Using laser light to temporarily inactivate a specific neuronal population, a team of researchers at The Scripps Research Institute (La Jolla, CA) have found that they can reverse the desire to drink in alcohol-dependent rats. The technique enabled them to reverse alcohol-seeking behavior and even reduce the physical symptoms of withdrawal.
Olivier George, Ph.D., an associate professor at Scripps Research and senior author of the research team's paper that describes the work, believes identifying these neurons opens the door to developing drug therapies or even gene therapies for alcohol addiction. "We need compounds that are specific to this neuronal circuitry," George says.
Previous work at Scripps Research has shown that transitioning from casual drinking to dependent drinking occurs alongside fundamental changes in how the brain sends signals. These signals drive the intense cravings that make it so difficult for many people to scale back their alcohol consumption.
George and his colleagues have been hunting for the brain cells that drive drinking in an alcohol-addicted rat model. In 2016, they reported that they had found a possible source: a neuronal "ensemble," or group of connected cells in a brain region called the central nucleus of the amygdala (CeA). This finding marked major progress in mapping the brain, but the researchers needed to characterize the identity of the neurons in this ensemble.
For the new study, they tested the role of a subset of neurons in the ensemble, called corticotropin-releasing factor (CRF) neurons. They had found that these CRF neurons make up 80% of the ensemble.
The researchers studied these neurons using optogenetics, a technique that involves the use of light to control cells in living tissue. Rats used in this study were surgically implanted with optic fibers aimed to shine light on the CRF neurons—to inactivate them at the flip of a switch.
First, the scientists established a baseline for how much the rats would drink before they got addicted to alcohol. The rats drank little this point—the equivalent of a glass of wine or one beer for a human. The scientists then spent several months increasing consumption in these rats to establish alcohol dependence.
The researchers then withdrew the alcohol, prompting withdrawal symptoms in the rats. When they offered alcohol again, the rats drank more than ever. The CeA neuronal ensemble was active, telling the rats to drink more.
Then, the scientists flipped on the lasers to inactivate the CRF neurons. The rats immediately returned to their pre-dependent drinking levels. The intense motivation to drink had gone away. Inactivating these neurons also reduced the physical symptoms of withdrawal, such as abnormal gait and shaking.
Confocal analysis at 63x magnification, followed by the three-dimensional reconstruction of neuronal cell bodies and branches. The image shows an example of eYFP and CRF in the same neuron. This rendered isosurface analysis demonstrated the colocalization of CRF immunoreactivity within CeA neurons that also expressed Cre-dependent eYFP and validates the crh-Cre rat as a tool to gain more direct access to CRF neurons to study their functional neuroanatomy. (Image credit: George lab)
"In this multidisciplinary study, we were able to characterize, target, and manipulate a critical subset of neurons responsible for excessive drinking." says Giordano de Guglielmo, Ph.D., first author of the study and staff scientist at Scripps Research.
George says the next step in translating this work to humans is to find a way to selectively inhibit only these specific CRF neurons, perhaps using a novel or repurposed compound identified using high-throughput screening of large libraries of compounds.
Meanwhile, de Guglielmo plans to take a closer look at the signaling pathways in the brain affected when the CRF neurons are deactivated. The new study shows that reduced drinking is tied to the CRF neurons that send projections to reach another brain region called the bed nucleus of the stria terminalis. De Guglielmo thinks other projections from these neurons may have different roles in alcohol addiction. He is also interested in identifying the role of these brain circuits in opioid addiction.
Full details of the work appear in the journal Nature Communications.