Area:
Addiction, behavioral pharmacology
We are testing a new system for linking grants to scientists.
The funding information displayed below comes from the
NIH Research Portfolio Online Reporting Tools and the
NSF Award Database.
The grant data on this page is limited to grants awarded in the United States and is thus partial. It can nonetheless be used to understand how funding patterns influence mentorship networks and vice-versa, which has deep implications on how research is done.
You can help! If you notice any innacuracies, please
sign in and mark grants as correct or incorrect matches.
Sign in to see low-probability grants and correct any errors in linkage between grants and researchers.
High-probability grants
According to our matching algorithm, Julie Broadbent is the likely recipient of the following grants.
Years |
Recipients |
Code |
Title / Keywords |
Matching score |
1996 — 1997 |
Broadbent, Julie |
R21Activity Code Description: To encourage the development of new research activities in categorical program areas. (Support generally is restricted in level of support and in time.) |
Sensitization of Ethanol Stimulated Locomotor Activity @ Oregon Health and Science University |
1 |
2000 — 2005 |
Broadbent, Julie |
R01Activity Code Description: To support a discrete, specified, circumscribed project to be performed by the named investigator(s) in an area representing his or her specific interest and competencies. |
Sensitization and Conditioning With Ethanol @ University of Michigan At Ann Arbor
DESCRIPTION: (Adapted from the Investigator's Abstract) The long-term goals of this project are to increase our understanding of the neural processes that underlie alcoholism, thereby accelerating development of effective treatment strategies. Individuals susceptible to alcoholism show a characteristic progression from intermittent social use of alcohol to compulsive drinking and frequent relapse, despite severe social and economic consequences. Thus, these individuals differ from the general population in their response to repeated alcohol exposure. Examination of neuroadaptive responses that develop from such drug exposure will, therefore, be valuable in shedding light on the neural mechanisms underlying this disease. The proposed 5-year project will examine sensitization, and conditioned responses to stimuli paired with drug administration, two neuroadaptive responses that have been accorded central roles in contemporary theories of drug abuse. Specifically, the experiments will assess the conditions under which sensitization develops, the neuropharmacological bases of sensitization, the contribution of conditioning processes to sensitization, and the impact of sensitization and conditioned responses on the behavioral effects of alcohol. Changes in locomotor activity in DBA/2J mice will be used as the experimental model. Initial experiments will examine the influence of alcohol dose and number of drug exposures on acquisition of sensitization. The neuropharmacological bases of sensitization will then be assessed by manipulating selected neurotransmitter systems using specific CNS lesions, dopamine and glutamate antagonists, and GABA agonists. Manipulations that alter sensitization will be examined further in studies that assess the contribution of conditioning processes to sensitization. Additional experiments will assess the impact of sensitization and conditioned responses on the rewarding effects of alcohol, and development of cross-sensitization between alcohol and other drugs. Finally, several mouse populations will be screened for development of sensitization in order to identify a second population with which parallel experiments can be conducted in the future. Such studies will increase the generality of findings in DBA/2J mice. The studies proposed in this application will provide valuable new information regarding the neural mechanisms underlying neuroadaptive responses to alcohol and the impact of these responses on the rewarding effects of alcohol.
|
1 |