Evidence map›Paper›PMID 42961528›Full record

ArticleMolecular biology reports2026

Berberine improves cognitive impairment in diabetic mice by mitigating 4-HNE-induced oxidative stress and enhancing hippocampal insulin sensitivity.

Mrinal Gupta, Mohammad Rumman, Abbas Ali Mahdi, Shivani Pandey

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Mrinal GuptaDepartment of Biochemistry, King George's Medical University, Lucknow, India.
Mohammad RummanDepartment of Biosciences, Integral University, Lucknow, India.
Abbas Ali MahdiDepartment of Biochemistry, King George's Medical University, Lucknow, India.
Shivani PandeyDepartment of Biochemistry, King George's Medical University, Lucknow, India. shivanipandey@kgmcindia.edu.

Funding

Department of Health and Research, New Delhi No.12013/19-2022-HR
6 · The paper itself

Abstract

backgroundBerberine (BBR), a component of the Chinese herb, is used for treating diabetes and diabetes-associated cognitive dysfunction (DACD), although the underlying mechanism is still unclear. Diabetes is a metabolic disease that raises the risk of developing cognitive impairment. The hippocampus within the forebrain has large number of insulin receptors linked to cognitive function and is crucial in the pathophysiology of neurodegenerative disorders. Herein, we examined whether BBR could improve DACD and explored the possible underlying mechanisms.

methodStreptozotocin (STZ) was used to induce diabetes in mice. BBR was administered before and after STZ administration for 4 weeks. The impact of BBR on 4-hydroxy 2-nonenal (4-HNE) adducts formation in diabetic mice was analyzed. Further, insulin signaling pathway was assessed to uncover the underlying molecular mechanism of BBR.

resultsBBR significantly ameliorates cognitive dysfunction in diabetic mice by decreasing 4-HNE adduct formation while increasing the levels of insulin and insulin receptor in the hippocampus of diabetic mice, indicating increased insulin uptake in the brain. BBR treatment increased the mRNA levels of PI3K, AKT, mTOR, and S6 kinase in the diabetic mice hippocampus, while decreasing BAD and NF-κB mRNA levels and tau hyperphosphorylation. Moreover, BBR increased the mRNA levels of CREB and CBP in the diabetic mice confirming the neuro-regenerative role of BBR.

conclusionBBR improves hippocampal insulin resistance by activating the PI3K/AKT/mTOR pathway and improving tau hyperphosphorylation in diabetic mice. Our study highlights a novel therapeutic target in DACD and a new mechanism of action of BBR.

Indexed as

BerberineCognitive DysfunctionDiabetes Mellitus, ExperimentalHippocampusInsulin ResistanceOxidative StressAldehydesAnimalsInsulinMaleMiceMice, Inbred C57BLReceptor, InsulinSignal TransductionStreptozocin4-hydroxy-2-nonenalAldehydesBerberineInsulinReceptor, InsulinStreptozocinApoptosisBerberineDiabetes-associated cognitive declineInsulin signaling pathwayStreptozotocinSynaptic Plasticity

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.