Evidence map›Paper›PMID 36819782›Full record

ArticleOxidative medicine and cellular longevity2023

A Multifunctional (-)-Meptazinol-Serotonin Hybrid Ameliorates Oxidative Stress-Associated Apoptotic Neuronal Death and Memory Deficits via Activating the Nrf2/Antioxidant Enzyme Pathway.

Faxue Zhao, Lin Zhao, Yan Zhou, Xiaofang Tan, Yang Yang, Wenwen Ni, Wei Zheng, Hongzhuan Chen, Yu Qiu, Juan Li

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
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

10 authors at 3 institutions in 1 country.

Faxue ZhaoDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Lin ZhaoDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Yan ZhouDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Xiaofang TanDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Yang YangDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Wenwen NiDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.
Wei ZhengNHC Key Laboratory of Reproduction Regulation, Shanghai Institute for Biomedical and Pharmaceutical Technologies, 2140 Xietu Road, Shanghai 200032, China.ORCID https://orcid.org/0000-0001-7731-8971
Hongzhuan ChenInstitute of Interdisciplinary Integrative Biomedical Research, Shanghai University of Traditional Chinese Medicine, 1200 Cailun Road, Shanghai 201210, China.
Yu QiuDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.ORCID https://orcid.org/0000-0002-1236-1941
Juan LiDepartment of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, 280 South Chongqing Road, Shanghai 200025, China.ORCID https://orcid.org/0000-0003-3321-7655
Shanghai Jiao Tong University · CNShanghai Institute of Pharmaceutical Industry · CNShanghai University of Traditional Chinese Medicine · CN

Funding

CSRD VA I01 CX002022
6 · The paper itself

Abstract

The pathogenesis of Alzheimer's disease (AD) involves multiple pathophysiological processes. Oxidative stress is a major cause of AD-associated neuronal injury. The current research was designed to examine whether a novel (-)-meptazinol-serotonin hybrid (Mep-S) with potent antioxidant activity and additional inhibitory properties for acetylcholinesterase (AChE) activity could attenuate oxidative neuronal damage and cognitive deficits. In human SH-SY5Y cells, Mep-S suppressed H

Indexed as

Alzheimer DiseaseMeptazinolNeuroblastomaAcetylcholinesteraseAnimalsAntioxidantsApoptosisGlutathioneHeme Oxygenase-1HumansHydrogen PeroxideKelch-Like ECH-Associated Protein 1Memory DisordersMiceMolecular Docking SimulationNF-E2-Related Factor 2AcetylcholinesteraseAntioxidantsGlutathioneHeme Oxygenase-1Hydrogen PeroxideKelch-Like ECH-Associated Protein 1MeptazinolNF-E2-Related Factor 2Proto-Oncogene Proteins c-aktReactive Oxygen SpeciesScopolamine DerivativesSerotonin

Identifiers

PMID36819782
PMCPMC9935814
OpenAlexW4319724949

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.