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甲基苯丙胺使用障碍患者外周血中α-突触核蛋白的增加。

Increase of α-Synuclein in the Peripheral Blood of Subjects with Methamphetamine Use Disorder.

作者信息

Choi Mi Ran, Chon Younghoon, Cho Joongbum, Han Changwoo, Jin Yeung-Bae, Lee Sang-Rae, Kim Dai-Jin

机构信息

Laboratory Animal Research Center, Ajou University School of Medicine, Suwon, Republic of Korea.

Department of Pharmacology, Ajou University School of Medicine, Suwon, Republic of Korea.

出版信息

Psychiatry Investig. 2025 Jul;22(7):786-795. doi: 10.30773/pi.2023.0389. Epub 2025 Jul 10.

Abstract

OBJECTIVE

Methamphetamine (MA) use has created significant public health problems worldwide. Its chronic abuse causes neurotoxicity resulting in disruption of neural plasticity and early onset of neurodegenerative diseases. Therefore, there is need for a biomarker to evaluate the neurotoxicity caused by MA. This study investigates the expression levels of α-synuclein (α-Syn), brain-derived neurotrophic factor (BDNF), and neuron-specific enolase (NSE) in the blood of patients with MA use disorder to identify potential biomarkers.

METHODS

We collected blood samples from 60 subjects (30 normal healthy controls and 30 patients with MA use disorder [MA group]). We used multiplex assay kits to analyze the expression levels of α-Syn, BDNF, and NSE in the blood of these subjects.

RESULTS

Beck Depression Inventory and Beck Anxiety Inventory scale scores were significantly different between the control and MA groups. The expression level of α-Syn in the MA group was significantly increased compared to that in the control group (z value=-1.986, p=0.0473). In contrast, BDNF in the MA group tended to increase as the duration of MA use increased (r=0.323, p=0.082).

CONCLUSION

We identified an increase of α-Syn in the blood of the MA group. This finding suggests that the α-Syn level increases in the brain after exposure to MA by passing through the blood brain barrier. This result provides useful information for potential biomarkers in diagnosis of neurodegenerative diseases caused by MA abuse.

摘要

目的

甲基苯丙胺(MA)的使用在全球范围内造成了严重的公共卫生问题。其长期滥用会导致神经毒性,进而破坏神经可塑性并引发神经退行性疾病的早期发作。因此,需要一种生物标志物来评估MA引起的神经毒性。本研究调查了MA使用障碍患者血液中α-突触核蛋白(α-Syn)、脑源性神经营养因子(BDNF)和神经元特异性烯醇化酶(NSE)的表达水平,以确定潜在的生物标志物。

方法

我们从60名受试者(30名正常健康对照者和30名MA使用障碍患者[MA组])中采集了血样。我们使用多重检测试剂盒分析这些受试者血液中α-Syn、BDNF和NSE的表达水平。

结果

对照组和MA组的贝克抑郁量表和贝克焦虑量表评分存在显著差异。MA组中α-Syn的表达水平与对照组相比显著升高(z值=-1.986,p=0.0473)。相比之下,MA组中的BDNF随着MA使用时间的增加而呈上升趋势(r=0.323,p=0.082)。

结论

我们发现MA组血液中α-Syn增加。这一发现表明,暴露于MA后,α-Syn水平通过血脑屏障进入大脑后升高。这一结果为诊断MA滥用所致神经退行性疾病的潜在生物标志物提供了有用信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/212b/12301680/c6666891d6e0/pi-2023-0389f1.jpg

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