Skip to content

Some Good News About The Aging Brain

Nice to hear that a new study found that across the lifespan, human brains are capable of producing new neurons (neurogenesis). Neurons are nerve cells, what we popularly call brain cells, and are the basic working unit of the nervous system. The human brain contains about 100 billion neurons.

The researchers did find some age differences (e.g. with age there was less neuroplasticity or the brain's ability to reorganize itself by forming new neural connections, and a decline in angiogenesis - the development of new blood vessels). But still... the findings are reassuring. Interesting how the researchers did the study. They examined 28 brains (specifically, newly formed neurons and the state of blood vessels within the hippocampus) right after death from previously healthy people (aged 14 to 79), who died suddenly.

While they found age differences, they did not find gender differences. The researchers summarized that healthy older subjects without cognitive impairment (meaning they were mentally healthy), neuropsychiatric disease, or treatment (e.g. depression drugs or psychotropic drugs) display preserved neurogenesis (produce new neurons) throughout life. From Science Daily:

Older adults grow just as many new brain cells as young people

Researchers show for the first time that healthy older men and women can generate just as many new brain cells as younger people.

There has been controversy over whether adult humans grow new neurons, and some research has previously suggested that the adult brain was hard-wired and that adults did not grow new neurons. This study, to appear in the journal Cell Stem Cell on April 5, counters that notion. Lead author Maura Boldrini, associate professor of neurobiology at Columbia University, says the findings may suggest that many senior citizens remain more cognitively and emotionally intact than commonly believed.

"We found that older people have similar ability to make thousands of hippocampal new neurons from progenitor cells as younger people do," Boldrini says. "We also found equivalent volumes of the hippocampus (a brain structure used for emotion and cognition) across ages. Nevertheless, older individuals had less vascularization and maybe less ability of new neurons to make connections."

The researchers autopsied hippocampi from 28 previously healthy individuals aged 14-79 who had died suddenly. This is the first time researchers looked at newly formed neurons and the state of blood vessels within the entire human hippocampus soon after death. (The researchers had determined that study subjects were not cognitively impaired and had not suffered from depression or taken antidepressants, which Boldrini and colleagues had previously found could impact the production of new brain cells.)

In rodents and primates, the ability to generate new hippocampal cells declines with age. Waning production of neurons and an overall shrinking of the dentate gyrus, part of the hippocampus thought to help form new episodic memories, was believed to occur in aging humans as well.

The researchers from Columbia University and New York State Psychiatric Institute found that even the oldest brains they studied produced new brain cells. "We found similar numbers of intermediate neural progenitors and thousands of immature neurons," they wrote. Nevertheless, older individuals form fewer new blood vessels within brain structures and possess a smaller pool of progenitor cells -- descendants of stem cells that are more constrained in their capacity to differentiate and self-renew.

Boldrini surmised that reduced cognitive-emotional resilience in old age may be caused by this smaller pool of neural stem cells, the decline in vascularization, and reduced cell-to-cell connectivity within the hippocampus. "It is possible that ongoing hippocampal neurogenesis sustains human-specific cognitive function throughout life and that declines may be linked to compromised cognitive-emotional resilience," she says.

Leave a Reply

Your email address will not be published. Required fields are marked *