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The effects of JWB1-84-1 on memory-related task performance by amyloid Aβ transgenic mice and by young and aged monkeys

  • Ajay Sood
    ,
  • J. Warren Beach
    ,
  • Scott J. Webster
    ,
  • ,
  • Jerry J. Buccafusco(corresponding author)
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

JWB1-84-1 is one of 50 tertiary amine analogs of choline synthesized with expectation that they would be high potency compounds for cytoprotection. As one of the more potent analogs in this regard, JWB1-84-1, a piperazine derivative, was selected for testing as a cognition-enhancing agent. The compound was evaluated for efficacy in Alzheimer's disease transgenic mice (B6C3-Tg(APPswe, PSEN1dE9)85Dbo/J). A separate cohort of mice (AD Tg) were first subjected to a behavioral test battery in which the transgenic strain was compared with the wild-type strain. AD Tg mice were shown to exhibit specific deficits in the acquisition of a working memory (5-trial/session radial arm water maze, RAWM) task at a time when the animals exhibited maximal cerebral amyloid burden. JWB1-84-1 produced a dose-dependent decrease in the number of errors made by well trained AD-Tg mice the RAWM task that was maximal after the 20 μg/kg dose. Aged macaques (20-32 y) were trained to proficiency in their performance of a computer-assisted delayed matching-to-sample task. Vehicle (normal saline) or JWB1-84-1 (5-150 μg/kg, i.m.) was administered 10 min before the initiating of testing. On average, JWB1-84-1 treatment significantly improved task accuracy after all but the lowest dose. The maximal degree of improvement was attained after animals received the 100 μg/kg dose. The drug's effects were restricted primarily to Medium and Long delay trials - the most difficult portions of the task, which were improved by up to 18% above control. In young macaques JWB1-84-1 treatment also significantly reversed the decrements in task accuracy associated with the random presentation of a task distractor. Thus JWB1-84-1exhibits the potential for treating the cognitive symptoms associated with neurodegenerative diseases and attention deficit disorders. Its cytoprotective action might also work to slow the progression of Alzheimer's disease.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 588-600 (13 pages)

Journal (Volume, Issue Number)

Neuropharmacology (Volume 53, Issue 5)

Publication milestones

  • Published - 10/2007

Publication status

Published - 10/2007

ISSN

0028-3908

Publication IDs

  • Scopus: 34848914887
  • PubMed: 17698153
  • ORCID: /0000-0003-2071-4767/work/68251978

Publication metrics

Metrics

SciVal
citations
34
Scopus
citations
SciVal
FWCI
0.67
SciVal
Author count
5
SciVal
Paper percentile
82
Fractional count
1
Fractional count
0.20
Fractional count
4
Fractional count
0.80
Fractional count
1
Fractional count
1

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Citation count
37
Captures
72

Funding Details

The authors would like to thank Nancy Kille, and Daniel Martin for their excellent assistance with the primate studies. This study was supported in part by the Institute for the Study of Aging, and the Veterans Administration Medical Center.
FundersFunding numbers
Institute for the Study of Aging
-
Vet. Administration Medical Center
-