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Ann N Y Acad Sci 1998 May 30;844:153-65

The impact of gender and estrogen on striatal dopaminergic neurotoxicity.

Miller DB, Ali SF, O'Callaghan JP, Laws SC
Toxiology & Molecular Biology Branch, CDC/NIOSH, Morgantown, West Virginia
26505-2888, USA. [log in to unmask]

The reproductive properties of estrogen are well established, but it is now
evident that this steroid hormone has substantial modulatory capabilities in
nonreproductive systems. For example, estrogen may be neuroprotective as
Alzheimer's disease progresses more slowly in women receiving hormone
replacement therapy, and Parkinson's disease affects more men than women.
Gender affects both the functional biochemical responses of the
nigral-striatal pathway to dopaminergically active compounds. To begin to
evaluate the possible neuroprotective effects of estrogen in this pathway,
we first determined if gender affected dopaminergic striatal neurotoxicity
induced by two different neurotoxicants,
1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and methamphetamine
(METH). Both agents induced greater neurotoxicity in males than females as
evidenced by greater striatal dopamine (DA) depletions. An examination of
striatal levels of 1-methyl-4-phenylpyridium ion (MPP+) following MPTP
treatment established that the observed gender differences were not due to
metabolic/pharmacokinetic variables. The neurotoxicity of MPTP was then
examined in ovariectomized (OVX) mice. Estrogen replacement reduced the DA,
dihydroxyphenylacetic acid (DOPAC) and homovanillic acid (HVA) depletions as
well as the glial fibrillary acidic protein (GFAP) elevation induced by
MPTP, which indicates that estrogen has neuroprotective properties in this
model of striatal dopaminergic neurotoxicity. Surprisingly, estrogen
supplementation did not protect against the neurotoxic effects of MPTP in
intact 2-yr-old intact female mice, suggesting that low endogenous levels of
estrogen may provide neuroprotection.

PMID: 9668673, UI: 98333270
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