Evidence map›Paper›PMID 41670033›Full record

ArticleJournal of diabetes investigation2026

Mechanisms of hesperetin in alleviating diabetic nephropathy: Network pharmacology, molecular docking, and experimental validation.

Yiwen Guo, Fengjiao Zhang, Yu Jin, Menglu Zhu, Zhiqiang Kang

Abstract read
In one paragraph

Article in Journal of diabetes investigation, 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

5 authors.

Yiwen GuoDepartment of Endocrinology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan, China.
Fengjiao ZhangDepartment of Endocrinology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan, China.
Yu JinDepartment of Cardio-Pulmonary Function, Zhengzhou Central Hospital, Zhengzhou, Henan, China.
Menglu ZhuDepartment of Endocrinology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan, China.
Zhiqiang KangDepartment of Endocrinology, Zhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan, China.ORCID https://orcid.org/0009-0009-8410-1688

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic nephropathy (DN) accounts for approximately 50% of chronic kidney disease cases. This study explored the potential regulatory mechanisms of hesperetin in DN.

methodsHigh glucose (HG)-treated HK-2 cells and streptozotocin (STZ)-induced diabetic mice were used as DN models. Impacts on cells were assessed by detecting viability, apoptosis, inflammatory cytokine release, and malondialdehyde (MDA), ferrous iron (Fe

resultsHesperetin increased cell viability and decreased apoptosis, the release of inflammatory cytokines, and the levels of MDA, Fe

conclusionsHesperetin alleviates DN progression by increasing cell viability and decreasing apoptosis, inflammatory cytokine release, and ferroptosis in HK-2 cells partially via modulating IGF1R expression.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic NephropathiesHesperidinMolecular Docking SimulationAnimalsApoptosisCell LineCell SurvivalHumansMaleMiceMice, Inbred C57BLNetwork PharmacologyOxidative StressReactive Oxygen SpeciesReceptor, IGF Type 1hesperetinHesperidinReactive Oxygen SpeciesReceptor, IGF Type 1Diabetic nephropathyHesperetinIGF1R

Identifiers

PMID41670033
PMCPMC13042708

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.