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J Am Assoc Lab Anim Sci. 2014 Mar;53(2):152-60.
2
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Cereb Cortex. 2015 Feb;25(2):516-27. doi: 10.1093/cercor/bht249. Epub 2013 Sep 17.
3
Chronic metabotropic glutamate receptor 5 inhibition corrects local alterations of brain activity and improves cognitive performance in fragile X mice.慢性代谢型谷氨酸受体 5 抑制可纠正脆性 X 小鼠大脑局部活动的改变,并改善其认知表现。
Biol Psychiatry. 2014 Feb 1;75(3):189-97. doi: 10.1016/j.biopsych.2013.05.038. Epub 2013 Jul 30.
4
Working memory deficits and related disinhibition of the cAMP/PKA/CREB are alleviated by prefrontal α4β2*-nAChRs stimulation in aged mice.前额叶α4β2*-nAChRs 刺激可减轻老年小鼠工作记忆缺陷和相关的 cAMP/PKA/CREB 去抑制。
Neurobiol Aging. 2013 Jun;34(6):1599-609. doi: 10.1016/j.neurobiolaging.2012.10.006. Epub 2013 Jan 23.
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Behav Brain Res. 2013 Aug 15;251:75-84. doi: 10.1016/j.bbr.2013.01.002. Epub 2013 Jan 14.
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Rescue of dendritic spine phenotype in Fmr1 KO mice with the mGluR5 antagonist AFQ056/Mavoglurant.使用代谢型谷氨酸受体5拮抗剂AFQ056/玛伐谷氨酸盐挽救脆性X智力低下蛋白1基因敲除小鼠的树突棘表型。
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Comprehensive analysis of ultrasonic vocalizations in a mouse model of fragile X syndrome reveals limited, call type specific deficits.全面分析脆性 X 综合征小鼠模型的超声发声,揭示了有限的、特定于叫声类型的缺陷。
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Variation in maternal and anxiety-like behavior associated with discrete patterns of oxytocin and vasopressin 1a receptor density in the lateral septum.外侧隔室中催产素和血管加压素 1a 受体密度的离散模式与母性行为和焦虑样行为的变化有关。
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The psychiatric presentation of fragile x: evolution of the diagnosis and treatment of the psychiatric comorbidities of fragile X syndrome.脆性 X 相关精神障碍的表现:脆性 X 综合征伴发精神共病的诊断和治疗演变。
Dev Neurosci. 2011;33(5):337-48. doi: 10.1159/000329421. Epub 2011 Sep 2.

早期社交丰富化可挽救脆性X综合征小鼠模型中的成年行为和大脑异常。

Early social enrichment rescues adult behavioral and brain abnormalities in a mouse model of fragile X syndrome.

作者信息

Oddi Diego, Subashi Enejda, Middei Silvia, Bellocchio Luigi, Lemaire-Mayo Valerie, Guzmán Manuel, Crusio Wim E, D'Amato Francesca R, Pietropaolo Susanna

机构信息

1] CNR, Cell Biology and Neurobiology Institute, Rome, Italy [2] IRCCS, Santa Lucia Foundation, Rome, Italy.

1] Université Bordeaux, INCIA, Talence, France [2] CNRS, INCIA, UMR5287, Talence, France.

出版信息

Neuropsychopharmacology. 2015 Mar 13;40(5):1113-22. doi: 10.1038/npp.2014.291.

DOI:10.1038/npp.2014.291
PMID:25348604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4367453/
Abstract

Converging lines of evidence support the use of environmental stimulation to ameliorate the symptoms of a variety of neurodevelopmental disorders. Applying these interventions at very early ages is critical to achieve a marked reduction of the pathological phenotypes. Here we evaluated the impact of early social enrichment in Fmr1-KO mice, a genetic mouse model of fragile X syndrome (FXS), a major developmental disorder and the most frequent monogenic cause of autism. Enrichment was achieved by providing male KO pups and their WT littermates with enhanced social stimulation, housing them from birth until weaning with the mother and an additional nonlactating female. At adulthood they were tested for locomotor, social, and cognitive abilities; furthermore, dendritic alterations were assessed in the hippocampus and amygdala, two brain regions known to be involved in the control of the examined behaviors and affected by spine pathology in Fmr1-KOs. Enrichment rescued the behavioral FXS-like deficits displayed in adulthood by Fmr1-KO mice, that is, hyperactivity, reduced social interactions, and cognitive deficits. Early social enrichment also eliminated the abnormalities shown by adult KO mice in the morphology of hippocampal and amygdala dendritic spines, namely an enhanced density of immature vs mature types. Importantly, enrichment did not induce neurobehavioral changes in WT mice, thus supporting specific effects on FXS-like pathology. These findings show that early environmental stimulation has profound and long-term beneficial effects on the pathological FXS phenotype, thereby encouraging the use of nonpharmacological interventions for the treatment of this and perhaps other neurodevelopmental diseases.

摘要

越来越多的证据支持使用环境刺激来改善各种神经发育障碍的症状。在非常早期的年龄应用这些干预措施对于显著减轻病理表型至关重要。在这里,我们评估了早期社会丰富化对Fmr1基因敲除小鼠的影响,Fmr1基因敲除小鼠是脆性X综合征(FXS)的一种基因小鼠模型,FXS是一种主要的发育障碍,也是自闭症最常见的单基因病因。通过为雄性基因敲除幼崽及其野生型同窝幼崽提供增强的社会刺激来实现丰富化,从出生到断奶将它们与母亲和另一只非哺乳期雌性一起饲养。成年后,对它们进行运动、社交和认知能力测试;此外,还评估了海马体和杏仁核中的树突改变,这两个脑区已知参与所检测行为的控制,并在Fmr1基因敲除小鼠中受脊柱病理影响。丰富化挽救了Fmr1基因敲除小鼠成年后表现出的类似FXS的行为缺陷,即多动、社交互动减少和认知缺陷。早期社会丰富化还消除了成年基因敲除小鼠在海马体和杏仁核树突棘形态上显示的异常,即未成熟型与成熟型密度增加。重要的是,丰富化并未在野生型小鼠中诱导神经行为变化,从而支持对类似FXS病理的特定影响。这些发现表明,早期环境刺激对病理性FXS表型具有深远而长期的有益影响,从而鼓励使用非药物干预来治疗这种疾病以及可能的其他神经发育疾病。