IF 1.7 4区 医学 Q4 NEUROSCIENCES Experimental Brain Research Pub Date : 2024-12-13 DOI:10.1007/s00221-024-06972-y
Halime Hanim Pence, Ertugrul Kilic, Birsen Elibol, Sibel Kuras, Mustafa Guzel, Yalcin Buyuk, Sadrettin Pence
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引用次数: 0

摘要

海洛因成瘾是影响许多基因和表观遗传系统的神经精神负担之一。虽然人们知道海洛因可能会在依赖过程中改变大脑中某些基因的表达,但目前还没有关于哪些基因主要受到影响的详细研究。因此,在本研究中,我们旨在确定大鼠大脑中 miRNA 图谱的变化,以便详细分析海洛因成瘾相关毒理学的分子机制。我们采用新一代全球 miRNA 测序技术,预测了静脉注射海洛因的大鼠前额叶皮层(PC)、海马、腹侧被盖区(VTA)、纹状体和纳氏核(NA)中潜在的 miRNAs。每天的总剂量从 2 毫克/千克开始,到第 10 天的 10 毫克/千克结束。在纹状体中,miR-18a、miR-17-5p、miR-20a-5p、miR-106a、miR-301a-3p、miR872-5p、miR-15a-5p、miR-500-3p和miR-339-5p的表达被海洛因上调了近2至4倍。海洛因成瘾大鼠海马 miR-153-3p、miR-130a-3p、miR-204-5p、miR-15b-5p 和 miR-137-3p 的表达,以及海洛因成瘾大鼠 VTA 中 miR-872、miR-183-5p、miR-20a-5p、miR-325-5p、miR-379-5p 和 miR-340-5p 的表达均增加了 2 倍。虽然 NA 中的 miR-129-1-3p 和 miR-3068-3p 表达量增加了近 2 倍,但 PC 中的 miR-129-1-3p 表达量却没有因海洛因而发生变化。在纹状体 miR-450b-3p 和 VTA 的 miR-103-1-5p 中,只观察到海洛因依赖性的表达下调。这些结果表明,海洛因成瘾可能通过改变细胞因子平衡、增加神经炎症和细胞凋亡对大脑造成伤害。此外,神经元也会通过不同脑区的多种 miRNAs 来增强神经发生和血管生成,以弥补这些异常。总之,本研究可为海洛因依赖症的临床诊断和治疗提供更全面的分子机制和潜在的生物标志物。
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Brain microRNA profiles after exposure to heroin in rats.

Heroin addiction is one of the neuropsychiatric burdens that affects many genetic and epigenetic systems. While it is known that heroin may change the expressions of some genes in the brain during dependence, there is no detailed study related to which gene are mostly affected. Therefore, in the current study, we aimed to determine alterations in the miRNA profiles of rats' brains for providing a detailed analysis of molecular mechanisms in heroin addiction-related toxicology. Next generation global miRNA sequencing was used to predict potential miRNAs in prefrontal cortex (PC), hippocampus, ventral tegmental area (VTA), striatum, and Nucleus accumbens (NA) of rats that exposed to heroin by intravenous injections. The total daily dose was started with 2 mg/kg and ended with 10 mg/kg on the 10th day. In the striatum, miR-18a, miR-17-5p, miR-20a-5p, miR-106a, miR-301a-3p, miR872-5p, miR-15a-5p, miR-500-3p, and miR-339-5p expressions were upregulated by nearly 2-to-4 times with heroin. The expressions of hippocampal miR-153-3p, miR-130a-3p, miR-204-5p, miR-15b-5p, and miR-137-3p and the expressions of miR-872, miR-183-5p, miR-20a-5p, miR-325-5p, miR-379-5p, and miR-340-5p in the VTA were 2-times higher in the heroin-addicted rats. While there was nearly 2-times increase in the miR-129-1-3p and miR-3068-3p expressions in the NA, no change was noted in the PC due to heroin. The only heroin-dependent downregulation was observed in the expressions of striatal miR-450b-3p and miR-103-1-5p of VTA. These results suggested that heroin addiction might give harm to brain by altering cytokine balance and increasing neuroinflammation and apoptosis. In addition, neurons also try to compensate these abnormalities by enhancing neurogenesis and angiogenesis through several miRNAs in the different brain regions. In conclusion, the present study may provide a more integrated view of the molecular mechanism and a potential biomarker that will aid in clinical diagnosis and treatment of heroin-dependence.

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来源期刊
CiteScore
3.60
自引率
5.00%
发文量
228
审稿时长
1 months
期刊介绍: Founded in 1966, Experimental Brain Research publishes original contributions on many aspects of experimental research of the central and peripheral nervous system. The focus is on molecular, physiology, behavior, neurochemistry, developmental, cellular and molecular neurobiology, and experimental pathology relevant to general problems of cerebral function. The journal publishes original papers, reviews, and mini-reviews.
期刊最新文献
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