Evidence map›Paper›PMID 35545730›Full record

ReviewMolecular neurobiology2022

Resveratrol and neuroprotection: an insight into prospective therapeutic approaches against Alzheimer's disease from bench to bedside.

Fahadul Islam, Mohamed H Nafady, Md Rezaul Islam, Susmita Saha, Salma Rashid, Aklima Akter, Md Harun- Or-Rashid, Muhammad Furqan Akhtar, Asma Perveen, Ghulam Md Ashraf and 2 more

Erratum issuedAbstract readReview
PubMed Publisher
In one paragraph

Review in Molecular neurobiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
10.2field-weighted citation impact, top 1% of its field
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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 7 institutions in 6 countries.

Fahadul IslamDepartment of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Mohamed H NafadyFaculty of Applied Health Science Technology, Misr University for Science and Technology, Giza, Egypt.
Md Rezaul IslamDepartment of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Susmita SahaDepartment of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Salma RashidDepartment of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Aklima AkterDepartment of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Md Harun- Or-RashidDepartment of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University, Dhaka, 1207, Bangladesh.
Muhammad Furqan AkhtarRiphah Institute of Pharmaceutical Sciences, Riphah International University Lahore Campus, Lahore, Pakistan.
Asma PerveenGlocal School of Life Sciences, Glocal University, Uttar Pradesh, Mirzapur Pole, Saharanpur, India.
Ghulam Md AshrafPre-Clinical Research Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah, 21589, Saudi Arabia.
Md Habibur RahmanDepartment of Pharmacy, Southeast University, Banani, Dhaka, 1213, Bangladesh.
Sherouk Hussein SweilamDepartment of Pharmacognosy, Faculty of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj 11942, Saudi Arabia. s.sweilam@psau.edu.sa.ORCID http://orcid.org/0000-0002-5352-4778
Daffodil International University · BDGlocal University · INKing Abdulaziz University · SAMisr University for Science and Technology · EGPrince Sattam Bin Abdulaziz University · SARiphah International University · PKYonsei University · KR

Funding

This publication was supported by the Deanship of Scientific Research at Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia, as well as Egyptian Russian University, Badr City, Egypt. Al-KharjThis publication was supported by the Deanship of Scientific Research at Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia, as well as Egyptian Russian University, Badr City, Egypt. as well as Egyptian Russian UniversityThis publication was supported by the Deanship of Scientific Research at Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia, as well as Egyptian Russian University, Badr City, Egypt. Badr CityThis publication was supported by the Deanship of Scientific Research at Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia, as well as Egyptian Russian University, Badr City, Egypt. Egypt.This publication was supported by the Deanship of Scientific Research at Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia, as well as Egyptian Russian University, Badr City, Egypt. Saudi ArabiaThis publication was supported by the Deanship of Scientific Research at Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia, as well as Egyptian Russian University, Badr City, Egypt. This publication was supported by the Deanship of Scientific Research at Prince Sattam Bin Abdulaziz University
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common cause of dementia and cognitive impairment; yet, there is currently no treatment. A buildup of Aβ, tau protein phosphorylation, oxidative stress, and inflammation in AD is pathogenic. The accumulation of amyloid-beta (Aβ) peptides in these neurocognitive areas is a significant characteristic of the disease. Therefore, inhibiting Aβ peptide aggregation has been proposed as the critical therapeutic approach for AD treatment. Resveratrol has been demonstrated in multiple studies to have a neuroprotective, anti-inflammatory, and antioxidant characteristic and the ability to minimize Aβ peptides aggregation and toxicity in the hippocampus of Alzheimer's patients, stimulating neurogenesis and inhibiting hippocampal degeneration. Furthermore, resveratrol's antioxidant effect promotes neuronal development by activating the silent information regulator-1 (SIRT1), which can protect against the detrimental effects of oxidative stress. Resveratrol-induced SIRT1 activation is becoming more crucial in developing novel therapeutic options for AD and other diseases that have neurodegenerative characteristics. This review highlighted a better knowledge of resveratrol's mechanism of action and its promising therapeutic efficacy in treating AD. We also highlighted the therapeutic potential of resveratrol as an AD therapeutic agent, which is effective against neurodegenerative disorders.

Indexed as

Alzheimer DiseaseNeuroprotective AgentsAmyloid beta-PeptidesAntioxidantsHumansNeuroprotectionResveratrolSirtuin 1Amyloid beta-PeptidesAntioxidantsNeuroprotective AgentsResveratrolSirtuin 1Alzheimer’s diseaseAutophagy inductionNeuroinflammationOxidative stressResveratrolSIRT1

Identifiers

PMID35545730
OpenAlexW4280643537

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.