Can't sleep? Blame these neurons
A “sleep switch” in the brain that helps explain why older people can't get a good night's rest
New research led by University of Toronto neurologist Andrew Lim sheds light on sleep disruption in aging adults.
"In many older people with insomnia and other patterns of sleep disruption, the underlying cause is unknown,” said Lim, assistant professor of neurology and neuroscientist at Sunnybrook Health Sciences.
“We provide evidence that loss of neurons in a particular region of the brain that controls sleep may be an important contributor to insomnia in many older individuals.”
Reported online August 20 in the journal Brain, the new findings demonstrate for the first time that a group of inhibitory neurons, whose loss leads to sleep disruption in experimental animals, is substantially diminished among the elderly and individuals with Alzheimer’s disease. (See the journal article.)
“These findings may one day lead to novel treatments for insomnia and other patterns of sleep disruption in old age, thereby improving quality of life,” said Lim. “And given recent evidence that sleep disruption may predispose to or potentiate the development of Alzheimer's disease, perhaps even prevent or slow the progression of Alzheimer's disease.”
On average, people in their seventies have about one hour less sleep per night than those in their twenties, said co-author Clifford B. Saper, MD, PhD, chairman of neurology at Beth Israel Deaconess Centre and James Jackson Putnam Professor of Neurology at Harvard Medical School.
“Sleep loss and sleep fragmentation is associated with a number of health issues, including cognitive dysfunction, increased blood pressure and vascular disease, and a tendency to develop type 2 diabetes," Saper said. "It now appears that loss of these neurons may be contributing to these various disorders as people age.”
In 1996, the Saper lab first discovered that a key cell group of inhibitory neurons was functioning as a “sleep switch” in rats, turning off the brain’s arousal systems to enable animals to fall asleep.
“Our experiments in animals showed that loss of these neurons produced profound insomnia, with animals sleeping only about 50 percent as much as normal and their remaining sleep being fragmented and disrupted,” he said.
A group of cells in the human brain is located in a similar location and has the same inhibitory neurotransmitter as the rats. The authors hypothesized that if the humans' intermediate nucleus was important for human sleep and was homologous to the animal’s ventrolateral preoptic nucleus, then it may also similarly regulate humans’ sleep-wake cycles.
In order to test this hypothesis, the investigators analyzed data from the Rush Memory and Aging Project, a community-based study of aging and dementia. The project began in 1997 and has been following a group of almost 1,000 subjects who entered the study as healthy 65-year-olds and are followed until their deaths, at which point their brains are donated for research.
"Since 2005, most of the subjects in the Memory and Aging Project have been undergoing actigraphic recording every two years. This consists of their wearing a small wristwatch-type device on their non-dominant arm for seven to 10 days,” said Lim, a former member of the Saper lab. The actigraphy device, which is waterproof, is worn 24 hours a day and thereby monitors all movements, large and small, divided into 15-second intervals.
“Our previous work had determined that actigraphic readings indicating absence of movement for five minutes or longer correlated with sleep intervals,” Lim said.
The authors examined the brains of 45 study subjects (with a median age at death of 89.2), identifying ventrolateral preoptic neurons by staining the brains for the neurotransmitter galanin. They then correlated the actigraphic rest-activity behaviour of the 45 individuals in the year prior to their deaths with the number of remaining ventrolateral preoptic neurons at autopsy.
“We found that in the older patients who did not have Alzheimer’s disease, the number of ventrolateral preoptic neurons correlated inversely with the amount of sleep fragmentation,” said Saper. “The fewer the neurons, the more fragmented the sleep became.”
The subjects with the largest number of neurons (greater than 6,000) spent 50 per cent or more of the sleep time in prolonged periods of non-movement, while subjects with the fewest ventrolateral preoptic neurons (fewer than 3,000) spent less than 40 per cent of their nights in extended periods of sleep. The results further showed that among Alzheimer’s patients, most sleep impairment seemed to be related to the number of ventrolateral preoptic neurons that had been lost.
Michael Kennedy writes about health issues for U of T News.