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Some people, no matter how old they get, never lose their beauty—they
merely move it from their faces into their hearts.”

Martin Buxbaum,
1912-1990



Home » Daily News

Feb. 4 - Estrogen Like Compound May Reduce Risk for Alzheimer's in Mice

New research accepted for publication in the journal Endocrinology reveals that mice with induced Alzheimer's like symptoms had improved cognitive function when given the synthetic estrogen-like hormone propylpyrazole triol (PPT).

"This synthetic hormone improved behavior much the way that estrogen does," said study leader Dr. Christian Pike, associate professor at the University of Southern California's School of Gerontology. But unlike estrogen, which enlarges the uterus and is a known risk factor for endometrial and breast cancer, PPT caused no obvious changes to the animals' reproductive tract.

"This may be a promising strategy to maximize hormone therapy benefits and minimize its risk," said Pike.

Estrogen based hormone therapy has long been studied as a therapeutic option for postmenopausal women to reduce the risk of several age-related disorders, including osteoporosis and Alzheimer's disease. Some studies have suggested that estrogen may lower the risk of Alzheimer's. This hormone, however, has also been associated with a number of adverse health effects.

A potential alternative approach to estrogen-based hormone therapy is a synthetic form of the hormone known as selective estrogen receptor modulators (SERMs). SERMs can have the same effect as estrogen, but specifically target certain tissues and certain parts of the body. Two recently developed SERMs PPT and diarylpropionitrile (DPN) have been shown to protect cultured neurons from damage.

For their study, the researchers examined the effects of estrogen, PPT, and DPN on female mice. The data confirmed previous studies showing that estrogen significantly reduced the buildup in the brain of the protein beta amyloid, which has been implicated in the development of Alzheimer's disease. Estrogen also reduced cognitive decline in the mice.

Source: Endocrine Society

 

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