The research on mice, led by University of California, Irvine professor Gregory Brewer, provides the first evidence that circadian rhythm-altering sleep disruptions similar to jet lag promote memory problems and chemical alterations in the brain.
Clinical application of this finding may lead to more emphasis on managing the sleep habits of people at risk for Alzheimer's disease and those with mild cognitive impairment.
People with Alzheimer's often have problems with sleeping or may experience changes in their slumber schedule. Scientists do not completely understand why these disturbances occur.
"It's a chicken-or-egg dilemma, but our research points to disruption of sleep as the accelerator of memory loss," said Brewer.
In order to examine the link between learning and memory and circadian disturbances, his team altered normal light-dark patterns with an eight-hour shortening of the dark period every three days for young mouse models of Alzheimer's disease and normal mice.
The resulting jet lag greatly reduced activity in both sets of mice, and the researchers found that in water maze tests, the AD mouse models had significant learning impairments absent in the AD mouse models not exposed to light-dark variations and in normal mice with jet lag.
Glutathione is a major antioxidant that helps prevent damage to essential cellular components.
Glutathione deficiencies produce redox changes in brain cells. Redox reactions involve the transfer of electrons, which leads to alterations in the oxidation state of atoms and may affect brain metabolism and inflammation.
Brewer pointed to the accelerated oxidative stress as a vital component in Alzheimer's-related learning and memory loss and noted that potential drug treatments could target these changes in redox reactions.
The study appears in the Journal of Alzheimer's Disease.
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