National Institute
on Drug Abuse (NIDA) Seeks Applications Using the JAX Diversity Outcross (DO)
Mice
Notice Number: NOT-DA-12-013
Key Dates
Release
Date: April 3, 2012
Issued by
National Institute on Drug Abuse (NIDA))
Purpose
The Genetics and Molecular
Neurobiology Research Branch (GMNRB) at the National Institute on Drug Abuse
(NIDA) seeks applications using the JAX Diversity Outcross (DO) mice to
identify genetic variants associated with substance abuse and addiction as well
as treatment response. To apply for grants within this area of interest,
refer to PA-11-026 Molecular Genetics of Drug Addiction and Related
Co-Morbidities (R01) (https://grants.nih.gov/grants/guide/pa-files/PA-11-026.html).
The diversity outcross mice permit fine mapping of genetic
loci for complex trait with far less effort and greater resolution than before
with other mouse resources. Papers highlighting this resource can
be found in the Feb 16, 2012 issues of Genetics www.genetics.org and G3:
Genes|Genomes|Genetics www.g3journal.org.
Identification the gene variants underlying the following
traits DO mice that are of interest to GMNRB include but are not limited to:
- Motivation
to work for a drug as measured by drug self-administration breakpoint.
- Persistence
of drug seeking behavior
- Compulsivity
of drug seeking behavior
- Preference
between drug and sucrose following drug self-administration and the absence of
any withdrawal symptoms
- Withdrawal
- Tolerance
- Sensitization
- Novelty
seeking
- Different
measures of impulsivity, e.g. 5CSRTT (five-choice serial reaction time
task) and reversal learning
- Goal
trackers vs. sign Trackers, i.e. difference in cue reactivity and auto-shaping.
- Measures
of anxiety associated with drug seeking behavior.
- Altered
brain circuitry following drug exposure
- Drug
Toxicity
- Pharmacokinetics
- Phenotypes
produced by GXE interactions that may affect substance abuse and addiction
phenoytpes such as maternal separation, victimization by aggression,
learned helplessness in utero exposure to drugs of abuse and environmental
toxins such as lead, and vulnerability to drugs of abuse during puberty
and early adulthood.
- Genetic
modifiers of knockout mouse phenotypes affecting drug response.
- Treatment
response to pharmacological agents that have potential for treating substance
abuse
- Nicotine,
cocaine, and heroin vaccine responses such antibody titer and amount of free
and bound drug in tissues.
The JAX:DO are available from The Jackson Laboratory (Bar
Harbor, ME), as JAXMice stock number 009376. Sibling information at each
generation is tracked and made available upon request. http://cgd.jax.org/datasets/phenotype/SvensonDO.shtml.
If interested in developing an application please contact
Dr. Jonathan Pollock.
Inquiries
Please direct all inquiries
to:
Jonathan D. Pollock, Ph.D.
Chief
Genetics and Molecular
Neurobiology Research Branch
Division of Basic
Neuroscience and Behavioral Research
National Institute on Drug
Abuse
6001 Executive Blvd. Rm 4103
Bethesda, MD 20892
(For Fedex Delivery the
address is Rockville, MD 20852)
Telephone: 301-435-1309
FAX: 301-594-6043
Email.
jpollock@mail.nih.gov