Citation

Steinmetz AB, Freeman JH. Neurobiol. Learn. Mem. 2018; ePub(ePub): ePub.

Affiliation

Department of Psychological and Brain Sciences, The University of Iowa, Iowa City, IA 52242 USA. Electronic address: john-freeman@uiowa.edu.

Copyright

(Copyright © 2018, Elsevier Publishing)

DOI

10.1016/j.nlm.2018.06.015

PMID

29964164

Abstract

Systemic administration of cannabinoid agonists impairs cerebellum- dependent motor learning. The cannabinoid-induced impairment of motor learning has been hypothesized to be due to disruption of Purkinje cell plasticity within the cerebellar cortex. In the current study, we tested this hypothesis in rats with localized microinfusions of cannabinoid agonists and antagonists into the cerebellar cortex during eyeblink conditioning, a type of cerebellum-dependent motor learning. Infusions of the cannabinoid agonists WIN55,212-2 or ACEA directly into the eyeblink conditioning microzone of the cerebellar cortex severely impaired acquisition of eyeblink conditioning, whereas the CB1R antagonist SR141716A did not produce a significant impairment. Infusions of WIN55,212-2 outside of the eyeblink conditioning microzone did not impair motor learning, establishing anatomical specificity for the agonist effects. The motor learning impairment caused by WIN55,212-2 and ACEA was rescued by SR141716A, indicating that the learning deficit was produced through CB1Rs. The current findings demonstrate that the effects of cannabinoid receptor agonists on motor learning are localized to CB1Rs within a discrete microzone of the cerebellar cortex.

Copyright © 2018. Published by Elsevier Inc.

Language: en

Keywords

Cannabinoid receptors; Cerebellum; Eye-blink conditioning; Learning; Purkinje cell