Understanding the complex nature of neuronal signaling at synapses could lead to better understanding of learning and memory, and novel treatments for relevant disorders, such as Alzheimer’s disease and schizophrenia.
Neurons in the hippocampus, one of the parts of the brain that is thought to have a critical function in learning and memory, communicate with each other at synapses by releasing various neurotransmitters, including acetylcholine and glutamate, which stimulate electrical signals in the adjacent neurons.
For years, neuroscientists have been working to determine which cellular processes allow humans to learn from experience and store memories, and how these processes are compromised by conditions such as schizophrenia and Alzheimer’s disease. Now, researchers from the National Institute of Environmental Health Sciences (NIEHS), which is part of the National Institutes of Health, believe they have found one such mechanism for synchronizing changes in the strength of synapses. The results of the study will be published online July 13 in the journal Neuron.
“We’ve demonstrated that when we stimulate the release of acetylcholine at just the right time in the hippocampus, we can induce a cellular change at synapses that use glutamate,” said Jerrel Yakel, Ph.D., a senior investigator in the NIEHS Laboratory of Neurobiology and co-author of the paper.
Previous work by other researchers had established that learning and memory is mediated by the strengthening or weakening of synapses, where electrical signals that last less than a hundredth of a second release neurotransmitters that change the electrical impulses of the connected neurons. In this study, Yakel and Zhenglin Gu, Ph.D., a research fellow in Yakel’s group and co-author of the publication, used molecular biology techniques to get some of the neurons in mouse brain cells to produce a special light-sensitive protein, and then used a laser to stimulate these neurons to release acetylcholine.
“A change of even a few hundredths of a second in the timing of acetylcholine release can make a difference,” said Gu. “No one had shown this was important until now.”
Yakel said the findings are also a potentially important step in the study of disorders that affect learning and memory, such as Alzheimer’s disease and schizophrenia, where the acetylcholine system and hippocampus are known to play critical roles. For example, amyloid beta peptide is the major component of plaques that form in the brains of Alzheimer’s patients and is thought to participate in the memory loss associated with Alzheimer’s disease. In this report, Yakel and Gu expand upon earlier findings that amyloid beta peptide disrupts acetylcholine’s ability to regulate synaptic strength.
The NIEHS supports research to understand the effects of the environment on human health and is part of NIH. For more information on environmental health topics, visit www.niehs.nih.gov. Subscribe to one or more of the NIEHS news lists to stay current on NIEHS news, press releases, grant opportunities, training, events, and publications.
About the National Institutes of Health (NIH): NIH, the nation’s medical research agency, includes 27 Institutes and Centers and is a component of the U.S. Department of Health and Human Services. NIH is the primary federal agency conducting and supporting basic, clinical, and translational medical research, and is investigating the causes, treatments, and cures for both common and rare diseases. For more information about NIH and its programs, visit www.nih.gov.
Reference: Gu Zhenglin, Yakel JL. 2011. Timing-dependent septal cholinergic induction of dynamic hippocampal synaptic plasticity. Neuron; doi:10.1016/j.neuron.2011.04.026 [Online 13 July 2011].