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Mystery Behind Long-lasting Memories In Mice Unravelled

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A new study by researchers at Wake Forest University School of Medicine may reveal how long-lasting memories form in the brain.

The researchers hope that the findings, now available online and scheduled to appear in an upcoming issue of Neuroscience, may one day help scientists develop treatments to prevent and treat conditions such as post-traumatic stress disorder.

“Although many things are known about memories that form from repeat experiences, not much is known with regard to how some memories form with just one exposure,” said Ashok Hegde, Ph.D., an associate professor of neurobiology and anatomy and the lead investigator on the study.

Scientists do know that people tend to remember extremely happy or sad occasions vividly because of the emotional connection, Hegde said. Extreme emotions trigger the release of a chemical in the brain called norepinephrine, which is related to adrenaline. That norepinephrine somehow helps memories last a long time – some even a lifetime.

For example, he said, when a person asks, “Where were you when the 9/11 attacks happened?” most people can recall immediately where they were and what they were doing when they heard the news. They remember the moment as if it just happened because a national tragedy arouses emotion and emotion somehow makes memories last for a long time, Hegde explained.

For the current study, Hegde and colleagues looked at how norepinephrine helps female mice remember the scent of their male partners after being exposed to it just once during mating.

The researchers studied the neural circuitry in the accessory olfactory bulb, the part of the brain where memory of the male partner’s scent is stored. They found that norepinephrine, released in mice while mating, activates an enzyme called Protein Kinase C (PKC), specifically, the “alpha” isoform of PKC, in the accessory olfactory bulb. The PKC enzyme has about a dozen forms, or isoforms, that exist in the brains of mammals, including humans.

“The fact that PKC-alpha is activated through the release of norepinephrine is an important discovery,” Hegde said. “It explains how strong memories form for specific sensory experiences.”

In female mice, the information about the partner’s scent is carried by a chemical called glutamate and the fact that mating has occurred is conveyed by the release of norepinephrine, Hegde explained. Previous studies have found that glutamate and norepinephrine together, but not individually, cause strong memory formation for the male’s scent.

“No one knew how this happened,” Hegde said. “Our findings indicate that the PKC-alpha enzyme tells the nerve cells in the brain that these two chemicals have arrived together. PKC-alpha is like the bouncer who lifts the rope blocking the entrance to an exclusive club for strong memories when glutamate and norepinephrine arrive together. If they arrive alone, they can’t get past the velvet rope.”

Hegde explained that, when memory is stored in the brain, the connections between nerve cells, called synapses, change. Strong memories are formed when synapses become stronger through structural changes that occur at the synapse. PKC-alpha works with glutamate and norepinephrine to create those changes.

Hegde said that the next step in this line of research is to learn exactly how PKC-alpha can turn genes on in nerve cells. Understanding the precise sequence of molecules that are activated by PKC-alpha will help researchers block the function of these molecules and test whether they block memory formation. This future research will not only explain strong pleasant memories, but also how strong unpleasant memories form in instances like post-traumatic stress disorder.

Neuroscience, 2009; DOI: 10.1016/j.neuroscience.2009.06.069
Protein kinase Cα mediates a novel form of plasticity in the accessory olfactory bulb.
C. Dong, D.W. Godwin, P.A. Brennan, A.N. Hegde.


Modification of synapses in the accessory olfactory bulb (AOB) is believed to underlie pheromonal memory that enables mate recognition in mice. The memory, which is acquired with single-trial learning, forms only with coincident noradrenergic and glutamatergic inputs to the AOB. The mechanisms by which glutamate and norepinephrine (NE) alter the AOB synapses are not well understood. Here we present results that not only reconcile the earlier, seemingly contradictory, observations on the role of glutamate and NE in changing the AOB synapses, but also reveal novel mechanisms of plasticity. Our studies suggest that initially, glutamate acting at Group II metabotropic receptors and NE acting at α2-adrenergic receptors inhibit N-type and R-type Ca2+ channels in mitral cells via a G-protein. The N-type and R-type Ca2+ channel inhibition is reversed by activation of α1-adrenergic receptors and protein kinase Cα (PKCα). Based on these results, we propose a hypothetical model for a new kind of synaptic plasticity in the AOB that accounts for the previous behavioral data on pheromonal memory. According to this model, initial inhibition of the Ca2+ channels suppresses the GABAergic inhibitory feedback to mitral cells, causing disinhibition and Ca2+ influx. NE also activates phospholipase C (PLC) through α1-adrenergic receptors generating inositol 1,4,5-trisphosphate and diacylglycerol (DAG). Calcium and DAG together activate PKCα which switches the disinhibition to increased inhibition of mitral cells. Thus, PKCα is likely to be a coincidence detector integrating glutamate and NE input in the AOB and bridging the short-term signaling to long-term structural changes resulting in enhanced inhibition of mitral cells that is thought to underlie memory formation.

Key words: glutamate; norepinephrine; pheromone memory; signal transduction; alpha adrenergic; metabotropic


Written by huehueteotl

August 13, 2009 at 7:23 am

Posted in Neuroscience

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