Shati/Nat8l knockout mice show behavioral deficits ameliorated by atomoxetine and methylphenidate

Behav Brain Res. 2018 Feb 26:339:207-214. doi: 10.1016/j.bbr.2017.11.040. Epub 2017 Dec 2.

Abstract

We previously identified a novel molecule, SHATI/NAT8L, as having an inhibitory effect on methamphetamine dependence. We generated Shati/Nat8l knockout (KO) mice and found that they showed neurochemical changes and behavioral abnormalities related to attention deficit/hyperactivity disorder (AD/HD). In this study, we assessed validities of the Shati/Nat8l KO mice as a new animal model for AD/HD through a behavioral pharmacology approach. We conducted a locomotor activity test in a novel environment, a cliff avoidance test, and an object-based attention assay using Shati/Nat8l KO mice at the ages of 4 and 8 weeks. We found that at the ages of both 4 and 8 weeks, Shati/Nat8l KO mice showed hyperactivity in locomotor activity test, shortened jumping latency in cliff avoidance test, and lower recognition index in object-based recognition test. Moreover, we evaluated the effects of atomoxetine (ATX) and methylphenidate (MPH) on the behavioral deficits in Shati/Nat8l KO mice. As the result, almost all behavioral deficits were improved by the treatment of both ATX and MPH. Our findings suggest that Shati/Nat8l KO mice have an impaired neural system similar to AD/HD pathophysiology. Shati/Nat8l KO mice might serve as a novel and a useful animal model for the pathophysiology of AD/HD.

Keywords: Atomoxetine; Attention deficit/hyperactivity disorder; Dopamine; Methylphenidate; SHATI/NAT8L.

MeSH terms

  • Acetyltransferases / genetics
  • Acetyltransferases / metabolism*
  • Amphetamine-Related Disorders / drug therapy*
  • Animals
  • Aspartic Acid / metabolism
  • Atomoxetine Hydrochloride / pharmacology*
  • Attention Deficit Disorder with Hyperactivity / drug therapy*
  • Behavior, Animal
  • Central Nervous System Stimulants / pharmacology
  • Methylphenidate / pharmacology*
  • Mice, Knockout
  • Motor Activity / drug effects*

Substances

  • Central Nervous System Stimulants
  • Methylphenidate
  • Aspartic Acid
  • Atomoxetine Hydrochloride
  • Acetyltransferases
  • Shati protein, mouse