In their experiments, Bettina Hartmann and her colleagues studied receptors called AMPA receptors, which are triggered by the neurotransmitter glutamate. Such receptors are protein switches that nestle in the membranes of nerve cells and, when triggered, induce either short-term or long-term changes in the nerve cells. A short-term change might be the triggering of a single nerve impulse; but AMPA receptors have been implicated in long-lasting changes such as adjusting the strength of nerve cell connections, or synapses, in learning and memory. AMPA receptors regulate nerve cell response by opening to enhance calcium flow into the cell, heightening the cells' sensitivity to producing nerve impulses when triggered.
According to Hartmann and her colleagues, studies of spinal cord tissue showed that AMPA receptors are found in spinal cord regions known to be responsible for pain sensing, or nociception. However, they said, there had been no studies that explored what role the receptors played in whole animals.
To study that role, the researchers genetically altered mice to lack one or another type of key component, or subunit, of the AMPA receptor protein. Knocking out one type of subunit, called GluR-A, would enhance AMPA permeability to calcium; and knocking out the other, called GluR-B, would reduce its permeability. Normally, the relative fraction of AMPA receptors with GluR-A or GluR-B on the surfaces of nerve cells would determine the cell's permeability to calcium.
Importantly, the researchers found that both of the types of deficient mice showed normal response to discomforting stimuli, such as heat. Thu
Contact: Heidi Hardman