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Estrogen as a neuromodulator of MPTP-induced neurotoxicity:
effects upon striatal dopamine release.
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The effects of estrogen upon MPTP-induced neurotoxicity were examined using
in vitro superfusion.

In Experiment 1, striatal tissue from ovariectomized rats was infused with
MPP+ (10 microM), a combination of MPP+ and 17beta-estradiol (300 nM), the
same dose of estradiol preceding MPP+, or no treatment infusion. The
effects of these treatments on dopamine release rates during the infusion
periods were determined. Infusion of MPP+ resulted in a significant
increase in dopamine release as compared to the control. Estradiol added to
the MPP+ infusion significantly attenuated this dopamine (DA) release,
while estradiol treatment preceding the MPP+ had no effect.

In Experiment 2, three different doses of estradiol (0.3, 3, or 300 nM)
were infused simultaneously with the MPP+. Doses of estradiol below 300 nM
did not attenuate the DA release.

In Experiment 3, estradiol alone (300 nM) was infused, to determine
dopamine release rate effects of the hormone itself.

There was no difference between estradiol treated and non-infused control
groups.

These results demonstrate that the gonadal steroid hormone estradiol can
modulate responses of striatal dopamine neurons to MPP+ by altering the
immediate increase in dopamine release which occurs in response to this
neurotoxin.

These modulating effects of estradiol are dose-dependent, and represent a
direct effect upon striatal neurons, most likely involving a non-genomic
mechanism of action.

These results implicate that hormonal modulation of nigrostriatal
dopaminergic neurotoxicity may represent an important variable responsible
for the sex differences which are reported in Parkinson's disease.


Brain Res 1997 Aug 1;764(1-2):9-16
Disshon KA, Dluzen DE
Northeastern Ohio Universities, Rootstown 44272-0095, Ohio, USA
PMID: 9295188, MUID: 97439632
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janet paterson - 50/9 - sinemet/selegiline/prozac - [log in to unmask]