Kcnn2 blockade reverses learning deficits in a mouse model of fetal alcohol spectrum disorders.
Shahid MohammadStephen J PageLi WangSeiji IshiiPeijun LiToru SasakiAiesha BashaAnna SalzbergZenaide QuezadoFumiaki ImamuraHirotaka NishiKeiichi IsakaJoshua G CorbinJudy S LiuYuka Imamura KawasawaMasaaki ToriiKazue Hashimoto-ToriiPublished in: Nature neuroscience (2020)
Learning disabilities are hallmarks of congenital conditions caused by prenatal exposure to harmful agents. These include fetal alcohol spectrum disorders (FASDs) with a wide range of cognitive deficiencies, including impaired motor skill development. Although these effects have been well characterized, the molecular effects that bring about these behavioral consequences remain to be determined. We previously found that the acute molecular responses to alcohol in the embryonic brain are stochastic, varying among neural progenitor cells. However, the pathophysiological consequences stemming from these heterogeneous responses remain unknown. Here we show that acute responses to alcohol in progenitor cells altered gene expression in their descendant neurons. Among the altered genes, an increase of the calcium-activated potassium channel Kcnn2 in the motor cortex correlated with motor learning deficits in a mouse model of FASD. Pharmacologic blockade of Kcnn2 improves these learning deficits, suggesting Kcnn2 blockers as a new intervention for learning disabilities in FASD.
Keyphrases
- mouse model
- gene expression
- traumatic brain injury
- alcohol consumption
- liver failure
- randomized controlled trial
- respiratory failure
- dna methylation
- spinal cord
- aortic dissection
- intensive care unit
- multiple sclerosis
- white matter
- blood brain barrier
- hepatitis b virus
- spinal cord injury
- resting state
- functional connectivity
- acute respiratory distress syndrome