The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA Exposure

ObjectiveTo explore the mechanism of myocardial toxicity caused by N-methyl-3,4-methyle-nedioxyamphetamine (MDMA), the changes of intracellular calcium oscillation mode and calcium handling proteins during acute exposure to different concentrations of MDMA were detected, and the involvement of nucle...

Full description

Saved in:
Bibliographic Details
Main Authors: WANG Rong-shuai, HUANG Si-zhe, WANG Yun-yun, DENG Yan-fei, DING Zi-jiao, ZHANG Jie, LIU Yong, REN Liang, LIU Liang
Format: Article
Language:zho
Published: Editorial Office of Journal of Forensic Medicine 2025-04-01
Series:Fayixue Zazhi
Subjects:
Online Access:http://www.fyxzz.cn/CN/10.12116/j.issn.1004-5619.2024.440503
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849239268506992640
author WANG Rong-shuai
HUANG Si-zhe
WANG Yun-yun
DENG Yan-fei
DING Zi-jiao
ZHANG Jie
LIU Yong
REN Liang
LIU Liang
author_facet WANG Rong-shuai
HUANG Si-zhe
WANG Yun-yun
DENG Yan-fei
DING Zi-jiao
ZHANG Jie
LIU Yong
REN Liang
LIU Liang
author_sort WANG Rong-shuai
collection DOAJ
description ObjectiveTo explore the mechanism of myocardial toxicity caused by N-methyl-3,4-methyle-nedioxyamphetamine (MDMA), the changes of intracellular calcium oscillation mode and calcium handling proteins during acute exposure to different concentrations of MDMA were detected, and the involvement of nuclear factor κB (NF-κB) and its effect on calcium handling proteins were investigated.MethodsPrimary rat cardiomyocytes were cultured to establish MDMA acute exposure model, and a control group was set up. The MDMA poisoning model was divided into three concentration groups of 10, 100 and 1 000 μmol/L. After 1 h of exposure, the morphological changes of cardiomyocytes were observed, the cytotoxicity and changes in calcium signals were measured, and the changes in calcium handling proteins RyR2, SERCA2a, PLN, NCX1 and Cav1.2 were detected. The changes of NF-κB activity and the expression of nucleoprotein p-p65 (Ser311) and PKCζ after MDMA exposure, and the intervention of NF-κB inhibitors pyrrolidine dithiocarbamate ammonium (PDTC) and protein kinase C (PKC) inhibitor chelerythrine (CHE) were detected by electrophoretic mobility shift assay (EMSA) and Western blotting. The effects of PDTC intervention on calcium signals, and the expressions of RyR2, SERCA2a, PLN, NCX1 and Cav1.2 after acute MDMA exposure were also observed.ResultsNo obvious changes were observed in the morphology of cardiomyocytes after acute exposure to MDMA, whereas the oscillation waveform of intracytoplasmic calcium ion showed irregular changes with increased oscillation amplitude, intense fluctuations, irregular frequency, and increased fluctuation range of relative optical density values. The expression of RyR2, SERCA2a and NCX1 increased, while the expression of Cav1.2 and PLN decreased. Acute MDMA exposure could increase NF-κB activity, while PDTC and CHE intervention could inhibit NF-κB activity. In MDMA exposed group, the expression of PKCζ and nucleoprotein p-p65 (Ser311) both increased and could be inhibited by CHE. After the intervention of PDTC to block NF-κB, the amplitude of calcium oscillation was lower than that of the MDMA exposed group, and the expression of RyR2, SERCA2a and NCX1 decreased. There was no significant change in PLN, while the expression of Cav1.2 increased.ConclusionMDMA can lead to an increase of calcium ion concentration in cardiomyocytes. Calcium ions are involved in myocardial toxicity of MDMA. The mechanism is related to changes in calcium handling proteins, mainly associated with the increased expression of RyR2. MDMA can up-regulate the intracellular activity of NF-κB through the PKCζ-NF-κB pathway and affect calcium handling proteins, which aggravate intracellular calcium overload during acute MDMA exposure.
format Article
id doaj-art-de0d2e0de052432ba1c9cb7786ed6d73
institution Kabale University
issn 1004-5619
language zho
publishDate 2025-04-01
publisher Editorial Office of Journal of Forensic Medicine
record_format Article
series Fayixue Zazhi
spelling doaj-art-de0d2e0de052432ba1c9cb7786ed6d732025-08-20T04:01:03ZzhoEditorial Office of Journal of Forensic MedicineFayixue Zazhi1004-56192025-04-0141214415110.12116/j.issn.1004-5619.2024.4405031004-5619(2025)02-0144-08The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA ExposureWANG Rong-shuai0HUANG Si-zhe1WANG Yun-yun2DENG Yan-fei3DING Zi-jiao4ZHANG Jie5LIU Yong6REN Liang7LIU Liang8Department of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaDepartment of Forensic Medicine, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, ChinaObjectiveTo explore the mechanism of myocardial toxicity caused by N-methyl-3,4-methyle-nedioxyamphetamine (MDMA), the changes of intracellular calcium oscillation mode and calcium handling proteins during acute exposure to different concentrations of MDMA were detected, and the involvement of nuclear factor κB (NF-κB) and its effect on calcium handling proteins were investigated.MethodsPrimary rat cardiomyocytes were cultured to establish MDMA acute exposure model, and a control group was set up. The MDMA poisoning model was divided into three concentration groups of 10, 100 and 1 000 μmol/L. After 1 h of exposure, the morphological changes of cardiomyocytes were observed, the cytotoxicity and changes in calcium signals were measured, and the changes in calcium handling proteins RyR2, SERCA2a, PLN, NCX1 and Cav1.2 were detected. The changes of NF-κB activity and the expression of nucleoprotein p-p65 (Ser311) and PKCζ after MDMA exposure, and the intervention of NF-κB inhibitors pyrrolidine dithiocarbamate ammonium (PDTC) and protein kinase C (PKC) inhibitor chelerythrine (CHE) were detected by electrophoretic mobility shift assay (EMSA) and Western blotting. The effects of PDTC intervention on calcium signals, and the expressions of RyR2, SERCA2a, PLN, NCX1 and Cav1.2 after acute MDMA exposure were also observed.ResultsNo obvious changes were observed in the morphology of cardiomyocytes after acute exposure to MDMA, whereas the oscillation waveform of intracytoplasmic calcium ion showed irregular changes with increased oscillation amplitude, intense fluctuations, irregular frequency, and increased fluctuation range of relative optical density values. The expression of RyR2, SERCA2a and NCX1 increased, while the expression of Cav1.2 and PLN decreased. Acute MDMA exposure could increase NF-κB activity, while PDTC and CHE intervention could inhibit NF-κB activity. In MDMA exposed group, the expression of PKCζ and nucleoprotein p-p65 (Ser311) both increased and could be inhibited by CHE. After the intervention of PDTC to block NF-κB, the amplitude of calcium oscillation was lower than that of the MDMA exposed group, and the expression of RyR2, SERCA2a and NCX1 decreased. There was no significant change in PLN, while the expression of Cav1.2 increased.ConclusionMDMA can lead to an increase of calcium ion concentration in cardiomyocytes. Calcium ions are involved in myocardial toxicity of MDMA. The mechanism is related to changes in calcium handling proteins, mainly associated with the increased expression of RyR2. MDMA can up-regulate the intracellular activity of NF-κB through the PKCζ-NF-κB pathway and affect calcium handling proteins, which aggravate intracellular calcium overload during acute MDMA exposure.http://www.fyxzz.cn/CN/10.12116/j.issn.1004-5619.2024.440503forensic pathologyforensic toxicologyn-methyl-3,4-methylenedioxyamphetamine (mdma)cytotoxicitycalcium homeostasiscalcium handling proteinnuclear factor κb (nf-κb)protein kinase c (pkc)
spellingShingle WANG Rong-shuai
HUANG Si-zhe
WANG Yun-yun
DENG Yan-fei
DING Zi-jiao
ZHANG Jie
LIU Yong
REN Liang
LIU Liang
The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA Exposure
Fayixue Zazhi
forensic pathology
forensic toxicology
n-methyl-3,4-methylenedioxyamphetamine (mdma)
cytotoxicity
calcium homeostasis
calcium handling protein
nuclear factor κb (nf-κb)
protein kinase c (pkc)
title The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA Exposure
title_full The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA Exposure
title_fullStr The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA Exposure
title_full_unstemmed The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA Exposure
title_short The Mechanism of Calcium Handling Proteins and NF-κB in Calcium Dyshomeostasis of Cardiomyocytes Caused by Acute MDMA Exposure
title_sort mechanism of calcium handling proteins and nf κb in calcium dyshomeostasis of cardiomyocytes caused by acute mdma exposure
topic forensic pathology
forensic toxicology
n-methyl-3,4-methylenedioxyamphetamine (mdma)
cytotoxicity
calcium homeostasis
calcium handling protein
nuclear factor κb (nf-κb)
protein kinase c (pkc)
url http://www.fyxzz.cn/CN/10.12116/j.issn.1004-5619.2024.440503
work_keys_str_mv AT wangrongshuai themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT huangsizhe themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT wangyunyun themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT dengyanfei themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT dingzijiao themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT zhangjie themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT liuyong themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT renliang themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT liuliang themechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT wangrongshuai mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT huangsizhe mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT wangyunyun mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT dengyanfei mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT dingzijiao mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT zhangjie mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT liuyong mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT renliang mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure
AT liuliang mechanismofcalciumhandlingproteinsandnfkbincalciumdyshomeostasisofcardiomyocytescausedbyacutemdmaexposure