Sexually inactive ("low-performing," LP) and
highly active ("high-performing," HP) rats were selected from a
sexually inexperienced population. Saline control LP rats (n = 44) lived
134.58 +/- 2.29 weeks, their HP peers (n = 49) lived 151.24 +/- 1.36
weeks. Life-long treatment with 0.25 mg/kg (-)deprenyl, a selective
inhibitor of MAO-B that also stimulates action potential-transmitter release
coupling in the catecholaminergic neurons in the brain (catecholaminergic
activity enhancer, CAE, effect), enhanced the sexual and learning
performance of both LP and HP rats and prolonged their life. LP rats (n =
48) treated with (-)deprenyl lived 152.54 +/- 1.36 weeks and HP rats on (-)deprenyl
(n = 50) lived 185.30 +/- 1.96 weeks. As an indicator of the basic
activity of catecholaminergic neurons, the resting release of dopamine from
the striatum, substantia nigra, and tuberculum olfactorium, and of
norepinephrine from the locus coeruleus, was measured in 2-, 4-, 8-, 16-,
and 32-week-old male and female rats. The release of transmitters
between weaning and the second month of age, i.e., during the crucial
developmental phase of life, was significantly higher than either before or
after that period, indicating that a CAE mechanism starts working with high
intensity after weaning, lasts until the completion of full scale sexual
development, and shows an unparalleled decay thereafter. It was
concluded that the CAE regulation in the brain, stimulated by (-)deprenyl,
controls general activity and consequently the longevity of rats.