Estrogen Deprivation Leads To Death Of Dopamine Cells In The Brain.
Estrogen deprivation leads to the death of dopamine cells in the brain, a
finding by Yale researchers that could have implications for
post-menopausal women. The cells can be regenerated if estrogen is
administered within 10 days, but by 30 days, the cells appear to be
permanently lost, said D. Eugene Redmond, Jr., professor of psychiatry and
neurosurgery at Yale School of Medicine and director of the Neural
Transplantation and Regeneration Program. Redmond is co-investigator and
spokesperson about the study published in the December issue of The Journal
of Neuroscience.
The principal investigator was Csaba Leranth, M.D., professor of obstetrics
and gynecology and neurobiology.
"Without estrogen, more than 30 percent of all the dopamine neurons
disappeared in a major area of the brain that produces the
neurotransmitter, dopamine, " Redmond said. "This finding is consistent
with a lot of observations for which there has been, until now, no
explanation. The results of the study shed light on why men, who have less
estrogen in their bodies and more androgen to antagonize it, are more
likely to develop Parkinson's Disease than pre-menopausal women, and why
post menopausal women are more likely then to develop the disease."
The discovery was made after the researchers removed the ovaries of female
monkeys, thereby depleting their bodies of estrogen and other gonadal
hormones. Within 10 days, key neurons in the brain that protect against
Parkinson's Disease disappeared. Redmond said monkeys were used in the
study because, unlike usual laboratory animals, they have real menstrual
cycles and many other close similarities to humans.
The researchers were interested in sexual differences in dopamine neurons
in the substantia nigra area of the midbrain, whose destruction is
associated with Parkinson's Disease and dementia. The researchers first
sought to determine whether circulating estrogen might have long term
effects by altering the number of dopamine neurons. The density of dopamine
neurons was calculated in the substantia nigra of intact male and female
primates; in female primates whose ovaries had been removed; and in female
primates whose ovaries had been removed but were receiving estrogen
replacement therapy.
"After both 10 and 30 days of estrogen deprivation, apparently 30 percent
of the total number of substantia nigra dopamine cells are lost," Redmond
said. "Furthermore, the density calculations showed that brief estrogen
replacement restores the density of the total number of neurons in that
area of the brain 10 days after the ovaries have been removed, but not 30
days later."
"These observations show the essential role of estrogen in maintaining the
integrity of the nigral dopamine system involved in muscle control and
higher brain functions. It suggests a new prevention or treatment strategy
for patients at risk of Parkinson's disease and certain forms of
memory-impairing disorders,"he said.
"This also provides another rationale for estrogen replacement therapy for
postmenopausal women. Thirty percent is a very significant number of cells
in this system. Maintenance, restoration, or loss of that many cells could
make the difference between severe parkinsonism and having no symptoms at
all." But Redmond cautioned that women should not use the results to make a
decision about estrogen replacement therapy until further studies look at
the effects on dopamine cells of much longer periods of estrogen
deprivation.
Redmond said the researchers also want to see if much larger doses of
estrogen or other hormones administered at 30 days and beyond of estrogen
deprivation would resuscitate the cells. All of this must be in the context
of possible side effects of hormone replacement that women should take into
account in consultation with their doctors.
Other investigators were Robert Roth, professor of psychiatry and
pharmacology; John Elsworth, senior research scientist, psychiatry;
Frederick Naftolin, M.D., professor of obstetrics and gynecology and of
molecular, cellular and developmental biology, and Tamas Horvath, associate
professor of obstetrics and gynecology and neurobiology.
The study was carried out at the St. Kitts Biomedical Research Foundation
in the West Indies.
Copyright © 1996-2000 The National Parkinson Foundation, Inc.
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