UCLA neuroscientists using a new MRI analysis technique to examine myelin sheaths that insulate the brain's wiring report that as people age, neural connections that develop last degenerate first. The computer-based analysis method is unique in its ability to examine specific brain structures in living people at millimeter resolution.
Published online by the Neurobiology of Aging earlier this year and scheduled to appear in the August 2004 print edition of the peer-reviewed journal, the study offers new insights into the role of myelin in brain aging and its contribution to the onset of Alzheimer's disease. In addition, the success of the MRI analysis technique opens new opportunities for studying the impact of lifestyle on brain aging and for developing medications that could slow aging or prevent Alzheimer's disease.
"The study increases our understanding of the role of myelin in brain development and degeneration, and demonstrates the usefulness of this MRI method for examining the single most powerful risk for Alzheimer's disease by far — age," said Dr. George Bartzokis, the study's lead investigator and visiting professor of neurology at the David Geffen School of Medicine at UCLA. He also is director of the UCLA Memory Disorders and Alzheimer's Disease Clinic and clinical core director of the UCLA Alzheimer's Disease Research Center.
Myelin is a sheet of lipid, or fat, with very high cholesterol content — the highest of any brain tissue. The high cholesterol content allows myelin to wrap tightly around axons, speeding messages through the brain by insulating these neural "wire" connections.
As the brain continues to develop in adulthood and as myelin is produced in greater and greater quantities, cholesterol levels in the brain grow and eventually promote the production of a toxic protein that together with other toxins attacks the brain. This toxic environment disrupts brain connections and eventually also leads to the brain/mind-destroying plaques and tangles visible years later in the cortex of Alzheimer's patients.
"The brain is not a computer, it is much more like the Internet," Bartzokis said. "The speed, quality and bandwidth of the connections determine its ability to process information, and all these depend in large part on the insulation that coats the brain's connecting wires.
"The results of our study show that in older age, the myelin insulation breaks down, resulting in a decline in the speed and efficiency of our Internet. Myelin and the cells that produce it are the most vulnerable component of our brain — the human brain's Achilles' heel," he said. "This safe, non-invasive technology can assess the development and degeneration of the brain's insulation in specific regions. Now that we can measure how brain aging proceeds in vulnerable regions, we can measure what treatments will slow aging down and thus begin in earnest to look at preventing Alzheimer's disease."
The UCLA research team examined the deterioration of myelin in the brain's splenium and genu regions of the corpus callosum, which connects the two sides of the brain. Neural connections important to vision develop early in life in the splenium, while connections important to decision‑making, memory, impulse control and other higher functions develop later in the genu.
The team found that the brain connections deteriorated three times as fast in the genu compared to the splenium. The study also notes that myelin deterioration is far greater throughout the brain of patients with Alzheimer's disease than in healthy older adults. The late myelinating regions are much more vulnerable and may be why the highest levels of reasoning and new memories are the first to go when one develops Alzheimer's disease, while movement and vision are unaffected until very late in the disease process.
We need a way to reseed the brain with the cells that make myelin. We also need ways to remove the accumulated toxic compounds that accumulate in the intercellular spaces as well as the toxic compounds (and junk that simply takes up increasing space) that accumulate inside cells. These are 3 of the 7 basic Strategies for Engineered Negligible Senescence (SENS) which you ought to read all about if you haven't already.
This result comes on the heels of another recent study that found brains older than 40 show lots of signs of damaged genes and expression of more repair and inflammation enzymes.
Update: Note how once again a new technique that enables the measurement of phenomena which were not previously measurable has enabled new discoveries to be made. While this initial discovery is interesting the technique itself will be more important in the long run because it will enable many more future discoveries. Better scientific tools are more important than any particular discoveries made with the tools.
|Share |||Randall Parker, 2004 July 13 03:25 PM Brain Aging|