Genetic instability is generally thought to underlie the process of ag
ing and is predominantly associated with meiosis and mitosis. This rev
iew will discuss DNA damage and repair, somatic mutations and somatic
recombination events in non-dividing neurons in relation to aging. In
general it can be concluded that mutagenesis operates at high frequenc
y in the brain. Present data do not provide clear evidence for accumul
ating DNA damage or a change in DNA repair activity in the brain with
age. However, a linear age-related increase in frameshift mutations ha
s been shown to occur in vasopressin neurons of the rat, revealing a n
ovel post-mitotic mechanism.