Rasagiline [R(+)-N-propargyl-1-aminoindane] is a selective irreversibl
e inhibitor of MAO-B which is not metabolised to amphetamine-like deri
vatives. Like deprenyl, when given to rats in a dose selective for inh
ibition of MAO-B, it does not affect striatal extracellular fluid dopa
mine levels, but when administered chronically (21 days) it increased
striatal microdialysate dopamine without reduction in deaminated metab
olites. Similarly to deprenyl, rasagiline (10(-6)M) increased the perc
entage of tyrosine hydroxylase positive cells in a primary culture of
rat fetal mesencephalic cells (6 days in culture). Rasagiline, but not
deprenyl, also increased the number of neurons per held in this organ
otypic culture.