A Role for GABAA Receptor β3 Subunits in Mediating Harmaline Tremor Suppression by Alcohol: Implications for Essential Tremor Therapy.

IF 2.5 Q2 CLINICAL NEUROLOGY Tremor and Other Hyperkinetic Movements Pub Date : 2024-04-26 eCollection Date: 2024-01-01 DOI:10.5334/tohm.834
Adrian Handforth, Ram P Singh, Hovsep P Kosoyan, Pournima A Kadam
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Abstract

Background: Essential tremor patients may find that low alcohol amounts suppress tremor. A candidate mechanism is modulation of α6β3δ extra-synaptic GABAA receptors, that in vitro respond to non-intoxicating alcohol levels. We previously found that low-dose alcohol reduces harmaline tremor in wild-type mice, but not in littermates lacking δ or α6 subunits. Here we addressed whether low-dose alcohol requires the β3 subunit for tremor suppression.

Methods: We tested whether low-dose alcohol suppresses tremor in cre-negative mice with intact β3 exon 3 flanked by loxP, and in littermates in which this region was excised by cre expressed under the α6 subunit promotor. Tremor in the harmaline model was measured as a percentage of motion power in the tremor bandwidth divided by overall motion power.

Results: Alcohol, 0.500 and 0.575 g/kg, reduced harmaline tremor compared to vehicle-treated controls in floxed β3 cre- mice, but had no effect on tremor in floxed β3 cre+ littermates that have β3 knocked out. This was not due to potential interference of α6 expression by the insertion of the cre gene into the α6 gene since non-floxed β3 cre+ and cre- littermates exhibited similar tremor suppression by alcohol.

Discussion: As α6β3δ GABAA receptors are sensitive to low-dose alcohol, and cerebellar granule cells express β3 and are the predominant brain site for α6 and δ expression together, our overall findings suggest alcohol acts to suppress tremor by modulating α6β3δ GABAA receptors on these cells. Novel drugs that target this receptor may potentially be effective and well-tolerated for essential tremor.

Highlights: We previously found with the harmaline essential tremor model that GABAA receptors containing α6 and δ subunits mediate tremor suppression by alcohol. We now show that β3 subunits in α6-expressing cells, likely cerebellar granule cells, are also required, indicating that alcohol suppresses tremor by modulating α6β3δ extra-synaptic GABAA receptors.

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GABAA 受体 β3 亚基在调解酒精对谐波震颤抑制中的作用:对基本震颤疗法的启示。
背景:本质性震颤患者可能会发现低量酒精会抑制震颤。一种候选机制是调节α6β3δ突触外 GABAA 受体,这种受体在体外对非毒性酒精水平有反应。我们以前曾发现,低剂量酒精可减少野生型小鼠的伤害性震颤,但不能减少缺乏δ或α6亚基的同窝小鼠的震颤。在此,我们探讨了低剂量酒精是否需要β3亚基来抑制震颤:我们测试了在loxP侧翼有完整β3外显子3的cre阴性小鼠和在α6亚基启动子下表达cre切除该区域的同窝小鼠中,低剂量酒精是否能抑制震颤。以震颤带宽中的运动能力除以总体运动能力的百分比来测量害马林模型中的震颤:结果:酒精(0.500 和 0.575 克/千克)与车辆处理的对照组相比,可减少失活的β3 cre- 小鼠的震颤,但对失活的β3 cre+ β3基因敲除的同窝小鼠的震颤没有影响。这并不是因为将 cre 基因插入到 α6 基因中可能干扰了 α6 的表达,因为非浮性 β3 cre+ 和 cre- 胎鼠在酒精作用下表现出相似的震颤抑制作用:讨论:由于α6β3δ GABAA受体对低剂量酒精敏感,而小脑颗粒细胞表达β3,并且是大脑中α6和δ共同表达的主要部位,我们的总体研究结果表明,酒精是通过调节这些细胞上的α6β3δ GABAA受体来抑制震颤的。以这种受体为靶点的新型药物可能对本质性震颤有效且耐受性良好:亮点:我们之前在哈马林本质性震颤模型中发现,含有α6和δ亚基的GABAA受体介导了酒精对震颤的抑制作用。我们现在发现,α6表达细胞(可能是小脑颗粒细胞)中的β3亚基也是必需的,这表明酒精是通过调节α6β3δ突触外GABAA受体来抑制震颤的。
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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
期刊最新文献
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