A new study has shown that estrogen reduces the mitochondria induced high levels of oxidative stress, believed to play a role in the pathogenesis of Alzheimer's disease, by increasing the ability of the mitochondria to generate energy.
As the major source of free radicals in cells, mitochondria contribute to the high levels of oxidative stress believed to play a role in the pathogenesis of Alzheimer's disease.
According to Dr. Roberta Brinton, University of Southern California, estrogen decreases this oxidative stress caused by the mitochondria while increasing the ability of the mitochondria to generate energy.
This increased ability to produce energy is important since there is usually an energy deficit in the Alzheimer brain, said Dr. Brinton.
Mitochondria, small organelles within the cells, use a process called Oxidative Phosphorylation to generate the vast majority of the adenosine triposphate (ATP) molecules that cells utilize to function properly. If the mitochondria become less efficient with age or disease, they use less up oxygen during this process.
This inefficiency produces a double hit against the brain: fewer energy molecules being produced and more free radicals being released, leading to damaging oxidative stress.
Using a combination of biochemical and proteomic (protein) approaches, Dr. Brinton's research team demonstrated how estrogen acts to regulate mitochondrial function in ways pivotal for protection against Alzheimer's disease.
These include: an increase of mitochondrial efficiency, enhancing the organelles' ability to generate energy-laden ATP molecules needed by the brain; increased expression of key proteins required for ATP generation; reduction of oxidative stress, protecting neurons from oxidative damage; prevention of excess apoptosis, or programmed cell death, of neurons of the brain; and protection of neurons from mitochondrial toxins, which can induce further mitochondrial dysfunction and cell death.
Dr. Brinton and her research team currently are validating the energy-production levels of mitochondria as a biomarker that could detect the presence of Alzheimer's in the earliest stages, when the neurodegenerative process might be stopped or slowed or therapeutics be more effective.
They believe this new information on how estrogen regulates mitochondrial function also sheds light on how to develop a new generation of effective Alzheimer therapeutics.
Dr. Brinton currently is developing new, brain specific molecules that promote neurological defense against Alzheimer's, using similar mechanisms as estrogen, but without estrogen's negative side effects.
The research presented at Experimental Biology 2008 was supported by the National Institutes of Health.