Accession Number:

ADA568600

Title:

The Role of Glucocorticoids and Neuroinflammation in Mediating the Effects of Stress on Drug Abuse

Descriptive Note:

Annual rept. 26 Sep 2011-25 Sep 2012

Corporate Author:

COLORADO UNIV AT BOULDER

Personal Author(s):

Report Date:

2012-10-01

Pagination or Media Count:

8.0

Abstract:

Drug abuse and misuse is a major health hazard in the military as well as in the population more generally. There have been major recent advances in our understanding of the alterations in the brain produced by drugs of abuse, and in how the addicted brain differs from the normal brain. However, many individuals who experience, or are exposed to a drug of abusedo not develop addiction, or abuse the drug. For example, the overwhelming majority of patients that receive opiates for painrelief while hospitalized do not develop opiate addiction. That is, use does not always develop into abuse, and the factors thmediate this transition are largely unknown. The development of an understanding of the factors and brain mechanisms that throw the balance towards the development of abuse from use would be a major step in the development of therapies that caameliorate addiction.The core hypothesis is that stressors, via their production of increased glucocorticoids GCs, sensitize microglia so that these cells produce excessively high levels of inflammatory mediators such as IL-1 when acted upon by drugs of abuse, and that this process is responsible, in whole or in part, for the increased vulnerability to drug abuse produceby stressful experiences. This is a novel, and previously unexplored hypothesis. The work, if successful, could lead to a reconceptualization of GCs as a sensitization factor that induces a vulnerability to neuroinflammatory processes and thereby open a new field of investigation into the role of stress and GCs in the etiology of substance abuse disorders.

Subject Categories:

  • Biochemistry
  • Medicine and Medical Research
  • Stress Physiology

Distribution Statement:

APPROVED FOR PUBLIC RELEASE