# Metformin improves RAN protein pathology, alternative splicing, and behavioral phenotypes in SCA8 mice

**Authors:** Lisa EL Romano, Setsuki Tsukagoshi, Emily E Davey-Osuch, Ramadan Ajredini, Kamat Manasi, Tala VR Ortiz, Eduardo Rijos, Nathan J Bourgon, S Elaine Ames, Timothy J Garrett, John D Cleary, Eric T Wang, Laura PW Ranum

PMC · DOI: 10.26508/lsa.202503555 · Life Science Alliance · 2026-03-02

## TL;DR

Metformin improves symptoms and pathology in SCA8 mice, suggesting potential for treating CAG•CTG expansion diseases.

## Contribution

Metformin reduces RAN proteins and neuroinflammation in SCA8 mice, offering a novel therapeutic approach.

## Key findings

- Metformin improves ambulatory performance in SCA8 mice using behavioral tests.
- Metformin reduces RAN protein levels and splicing abnormalities without altering RNA levels.
- Metformin decreases neuroinflammation and glial activation in SCA8 mice.

## Abstract

Spinocerebellar ataxia type 8, a debilitating neurological disease with no effective treatment, is caused by a CAG•CTG expansion mutation. In SCA8 mice, metformin decreases repeat-associated non-AUG proteins and neuroinflammation, improves behavior, and partially corrects splicing abnormalities.

Spinocerebellar ataxia type 8 (SCA8) is a member of a group of dominantly inherited, debilitating neurological diseases caused by CAG•CTG expansions for which there are no effective treatments. RAN translation, which was discovered in SCA8, has previously been shown to occur across CAG and CUG expansion transcripts, making treatments for SCA8 potentially relevant to a broad group of diseases, including SCA1, SCA2, SCA3, SCA6, SCA7, SCA12, Huntington’s disease, and myotonic dystrophy type 1. In addition, CUG and CAG expansion transcripts have been reported to cause RNA gain-of-function effects. Using SCA8 BAC transgenic mice as a model for CAG•CTG expansion diseases, we now show that metformin improves ambulatory performance using rotarod, DigiGait, and open-field testing. At the molecular level, metformin-treated mice show reduced RAN protein levels and improved splicing, without altering sense or antisense RNA levels. Metformin-treated mice also show decreased neuroinflammation, with reduced astrogliosis and fewer activated microglia. These data provide strong preclinical support for testing metformin in clinical trials for SCA8 and potentially the broader group of CAG•CTG repeat expansion disorders.

## Linked entities

- **Chemicals:** metformin (PubChem CID 4091)
- **Diseases:** Spinocerebellar ataxia type 8 (MONDO:0012116), Huntington’s disease (MONDO:0007739), myotonic dystrophy type 1 (MONDO:0008056), SCA1 (MONDO:0008119), SCA2 (MONDO:0008458), SCA3 (MONDO:0007182), SCA6 (MONDO:0008457), SCA7 (MONDO:0016163), SCA12 (MONDO:0011439)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Alb (albumin) [NCBI Gene 11657] {aka Alb-1, Alb1, BCL001, BCL002, BPL001}, Gfap (glial fibrillary acidic protein) [NCBI Gene 14580], Dnase1 (deoxyribonuclease I) [NCBI Gene 13419] {aka DNaseI, Dnl1}, ATXN3 (ataxin 3) [NCBI Gene 4287] {aka AT3, ATX3, JOS, MJD, MJD1, SCA3}, ATXN8OS (ATXN8 opposite strand lncRNA) [NCBI Gene 6315] {aka KLHL1AS, NCRNA00003, SCA8}, Eif2ak2 (eukaryotic translation initiation factor 2-alpha kinase 2) [NCBI Gene 19106] {aka 2310047A08Rik, 4732414G15Rik, Pkr, Prkr, Tik}, CACNA1A (calcium voltage-gated channel subunit alpha1 A) [NCBI Gene 773] {aka APCA, BI, CACNL1A4, CAV2.1, DEE42, EA2}, Adarb1 (adenosine deaminase, RNA-specific, B1) [NCBI Gene 110532] {aka 1700057H01Rik, Adar2, D10Bwg0447e, Red1}, BY367451 (cDNA sequence, BY367451) [NCBI Gene 108639] {aka Atxn8os, Klhl1as, Sca8}, Rbm3 (RNA binding motif (RNP1, RRM) protein 3) [NCBI Gene 19652] {aka 2600016C11Rik}, Baiap2 (brain-specific angiogenesis inhibitor 1-associated protein 2) [NCBI Gene 108100] {aka IRSp53}, Atxn3 (ataxin 3) [NCBI Gene 110616] {aka 2210008M02Rik, ATX3, MJD1, Mjd, Sca3, ataxin-3}, Atxn7 (ataxin 7) [NCBI Gene 246103] {aka A430107N12Rik, Sca7, ataxin-7}, Cacna1b (calcium channel, voltage-dependent, N type, alpha 1B subunit) [NCBI Gene 12287] {aka BIII, Cav2.2, Cchn1a, alpha(1B)}, Atxn2 (ataxin 2) [NCBI Gene 20239] {aka 9630045M23Rik, ATX2, Sca2}, Unc13b (unc-13 homolog B) [NCBI Gene 22249] {aka Munc13-1, Munc13-2, Unc13a, Unc13h1, Unc13h2}, Pms2 (PMS1 homolog2, mismatch repair system component) [NCBI Gene 18861] {aka Pmsl2}, Rad52 (RAD52 homolog, DNA repair protein) [NCBI Gene 19365] {aka Rad52yh}, RAN (RAN, member RAS oncogene family) [NCBI Gene 5901] {aka ARA24, Gsp1, TC4}, ATXN7 (ataxin 7) [NCBI Gene 6314] {aka ADCAII, OPCA3, SCA7, SGF73}, C9orf72 (C9orf72-SMCR8 complex subunit) [NCBI Gene 203228] {aka ALSFTD, DENND9, DENNL72, FTDALS, FTDALS1}, Tardbp (TAR DNA binding protein) [NCBI Gene 230908] {aka 1190002A23Rik, TDP-43, Tdp43}, Iba1 (induction of brown adipocytes 1) [NCBI Gene 114737], Cacna1a (calcium channel, voltage-dependent, P/Q type, alpha 1A subunit) [NCBI Gene 12286] {aka APCA, BI, Caca1a, Cacnl1a4, Cav2.1, Ccha1a}, Ran (RAN, member RAS oncogene family) [NCBI Gene 19384], ATXN2 (ataxin 2) [NCBI Gene 6311] {aka ATX2, SCA2, TNRC13}, Tbccd1 (TBCC domain containing 1) [NCBI Gene 70573] {aka 5730478M09Rik}, Kcnq2 (potassium voltage-gated channel, subfamily Q, member 2) [NCBI Gene 16536] {aka HNSPC, KQT2, Nmf134}, Celf4 (CUGBP, Elav-like family member 4) [NCBI Gene 108013] {aka A230070D14Rik, BRUNOL-4, Brul4, Brunol4, C130060B05Rik}, ATXN8 (ataxin 8) [NCBI Gene 724066], Ppp2r5c (protein phosphatase 2, regulatory subunit B', gamma) [NCBI Gene 26931] {aka 2610043M05Rik, 2700063L20Rik, D12Bwg0916e}, Atxn1 (ataxin 1) [NCBI Gene 20238] {aka 2900016G23Rik, Atx1, Gm10786, Sca1}, Nfib (nuclear factor I/B) [NCBI Gene 18028] {aka 6720429L07Rik, CTF, E030026I10Rik, NF-I/B, NF1-B, NFI-B}, Clcc1 (chloride channel CLIC-like 1) [NCBI Gene 229725] {aka ERAC1, Mclc}, Mbnl1 (muscleblind like splicing regulator 1) [NCBI Gene 56758] {aka Mbnl, mKIAA0428}
- **Diseases:** Spinocerebellar ataxia type 8 (MESH:D020754), gastrointestinal issues (MESH:D005767), lethargy (MESH:D053609), toxicity (MESH:D064420), DigiGait abnormalities (MESH:D000014), amyotrophic lateral sclerosis (MESH:D000690), astrogliosis (MESH:D005911), FECD (MESH:C535478), ataxia (MESH:D001259), FTD (MESH:D057180), MS (MESH:D009103), CANVAS (MESH:C000726747), ALS (MESH:D008113), type 2 diabetes (MESH:D003924), behavioral defects (MESH:D001523), AD (MESH:D000544), cancer (MESH:D009369), lactic acidosis (MESH:D000140), HD (MESH:D006816), diabetic (MESH:D003920), neuroinflammation (MESH:D000090862), DM1 (MESH:D009223), inflammatory (MESH:D007249), CAG CTG diseases (MESH:D004194), neurodegenerative disorders (MESH:D019636), AS (MESH:C536589), CAG CTG expansion disorders (OMIM:616452), PD (MESH:D010300), gastrointestinal distress (MESH:D012128), oligodendrocyte abnormalities (MESH:D056784), neurological disease (MESH:D020271)
- **Chemicals:** H2O2 (MESH:D006861), C4H11N5 HCl (-), zirconium (MESH:D015040), PBS (MESH:D007854), 3,3'-diaminobenzidine (MESH:D015100), alcohol (MESH:D000438), formalin (MESH:D005557), citrate (MESH:D019343), xylene (MESH:D014992), xylazine (MESH:D014991), EDTA (MESH:D004492), acetonitrile (MESH:C032159), paraffin (MESH:D010232), methanol (MESH:D000432), ammonium formate (MESH:C030544), CaCl2 (MESH:D002122), ethanol (MESH:D000431), water (MESH:D014867), Metformin (MESH:D008687), TRIzol (MESH:C411644)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]
- **Mutations:** K296R

## Full text

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## Figures

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## References

66 references — full list in the complete paper: https://tomesphere.com/paper/PMC12954051/full.md

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Source: https://tomesphere.com/paper/PMC12954051