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Vol. 289, Issue 1, 334-345, April 1999
Department of Pharmacology and Cancer Biology, Duke University
Medical Center, Durham, North Carolina (T.A.S., E.C.M., J.Z., F.J.S.);
Health Effects Laboratory Division, Centers for Disease
Control/National Institute of Occupational Safety and Health,
Morgantown, West Virginia (D.B.M.);
Center of Neuropharmacology,
Institute of Pharmacological Sciences, Milan, Italy (F.F.); and
Department of Psychiatry and Human Behavior, University of Mississippi
Medical Center, Jackson, Mississippi (G.B.)
Geriatric depression exhibits biological and therapeutic differences
relative to early-onset depression. We studied olfactory bulbectomy
(OBX), a paradigm that shares major features of human depression, in
young versus aged rats to determine mechanisms underlying these
differences. Young OBX rats showed locomotor hyperactivity and a loss
of passive avoidance and tactile startle. In contrast, aged OBX animals
maintained avoidance and startle responses but showed greater locomotor
stimulation; the aged group also exhibited decreased grooming and
suppressed feeding with novel presentation of chocolate milk, effects
which were not seen in young OBX. These behavioral contrasts
were accompanied by greater atrophy of the frontal/parietal cortex and
midbrain in aged OBX. Serotonin transporter sites were increased in the
cortex and hippocampus of young OBX rats, but were decreased in the
aged OBX group. Cell signaling cascades also showed age-dependent
effects, with increased adenylyl cyclase responses to monoaminergic
stimulation in young OBX but no change or a decrease in aged OBX. These
data indicate that there are biological distinctions in effects of OBX
in young and aged animals, which, if present in geriatric depression,
provide a mechanistic basis for differences in biological markers and drug responses. OBX may provide a useful animal model with which to
test therapeutic interventions for geriatric depression.
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