In the October 28, 2020 issue of the Journal of Neuroscience, researchers from the Medical University of South Carolina and the National Institutes of Health describe how reminders of drug use can change specific brain cells responsible for motivation, increasing the desire to seek drugs.
Connections between these and other brain cells strengthen because the dendritic spines, the parts of the brain cells that receive messages from other neurons, enlarge in response to intercellular communication by molecules in the brain.
This enhanced connectivity increases the urge to engage in drug use, making relapse more likely. Understanding this communication pathway could lead to more targeted treatments for drug addiction.
The study was led by MUSC Department of Neuroscience professor Peter W. Kalivas, Ph.D., and assistant professor Constanza Garcia-Keller, Ph.D., who works in the Kalivas lab.
For decades, the Kalivas laboratory has been studying the mechanisms behind drug addiction. In previous studies, Kalivas and his team have shown that an increase in the size of these spines correlates with how much an animal will work for a drug, such as cocaine.
Interestingly, these spines enlarge in response to signals sent not from other neurons but from the extracellular matrix that surrounds these cells. They found that these signals from outside the brain cells lead to internal changes in the neurons to change their connections to other neurons.
"The key finding is that enlargement of spines is necessary and induced by cues that are associated with addictive drugs, not cues that are associated with natural rewards," explained Kalivas.
That's an important distinction because it means that treatments can be developed to diminish the cravings for drugs without depriving patients of pleasurable experiences.
The researchers were able to image the fine details of the neurons in the nucleus accumbens of the brain, a region that has been implicated in driving drug addiction, with high-resolution confocal microscopy. They could see how the spines changed under different conditions and could even visualize the signaling molecules inside the cells that led to an increase in spine size.
One of these molecules in the neurons is focal adhesion kinase (FAK). When Kalivas and his team inhibited this protein with a drug, the animals did not seek cocaine when exposed to a reminder of the drug.
In addition, they showed that modifications to this kinase and the actin-binding protein cofilin led to spine enlargement and enhanced connections in a specific cell type in the brain known as D1-medium spiny neurons -neurons in the nucleus accumbens that motivate behavior.
"There are actually two cell groups in the nucleus accumbens. One motivates, and the other puts the brakes on behavior," said Kalivas. "Our study showed that this signaling is going through the cell group that promotes motivating behavior and not so much the cell group that is responsible for inhibiting behavior."
In other words, the cocaine is changing brain structure and function, especially in D1-medium spiny neurons, to motivate the animal to seek more cocaine.
A better understanding of how drug reminders change the neuronal structure by altering brain signaling will be crucial to developing effective therapies to avoid relapse.
The long-range goal is to establish therapies to help to prevent or reduce this relapse event that happens in people who try to recover. However, we first need to understand the signaling system better before we devise novel pharmacological treatments."
Constanza Garcia-Keller, PhD, Assistant Professor, Medical University of South Carolina
Garcia-Keller, C., et al. (2020) Relapse-Associated Transient Synaptic Potentiation Requires Integrin-Mediated Activation of Focal Adhesion Kinase and Cofilin in D1-Expressing Neurons. Journal of Neuroscience. doi.org/10.1523/JNEUROSCI.2666-19.2020.