Abstract
Psychostimulants such as amphetamine target dopamine neuron synapses to engender drug-induced plasticity. While dopamine neurons modulate the activity of striatal cholinergic interneurons (ChIs) with regional heterogeneity, how amphetamine affects ChI activity has not been elucidated. Here, we applied quantitative fluorescence imaging approaches to map the dose-dependent effects of a single dose of amphetamine on ChI activity at 2.5 and 24 hours after injection across the mouse striatum using the activity-dependent marker phosphorylated ribosomal protein S6 (p-rpS6240/244). Amphetamine did not affect the distribution or morphology of ChIs in any striatal subregion. While amphetamine at either dose had no effect on ChI activity after 2.5 hours, ChI activity was dose-dependently reduced after 24 hours specifically in the ventral striatum/nucleus accumbens, a critical site of psychostimulant action. Amphetamine at either dose did not affect the spontaneous firing of ChIs. Altogether this work demonstrates that a single dose of amphetamine has delayed regionally heterogeneous effects on ChI activity, which most likely involves extra-striatal synaptic input.
Significance statement
Using the activity dependent marker phosphorylated ribosomal protein S6 (p-rpS6240/244), we mapped amphetamine effects on the activity of cholinergic interneurons (ChIs) across the striatum. Amphetamine reduced ChI activity in dose-dependent manner in the ventral striatum/nucleus accumbens, a critical site of psychostimulant action.
Footnotes
The authors declare no competing financial interests.
We thank Susana Mingote, Leora Yetnikoff and Vlad Velicu for technical help and advice. This work was supported by NIH R01 DA038966 and R01 MH117128 (SR), Philippe Foundation (SZ) and by ARC DP190102511, ARC DP210102700 and NHMRC APP1165990 (JBG and MM) and FT200100502 (JBG).
This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.






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