The rapidly advancing technology in the area of molecular neuroscience
has greatly expanded the tools available to behavioural pharmacologis
ts for investigating the molecular bases underlying the interrelation
of pharmacological agents and behaviour, Strategies such as gene targe
ted knockout mutations, expression of an exogenous transgene, as well
as the disruption of the cellular expression of genes with antisense o
ligonucleotides, are being successfully used to study normal and impai
red behavioural function. Advantages of these genetic methods include
the ability to manipulate systems for which selective pharmacological
ligands do not exist, and the opportunity to study the interaction bet
ween genotype and environment without having to rely on spontaneously
occurring mutants or selective breeding programmes. By targeting parti
cular genes, questions can be asked about how genes control neuronal f
unction and how manipulations of these genes affect behaviour, In part
icular, these strategies have been applied to studies of the molecular
bases for disrupted behaviours, the behavioural actions of psychoacti
ve drugs, and models of neuropsychiatric and neuropathological disorde
rs, These emerging molecular biological techniques complement traditio
nal pharmacological analysis to provide a very powerful approach with
which to study the molecular correlates of behavioural pharmacology.