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

Title: A Role for GABAA Receptor β3 Subunits in Mediating Harmaline Tremor Suppression by Alcohol: Implications for Essential Tremor Therapy
Authors: Handforth, Adrian; Singh, Ram P; Kosoyan, Hovsep P; Kadam, Pournima A
Source: Tremor and Other Hyperkinetic Movements, vol 14, iss 1
Publisher Information: eScholarship, University of California
Publication Year: 2024
Collection: University of California: eScholarship
Subject Terms: 5202 Biological Psychology (for-2020); 3214 Pharmacology and Pharmaceutical Sciences (for-2020); 32 Biomedical and Clinical Sciences (for-2020); 52 Psychology (for-2020); Neurosciences (rcdc); Substance Misuse (rcdc); Alcoholism; Alcohol Use and Health (rcdc); Genetics (rcdc); Animals (mesh); Receptors; GABA-A (mesh); Harmaline (mesh); Essential Tremor (mesh); Mice (mesh); Ethanol (mesh); Central Nervous System Depressants (mesh); Disease Models; Animal (mesh); Male (mesh); Mice; Knockout (mesh); tremor; cerebellum; alcohol; GABA A receptor; harmaline; GABAA receptor
Description: 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.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: unknown
Relation: qt453569vs; https://escholarship.org/uc/item/453569vs; https://escholarship.org/content/qt453569vs/qt453569vs.pdf
DOI: 10.5334/tohm.834
Availability: https://escholarship.org/uc/item/453569vs; https://escholarship.org/content/qt453569vs/qt453569vs.pdf; https://doi.org/10.5334/tohm.834
Rights: CC-BY
Accession Number: edsbas.7C9674F0
Database: BASE