NEUROLOGISTS DECODE BRAIN MAPS TO DISCOVER HOW WE TAKE AIM

Serena Williams won her third consecutive US Open title a few days ago, thanks to reasons including obvious ones like physical strength and endurance. But how much did her brain and its egocentric and allocentric functions help the American tennis star retain the cup?

Quite significantly, according to York University neuroscience researchers whose recent study shows that different regions of the brain help to visually locate objects relative to one's own body (self-centred or egocentric) and those relative to external visual landmarks (world-centred or allocentric).

"The current study shows how the brain encodes allocentric and egocentric space in different ways during activities that involve manual aiming," explains Distinguished Research Professor Doug Crawford, in the Department of Psychology. "Take tennis for example. Allocentric brain areas could help aim the ball toward the opponent's weak side of play, whereas the egocentric areas would make sure your muscles return the serve in the right direction."

The study finding will help healthcare providers to develop therapeutic treatment for patients with brain damage in these two areas, according to the neuroscientists at York Centre for Vision Research. "As a neurologist, I am excited by the finding because it provides clues for doctors and therapists how they might design different therapeutic approaches," says Ying Chen, lead researcher and PhD candidate in the School of Kinesiology and Health Science.

The study, "Allocentric versus Egocentric Representation of Remembered Reach Targets in Human Cortex," published in the Journal of Neuroscience, was conducted using the state-of-the-art fMRI scanner at York U's Sherman Health Science Research Centre. A dozen participants were tested using the scanner, which Chen modified to distinguish brain areas relating to these two functions.

The participants were given three different tasks to complete when viewing remembered visual targets: egocentric reach (remembering absolute target location), allocentric reach (remembering target location relative to a visual landmark) and a nonspatial control, colour report (reporting color of target).

When participants remembered egocentric targets' locations, areas in the upper occipital lobe (at the back of the brain) encoded visual direction. In contrast, lower areas of the occipital and temporal lobes encoded object direction relative to other visual landmarks. In both cases, the parietal and frontal cortex (near the top of the brain) coded reach direction during the movement.

SCIENTISTS DISCOVER DIMMER SWITCH FOR MOOD DISORDERS

Researchers at University of California, San Diego School of Medicine have identified a control mechanism for an area of the brain that processes sensory and emotive information that humans experience as "disappointment.

The discovery of what may effectively be a neurochemical antidote for feeling let-down is reported Sept. 18 in the online edition of Science.

"The idea that some people see the world as a glass half empty has a chemical basis in the brain," said senior author Roberto Malinow, MD, PhD, professor in the Department of Neurosciences and neurobiology section of the Division of Biological Sciences. "What we have found is a process that may dampen the brain's sensitivity to negative life events."

Because people struggling with depression are believed to register negative experiences more strongly than others, the study's findings have implications for understanding not just why some people have a brain chemistry that predisposes them to depression but also how to treat it.

Specifically, in experiments with rodents, UC San Diego researchers discovered that neurons feeding into a small region above the thalamus known as the lateral habenula (LHb) secrete both a common excitatory neurotransmitter, glutamate, and its opposite, the inhibitory neurotransmitter GABA.

Excitatory neurotransmitters promote neuronal firing while inhibitory ones suppress it, and although glutamate and GABA are among two of the most common neurotransmitters in the mammalian brain, neurons are usually specialists, producing one but not both kinds of chemical messengers.

Indeed, prior to the study, there were only two other systems in the brain where neurons had been observed to co-release excitatory and inhibitory neurotransmitters -- in a particular connection in the hippocampus and in the brainstem during development of the brain's auditory map.

"Our study is one of the first to rigorously document that inhibition can co-exist with excitation in a brain pathway," said lead author Steven Shabel, a postdoctoral researcher with Department of Neurosciences and neurobiology section of the Division of Biological Sciences. "In our case, that pathway is believed to signal disappointment."

The LHb is a small node-like structure in the epithalamus region of the brain that is critical for processing a variety of inputs from the basal ganglia, hypothalamus and cerebral cortex and transmitting encoded responses (output) to the brainstem, an ancient part of the brain that mammals share with reptiles.

Experiments with primates have shown that activity in the LHb increases markedly when monkeys are expecting but don't get a sip of fruit juice or other reward, hence the idea that this region is part of a so-called disappointment pathway.

Proper functioning of the LHb, however, is believed to be important in much more than just disappointment and has been implicated in regulating pain responses and a variety of motivational behaviors. It has also been linked to psychosis.

Depression, in particular, has been linked to hyperactivity of the LHb, but until this study, researchers had little empirical evidence as to how this overstimulation is prevented in healthy individuals given the apparent lack of inhibitory neurons in this region of the brain.

"The take-home of this study is that inhibition in this pathway is coming from an unusual co-release of neurotransmitters into the habenula," Shabel said. Researchers do not know why this region of the brain is controlled in this manner, but one hypothesis is that it allows for a more subtle control of signaling than having two neurons directly counter-acting each other.

Researchers were also able to show that neurons of rodents with aspects of human depression produced less GABA, relative to glutamate. When these animals were given an antidepressant to raise their brain's serotonin levels, their relative GABA levels increased.

"Our study suggests that one of the ways in which serotonin alleviates depression is by rebalancing the brain's processing of negative life events vis-à-vis the balance of glutamate and GABA in the habenula," Shabel said. "We may now have a precise neurochemical explanation for why antidepressants make some people more resilient to negative experiences."

Funding for this project came, in part, from the National Institutes of Health (grant NS047101).

Co-authors include Christophe Proulx, UC San Diego, and Joaquin Piriz, Universidad de Buenos Aires, Argentina.