1241 GMT May 27, 2018
The researchers studied the brains of Nile grass rats (which, like humans, are diurnal and sleep at night) after exposing them to dim and bright light for four weeks, according to sciencedaily.com.
The rodents exposed to dim light lost about 30 percent of capacity in the hippocampus, a critical brain region for learning and memory, and performed poorly on a spatial task they had trained on previously.
The rats exposed to bright light, on the other hand, showed significant improvement on the spatial task.
Further, when the rodents that had been exposed to dim light were then exposed to bright light for four weeks (after a month-long break), their brain capacity — and performance on the task — recovered fully.
The study, funded by the National Institutes of Health, is the first to show that changes in environmental light, in a range normally experienced by humans, leads to structural changes in the brain. Americans, on average, spend about 90 percent of their time indoors, according to the Environmental Protection Agency.
Antonio ‘Tony’ Nunez, psychology professor and co-investigator on the study, said, "When we exposed the rats to dim light, mimicking the cloudy days of Midwestern winters or typical indoor lighting, the animals showed impairments in spatial learning.
"This is similar to when people can't find their way back to their cars in a busy parking lot after spending a few hours in a shopping mall or movie theater."
Nunez collaborated with Lily Yan, associate professor of psychology and principal investigator on the project, and Joel Soler, a doctoral graduate student in psychology.
Soler is also lead author of a paper on the findings published in the journal Hippocampus.
Soler said that sustained exposure to dim light led to significant reductions in a substance called brain derived neurotrophic factor — a peptide that helps maintain healthy connections and neurons in the hippocampus — and in dendritic spines, or the connections that allow neurons to ‘talk’ to one another.
He said, "Since there are fewer connections being made, this results in diminished learning and memory performance that is dependent upon the hippocampus.
"In other words, dim lights are producing dimwits."
Interestingly, light does not directly affect the hippocampus, meaning it acts first other sites within the brain after passing through the eyes.
Yan said the research team is investigating one potential site in the rodents' brains — a group of neurons in the hypothalamus that produce a peptide called orexin that's known to influence a variety of brain functions.
One of their major research questions: If orexin is given to the rats that are exposed to dim light, will their brains recover without being re-exposed to bright light?
The project could have implications for the elderly and people with glaucoma, retinal degeneration or cognitive impairments.
Yan said, "For people with eye disease who don't receive much light, can we directly manipulate this group of neurons in the brain, bypassing the eye, and provide them with the same benefits of bright light exposure?
"Another possibility is improving the cognitive function in the aging population and those with neurological disorders. Can we help them recover from the impairment or prevent further decline?"