Addiction Neuroscience Laboratory
The Addiction Neuroscience Group studies how alcohol and other drugs change the brain’s chemistry, structure and function.
We continue to unravel the circuitry and brain chemistry implicated in stress-induced relapse to alcohol-seeking by interrogating how and where in the brain specific peptide systems interact to regulate reward-seeking. So far we have identified a novel neural signalling system in the brain for the regulation of stress-induced relapse to alcohol-seeking. Specifically, we have shown that relaxin-3 inputs (likely from the nucleus incertus, NI) to the bed nucleus of the stria terminalis (BNST) are critical for stress-induced relapse to alcohol-seeking in rats. We are extending this innovative work which will lead the field by further delineating the circuitry and brain chemistry implicated in stress-driven relapse, the major stumbling block in the successful treatment of substance abuse clients. Given the scale and costs of substance abuse disorders, the identification of improved therapeutic approaches will have immediate and sustained impact.
Another related project involves a model of voluntary abstinence from alcohol that is precipitated by the presentation of an adverse consequence following drug use (as occurs in the human situation). We are characterising the circuitry that underpins context-induced relapse to alcohol-seeking following voluntary abstinence. We have identified a potentially critical neural mechanism by which alcohol associated environments promote alcohol seeking during abstinence. We will further unravel the brain mechanisms of relapse to alcohol seeking, and will identify novel brain areas and circuits that future clinical studies can target in treatment-seeking alcoholics.
There is a strong negative correlation between cognitive function and treatment outcome for addicts. An often overlooked factor is that long term alcohol abuse is strongly associated with an accelerated rate of cognitive decline and dementia. Dr Christina Perry has recently been awarded an NHMRC Dementia Fellowship to directly study this problem using validated animal models, with the translationally accepted touchscreen cognitive behavioural platform. Going forwards we will undertake the first comprehensive and systematic analysis of how long term chronic intermittent exposure to alcohol leads to precipitation of behavioural and neuropathological symptoms of dementia. Importantly, we will establish the extent to which these symptoms can be rescued with abstinence, and whether a relatively simple behavioural intervention can enhance this recovery. This study will provide the field with a road map for alcohol-induced cognitive decline. Our results will have important therapeutic applications for an aging population.
Obesity has reached pandemic proportions and is rapidly surpassing smoking as the number one killer in the industrialized world. Dr Robyn Brown (Doherty Fellow), has generated compelling evidence, based on complementary behavioural and electrophysiological approaches, which show that rats prone to diet-induced obesity display ‘addiction-like’ behaviour towards palatable food. Moreover, for the first time we provide evidence of dysregulated glutamate physiology at accumbal synapses in rats prone to obesity. This provides important preliminary evidence to support our central hypothesis that the pathological over-eating commonly observed in diet-induced obesity shares common features with compulsive drug-taking observed in drug addiction. This finding suggests that the management of obesity should incorporate “relapse-prevention” strategies in parallel to weight loss programs, as an adjunct to help reduce episodes of over-eating.
Brain health affects all Australians. You can support our research by making a donation or a bequest.