Catechol-O-methyltransferase (COMT) inactivates dopamine in prefrontal cortex and is associated clinically with a schizophrenia endophenotype. Using an ethologically based approach, the phenotype of mice with heterozygous COMT deletion was characterised by decreased rearing with increased sifting and chewing. Heterozygous COMT deletion is associated with a distinctive phenotype. This differs from that which we have reported previously for heterozygous deletion of the schizophrenia risk gene neuregulin-1.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.bbr.2007.07.006 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!