Such differences are usually not accounted for in laboratory studies, but could lead to more successful clinical treatments. “PTSD significantly increases the risk of alcohol use disorder as individuals use alcohol to manage stress and anxiety. However, the underlying biology of comorbid disorders is generally not well understood, ”says Dean Kirson, PhD, a postdoctoral fellow in neurophysiology in the laboratory of Professor Marisa Roberto, PhD, and a co-lead author with Michael Steinman, PhD.
“We hope that our new knowledge of gender changes in the brain will help fuel the development of more targeted treatments.” According to the Department of Veterans Affairs, approximately 7 to 8 percent of the country’s population will suffer from PTSD at some point in their lives. Causes include combat exposure, physical abuse, an accident, or other forms of trauma. Alcohol abuse disorder is also common, affecting approximately 15 million people in the United States. People with stress and anxiety disorders like PTSD not only abuse alcohol more often, they also have increased alcohol withdrawal symptoms and a higher risk of relapse.
“Most people know or know someone who is struggling with one or both of these disorders and may be trying to help them. However, there are very few effective treatments currently available, ”says Roberto. “Both are complex disorders that affect similar brain circuits. My lab looked at addiction and stress separately. That’s why we’ve teamed up with the Zorrilla Laboratory to apply a novel translationally relevant behavioral model to investigate what changes occur when these disorders are comorbid. “” The joint study by Roberto and Eric Zorrilla, PhD, who are co-senior authors, looked at behavior, sleep patterns, inflammatory immune responses, and levels of a neurotransmitter called GABA (short for gamma-aminobutyric acid) that lowers anxiety and increases feelings of anxiety of relaxation and is a common feature of alcohol addiction.
In both male and female rats, traumatic stress and alcohol exacerbated other behaviors common in PTSD, such as: B. shock reactions in social avoidance and defensive behavior. Those identified as “at risk of drinking” prior to the trauma were most likely to show avoidance of traumatic locations. However, the scientists found significant differences in the behavior of men and women after trauma and saw significantly different patterns of GABA signal transmission. For example, men showed increased GABA receptor function while women showed increased GABA release.
“This can be important as there is a growing awareness that drugs may have different levels of effectiveness in male and female patients, and an understanding of the biology that explains why these differences exist could improve outcomes,” Steinman says. The team also found that men had immune-based biomarkers – small proteins called cytokines that are secreted by immune cells – that determined susceptibility to an alcohol use disorder. The women didn’t. “We identified profiles of specific cytokines, many of which have not been previously associated with stressful behavior and which are strongly related to poor drinking outcomes,” said Zorilla, associate professor in the Department of Molecular Medicine. “These may be clinically or even mechanistically important, but they were only found in men. So we still have to find similar biomarkers for women. ”
Roberto and Zorrilla’s labs plan to conduct additional research into the mechanisms behind the biological changes observed and test which brain systems can be used to treat PTSD and alcohol abuse. “We also plan to further investigate the role of the immune system in these disorders,” says Roberto. “These different biomarkers can be helpful for targeted treatment.” (ANI)
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