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本文引用的文献

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Enhancement of Anandamide-Mediated Endocannabinoid Signaling Corrects Autism-Related Social Impairment.增强花生四烯酸乙醇胺介导的内源性大麻素信号可纠正自闭症相关的社交障碍。
Cannabis Cannabinoid Res. 2016 Feb 1;1(1):81-89. doi: 10.1089/can.2015.0008. eCollection 2016.
2
Targeting anandamide metabolism rescues core and associated autistic-like symptoms in rats prenatally exposed to valproic acid.靶向花生四烯酸乙醇胺代谢可挽救产前暴露于丙戊酸的大鼠的核心及相关自闭症样症状。
Transl Psychiatry. 2016 Sep 27;6(9):e902. doi: 10.1038/tp.2016.182.
3
Pharmacological inhibition of fatty acid amide hydrolase attenuates social behavioural deficits in male rats prenatally exposed to valproic acid.脂肪酸酰胺水解酶的药理学抑制作用可减轻产前暴露于丙戊酸的雄性大鼠的社会行为缺陷。
Pharmacol Res. 2016 Nov;113(Pt A):228-235. doi: 10.1016/j.phrs.2016.08.033. Epub 2016 Aug 31.
4
Possible Therapeutic Doses of Cannabinoid Type 1 Receptor Antagonist Reverses Key Alterations in Fragile X Syndrome Mouse Model.大麻素 1 型受体拮抗剂的可能治疗剂量可逆转脆性 X 综合征小鼠模型中的关键改变。
Genes (Basel). 2016 Aug 31;7(9):56. doi: 10.3390/genes7090056.
5
Deficient adolescent social behavior following early-life inflammation is ameliorated by augmentation of anandamide signaling.早年炎症后青少年社交行为缺陷可通过增强花生四烯酸乙醇胺信号传导得到改善。
Brain Behav Immun. 2016 Nov;58:237-247. doi: 10.1016/j.bbi.2016.07.152. Epub 2016 Jul 21.
6
Excitation/Inhibition Imbalance in Animal Models of Autism Spectrum Disorders.自闭症谱系障碍动物模型中的兴奋/抑制失衡。
Biol Psychiatry. 2017 May 15;81(10):838-847. doi: 10.1016/j.biopsych.2016.05.011. Epub 2016 May 20.
7
The CB receptor and its role as a regulator of inflammation.CB受体及其作为炎症调节因子的作用。
Cell Mol Life Sci. 2016 Dec;73(23):4449-4470. doi: 10.1007/s00018-016-2300-4. Epub 2016 Jul 11.
8
Genetic and non-genetic animal models for autism spectrum disorders (ASD).自闭症谱系障碍(ASD)的遗传和非遗传动物模型。
Reprod Toxicol. 2016 Sep;64:116-40. doi: 10.1016/j.reprotox.2016.04.024. Epub 2016 Apr 30.
9
Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.当前自闭症谱系障碍动物模型的临床与神经生物学相关性
Biomol Ther (Seoul). 2016 May 1;24(3):207-43. doi: 10.4062/biomolther.2016.061.
10
Endocannabinoids and endocannabinoid-related mediators: Targets, metabolism and role in neurological disorders.内源性大麻素和内源性大麻素相关介质:靶点、代谢及其在神经障碍中的作用。
Prog Lipid Res. 2016 Apr;62:107-28. doi: 10.1016/j.plipres.2016.02.002. Epub 2016 Mar 7.

内源性大麻素系统与自闭症谱系障碍:动物模型的启示。

The Endocannabinoid System and Autism Spectrum Disorders: Insights from Animal Models.

机构信息

Department of Biotechnology and Life Sciences (DBSV), University of Insubria, 21052 Busto Arsizio (VA), Italy.

Zardi Gori Foundation, 20122 Milan, Italy.

出版信息

Int J Mol Sci. 2017 Sep 7;18(9):1916. doi: 10.3390/ijms18091916.

DOI:10.3390/ijms18091916
PMID:28880200
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5618565/
Abstract

Autism spectrum disorder (ASD) defines a group of neurodevelopmental disorders whose symptoms include impaired communication and social interaction with restricted or repetitive motor movements, frequently associated with general cognitive deficits. Although it is among the most severe chronic childhood disorders in terms of prevalence, morbidity, and impact to the society, no effective treatment for ASD is yet available, possibly because its neurobiological basis is not clearly understood hence specific drugs have not yet been developed. The endocannabinoid (EC) system represents a major neuromodulatory system involved in the regulation of emotional responses, behavioral reactivity to context, and social interaction. Furthermore, the EC system is also affected in conditions often present in subsets of patients diagnosed with ASD, such as seizures, anxiety, intellectual disabilities, and sleep pattern disturbances. Despite the indirect evidence suggestive of an involvement of the EC system in ASD, only a few studies have specifically addressed the role of the EC system in the context of ASD. This review describes the available data on the investigation of the presence of alterations of the EC system as well as the effects of its pharmacological manipulations in animal models of ASD-like behaviors.

摘要

自闭症谱系障碍(ASD)定义了一组神经发育障碍,其症状包括沟通和社交互动受损,以及受限或重复的运动动作,通常伴有一般认知缺陷。尽管它是最严重的慢性儿童疾病之一,其患病率、发病率和对社会的影响都很高,但目前还没有针对 ASD 的有效治疗方法,这可能是因为其神经生物学基础尚不清楚,因此尚未开发出特定的药物。内源性大麻素(EC)系统是一个主要的神经调制系统,参与调节情绪反应、对环境的行为反应和社交互动。此外,EC 系统在经常出现在 ASD 诊断患者亚组中的一些疾病中也受到影响,如癫痫发作、焦虑、智力障碍和睡眠模式紊乱。尽管有间接证据表明 EC 系统参与了 ASD,但只有少数研究专门探讨了 EC 系统在 ASD 背景下的作用。这篇综述描述了现有的关于 EC 系统改变的存在以及其在 ASD 样行为的动物模型中的药理学干预的研究数据。