Protein deposits associated with dementia influence brain activity during sleep.
Alzheimer’s patients frequently suffer from sleep disorders, mostly even before they become forgetful. Furthermore, it is known that sleep plays a very important role in memory formation. Researchers from the Technical University of Munich (TUM) have now been able to show for the first time how the pathological changes in the brain act on the information-storing processes during sleep. Using animal models, they were able to decode the exact mechanism and alleviate the impairment with medicinal agents.
The sleep slow waves, also known as slow oscillations, which our brain generates at night, have a particular role in consolidating what we have learned and in shifting memories into long-term storage. These waves are formed via a network of nerve cells in the brain’s cortex, and then spread out into other parts of the brain, such as the hippocampus.
“These waves are a kind of signal through which these areas of the brain send mutual confirmation to say ‘I am ready, the exchange of information can go ahead’. Therefore, there is a high degree of coherence between very distant nerve cell networks during sleep”, explains Dr. Marc Aurel Busche, scientist at the Department of Psychiatry and Psychotherapy at TUM University Hospital Klinikum rechts der Isar and TUM Institute of Neuroscience. Together with Dr. Arthur Konnerth from the Institute of Neurosciences, he headed the study which was published in the journal Nature Neuroscience.
Disrupted spread of sleep waves in Alzheimer models
As the researchers discovered, this coherence process is disrupted in Alzheimer’s disease. In their study, they used mouse models with which the defects in the brains of Alzheimer’s patients can be simulated. The animals form the same protein deposits, known as β-amyloid plaques, which are also visible in human patients. The scientists were now able to show that these plaques directlyimpair the slow wave activity. “The slow oscillations do still occur, but they are no longer able to spread properly – as a result, the signal for the information cross-check is absent in the corresponding regions of the brain,” is how Marc Aurel Busche summarizes it.
The scientists also succeeded in decoding this defect at the molecular level: correct spread of the waves requires a precise balance to be maintained between the excitation and inhibition of nerve cells. In the Alzheimer models, this balance was disturbed by the protein deposits, so that inhibition was reduced.
Low doses of sleep-inducing drugs as possible therapy
Busche and his team used this knowledge to treat the defect with medication. One group of sleep-inducing drugs, the benzodiazepines, is known to boost inhibitory influences in the brain. If the scientists gave small amounts of this sleep medication to the mice (approximately one-tenth of the standard dose), the sleep slow waves were able to spread out correctly again. In subsequent behavioral experiments, they were able to demonstrate that learning performance had now improved as well.
For the researchers, of course, these results are just a first step on the way to a suitable treatment of Alzheimer’s disease. “But, these findings are of great interest for two reasons: firstly, mice and humans have the same sleep oscillations in the brain – the results are thus transferrable. Secondly, these waves can be recorded with a standard EEG monitor, so that any impairment may also be diagnosed at an early stage”, concludes the scientist.
About this Alzheimer’s disease research
Source: Marc Aurel Busche- TUM Image Credit: The image is credited to Marc Aurel Busche / TUM Original Research:Abstract for “Rescue of long-range circuit dysfunction in Alzheimer’s disease models” by Marc Aurel Busche, Maja Kekuš, Helmuth Adelsberger, Takahiro Noda, Hans Förstl, Israel Nelken and Arthur Konnerth in Nature Neuroscience. Published online October 12 2015 doi:10.1038/nn.4137
Rescue of long-range circuit dysfunction in Alzheimer’s disease models
Alzheimer’s disease (AD) is associated with defects of synaptic connectivity. Such defects may not be restricted to local neuronal interactions but may extend to long-range brain activities, such as slow-wave oscillations that are particularly prominent during non–rapid eye movement (non-REM) sleep and are important for integration of information across distant brain regions involved in memory consolidation. There is increasing evidence that sleep is often impaired in AD, but it is unclear whether this impairment is directly related to amyloid-β (Aβ) pathology. Here we demonstrate that slow-wave activity is severely altered in the neocortex, thalamus and hippocampus in mouse models of AD amyloidosis. Most notably, our results reveal an Aβ-dependent impairment of slow-wave propagation, which causes a breakdown of the characteristic long-range coherence of slow-wave activity. The finding that the impairment can be rescued by enhancing GABAAergic inhibition identifies a synaptic mechanism underlying Aβ-dependent large-scale circuit dysfunction.
“Rescue of long-range circuit dysfunction in Alzheimer’s disease models” by Marc Aurel Busche, Maja Kekuš, Helmuth Adelsberger, Takahiro Noda, Hans Förstl, Israel Nelken and Arthur Konnerth in Nature Neuroscience. Published online October 12 2015 doi:10.1038/nn.4137