is located in the limbic lobe. Recent research has found neurons here that are responsive to landmarks.
Do older adults forget as much as they think, or is it rather that they ‘misremember’?
A small study adds to evidence that gist memory plays an important role in false memories at any age, but older adults are more susceptible to misremembering because of their greater use of gist memory.
A meta-analysis of studies reporting brain activity in individuals with a diagnosis of PTSD has revealed differences between the brain activity of individuals with PTSD and that of groups of both trauma-exposed (those who had experienced trauma but didn't have a diagnosis of PTSD) and trauma-naïve (those who hadn't experienced trauma) participants.
The critical difference between those who developed PTSD and those who experienced trauma but didn't develop PTSD lay in the basal ganglia. Specifically:
September 2009
A study using healthy older adults from Holland's long-term Maastricht Aging Study found that the 35 cognitively healthy people who stayed free of dementia showed no significant decline in gray matter, but the 30 people who showed substantial cognitive decline although still dementia-free showed a significant reduction in brain tissue in the hippocampus and parahippocampal areas, and in the frontal and cingulate cortices. The findings suggest that atrophy in the normal older brain may have been over-estimated in earlier studies, by not screening out people whose undetected, slowly developing brain disease was killing off cells in key areas.
Burgmans, S. et al. 2009. The Prevalence of Cortical Gray Matter Atrophy May Be Overestimated In the Healthy Aging Brain. Neuropsychology, 23 (5), 541-550.
http://www.eurekalert.org/pub_releases/2009-09/apa-hob090309.php
June 2009
An imaging study has revealed that when people were shown a composite image with a face surrounded by "place" images, such as a house, and asked to identify the gender of the face, those in whom a bad mood had been induced didn’t process the places in the background. However, those in a good mood took in both the focal and background images. These differences in perception were coupled with differences in activity in the parahippocampal place area. Increasing the amount of information is of course not necessarily a good thing, as it may result in more distraction.
Schmitz, T.W., De Rosa, E. & Anderson, A.K. 2009. Opposing Influences of Affective State Valence on Visual Cortical Encoding. Journal of Neuroscience, 29 (22), 7199-7207.
http://www.eurekalert.org/pub_releases/2009-06/uot-pww060309.php
January 2006
A study of 54 postmenopausal women (aged 58 to 80) suggests that being physically fit offsets cognitive declines attributed to long-term hormone-replacement therapy. It was found that gray matter in four regions (left and right prefrontal cortex, left parahippocampal gyrus and left subgenual cortex) was progressively reduced with longer hormone treatment, with the decline beginning after more than 10 years of treatment. Therapy shorter than 10 years was associated with increased tissue volume. Higher fitness scores were also associated with greater tissue volume. Those undergoing long-term hormone therapy had more modest declines in tissue loss if their fitness level was high. Higher fitness levels were also associated with greater prefrontal white matter regions and in the genu of the corpus callosum. The findings need to be replicated with a larger sample, but are in line with animal studies finding that estrogen and exercise have similar effects: both stimulate brain-derived neurotrophic factor.
Erickson, K.I., Colcombe, S.J., Elavsky, S., McAuley, E., Korol, D., Scalf, P.E. & Kramer, A.F. 2006. Interactive effects of fitness and hormone treatment on brain health in postmenopausal women. Neurobiology of Aging, In Press, Corrected Proof, Available online 6 January 2006
http://www.eurekalert.org/pub_releases/2006-01/uoia-fcc012406.php
September 2003
Researchers monitored signals from individual brain cells as patients played a computer game in which they drove around a virtual town in a taxi, searching for passengers who appeared in random locations and delivering them to their destinations. Previous research has found specific cells in the brains of rodents that respond to “place”, but until now we haven’t known whether humans have such specific cells. This study identifies place cells (primarily found in the hippocampus), as well as “view” cells (responsive to landmarks; found mainly in the parahippocampal region) and “goal” cells (responsive to goals, found throughout the frontal and temporal lobes). Some cells respond to combinations of place, view and goal — for example, cells that responded to viewing an object only when that object was a goal.
Ekstrom, A.D., Kahana, M.J., Caplan, J.B., Fields, T.A., Isham, E.A., Newman, E.L. & Fried, I. 2003. Cellular networks underlying human spatial navigation.Nature, 425 (6954), 184-7.
http://www.eurekalert.org/pub_releases/2003-09/uoc--vgu091003.php
A pilot study involving 17 older adults with mild cognitive impairment and 18 controls (aged 60-88; average age 78) has found that a 12-week exercise program significantly improved performance on a semantic memory task, and also significantly improved brain efficiency, for both groups.
I’ve reported before on how London taxi drivers increase the size of their posterior hippocampus by acquiring and practicing ‘the Knowledge’ (but perhaps at the expense of other functions). A new study in similar vein has looked at the effects of piano tuning expertise on the brain.
Back when I was young, sleep learning was a popular idea. The idea was that a tape would play while you were asleep, and learning would seep into your brain effortlessly. It was particularly advocated for language learning. Subsequent research, unfortunately, rejected the idea, and gradually it has faded (although not completely). Now a new study may presage a come-back.
Memory begins with perception. We can’t remember what we don’t perceive, and our memory of things is influenced by how we perceive them.
Our ability to process visual scenes has been the subject of considerable research. How do we process so many objects? Some animals do it by severely limiting what they perceive, but humans can perceive a vast array of features. We need some other way of filtering the information. Moreover, it’s greatly to our advantage that we can process the environment extremely quickly. So that’s two questions: how do we process so much, and so fast?
A two-year study involving 53 older adults (60+) has found that those with a mother who had Alzheimer's disease had significantly more brain atrophy than those with a father or no parent with Alzheimer's disease. More specifically, they had twice as much gray matter shrinkage, and about one and a half times more whole brain shrinkage per year.
This atrophy was particularly concentrated in the precuneus and parahippocampal gyrus. Those with the APOE4 gene also had more atrophy in the frontal cortex than those who didn’t carry the ‘Alzheimer’s gene’.
Comparison of 17 people with severe obstructive sleep apnea (OSA) with 15 age-matched controls has revealed that those with OSA had reduced gray matter in several brain regions, most particularly in the left parahippocampal gyrus and the left posterior parietal cortex, as well as the entorhinal cortex and the right superior frontal gyrus. These areas were associated with deficits in abstract reasoning and executive function. Deficits in the left posterior parietal cortex were also associated with daytime sleepiness.
A study involving young (average age 22) and older adults (average age 77) showed participants pictures of overlapping faces and places (houses and buildings) and asked them to identify the gender of the person. While the young adults showed activity in the brain region for processing faces (fusiform face area) but not in the brain region for processing places (parahippocampal place area), both regions were active in the older adults.