Therapeutic potential of GABAA receptor subunit expression abnormalities in fragile X syndrome

Mathijs B. van der Lei, R. Kooy
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引用次数: 1

Abstract

ABSTRACT Introduction Many studies have reported brain region and age-dependent alterations in the expression of several subunits of the GABAA receptor in Fmr1 KO mice. GABAA receptors are located synaptic and extrasynaptic with differential subunit compositions and characteristics. Interestingly, the activity of many subunits of the GABAA receptor is amendable by differential pharmacological treatment. Areas Covered The purpose of this review is to summarize the expression of GABAA receptor subunits in different brain regions of Fmr1 KO mice across different ages. The decreased expression of the synaptic α2 subunit in juvenile, and the decreased expression of the extrasynaptic δ subunit in both juvenile and adult Fmr1 KO mice, are among the most consistent abnormalities reported. Both subunits are suitable for treatment and currently available compounds are discussed in this review along with their therapeutic potential. Expert Opinion Pharmacological treatment targeting specific subunits of the GABAA receptor has shown selective improvements in fragile X syndrome. To our knowledge, combinatorial therapies targeting multiple subunits of the GABAA receptor have not been explored. We here argue that such a combination therapy could induce a synergistic effect to ameliorate the clinical symptoms of fragile X syndrome.
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脆性X综合征GABAA受体亚单位表达异常的治疗潜力
许多研究报道了Fmr1 KO小鼠中GABAA受体几个亚基表达的脑区域和年龄依赖性改变。GABAA受体位于突触和突触外,具有不同的亚基组成和特征。有趣的是,GABAA受体的许多亚基的活性可以通过不同的药物治疗来改变。本综述的目的是总结不同年龄Fmr1 KO小鼠不同脑区GABAA受体亚基的表达。幼年期Fmr1 KO小鼠突触α2亚基的表达减少,以及幼年期和成年期Fmr1 KO小鼠突触外δ亚基的表达减少,是报道的最一致的异常。这两种亚基都适合治疗,目前可用的化合物在这篇综述中讨论了它们的治疗潜力。针对GABAA受体特定亚基的药物治疗已显示出脆性X综合征的选择性改善。据我们所知,针对GABAA受体多个亚基的联合治疗尚未被探索。我们认为,这种联合治疗可以诱导协同作用,改善脆性X综合征的临床症状。
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来源期刊
CiteScore
2.30
自引率
0.00%
发文量
9
期刊介绍: Expert Review of Precision Medicine and Drug Development publishes primarily review articles covering the development and clinical application of medicine to be used in a personalized therapy setting; in addition, the journal also publishes original research and commentary-style articles. In an era where medicine is recognizing that a one-size-fits-all approach is not always appropriate, it has become necessary to identify patients responsive to treatments and treat patient populations using a tailored approach. Areas covered include: Development and application of drugs targeted to specific genotypes and populations, as well as advanced diagnostic technologies and significant biomarkers that aid in this. Clinical trials and case studies within personalized therapy and drug development. Screening, prediction and prevention of disease, prediction of adverse events, treatment monitoring, effects of metabolomics and microbiomics on treatment. Secondary population research, genome-wide association studies, disease–gene association studies, personal genome technologies. Ethical and cost–benefit issues, the impact to healthcare and business infrastructure, and regulatory issues.
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