以胆碱能和内源性大麻素系统为靶点,对自闭症模型中与自闭症相关的核心表型进行治疗干预:系统综述。

Princewill Sopuluchukwu Udodi, Godson Emeka Anyanwu, Ebube Roseline Udodi, Damian Nnabuihe Ezejindu
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引用次数: 0

摘要

引言自闭症谱系障碍(ASD)是一种神经发育障碍,与胆碱能和内源性大麻素(EC)系统失调有关。本研究系统回顾了目前有关旨在增强 ASD 模型中这两个系统活性的治疗策略的文献:我们按照《系统综述和荟萃分析首选报告项目》(Preferred Reporting Items for Systematic Reviews and Meta-Analyses,PRISMA)核对表提供的指南,对研究不同治疗干预措施对 ASD 模型中胆碱能和内源性大麻素系统成分的影响的文献进行了系统评估。检索了四个数据库:Google Scholar、Web of science、EMBASE 和 MEDLINE/PubMed,检索时间为 2012 年 8 月至 2023 年 2 月。同时还检查了所选研究论文的参考文献。本研究审查了 12 篇论文(其中 5 篇涉及胆碱能系统,6 篇涉及心血管系统,1 篇涉及这两个系统),以了解之前影响这两个系统的相关治疗策略。共有 77 项研究被引用:结果:大多数研究显示,不同的治疗干预措施会下调大麻素 1(CB1)受体和系统水解酶,上调胆碱能系统、α7 烟碱乙酰胆碱受体(α7 nAChR)和乙酰胆碱信号分子。治疗药物对胆碱能和EC系统成分的调节普遍增强了ASD模型的行为:结论:有可能在其中一个系统中评估的治疗干预措施可有效治疗与 ASD 相关的核心表型。本研究中审查的治疗干预措施的益处需要在随机、盲法、安慰剂对照临床试验中进一步研究。
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Targeting cholinergic and endocannabinoid system as a therapeutic intervention for core asd associated phenotypes in autism model: a systematic review.

Introduction: Autism spectrum disorder (ASD) is a neurodevelopmental disorder that has been linked to the dysregulation in the cholinergic and endocannabinoid (EC) system. This study systematically reviews the present literature on treatment strategies aimed at enhancing the activity of both systems in ASD models.

Method: We performed a systematic evaluation of literatures that investigated the effects of different therapeutic interventions on the components of the cholinergic and EC systems in ASD models, following the guidelines provided by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) checklist. Four databases were searched: Google Scholar, Web of science, EMBASE and MEDLINE/PubMed, between August 2012 and February 2023. The selected research papers' references were also examined. Twelve papers (five for cholinergic system, six for EC system and one for the two systems) were reviewed in this study of prior relevant treatment strategies that impact both systems. There were 77 studies cited in total.

Results: The majority of research revealed that different therapeutic interventions down-regulated cannabinoid 1 (CB1) receptors, and the systems hydrolyzing enzymes and up-regulated EC, Alpha7 nicotinic acetylcholine receptor (α7 nAChR), and acetylcholine signaling molecules. The regulation of the components of the cholinergic and EC systems by the therapeutics generally enhanced behaviors in ASD models.

Conclusion: It is possible that there are therapeutic interventions assessed in one of the systems that may be effective in treating the core ASD-associated phenotype. The benefits of the reviewed therapeutic interventions in this study need to be further investigated in randomized, blind, placebo-controlled clinical trials.

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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
32
审稿时长
13 weeks
期刊介绍: Information not localized
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