Both drinking and withdrawal from chronic drinking can raise circulating glucocorticoid levels, known as cortisol in humans and corticosterone in rodents. Prolonged and high concentrations of glucocorticoids can have damaging effects on neuronal function and cognition. Evidence shows that glucocorticoids are associated with neurotoxicity during abstinence after withdrawal from alcohol dependence (AD), and that glucocorticoid receptor antagonism may represent a pharmacological option for recovery.
"Prolonged and elevated levels of glucocorticoid hormones can damage or destroy neurons, and lead to an increased vulnerability to other situations that can damage neurons, such as raised excitatory amino acid activity," explained A.K. Rose, a lecturer in psychology at the University of Liverpool and corresponding author for the review. "This can underlie loss of memory functions."
"High levels of brain cortisol associated with stress have long been linked to deficits in neuronal function, which can be seen in aging," added John Littleton, a professor in the department of pharmaceutical sciences at the University of Kentucky.=20
Among the review's key points:
Brain glucocorticoid concentrations increase and glucocorticoid receptor occupancy decreases during prolonged abstinence after withdrawal from alcohol.
"Our evidence shows that brain concentrations of corticosterone remain raised for long periods after alcohol withdrawal, even after the blood concentrations return to normal levels," said H.J. Little, a professor in addiction science at King's College London and who conducted this research. "Further more, the corticosterone concentrations remained increased in rodent brains for up to two months, approximately five human years, following cessation of prolonged alcohol drinking."
"One of the most important questions for research and treatment is why alcoholics can relapse after many months of abstinence," observed Littleton. "Partly this can be attributed to the effects of conditioning in which 'cues' provoke craving for alcohol, as well as a 'protracted withdrawal syndrome' which includes anxiety, sleep disturbances, and general feelings of being unwell. Prolonged high levels of brain cortisol after withdrawal from alcohol may explain the strength of these cues, and many of the symptoms of protracted withdrawal."
Increased glucocorticoid levels in the brain after alcohol treatment are associated with cognitive deficits seen during abstinence, affecting both treatment efficacy and quality of life.
"Cessation of drinking is clearly linked to cognitive deficits," said Little. "For example, visuospatial learning can be worse in abstinent alcoholics than in those still intoxicated, and memory and learning deficits have been found in rats after alcohol withdrawal, but not during alcohol intake. Furthermore, greater neuronal degeneration has been reported after cessation of chronic alcohol intake than during its consumption, and multiple withdrawal episodes cause greater neuronal damage than a single withdrawal episode."
"If cognitive impairments could be reduced, patients would be more likely to engage in, and thus benefit from, psychosocial treatments," added Rose. "Better cognitive function coupled with better treatment engagement is likely to produce better treatment outcomes and quality of life. A person with greater cognitive function is likely to be more able to find work and re-build relationships.
"In summary," said Littleton," stress, the hypothalamo-pituitary adrenal axis, and cortisol are very important determinants of the natural history of alcoholism - affecting an individual's drinking behavior, the effects on cognition and memory, and the likelihood of relapsing into alcoholism during abstinence. We can also see that hypotheses applicable to animals can now be applied to inform new human research."
For further information contact:
Dr Abigail K. Rose,
Division of Psychological Medicine and Psychiatry,
Section of Alcohol Research,
National Addiction Centre,
Institute of Psychiatry,
King's College London,