Cocaine remains an important drug of abuse in the United States, and aside from producing profound behavioral effects, cocaine also disrupts neuroendocrine function in many species. Knowledge of the effects of drugs of abuse on neuroendocrine function is of fundamental importance because it provides information on the pathophysiological changes that can occur with drug use. Cocaine stimulates the hypothalamo-pituitary-adrenal (HPA) axis, and disruption of the normal regulation of the HPA axis can affect the maintenance of physiologic homeostasis by altering the metabolism of glucose, proteins and fats. In addition, immune function can be compromised as well as the reaction and adaptation to acute and chronic stress. Recently it has become apparent that exposure to stressors as well as pharmacological manipulation of the HPA axis can affect the responses to and the reinforcing properties of some drugs of abuse. Thus, exposure to stressors and subsequent activation of the HPA axis might play a critical role in determining """"""""vulnerability"""""""" to drug self-administration. Although numerous preclinical studies examining the effects of cocaine on neuroendocrine function have been published, little is known about the effects of the self-administration of cocaine on neuroendocrine function. The overall goal of the proposed experiments is to utilize an experimental system where blood can be sampled for hormones in rats during the self-administration of cocaine in order to obtain potentially important information on the relationships between activation of the HPA axis and drug self-administration. The proposed studies will characterize the relationships between self-administered cocaine and activation of the HPA axis by generating dose response and time course data during the acquisition, maintenance, extinction and re-initiation phases of cocaine self-administration. The hypothesis that the active (response contingent) versus passive (response non-contingent) administration of cocaine differentially affects the HPA axis will be tested by comparing subjects that receive cocaine under different response contingencies. The proposed studies also will generate new information on whether prior activation of the HPA axis through pharmacologic and non-pharmacologic means alters the effects of self-administered cocaine on the HPA axis and the reinforcing properties of cocaine. The results of these experiments could provide new and important insights on the relationships between stress and drug seeking behavior.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
1R01DA010830-01A2
Application #
2628861
Study Section
Human Development Research Subcommittee (NIDA)
Program Officer
Thadani, Pushpa
Project Start
1998-04-01
Project End
2001-02-28
Budget Start
1998-04-01
Budget End
1999-02-28
Support Year
1
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Louisiana State University Hsc New Orleans
Department
Pharmacology
Type
Schools of Medicine
DUNS #
782627814
City
New Orleans
State
LA
Country
United States
Zip Code
70112
Galici, R; Pechnick, R N; Poland, R E et al. (2000) Comparison of noncontingent versus contingent cocaine administration on plasma corticosterone levels in rats. Eur J Pharmacol 387:59-62