A large number of investigators at Virginia Commonwealth University (VCU) have made significant contributions to our knowledge of drugs of abuse and related phenomena during the past two decades. The interests of these researchers encompass behavioral, pharmacokinetic, neurochemical, and pharmacological characterization of all classes of abused drugs. While there have always been active collaborations among these investigators, the drug abuse research effort at VCU has been enhanced by the creation of the NIDA Center on Drug Abuse Research. The primary objective of the Center is to foster interdisciplinary research on drug abuse at VCU. The Center will continue to provide a mechanism for bringing together scientists from many different disciplines (pharmacology, toxicology, physiology, histology, biostatistics, neurology, medicinal chemistry, microbiology, pediatrics, substance abuse medicine, etc.) who have had the opportunity to share information and ideas regarding abused drugs. Another major contribution has been to facilitate the training and development of young scientists in drug abuse research. Our success in stimulating collaborative research as well as in recruiting young investigators into drug abuse research is reflected in the growth of the Center which is composed of a core and eight research projects. The role of the Core is to provide program management and facilitate interaction and cooperation among the participants through its administrative, drug synthesis, instrumentation and statistical components. The objective of Project 1 is to test the dopamine hypothesis of the mechanism of action of cocaine through structure-activity relationship studies in rats. Project 2 is designed to verify that there is an increased incidence of apnea in infants exposed in utero to drugs of abuse and to devise effective treatment strategies. The objective of Project 3 is to understand in a comprehensive manner how cocaine affects the cerebral circulation and microvascular function. The evaluation of the functional role of central nicotine receptors will be carried out in Project 4. The hypothesis to be tested is that nicotine agonists and antagonists act through two distinct receptor systems which have not yet been fully characterized. Studies will be conducted in both normal and brain-injured adults as well as in neonatal animals. The impact of opioid exposure on the fetus during pregnancy has not been fully explored. Therefore, the effects of in utero methadone exposure on brain neurochemistry will continue to be evaluated in Project 5. The growing concern as to when and how pain in newborns should be treated forms the basis of Project 6. The emphasis will be placed upon the assessment of the development of opioid tolerance and dependence in neonatal rats. Project 7 will be devoted to the cloning of cannabinoid receptors and subsequent pharmacological characterization in order to establish the functional role of these receptor in the central nervous system. Finally, the objective of Project 8 will be the elucidation of the antinociceptive mechanism(s) of cannabinoids with particular emphasis on second messenger systems.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Specialized Center (P50)
Project #
5P50DA005274-07
Application #
2117536
Study Section
Special Emphasis Panel (SRCD (48))
Project Start
1988-09-30
Project End
1996-07-31
Budget Start
1994-09-01
Budget End
1995-07-31
Support Year
7
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Bagdas, Deniz; Alkhlaif, Yasmin; Jackson, Asti et al. (2018) New insights on the effects of varenicline on nicotine reward, withdrawal and hyperalgesia in mice. Neuropharmacology 138:72-79
Jackson, Kia J; Muldoon, Pretal P; Walters, Carrie et al. (2016) Neuronal calcium/calmodulin-dependent protein kinase II mediates nicotine reward in the conditioned place preference test in mice. Behav Pharmacol 27:50-6
Nass, Sara R; Long, Jonathan Z; Schlosburg, Joel E et al. (2015) Endocannabinoid Catabolic Enzymes Play Differential Roles in Thermal Homeostasis in Response to Environmental or Immune Challenge. J Neuroimmune Pharmacol 10:364-70
Muldoon, P P; Chen, J; Harenza, J L et al. (2015) Inhibition of monoacylglycerol lipase reduces nicotine withdrawal. Br J Pharmacol 172:869-82
Poklis, Justin L; Devers, Kelly G; Arbefeville, Elise F et al. (2014) Postmortem detection of 25I-NBOMe [2-(4-iodo-2,5-dimethoxyphenyl)-N-[(2-methoxyphenyl)methyl]ethanamine] in fluids and tissues determined by high performance liquid chromatography with tandem mass spectrometry from a traumatic death. Forensic Sci Int 234:e14-20
Poklis, Justin L; Nanco, Carol R; Troendle, Michelle M et al. (2014) Determination of 4-bromo-2,5-dimethoxy-N-[(2-methoxyphenyl)methyl]-benzeneethanamine (25B-NBOMe) in serum and urine by high performance liquid chromatography with tandem mass spectrometry in a case of severe intoxication. Drug Test Anal 6:764-9
Ignatowska-Jankowska, B M; Ghosh, S; Crowe, M S et al. (2014) In vivo characterization of the highly selective monoacylglycerol lipase inhibitor KML29: antinociceptive activity without cannabimimetic side effects. Br J Pharmacol 171:1392-407
Bagdas, Deniz; Muldoon, Pretal P; Zhu, Andy Z X et al. (2014) Effects of methoxsalen, a CYP2A5/6 inhibitor, on nicotine dependence behaviors in mice. Neuropharmacology 85:67-72
Wolf, Carl E; Goldstein, Ashley; Poklis, Justin L et al. (2014) Evaluation of an enzyme immunoassay for the detection of methadone metabolite EDDP [2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine] in urine. J Clin Lab Anal 28:136-40
Burston, James J; Sagar, Devi Rani; Shao, Pin et al. (2013) Cannabinoid CB2 receptors regulate central sensitization and pain responses associated with osteoarthritis of the knee joint. PLoS One 8:e80440

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