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M4 Positive Allosteric Modulator VU0467154 Impacts Amphetamine Sensitization and Spontaneous Locomotion in Male Mice
Anna Berezovskaia1,2, Craig Lindsley3, Anders Fink-Jensen1,2,4
1Laboratory of Neuropsychiatry, Mental Health Centre Copenhagen, Mental Health Services in the Capital Region of Denmark and University of Copenhagen, Frederiksberg 2000, Denmark.
Abstract:
This study investigates the effects of the muscarinic acetylcholine receptor subtype 4 (M4) positive allosteric modulator (PAM) VU0467154 on the development, incubation, and expression of amphetamine sensitization in mice, the expression of immediate early genes in the medial prefrontal cortex after induction and expression of sensitization, as well as on spontaneous locomotion and several aspects of sensorimotor function. Mice were pretreated with VU0467154 during the induction phase, before the challenge test, or both. A separate cohort was treated during the incubation period. Tests of spontaneous locomotion and sensorimotor function were conducted after VU0467154 administration to evaluate potential side effects. Treatment with VU0467154 inhibited the development and expression of amphetamine sensitization. This was paralleled by effects on immediate early gene expression in the medial prefrontal cortex. Additionally, previous pretreatment with VU0467154 during the induction phase attenuated the expression of sensitization after a two-week incubation period. However, treatment with VU0467154 during the incubation period did not affect the expression of a sensitized response. VU0467154 significantly reduced spontaneous locomotion without impairing other aspects of sensorimotor function, as assessed by the mesh, adhesive removal, horizontal bar, and negative geotaxis tests. Global M4 knockout mice confirmed that the inhibitory effect on spontaneous locomotion was specific to M4 receptors. Our findings provide new insights into the therapeutic potential of M4 PAMs in modulating the neuroadaptations associated with psychostimulant abuse. Collectively, these results suggest that activation of M4 receptors could be a promising strategy for modulating dopaminergic signaling and reducing some behaviors associated with substance use disorder.
Insights
The muscarinic acetylcholine receptor subtype 4 (M4) positive allosteric modulator VU0467154 inhibits amphetamine sensitization and reduces locomotion in mice, suggesting therapeutic potential for substance use disorders.
Area of Science:
- Neuroscience
- Pharmacology
- Addiction Research
Background:
- Amphetamine sensitization is a key neurobiological model for studying psychostimulant addiction.
- Muscarinic acetylcholine receptors, particularly M4, are implicated in modulating dopamine signaling and reward pathways.
- Positive allosteric modulators (PAMs) offer a targeted approach to enhance receptor function.
Purpose of the Study:
- To investigate the effects of the M4 PAM VU0467154 on amphetamine-induced sensitization in mice.
- To examine the impact of VU0467154 on immediate early gene expression in the medial prefrontal cortex.
- To assess the influence of VU0467154 on spontaneous locomotion and sensorimotor function.
Main Methods:
- Mice were treated with VU0467154 during different phases (induction, challenge, incubation) of amphetamine sensitization.
- Immediate early gene expression was analyzed in the medial prefrontal cortex.
- Spontaneous locomotion and sensorimotor tests (mesh, adhesive removal, horizontal bar, negative geotaxis) were performed.
- M4 knockout mice were used to confirm receptor specificity.
Main Results:
- VU0467154 significantly inhibited the development and expression of amphetamine sensitization.
- Effects on sensitization were associated with changes in medial prefrontal cortex immediate early gene expression.
- Pretreatment during induction attenuated sensitization expression after incubation, but incubation treatment alone did not.
- VU0467154 reduced spontaneous locomotion, a M4 receptor-dependent effect, without impairing other sensorimotor functions.
Conclusions:
- M4 PAMs, like VU0467154, show potential in modulating neuroadaptations underlying psychostimulant abuse.
- Activation of M4 receptors may offer a therapeutic strategy for substance use disorders by influencing dopaminergic signaling.
- Targeting M4 receptors could help reduce behaviors associated with substance use.
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