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Effect of Metformin on tau pathology and proteostasis in cellular and a Drosophila model of Tauopathy
Paruchuri S, Sivanantharajah L, Mudher A, Chatterjee S.. Research Square, 2026-10-29
Topic: Disease mechanisms in lab and animal studies
Alzheimer’s disease is increasingly linked to metabolic dysfunction, with insulin resistance emerging as a key contributor to tau pathology. The antidiabetic drug Metformin has shown conflicting effects in neurodegeneration, underscoring the need to resolve its mechanistic impact on tau regulation. This study combines insulin-resistant neuroblastoma cells with Drosophila models of tauopathy to define how Metformin modulates tau phosphorylation via underlying signalling pathways. Metformin treatment increased total tau levels while consistently reducing hyperphosphorylated tau at disease-relevant epitopes in endogenous neuroblastoma cells. This dissociation was associated with enhanced activation of AKT and AMPK signalling and maintenance of basal phosphatase activity. We further observed that Metformin at low concentrations promoted autophagic activity, whereas higher concentrations impaired autophagic clearance. In the Tauopathy models, Metformin selectively ameliorated tau-induced neurodegeneration and tau-hyperphosphorylation in tau-0N4R but not in more pathogenic tau variants (tau-2N4R and tau-E14). The alteration in pathological tau levels did not correlate directly with the status of autophagy. On the contrary, autophagic status was influenced by diet and sex of these organisms. Together, our findings demonstrate that Metformin modulates tau phosphorylation independently of total tau levels and reveals a critical dissociation between upstream metabolic signalling and downstream proteostatic outcomes.
Key findings
- This dissociation was associated with enhanced activation of AKT and AMPK signalling and maintenance of basal phosphatase activity.
- Together, our findings demonstrate that Metformin modulates tau phosphorylation independently of total tau levels and reveals a critical dissociation between upstream metabolic signalling and downstream proteostatic outcomes.
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Study details
- Evidence strengthLow
How this study scored 16/100
Preprint — not yet peer-reviewed. It scored 21 on the same rubric, but non-peer-reviewed sources are capped at 16, so it shows as 16. Scored zero for study design, sample size, effect reported and randomised / blinded because the record does not state it. We have no data on times cited, citations per year, impact for its field and year, cited by studies here, still being cited, senior author's track record, institution's track record and multi-centre collaboration, so those were left out: it earned 13 of the 62 points we could judge it on, which is 21 out of 100.
| Component | Points | Why |
|---|---|---|
| Journal tier | 2 / 10 | Tier 4 — not a peer-reviewed journal (Research Square) |
| Journal's citation record | 0 / 4 | Not a journal article, so the journal's record does not count |
| Study design | 0 / 12 | No study design recorded — scores zero, not guessed (not stated in the record — scored 0) |
| Strength of evidence | 1 / 5 | Rated “low” in our summary |
| Peer-review validation | 4 / 10 | Preprint — not yet peer-reviewed. Hosted on a preprint server. |
| How recent | 5 / 5 | 2026 — within 1 year(s) of the newest study here |
| Sample size | 0 / 4 | Participant count not stated — scores zero (not stated in the record — scored 0) |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 0 / 3 | Laboratory or animal study (title names “drosophila”) — scores zero |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | — / 7 | No citation count (not found in OpenAlex) — left out of this score |
| Citations per year | — / 5 | No citation count or no year — left out of this score |
| Impact for its field and year | — / 6 | No field-weighted citation impact (OpenAlex has none yet) — left out of this score |
| Cited by studies here | — / 6 | Not yet checked against this library's citation graph — left out of this score |
| Still being cited | — / 4 | No yearly citation counts — left out of this score |
| Senior author's track record | — / 4 | Senior author's record not available — left out of this score |
| Institution's track record | — / 3 | No institution listed in OpenAlex — left out of this score |
| Multi-centre collaboration | — / 3 | Institutions not listed — left out of this score |
| Indexed in PubMed | 1 / 2 | Not in PubMed, but has a DOI |
| Free to read | 0 / 2 | Behind a paywall — scores zero |
| Points | 13 / 62 | Scored on 12 of 20 parts. We have no data for the rest, so they are left out: 13 of the 62 points we could judge it on is 21 out of 100. |
| Total | 21 / 100 | Capped to 16 because this is not a peer-reviewed article. |
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Cite this study APA, Vancouver, BibTeX · download .bib or .ris
Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. Check the citation against the original before you use it.
APA 7th
Paruchuri, S., Sivanantharajah, L., Mudher, A., & Chatterjee, S. (2026). Effect of Metformin on tau pathology and proteostasis in cellular and a Drosophila model of Tauopathy. Research Square. https://doi.org/10.21203/rs.3.rs-10786020/v1
Vancouver
Paruchuri S, Sivanantharajah L, Mudher A, Chatterjee S. Effect of Metformin on tau pathology and proteostasis in cellular and a Drosophila model of Tauopathy. Research Square. 2026. doi:10.21203/rs.3.rs-10786020/v1.
BibTeX
@article{paruchuri2026-a6042b4b,
author = {Paruchuri, S. and Sivanantharajah, L. and Mudher, A. and Chatterjee, S.},
title = {{Effect of Metformin on tau pathology and proteostasis in cellular and a Drosophila model of Tauopathy}},
journal = {Research Square},
year = {2026},
doi = {10.21203/rs.3.rs-10786020/v1},
url = {https://doi.org/10.21203/rs.3.rs-10786020/v1}
}
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