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Nicotinic ligands as multifunctional agents for the treatment of neuropsychiatric disorders

  • Alvin V. Terry(corresponding author)
    ,
  • Patrick M. Callahan
    ,
  • Caterina M. Hernandez
*Corresponding author for this work
Scholary Output:
Contribution to journal
Review article
Peer-review

Open access

Abstract

challenges associated with developing more effective treatments for neurologic and psychiatric illness such as Alzheimer's disease and schizophrenia are considerable. Both the symptoms and the pathophysiology of these conditions are complex and poorly understood and the clinical presentations across different patients can be very heterogeneous. Moreover, it has become apparent that the reductionist approach to drug discovery for these illnesses that has dominated the field for decades (i.e., the development of highly selective compounds or other treatment modalities focused on a very specific pathophysiologic target) has not been widely successful. Accordingly, a variety of new strategies have emerged including the development of "multitarget-directed ligands" (MTDLs), the development and/or identification of compounds that exhibit "multifunctional" activity (e.g., pro-cognitive plus neuroprotective, pro-cognitive plus antipsychotic activity), "repurposing" strategies for existing compounds that have other clinical indications, and novel "adjunctive" treatment strategies that might enhance the efficacy of the currently available treatments. Interestingly, a variety of ligands at nicotinic acetylcholine receptors (nAChRs) appear to have the potential to fulfill one or more of these desirable properties (i.e., multifunctional, repurposing, or adjunctive treatment potential). The purpose of this review (while not all-inclusive) is to provide an overview of a variety of nAChR ligands that demonstrate potential in these categories, particularly, "multifunctional" properties. Due to their densities in the mammalian brain and the amount of literature available, the review will focus on ligands of the high affinity α4β2 nAChR and the low affinity α7 nAChR.

Publication Information

Output type

Scholary Output:
Contribution to journal
Review article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 388-398 (11 pages)

Journal (Volume, Issue Number)

Biochemical Pharmacology (Volume 97, Issue 4)

Publication milestones

  • Published - 10/15/2015

Publication status

Published - 10/15/2015

ISSN

0006-2952

Publication IDs

  • Scopus: 84943357229
  • PubMed: 26231940

Publication metrics

Metrics

Scopus
citations
SciVal
citations
29
Fractional count
3
Fractional count
1
Fractional count
3
Fractional count
1
SciVal
FWCI
1.00
SciVal
Author count
3
SciVal
Paper percentile
89

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Citation count
40
Captures
61

Funding Details

The authors would like to thank Ms. Ashley Davis for her administrative assistance in preparing this article. This corresponding author’s laboratories are supported by the National Institute on Drug Abuse ( DA029127 ), the National Institute of Environmental Health Sciences ( ES012241 ), and the Department of Defense / US Army Medical Research Acquisition Activity (USAMRAA) W81XWH-12-1-0536 . The corresponding author has also provided consultation or performed research (relevant to this article) in the last three years either contractually or in collaboration with several pharmaceutical companies including AbbVie Inc., Institut de Recherches Servier, and Comentis, Inc.
FundersFunding numbers
DOD
-
NIDA
R01DA029127
NIEHS
ES012241
USAMRAA
W81XWH-12-1-0536