APR 12, 2017 9:31 AM PDT

Surprising Brain Change Appears to Drive Alcohol Dependence

Image Credit: Pixabay

LA JOLLA, CA – April 12, 2017 – A new study led by scientists at The Scripps Research Institute (TSRI) could help researchers develop personalized treatments for alcoholism and alcohol use disorder.

The research reveals a key difference between the brains of alcohol-dependent versus nondependent rats. When given alcohol, both groups showed increased activity in a region of the brain called the central amygdala (CeA)—but this activity was due to two completely different brain signaling pathways.

TSRI Professor Marisa Roberto, senior author of the new study, said the findings could help researchers develop more personalized treatments for alcohol dependence, as they evaluate how a person’s brain responds to different therapeutics.

The findings were published recently online ahead of print in The Journal of Neuroscience.

Researchers Find Brain’s Alcohol Response ‘Switch’

The new research builds on the Roberto lab’s previous discovery that alcohol increases neuronal activity in the CeA. The researchers found increased activity both nondependent, or naïve, and alcohol-dependent rats.

As they investigated this phenomenon in the new study, Roberto and her colleagues were surprised to find that the mechanisms underlying this increased activity differed between the two groups.

By giving naïve rats a dose of alcohol, the researchers engaged proteins called calcium channels and increased neuronal activity. Neurons fired as the specific calcium channels at play, called L-type voltage-gated calcium channels (LTCCs), boosted the release of a neurotransmitter called GABA. Blocking these LTCCs reduced voluntary alcohol consumption in naïve rats.

But in alcohol-dependent rats, the researchers found decreased abundance of LTCCs on neuronal cell membranes, disrupting their normal ability to drive a dose of alcohol’s effects on CeA activity. Instead, increased neuronal activity was driven by a stress hormone called corticotropin-releasing factor (CRF) and its type 1 receptor (CRF1). The researchers found that blocking CeA CRF1s reduced voluntary alcohol consumption in the dependent rats.

Studying these two groups shed light on how alcohol functionally alters the brain, Roberto explained.

“There is a switch in the molecular mechanisms underlying the CeA’s response to alcohol (from LTCC- to CRF1-driven) as the individual transitions to the alcohol-dependent state,” she said.

The cellular and molecular experiments were led by TSRI Research Associate and study first author Florence Varodayan. The behavioral tests were conducted by TSRI Research Associate Giordano de Guglielmo in the lab of TSRI Associate Professor Olivier George.

Roberto hopes the findings lead to better ways to treat alcohol dependence. Alcohol use disorder appears to have many different root causes, but the new findings suggest doctors could analyze certain symptoms or genetic markers to determine which patients are likely to have CRF-CRF1 hyperactivation and benefit from the development of a novel drug that blocks that activity.

In addition to Roberto, Varodayan and de Guglielmo, authors of the study, “Alcohol dependence disrupts amygdalar L-type voltage-gated calcium channel mechanisms,” were Marian Logrip and Olivier George of TSRI.

The study was supported by the National Institutes of Health (grants AA015566, AA021491, AA017447, AA006420, AA013498, AA020608, AA022977 and AA021802).

This article was originally published on Scripps.edu.

About the Author
  • The Scripps Research Institute (TSRI) is one of the world's largest independent, not-for-profit organizations focusing on research in the biomedical sciences. TSRI is internationally recognized for its contributions to science and health, including its role in laying the foundation for new treatments for cancer, rheumatoid arthritis, hemophilia, and other diseases. An institution that evolved from the Scripps Metabolic Clinic founded by philanthropist Ellen Browning Scripps in 1924, the institute now employs about 2,700 people on its campuses in La Jolla, CA, and Jupiter, FL, where its renowned scientists-including two Nobel laureates-work toward their next discoveries. The institute's graduate program, which awards PhD degrees in biology and chemistry, ranks among the top ten of its kind in the nation. For more information, see www.scripps.edu.
You May Also Like
NOV 06, 2019
Cell & Molecular Biology
NOV 06, 2019
Brains are More Symmetrical in People With Autism
The two halves of the brain and typically assymterical, but that may be less true for individuals with autism spectrum disorder....
NOV 26, 2019
Neuroscience
NOV 26, 2019
Air Pollution Linked to Alzheimer's, Study Finds
Worldwide, 9 in every 10 people breathe highly polluted air. A known contributing factor for many respiratory illnesses such as lung cancer, an increasing ...
NOV 30, 2019
Genetics & Genomics
NOV 30, 2019
Depression is Not Caused By Genetics
Since the discovery of DNA, attributing the cause of illnesses to genetic reasons became trendy. Depression was no exception- with hundreds of studies havi...
DEC 04, 2019
Neuroscience
DEC 04, 2019
Antibiotic Usage May Cause Parkinson's, Study Finds
A study from Helsinki University Hospital, Finland suggests that excessive usage of certain antibiotics may increase one’s risk of developing Parkins...
DEC 27, 2019
Drug Discovery & Development
DEC 27, 2019
Acne Drug Linked to 10 Suicides
UK regulators claim to have found a link between at least ten suicides and a powerful acne drug, manufactured under the names Roaccutane and Accutane. Alth...
JAN 07, 2020
Cell & Molecular Biology
JAN 07, 2020
Cancer-Like Metabolism Can Fuel Brain Growth
During evolution, the size of the human brain increased significantly compared to other primates....
Loading Comments...