TY - JOUR
T1 - M4 Positive Allosteric Modulator VU0467154 Impacts Amphetamine Sensitization and Spontaneous Locomotion in Male Mice
AU - Berezovskaia, Anna
AU - Lindsley, Craig
AU - Fink-Jensen, Anders
AU - Wörtwein, Gitta
PY - 2025
Y1 - 2025
N2 - 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.
AB - 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.
KW - Animals
KW - Male
KW - Receptor, Muscarinic M4/genetics
KW - Locomotion/drug effects
KW - Amphetamine/pharmacology
KW - Mice
KW - Central Nervous System Stimulants/pharmacology
KW - Prefrontal Cortex/drug effects
KW - Allosteric Regulation/drug effects
KW - Mice, Inbred C57BL
KW - Central Nervous System Sensitization/drug effects
KW - Motor Activity/drug effects
KW - Thiophenes/pharmacology
KW - Pyridines
U2 - 10.1021/acschemneuro.4c00795
DO - 10.1021/acschemneuro.4c00795
M3 - Journal article
C2 - 39982140
SN - 1948-7193
VL - 16
SP - 868
EP - 879
JO - ACS Chemical Neuroscience
JF - ACS Chemical Neuroscience
IS - 5
ER -