Sunday, September 23, 2012

Brain Aging: What's Rise of Nations Got To Do With It?

The brain is a profoundly interconnected organ. It is made up of approximately 60% white matter and 40% gray matter (1). The white matter, which makes up the central core of the brain, is widely responsible for interneuron communication at different locations. In the human lifespan, the brain undergoes a lot of morphological changes including aging and atrophy. This atrophy includes decline in white matter integrity as well as in cortical thickness.

Dr. Maren Strenziok, a post-doctoral fellow at George Mason University's Arch Lab presented the research that she and numerous other faculty and students are currently involved in. The backbone of their research consists of conducting training and longitudinal studies in healthy aging. These studies are vital as they attempt to make sense of why the brain undergoes decline with age. Decline begins at the age of 30-40 years and is steady in terms of brain tissue integrity. On average, cognitive function and fluid abilities and intelligence decline, but this does not occur in everyone. About 30-50% of people show no decline in cognitive function. Different factors including diet, exercise, education, and genetic and social factors are studied for any correlation and to help explain this phenomenon (2).


This image is of a diffusion tensor imaging scan. DTI scans of
a healthy brain add color to its white matter.
http://www.dana.org/news/brainwork/detail.aspx?id=5322

Brain aging has been studied using magnetic resonance imaging (MRI). Dr. Strenziok introduced the techniques used and focused mainly on two types of MRI techniques: diffusion tensor imaging (DTI) and functional magnetic resonance imaging (fMRI). DTI is an MRI technique that allows for the measurement of fractional anisotropy, the random diffusion of water molecules in the brain. Higher fractional anisotropy (FA) reflects better white matter fiber integrity while a decline in FA is indicative of decreasing white matter health. Functional MRI is a technique that helps in mapping the specific regions of the brain engaged in certain tasks, processes or emotions. It works by detecting changes in blood flow related to neural activity of brain cells. It was used to measure the functional connectivity of the brain when in default mode network (DMN).
                        
This image depicts four fMRI brain scans obtained during a visual memory task.
http://berkeley.edu/news/media/releases/2000/11/20_mri.html

In the study conducted at the Arch Lab, a video game known as 'Rise of Nations' was used. This video game was previously shown to have benefited older people and an increase in white matter integrity and improved intellectual ability have been noted. Training was conducted in individuals over the age of 60 and the study lasted 8 weeks. Participants trained 6 times a week; 3 times were supervised in the lab and 3 times were at home. Each session lasted for 1 hour. There were 10 trained subjects and 8 control subjects. Experimenters engaged in motivational speech with the participants. A fixed order of games was used and an emphasis was placed on using a variety of strategies. Pre and post-training performance differences were measured across participants (2).

Rise of Nations: Rise of Legends Preview
http://pcmedia.gamespy.com/pc/image/article/685/685658/rise-of-nations-rise-of-legends-20060203034016276-000.jpg


The results of the experiment were not as expected. Corpus callosum FA was lower post-training in trained individuals. This was a surprise as white matter integrity is expected to increase and a greater FA should mean better performance. This is not always the case however as was found in a study in which Williams Syndrome patients were tested. Although these participants were found to have higher FA post-training, they did worse on tests. It can be concluded therefore, that FA can decrease with expertise, as well as with age. In functional connectivity tests, superior parietal connectivity was higher post-training in trained individuals. It was noted that participants exhibited more reliance on intrahemispheric integration and less reliance on interhemispheric integration. A correlation was also made between lower FA and higher functional connectivity in the same participants. In the future, the team at Arch lab hope to create an index to measure improvement over time in game performance (2). They also hope to further analyze cortical thickness and how it degenerates with age.

Overall, I found Dr. Strenziok's lecture to be informative and thought-provoking and her presentation style was also effective. The research that is being conducted at the Arch lab is vital and can help in better understanding abnormalities of the brain associated with different psychiatric disorders such as obsessive compulsive disorder and depression. By providing insight into the abnormalities and faulty neural connections associated with such disorders, techniques such as fMRI and DTI can provide clues to recovery. By employing these techniques in people at risk but not yet suffering from a developmental disorder, it might possibly enable treatment before the onset of symptoms (3). Patients with traumatic brain injuries (TBI) have symptoms that manifest themselves in different ways. Would it be possible to use fMRI scans to predict how patients with TBI will respond to different rehabilitation strategies?







References:

1. http://www.nursingassistantcentral.com/blog/2008/100-fascinating-facts-you-never-knew-about-the-human-brain/
2. Strenziok, Dr. Maren. "Brain Connectivity: Neural Substrates of Cognitive Function in Healthy Aging", Arch Lab/Cognitive Genetics Research Group – Psychology. 20 September 2012. Lecture.
3. http://www.dana.org/news/brainwork/detail.aspx?id=5322&p=1
4. http://www.dana.org/news/publications/detail.aspx?id=14442





Sunday, September 2, 2012

Exploring Neuromorphology


The lecture focused broadly on means in which neuroscience related knowledge can be cataloged and analyzed. Similar to the Human Genome Project, the Hippocampome Project is an attempt to improve data analysis of the many different neuron types found in the hippocampus by collecting and cataloging the deluge of information found regarding the function of this brain region. This project will allow for more open sharing of data regarding the function of the hippocampus and by utilizing and understanding the information gathered, it may also open doors for treatment of the many disorders and diseases associated with the hippocampus. NeuroMorpho.org is a site that also attempts to make sense of the deluge of information known about neurons and presents reconstructions of neuronal morphologies. Both of these projects are invaluable in that they are the basis of secondary research and discovery. 

Dr. Ascoli began his talk by mentioning the striking resemblance between a seahorse and the hippocampus, a small but vital structure found deep in the medial temporal lobe of the brain. The role of the hippocampus is so fundamental to our daily functions. Known as the GPS of our mind, the hippocampus works by maintaining cognitive navigation maps and is also involved in the formation and storage of memories. It is important for
the processing of different mental states including episodic, autobiographic, and declarative. The hippocampus is one of the most prolific grounds for study and is the key area for many diseases including stroke, epilepsy, and Alzheimer's. 

The hippocampus is made up of various types of neurons, a few classes being much more abundant than others. The organization and connectivity of these neurons is very important as it determines how information is processed. Each neuron is unique with respect to its axonal and dendritic patterns. Analyzing neuronal morphologies is essential to understanding how neurons give rise to recognition. Dr. Parekh went more into detail about just how neuronal morphologies are analyzed. The process includes labeling the tissue with a stain or dye to examine the connectivity of particular regions. Visualizing is done under a microscope and tracing follows using pencil and paper, digitizing tablets, or computational algorithms. Reconstructions are then generated automatically. 

Collecting and cataloging such vital information into a knowledge base or user-friendly site is extremely advantageous. These sources may bring us one step closer to understanding the precise mechanism that triggers clinical depression. A treatment for pediatric epilepsy can be developed. These possibilities may be further explored by observing outlier neurons that appear to differ from the norm, for instance. My question is this: By utilizing these sources that catalog vital information, will it be possible for us to finally understand how and why a disease such as Alzheimer's begins? 






http://ars.els-cdn.com/content/image/1-s2.0-S0014488605002372-gr2.jpg