Literature DB >> 23272693

Emerging approaches for treatment of schizophrenia: modulation of cholinergic signaling.

Daniel J Foster1, Carrie K Jones, P Jeffrey Conn.   

Abstract

Currently available therapeutic agents for treatment of schizophrenia target signaling by monoaminergic neurotransmitters; however, these treatments do not adequately treat the range of symptoms observed in patients. While these therapies treat the positive symptoms, they do not have efficacy in treating the negative symptoms and cognitive deficits that are associated with the disease. Evidence suggests that molecules that modulate signaling by the neurotransmitter acetylcholine (ACh) could provide a more comprehensive treatment of schizophrenia than currently prescribed antipsychotics. Molecules that broadly increase ACh-signaling have been demonstrated to have efficacy in treating numerous symptom clusters in schizophrenia patients. Unfortunately, these compounds induce adverse effects via activation of peripheral receptors that limit their clinical utility. One proposed strategy for retaining the efficacy of cholinergic treatments, without the adverse effects, is to target specific cholinergic receptor subtypes in the brain. Several cholinergic receptors are able to modulate brain circuits that are dysregulated in schizophrenia patients including receptors belonging to both the muscarinic family (i.e., M1, M4, and M5), and the nicotinic family (i.e., α7, α4β2). Recently, great strides have been made in developing small molecules with high specificity for these receptors, and several of these novel molecules have robust efficacy in several preclinical models predictive of both anti-psychotic and pro-cognitive effectiveness. Promising studies suggest that targeting M1 and α7 may be beneficial for pro-cognitive effects, while molecules that target M4 may be ideally suited to address the positive symptoms. Since these receptor subtypes are distinct from those responsible for the adverse effects observed with non-selective cholinergic treatments, there is hope that molecules targeting these receptors could provide novel therapeutics. Further research is needed to examine the utility of such compounds as therapeutics that could be used either alone, or in combination with existing medications, to better treat schizophrenia.

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Year:  2012        PMID: 23272693      PMCID: PMC3726271     

Source DB:  PubMed          Journal:  Discov Med        ISSN: 1539-6509            Impact factor:   2.970


  75 in total

1.  Muscarinic receptors induce LTD of NMDAR EPSCs via a mechanism involving hippocalcin, AP2 and PSD-95.

Authors:  Jihoon Jo; Gi Hoon Son; Bryony L Winters; Myung Jong Kim; Daniel J Whitcomb; Bryony A Dickinson; Youn-Bok Lee; Kensuke Futai; Mascia Amici; Morgan Sheng; Graham L Collingridge; Kwangwook Cho
Journal:  Nat Neurosci       Date:  2010-09-19       Impact factor: 24.884

2.  AGAP1/AP-3-dependent endocytic recycling of M5 muscarinic receptors promotes dopamine release.

Authors:  Jacob Bendor; José E Lizardi-Ortiz; Robert I Westphalen; Markus Brandstetter; Hugh C Hemmings; David Sulzer; Marc Flajolet; Paul Greengard
Journal:  EMBO J       Date:  2010-07-27       Impact factor: 11.598

3.  Orthosteric and allosteric modes of interaction of novel selective agonists of the M1 muscarinic acetylcholine receptor.

Authors:  Vimesh A Avlani; Christopher J Langmead; Elizabeth Guida; Martyn D Wood; Ben G Tehan; Hugh J Herdon; Jeannette M Watson; Patrick M Sexton; Arthur Christopoulos
Journal:  Mol Pharmacol       Date:  2010-04-22       Impact factor: 4.436

4.  Impact of species variability and 'probe-dependence' on the detection and in vivo validation of allosteric modulation at the M4 muscarinic acetylcholine receptor.

Authors:  S Suratman; K Leach; Pm Sexton; Cc Felder; Re Loiacono; A Christopoulos
Journal:  Br J Pharmacol       Date:  2011-04       Impact factor: 8.739

Review 5.  Neural systems governed by nicotinic acetylcholine receptors: emerging hypotheses.

Authors:  Julie M Miwa; Robert Freedman; Henry A Lester
Journal:  Neuron       Date:  2011-04-14       Impact factor: 17.173

6.  A subpopulation of neuronal M4 muscarinic acetylcholine receptors plays a critical role in modulating dopamine-dependent behaviors.

Authors:  Jongrye Jeon; Ditte Dencker; Gitta Wörtwein; David P D Woldbye; Yinghong Cui; Albert A Davis; Allan I Levey; Günther Schütz; Thomas N Sager; Arne Mørk; Cuiling Li; Chu-Xia Deng; Anders Fink-Jensen; Jürgen Wess
Journal:  J Neurosci       Date:  2010-02-10       Impact factor: 6.167

7.  Heterobiaryl and heterobiaryl ether derived M5 positive allosteric modulators.

Authors:  Thomas M Bridges; J Phillip Kennedy; Corey R Hopkins; P Jeffrey Conn; Craig W Lindsley
Journal:  Bioorg Med Chem Lett       Date:  2010-08-12       Impact factor: 2.823

8.  Role of specific muscarinic receptor subtypes in cholinergic parasympathomimetic responses, in vivo phosphoinositide hydrolysis, and pilocarpine-induced seizure activity.

Authors:  Frank P Bymaster; Petra A Carter; Masahisa Yamada; Jesus Gomeza; Jürgen Wess; Susan E Hamilton; Neil M Nathanson; David L McKinzie; Christian C Felder
Journal:  Eur J Neurosci       Date:  2003-04       Impact factor: 3.386

9.  Striatal muscarinic receptors promote activity dependence of dopamine transmission via distinct receptor subtypes on cholinergic interneurons in ventral versus dorsal striatum.

Authors:  Sarah Threlfell; Michael A Clements; Tansi Khodai; Ilse S Pienaar; Richard Exley; Jürgen Wess; Stephanie J Cragg
Journal:  J Neurosci       Date:  2010-03-03       Impact factor: 6.167

10.  Facilitation of long-term potentiation by muscarinic M(1) receptors is mediated by inhibition of SK channels.

Authors:  Katherine A Buchanan; Milos M Petrovic; Sophie E L Chamberlain; Neil V Marrion; Jack R Mellor
Journal:  Neuron       Date:  2010-12-09       Impact factor: 17.173

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  22 in total

Review 1.  Cholinergic interneurons in the dorsal and ventral striatum: anatomical and functional considerations in normal and diseased conditions.

Authors:  Kalynda K Gonzales; Yoland Smith
Journal:  Ann N Y Acad Sci       Date:  2015-04-15       Impact factor: 5.691

2.  An Integrative and Mechanistic Model of Impaired Belief Updating in Schizophrenia.

Authors:  Merage Ghane; Tim Sparer
Journal:  J Neurosci       Date:  2019-07-17       Impact factor: 6.167

3.  M5 receptor activation produces opposing physiological outcomes in dopamine neurons depending on the receptor's location.

Authors:  Daniel J Foster; Patrick R Gentry; Jose E Lizardi-Ortiz; Thomas M Bridges; Michael R Wood; Colleen M Niswender; David Sulzer; Craig W Lindsley; Zixiu Xiang; P Jeffrey Conn
Journal:  J Neurosci       Date:  2014-02-26       Impact factor: 6.167

4.  M4 mAChR-mediated modulation of glutamatergic transmission at corticostriatal synapses.

Authors:  Tristano Pancani; Caroline Bolarinwa; Yoland Smith; Craig W Lindsley; P Jeffrey Conn; Zixiu Xiang
Journal:  ACS Chem Neurosci       Date:  2014-02-27       Impact factor: 4.418

Review 5.  Muscarinic acetylcholine receptors: novel opportunities for drug development.

Authors:  Andrew C Kruse; Brian K Kobilka; Dinesh Gautam; Patrick M Sexton; Arthur Christopoulos; Jürgen Wess
Journal:  Nat Rev Drug Discov       Date:  2014-06-06       Impact factor: 84.694

6.  Long-term effects of maternal choline supplementation on CA1 pyramidal neuron gene expression in the Ts65Dn mouse model of Down syndrome and Alzheimer's disease.

Authors:  Melissa J Alldred; Helen M Chao; Sang Han Lee; Judah Beilin; Brian E Powers; Eva Petkova; Barbara J Strupp; Stephen D Ginsberg
Journal:  FASEB J       Date:  2019-06-10       Impact factor: 5.191

7.  Total RNA Sequencing of Rett Syndrome Autopsy Samples Identifies the M4 Muscarinic Receptor as a Novel Therapeutic Target.

Authors:  Rocco G Gogliotti; Nicole M Fisher; Branden J Stansley; Carrie K Jones; Craig W Lindsley; P Jeffrey Conn; Colleen M Niswender
Journal:  J Pharmacol Exp Ther       Date:  2018-03-09       Impact factor: 4.030

8.  Crystal structures of the M1 and M4 muscarinic acetylcholine receptors.

Authors:  David M Thal; Bingfa Sun; Dan Feng; Vindhya Nawaratne; Katie Leach; Christian C Felder; Mark G Bures; David A Evans; William I Weis; Priti Bachhawat; Tong Sun Kobilka; Patrick M Sexton; Brian K Kobilka; Arthur Christopoulos
Journal:  Nature       Date:  2016-03-09       Impact factor: 49.962

Review 9.  Opportunities and challenges in the discovery of allosteric modulators of GPCRs for treating CNS disorders.

Authors:  P Jeffrey Conn; Craig W Lindsley; Jens Meiler; Colleen M Niswender
Journal:  Nat Rev Drug Discov       Date:  2014-09       Impact factor: 84.694

10.  Homozygous Deletion of Glutathione Peroxidase 1 and Aldehyde Dehydrogenase 1a1 Genes Is Not Associated with Schizophrenia-Like Behavior in Mice.

Authors:  Xiang Bai; Elizabeth Fermandez; Georgianna Gould; Randy Strong
Journal:  J Biochem Pharmacol Res       Date:  2013-12-01
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