A Systematic Review of the Molecular and Cellular Alterations Induced by Cannabis That May Serve as Risk Factors for Bipolar Disorder.

IF 4.5 2区 医学 Q1 CLINICAL NEUROLOGY
Alejandra Delgado-Sequera, Clara Garcia-Mompo, Ana Gonzalez-Pinto, Maria Hidalgo-Figueroa, Esther Berrocoso
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Abstract

Background: Cannabis use is a risk factor of psychiatric illness, such as bipolar disorder type-I (BDI). Indeed, cannabis use strongly influences the onset and clinical course of BDI, although the biological mechanisms underlying this interaction remain unknown. Therefore, we have reviewed the biological mechanisms affected by cannabis use that may trigger BD.

Methods: A systematic review was carried out of articles in which gene expression was studied in cannabis users or human-derived cells exposed to tetrahydrocannabinol (THC) or cannabidiol (CBD). A second systematic review was then performed to identify articles in which gene expression was studied in BDI samples, highlighting those that described alterations to the same molecular and cellular mechanisms affected by cannabis/THC/CBD.

Results: The initial search identified 82 studies on cannabis and 962 on BDI. After removing duplicates and applying the inclusion/exclusion criteria, 9 studies into cannabis and 228 on BDI were retained. The molecular and cellular mechanisms altered by cannabis use or THC/CBD exposure were then identified, including neural development and function, cytoskeletal function, cell adhesion, mitochondrial biology, inflammatory related pathways, lipid metabolism, the endocannabinoid system, the hypocretin/orexin system, and apoptosis. Alterations to those activities were also described in 19 of 228 focused on BDI.

Conclusions: The biological mechanisms described in this study may be good candidates to the search for diagnostic biomarkers and therapeutic targets for BDI. Because cannabis use can trigger the onset of BD, further studies would be of interest to determine whether they are involved in the early development of the disorder, prompting early treatment.

大麻诱发的分子和细胞变化可能成为躁郁症风险因素的系统回顾。
背景:吸食大麻是罹患躁郁症(BDI)等精神疾病的风险因素之一。事实上,吸食大麻对躁狂症的发病和临床过程有很大影响,但这种相互作用的生物机制仍不清楚。因此,我们回顾了受大麻使用影响而可能引发躁郁症的生物机制:方法:我们对研究大麻使用者或暴露于四氢大麻酚或 CBD 的人源细胞基因表达的文章进行了系统综述。然后进行了第二次系统综述,以确定对 BDI 样本中基因表达进行研究的文章,重点是那些描述了受大麻/四氢大麻酚/CBD 影响的相同分子和细胞机制变化的文章:初步搜索确定了 82 项关于大麻的研究和 962 项关于 BDI 的研究。在去除重复内容并应用纳入/排除标准后,保留了 9 项关于大麻的研究和 228 项关于 BDI 的研究。然后确定了因吸食大麻或接触四氢大麻酚/CBD 而改变的分子和细胞机制,包括:神经发育和功能、细胞骨架功能、细胞粘附、线粒体生物学、炎症相关途径、脂质代谢、内源性大麻素系统、视网膜下素/视黄醇系统和细胞凋亡。在 228 项关注 BDI 的研究中,有 19 项也描述了这些活动的改变:本研究中描述的生物机制可能是寻找 BDI 诊断生物标志物和治疗目标的良好候选者。由于吸食大麻可诱发 BD 发病,进一步的研究将有助于确定它们是否参与了该疾病的早期发展,从而促进早期治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.40
自引率
2.10%
发文量
230
审稿时长
4-8 weeks
期刊介绍: The central focus of the journal is on research that advances understanding of existing and new neuropsychopharmacological agents including their mode of action and clinical application or provides insights into the biological basis of psychiatric disorders and thereby advances their pharmacological treatment. Such research may derive from the full spectrum of biological and psychological fields of inquiry encompassing classical and novel techniques in neuropsychopharmacology as well as strategies such as neuroimaging, genetics, psychoneuroendocrinology and neuropsychology.
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