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Published on: July 3, 2013
Oxidative stress in rat kidneys due to 3,4-methylenedioxymetamphetamine (ecstasy) toxicity
Milica Ninković1, Vesna Selaković, Mirjana Dukić
1Institute of Medical Research, Military Medical Academy, Department of Toxicology, Faculty of Pharmacy, Belgrade, Serbia. ninkomj@ptt.yu
Aim:
The mechanism of MDMA (3,4-methylenedioxymethamphetamine)-induced toxicity is believed to be, in part, due to enhanced oxidative stress. As MDMA is eliminated via the kidney, the aim of this study was to investigate whether MDMA created conditions of oxidative stress within rat kidney.
Methods:
Adult male Wistar rats were divided into three groups, control treatment (water), acute MDMA administration (single oral dose: 5, 10, 20 or 40 mg/kg body weight) and subacute MDMA administration (5, 10, or 20 mg/kg body weight per day during 14 days). Animals were sacrificed 8 h after the single oral MDMA administration in the acute MDMA administration group and after the last MDMA administration in the subacute MDMA administration group. Rectal temperature measurements, oxidative stress status parameters and histological examinations were performed.
Results:
In all MDMA-administered rats, rectal temperature markedly increased peaking approximately 1 h after MDMA ingestion. Superoxide dismutase activity and thiobarbituric acid reactive substances increased after MDMA administration. Histological examinations of the kidney revealed dose-dependent disruption of tissue structure in subacute MDMA-administered rats. The latter was not observed in acute MDMA-administered rats.
Insights
MDMA (3,4-methylenedioxymethamphetamine) causes oxidative stress in rat kidneys, especially with repeated exposure. This study investigated MDMA
Area of Science:
- Toxicology
- Pharmacology
- Nephrology
Background:
- 3,4-methylenedioxymethamphetamine (MDMA) toxicity is linked to oxidative stress.
- MDMA is primarily eliminated by the kidneys, suggesting potential renal impact.
Purpose of the Study:
- To investigate if MDMA induces oxidative stress in rat kidneys.
- To assess the effects of acute and subacute MDMA administration on renal oxidative stress parameters.
Main Methods:
- Adult male Wistar rats received acute (single dose) or subacute (14-day) oral MDMA.
- Measurements included rectal temperature, oxidative stress markers (superoxide dismutase, thiobarbituric acid reactive substances), and kidney histology.
- Animals were analyzed 8 hours after the last dose or single administration.
Main Results:
- MDMA administration caused a significant increase in rectal temperature.
- Superoxide dismutase activity and thiobarbituric acid reactive substances levels were elevated post-MDMA.
- Subacute MDMA exposure led to dose-dependent kidney tissue damage, not observed with acute exposure.
Conclusions:
- MDMA induces oxidative stress in rat kidneys.
- Subacute MDMA administration poses a greater risk for renal tissue damage compared to acute exposure.
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