a third significant finding was the aging hotspot, an area in the brain that experienced a high level of inflammation and decreased brain cell function: the hypothalamus. this section manages internal functions in the body, including those performed by the autonomic nervous system, such as heart rate, blood pressure, and body temperature. it also controls appetite, salt and water balance, hormone production and regulation, mood, memory, behaviour, sleep regulation, and sexual health.
the researchers then discovered that these gene expression changes were even more significant in a specific area of the hypothalamus known as the third ventricle. this area is responsible for energy homeostasis, metabolism, and food intake. because of its prominent role in brain changes caused by aging, it was dubbed the aging hotspot.
due to the third ventricle’s functional support of how the body utilizes energy and nutrients, the researchers now believe that lifestyle, diet, and brain aging are strongly connected to the risk of age-related brain disorders.
“our hypothesis is that those cell types are getting less efficient at integrating signals from our environment or from things that we’re consuming,” said kelly jin, ph.d., a scientist at the allen institute for brain science and lead author of the study in a press release. “and that loss of efficiency somehow contributes to what we know as aging in the rest of our body. i think that’s pretty amazing, and i think it’s remarkable that we’re able to find those very specific changes with the methods that we’re using.”
what this means for the aging population
the target outlined by this study is one that many medical professionals have known to be associated with ailing health: lifestyle and diet. the role of diet has long been seen as a precursor to good health and an effective tool to reduce the risk of other diseases, including heart disease and type 2 diabetes. now, they know that aging is another aspect of health strongly associated with what you choose to fuel yourself with because of these cell changes.