that blood glucose increased after a single dose of MDMA administration in group C and it is consistent with the findings of Graham et al. (16), that serum corticosterone and glucose increased significantly after an acute exposure to MDMA, in male and female rats. This response might be due to the effects of MDMA on hypothalamic-pituitary-adrenal (HPA) axis, which affects the serum corticosterone and glucose levels. In axis stress, catecholamine release causes epinephrine increase which leads to potent stimulatory effects on glucose production, mainly by enhancing hepatic glycogenolysis (17), resulting in blood sugar increase.
Investigation revealed that a cooperative contribution of monoamines such as dopamine and serotonin in the cyclic centre of secretion releases gonadotropins, which makes up a base for forming adaptive (sexual, feeding, and aggressive-defensive) behavior and stress reaction (18). Moreover, studies exhibited a significant prevalence of DNA injuries in sperms, tubular degeneration, and interstitial edema in male rats with chronic exposure to MDMA (19). Acute MDMA has some dominant neurohormonal effect such as increasing oxytocin, testosterone, and other hormone levels, which may facilitate psychotherapy.
On the other hand, MDMA administration is followed by a period of neurochemical recovery when low serotonin levels are often accompanied by lethargy and depression (20). Soto-Montenegro et al. (21) reported that a single dose of MDMA had hypoglycemic effects on rats, but repeated doses of MDMA did not alter their blood glucose level (22). However, our findings are not consistent with those of Soto-Montenegro et al. (21). This difference might be due to different dosages of ecstasy and their administration time. Our results are similar to those of Pourahmad et al. (23) who reported that metabolic reductive foundation of MDMA could probably induce liver toxicity through a mitochondrial/lysosomal toxic in isolated rat hepatocytes. On the other hand, our result is similar to those found by Pachmerhiwala et al. (24) that MDMA administration in rats caused an increase in blood glucose level in multiple brain regions. and the fact that this response involves both serotonergic and noradrenergic mechanisms by increased glycogenolysis.
Our study showed that repeated doses of MDMA administration caused an increase in AST and ALT value in group D1 compared with the control group. This finding is consistent with findings of Pontes et al. in 2010 (25) who reported that MDMA and ethanol are mainly metabolized in the liver with formation of toxic metabolites. In addition, our conclusion is in agreement with that of Ninković et al. (12) reporting that single and repeated administration of MDMA cause increased hepatic oxide-reductive status in the rat liver. Andreu et al. (5) explained that ecstasy was the most common substance targeting liver damage in patients under the age of 25. Custodio et al. (26) reported that MDMA and 4-methylthioamphetamine (MTA) induce different systemic and organ-specific effects like hepatotoxicity.
The mechanisms underlying MDMA and MTA-induced hepatotoxicity are multifactors. Beitia et al. (14) reported that ALT and AST serum activities as indicators of liver injury and their value did not alter 3 hours after a single dose of MDMA administration, but a significant increase in ALT and AST activities happened 6 hours after repeated dose administration. AST and ALT are liver enzyme markers, which indicate the health condition of these structures. Their significant increase observed in D1 and D2 compared with other groups is an indication of organ disruption (14). They also showed that repeated administration of MDMA resulted in liver injuries by increasing liver enzymes, which may lead to liver necrosis. ALK-P values in group D1, D2 and C were not significantly different to those of A and B, a major indicator of liver cholestasis. The findings, however, showed that chronic repeated dose did not induce cholestasis in the liver of treated groups of D1 and D2. Our findings pointed out that oral dose administration of ecstasy increased blood glucose and damaged liver, which results in liver necrosis. However, the mechanism behind the action is unknown yet.
