Medical College of Wisconsin
CTSICores SearchResearch InformaticsREDCap

N-Acetylcysteine treatment during acute stress prevents stress-induced augmentation of addictive drug use and relapse. Addict Biol 2020 Sep;25(5):e12798

Date

07/10/2019

Pubmed ID

31282090

Pubmed Central ID

PMC7439767

DOI

10.1111/adb.12798

Scopus ID

2-s2.0-85068669997 (requires institutional sign-in at Scopus site)   29 Citations

Abstract

Converging epidemiological studies show that a life-threatening event increases the incidence of posttraumatic stress disorder (PTSD), which carries 30% to 50% comorbidity with substance use disorders (SUDs). Such comorbidity results in greater drug use and poorer treatment outcomes. There is overlap between the enduring synaptic neuroadaptations produced in nucleus accumbens core (NAcore) by acute restraint stress and cocaine self-administration. Because of these coincident neuroadaptations, we hypothesized that an odor paired with acute restraint stress would reinstate drug seeking and chose two mechanistically distinct drugs of abuse to test this hypothesis: alcohol and cocaine. Rats were trained to self-administer either drug beginning 3 weeks after odor pairing with acute stress or sham, and acute restraint stress increased alcohol consumption. Following context extinction training, the stress-paired odor reinstated both alcohol and cocaine seeking, while an unpaired odor had no effect. N-Acetylcysteine (NAC) restores drug and stress-induced reductions in glial glutamate transporter-1 and has proven effective at reducing cue-induced reinstatement of drug seeking. We administered NAC for 5 days prior to reinstatement testing and abolished the capacity of the stress-paired odor to increase alcohol and cocaine seeking. Importantly, daily NAC given during or just following experiencing acute restraint stress also prevented the capacity of stress-paired odors to reinstate alcohol and cocaine seeking and prevented stress-induced deficits in behavioral flexibility. These data support using daily NAC treatment during or immediately after experiencing a strong acute stress to prevent subsequent conditioned stress responding, in particular relapse and cognitive deficits induced by stress-conditioned stimuli.

Author List

Garcia-Keller C, Smiley C, Monforton C, Melton S, Kalivas PW, Gass J

Author

Constanza Garcia Keller PhD Assistant Professor in the Pharmacology and Toxicology department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Acetylcysteine
Acute Disease
Alcohol-Related Disorders
Animals
Cocaine
Cocaine-Related Disorders
Cues
Disease Models, Animal
Drug-Seeking Behavior
Ethanol
Free Radical Scavengers
Male
Rats
Rats, Sprague-Dawley
Recurrence
Self Administration
Stress, Psychological