Neurogenesis (the birth of new neurons) continues postnatally and into adul
thood in the brains of many animal species, including humans. This is parti
cularly prominent in the dentate gyrus of the hippocampal formation. One of
the factors that potently suppresses adult neurogenesis is stress, probabl
y due to increased glucocorticoid release. Complementing this, we have rece
ntly found that increasing brain levels of serotonin enhance the basal rate
of dentate gyrus neurogenesis. These and other data have led us to propose
the following theory regarding clinical depression. Stress-induced decreas
es in dentate gyrus neurogenesis are an important causal factor in precipit
ating episodes of depression. Reciprocally, therapeutic interventions for d
epression that increase serotonergic neurotransmission act at least in part
by augmenting dentate gyrus neurogenesis and thereby promoting recovery fr
om depression. Thus, we hypothesize that the waning and waxing of neurogene
sis in the hippocampal formation are important causal factors, respectively
, in the precipitation of, and recovery from, episodes of clinical depressi
on.