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Deprenyl increases the life span as well
as activities of superoxide dismutase and catalase but not of glutathione
peroxidase in selective brain regions in Fischer rats
Kitani K, Kanai S, Carrillo MC, Ivy GO
Radioisotope Research Institute
Faculty of Medicine
University of Tokyo, Japan
Ann N Y Acad Sci 1994 Jun 30; 717:60-71
ABSTRACT
(-)Deprenyl, a MAO-B inhibitor that is also
known to be effective for symptoms of Parkinson's disease, when injected
subcutaneously (sc) in male Fischer-344 rats at a dose of 0.5 mg/kg per day
(3 times a week) from 18 months of age, significantly increased the
remaining life expectancy. The average life span after 24 months was 34%
greater in treated rats than in saline-treated control animals. Furthermore,
a short-term (3 wk) continuous sc infusion of deprenyl significantly
increased activities of superoxide dismutase and catalase but not of
glutathione peroxidase in selective brain regions such as s. nigra,
striatum, and cerebral cortex, but not in hippocampus or cerebellum, or the
liver. The optimal dose for increasing these activities, however, differed
greatly depending on the sex and age of animals, with a 10-fold lower value
for young female than male rats. Interestingly, aging caused an increase and
a decrease in the optimal dose in female and male rats, respectively. In
addition, treatment for a longer term tended to reduce the optimal dosage in
the same animal group. The results clearly demonstrate that deprenyl
increases antioxidant enzyme activities in selective brain regions.
If this
effect of deprenyl is causally related to its life-prolonging effect, the
dosage to be used for any life span study would be a critical factor, with
the dosage differing widely depending on sex, age of animal, and mode and
duration of drug administration.
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