Ibogaine is claimed to be an effective treatment for opiate and stimul
ant addiction. O'Hearn and Molliver, however, showed that ibogaine cau
ses degeneration of cerebellar Purkinje cells in rats. The present stu
dy re-examined cerebellar responses to the high doses of ibogaine used
by O'Hearn and Molliver (100 mg/kg or 3 x 100 mg/kg) and sought to de
termine whether a lower dose (40 mg/kg), one effective in reducing mor
phine and cocaine self-administration, produced similar responses. Pur
kinje cell degeneration was evaluated with a Fink-Heimer II stain, and
enhanced glial cell activity with an antibody to glial fibrillary aci
dic protein. Every rat treated with the high dose of ibogaine displaye
d clear evidence of Purkinje cell degeneration. The degeneration consi
stently occurred in the intermediate and lateral cerebellum, as well a
s the vermis. Purkinje cells in lobules 5 and 6 were particularly susc
eptible. Given the response properties of cells in these lobules, this
finding suggests any long-term motor deficits produced by ibogaine-in
duced degeneration should preferentially affect the head and upper ext
remity. In marked contrast, rats given the smaller dose of ibogaine di
splayed no degeneration above the level seen in saline-treated animals
. When combined with information on other compounds, these data sugges
t that the degenerative and 'anti-addictive' properties of ibogaine re
flect different actions of the drug.