LAUSR

Highlights3‐Acetylpyridine leads to changes in both balance and gait in mice.Mice are less sensitive to the neurotoxic effects of 3‐acetylpyridine than rats.3‐Acetylpyridine led to a loss of neurons several subregions within the inferior olive.Rotorod performance was related to neuronal loss in the rostral medial nucleus, ventrolateral protrusion, and cap of Kooy. Abstract 3‐acetylpyridine (3‐AP) is a metabolic antagonist used in research to decrease levels of nicotinamide (niacinamide) in laboratory animals. The administration of 3‐AP followed by nicotinamide to rats leads to the selective destruction of neurons in the medial inferior olive, resulting in a loss of climbing fibers innervating cerebellar Purkinje cells and a consequent ataxia manifest by alterations in both balance and gait. Although 3‐AP has also been administered to mice to destroy neurons in the inferior olive, there are limited studies quantifying the consequent effects on balance, and no studies on gait. Further, the relationship between 3‐AP‐induced lesions of the inferior olive and behavior has not been elucidated. Because 3‐AP continues to be used for experiments involving mice, this study characterized the effects of this toxin on both balance and gait, and on the neuronal integrity of several brain regions involved in motor coordination. Results indicate that C57BL/6 mice are less sensitive to the neurotoxic effects of 3‐AP than rats, and a dose more than 6.5 times that used for rats produces deficits in both balance and gait comparable to those in rats. This dose led to a significant (p < 0.05) loss of NeuN(+) neurons in several subregions of the inferior olive including the rostral medial nucleus, dorsomedial cell column, ventrolateral protrusion, and cap of Kooy. Further, the number of NeuN(+) neurons in these subregions, with the exception of the dorsomedial cell column, was significantly (p < 0.05) related to rotorod performance, implicating their involvement in this behavior.