Evidence map›Paper›PMID 42412302›Full record

ArticleJournal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology2026

Study on the Effects and Mechanisms of Resveratrol in Improving Cognitive Impairment in Aβ

Chu Zhang, Yunhan Ma, Zhidan Shi, Xinqi He, Jiayi Hu, Shuting Chen, Hao Wu, Meng Tian, Chuang Yan, Mengtao Xing and 1 more

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Article in Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology, 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

11 authors.

Chu Zhang *Department of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Yunhan Ma *Department of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Zhidan ShiDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Xinqi HeDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Jiayi HuDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Shuting ChenDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Hao WuDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Meng TianDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Chuang YanDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China.
Mengtao XingDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China. 1020202612@cpu.edu.cn.ORCID http://orcid.org/0000-0003-3816-4214
Ling HeDepartment of Pharmacology, School of Pharmacy, China Pharmaceutical University, Nanjing, 210009, China. heling92@hotmail.com.ORCID http://orcid.org/0000-0003-3564-8862

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging is a major risk factor for neurodegenerative diseases, including Alzheimer's disease (AD). Targeting cellular senescence has therefore emerged as a promising therapeutic strategy. Resveratrol (RV), a natural polyphenolic compound, exhibits anti-aging properties through the regulation of autophagy and oxidative stress; however, its mechanisms in AD remain incompletely understood. In this study, we investigated the effects and underlying mechanisms of RV in an Aβ1-42-induced AD model. In vivo, RV administration significantly reduced the expression of aging-related markers and activated autophagy-associated signaling pathways. In vitro, RV treatment markedly attenuated Aβ1-42-induced cell viability loss and excessive reactive oxygen species (ROS) production. Further mechanistic analyses demonstrated that RV-induced autophagy activation was closely associated with the AMP-activated protein kinase/UNC-51-like kinase 1 (AMPK/ULK1) and silent information regulator 1/nuclear factor-kappaB (SIRT1/NF-κB) pathways. Collectively, these findings suggest that RV alleviates AD-related pathological processes by promoting autophagy and delaying cellular senescence, highlighting its potential as a therapeutic agent for age-related neurodegenerative diseases.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAntioxidantsCognitive DysfunctionPeptide FragmentsResveratrolAnimalsAutophagyDisease Models, AnimalMaleMiceMice, Inbred C57BLOxidative StressAmyloid beta-Peptidesamyloid beta-protein (1-42)AntioxidantsPeptide FragmentsResveratrolAgingAlzheimer’s diseaseResveratrolβ-amyloid

Identifiers

PMID42412302

What Socratic 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 Socratic graph.