Evidence map›Paper›PMID 39004669›Full record

ArticleBiological trace element research2025

Zinc Supplementation Reduces ROS Production and Prevents MDMA-Induced Apoptosis in TM3 Leydig Cells via the Inhibition of Pro-Apoptotic Proteins.

Salar Mahmoudi-Nejad, Sina Ahmadi, Mahssa Hassan-Nejhad, Mahdieh Azimi, Hanieh Dadvand, Morteza Bagheri

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Article in Biological trace element research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Salar Mahmoudi-NejadStudent Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Sina AhmadiStudent Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Mahssa Hassan-NejhadStudent Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Mahdieh AzimiStudent Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Hanieh DadvandStudent Research Committee, Urmia University of Medical Sciences, Urmia, Iran.
Morteza BagheriStudent Research Committee, Urmia University of Medical Sciences, Urmia, Iran. mortezabagheri@umsu.ac.ir.

Funding

Student Research Committee, Urmia University of Medical Sciences,Urmia, Iran 3303
6 · The paper itself

Abstract

MDMA can cause serious adverse effects on vital organs such as the heart, brain, and liver. Additionally, MDMA consumption can also potentially cause various endocrine system dysfunctions. The previous study has shown that pre-treatment of zinc can reduce the cytotoxicity of MDMA on the Leydig cell line (TM3). In this study, we investigated the mechanisms involved in the treatment with MDMA on the apoptosis of TM3 cells and the effects of zinc pre-treatment on reducing the apoptotic effects of MDMA. TM3 cells were incubated with MDMA (5 mM), zinc (8 µM), and zinc (8 µM) prior to MDMA (5 mM) for 48 h. The cells were pre-treated with zinc for 24 h prior to the administration of MDMA, and the total culture time was 48h. The effect of different treatment groups in causing oxidative stress and apoptosis in TM3 cells was measured by DCF, TUNNEL, and western blot tests, respectively. Our results revealed that the number of DCF and tunnel-positive cells increases as a result of MDMA treatment. In addition, the treatment with MDMA increased the expression of pro-apoptotic proteins caspase 3, Bax, and p53. Conversely, the expression of anti-apoptotic protein Bcl-2 decreased. Zinc pre-treatment significantly decreased the expression of pro-apoptotic proteins and the number of tunnels and DCF-positive cells compared to the MDMA-only group. It is concluded that MDMA has a toxic effect and causes apoptosis on TM3 cells, and also, pre-treatment with zinc mitigates the ROS production and toxic effect of MDMA and MDMA-induced apoptosis in TM3 cells.

Indexed as

ApoptosisApoptosis Regulatory ProteinsLeydig CellsN-Methyl-3,4-methylenedioxyamphetamineReactive Oxygen SpeciesZincAnimalsbcl-2-Associated X ProteinCaspase 3Cell LineMaleMiceOxidative StressTumor Suppressor Protein p53Apoptosis Regulatory Proteinsbcl-2-Associated X ProteinCaspase 3N-Methyl-3,4-methylenedioxyamphetamineReactive Oxygen SpeciesTumor Suppressor Protein p53ZincApoptosisLeydig cell lineMDMAROSZinc

Identifiers

PMID39004669

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