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Electrical implants that shut down excessive activity in brain cells hold great potential for treating epilepsy and chronic pain. Likewise, devices that enhance neurons’ activity may help restore function to people with nerve damage. A new technology developed at MIT and Harvard Medical School may overcome the primary drawback to this approach, known as functional electrical stimulation: When electrical current is applied, it can spread to nearby nerves, causing painful side effects. Nerves, the long bundles of neuronal extensions that carry instructions to the muscles — as well as sensory information such as pain — communicate via extremely rapid electrical signals. By manipulating the concentration of charged ions surrounding a nerve, the researchers were able to dramatically reduce the current needed to keep an impulse going; they could also interrupt an impulse as it traveled along a nerve.
This Artificial Rat Brain Has 12 Seconds of Short-term Memory Ashwin Vishwanathan, Guo-Qiang Bi and Henry C. Zeringue, University of Pittsburgh It’s not artificial intelligence in the Turing test sense, but the technicolor ring you see above is actually an artificial microbrain, derived from rat brain cells --just 40 to 60 neurons in total--that is capable of about 12 seconds of short-term memory. Developed by a team at the University of Pittsburgh, the brain was created in an attempt to artificially nurture a working brain into existence so that researchers could study neural networks and how our brains transmit electrical signals and store data so efficiently. The did so by attaching a layer of proteins to a silicon disk and adding brain cells from embryonic rats that attached themselves to the proteins and grew to connect with one another in the ring seen above.
I n a scientific first that could shed light on how signals travel in the brain and the effects of learning on neural pathways, scientists at Harvard have created genetically altered neurons that light up as they fire. The work may also lead to speedier drug development. Led by John L. Loeb Associate Professor of the Natural Sciences Adam Cohen and described in Nature Methods on Nov. 27, the research involved using a gene from a Dead Sea microorganism to produce a protein that, when exposed to the electrical signal in a neuron, fluoresces, allowing scientists to trace the propagation of signals through the cell. “It’s very exciting,” Cohen said.
N euron transplants have repaired brain circuitry and substantially normalized function in mice with a brain disorder, an advance indicating that key areas of the mammalian brain are more reparable than was widely believed. Collaborators from Harvard University , Massachusetts General Hospital (MGH), Beth Israel Deaconess Medical Center (BIDMC) and Harvard Medical School (HMS) transplanted normally functioning embryonic neurons at a carefully selected stage of their development into the hypothalamus of mice unable to respond to leptin, a hormone that regulates metabolism and controls body weight. These mutant mice usually become morbidly obese, but the neuron transplants repaired defective brain circuits, enabling them to respond to leptin and thus experience substantially less weight gain.