Evidence map›Paper›PMID 27327269›Full record

ReviewAnnals of the New York Academy of Sciences2016

Efforts toward treatments against aging of organophosphorus-inhibited acetylcholinesterase.

Qinggeng Zhuang, Amneh Young, Christopher S Callam, Craig A McElroy, Özlem Dogan Ekici, Ryan J Yoder, Christopher M Hadad

Open access · greenAbstract readReview
In one paragraph

Review in Annals of the New York Academy of Sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. FDA-Approved Oximes and Their Significance in Medicinal Chemistry.Pharmaceuticals (Basel, Switzerland) · 2022
    Review
  12. Review
  13. Review
  14. Article
  15. Review
  16. Resurrection and Reactivation of Acetylcholinesterase and Butyrylcholinesterase.Chemistry (Weinheim an der Bergstrasse, Germany) · 2019
    Review
  17. Study ofACS medicinal chemistry letters · 2017
    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

7 authors at 3 institutions in 1 country.

Qinggeng ZhuangDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
Amneh YoungDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
Christopher S CallamDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
Craig A McElroyCollege of Pharmacy, The Ohio State University, Columbus, Ohio.
Özlem Dogan EkiciDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
Ryan J YoderDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
Christopher M HadadDepartment of Chemistry and Biochemistry, The Ohio State University, Columbus, Ohio.
The Ohio State University · USThe Ohio State University at Marion · USThe Ohio State University Newark · US

Funding

Reactivation of Aged Acetylcholinesterase: Design and Development of Novel TherapU01NS087983 · NINDS · OHIO STATE UNIVERSITY · PI HADAD, CHRISTOPHER M. · 2014 to 2016
$1.1M
NINDS NIH HHS U01 NS087983
6 · The paper itself

Abstract

Aging is a dealkylation reaction of organophosphorus (OP)-inhibited acetylcholinesterase (AChE). Despite many studies to date, aged AChE cannot be reactivated directly by traditional pyridinium oximes. This review summarizes strategies that are potentially valuable in the treatment against aging in OP poisoning. Among them, retardation of aging seeks to lower the rate of aging through the use of AChE effectors. These drugs should be administered before AChE is completely aged. For postaging treatment, realkylation of aged AChE by appropriate alkylators may pave the way for oxime treatment by neutralizing the oxyanion at the active site of aged AChE. The other two strategies, upregulation of AChE expression and introduction of exogenous AChE, cannot resurrect aged AChE but may compensate for lowered active AChE levels by in situ production or external introduction of active AChE. Upregulation of AChE expression can be triggered by some peptides. Sources of exogenous AChE can be whole blood or purified AChE, either from human or nonhuman species.

Indexed as

AcetylcholinesteraseAnimalsCholinesterase InhibitorsHumansModels, BiologicalOrganophosphorus CompoundsUp-RegulationAcetylcholinesteraseCholinesterase InhibitorsOrganophosphorus Compoundsacetylcholinesteraseagingexogenousrealkylationresurrectionupregulation

Identifiers

PMID27327269
PMCPMC4940266
OpenAlexW2473053464

What OpenQuestion holds

Textmetadata
LicenceTDM
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.