The long term objectives of the work proposed herein are (a) elucidation of the mechanism of action of hallucinogenic agents (with particular emphasis on derivatives of phenalkylamines and indolealkylamines), (b) determination of the role of the neurotransmitter substance serotonin (5-HT) in such a mechanism, and (c) identification of structural characteristics required by a molecule in order for it to be hallucinogenic (achievement of this latter goal would allow the potential identification of those new drugs and abnormally produced endogenous substances which might possess hallucinogenic liability).
The specific aims of this present proposal are to identify those phenalkylamines (PAA) and indolealkylamines (IAA) that produce qualitatively similar behavioral effects and to then limit mechanistic studies to these agents. Using the discriminative stimulus paradigm, PAA and IAA derivatives will be administered to rats trained to discriminate DOM or amphetamine from saline. Generalization studies will provide information as to the """"""""DOM-likeness,"""""""" for example, of each of these agents. These data will then be compared with 5-HT receptor affinities (previously determined in these laboratories) and with 5-HT1 and 5-HT2 brain binding data in order to determine the role of these binding sites in the mechanism of action of the hallucinogens being studied (and in order to determine if fundus 5-HT receptors are similar to either of these binding sites). Finally, because it appears that hallucinogenic PPAs and IAAs might be acting in vivo as 5-HT agonists, several novel serotonergic agents, including latent 5-HT analogs, will be synthesized and evaluated to challenge this hypothesis. The novelty of our approach is (a) that an in vivo """"""""drug detection"""""""" paradigm is being used (to obtain qualitative as well as quantitative data) in order to assure that each of the agents under study is producing a common effect, and (b) that medicinal chemical principles are being employed to design and synthesize agents that will aid in determining the role of 5-HT1 vs. 5-HT2 binding as it relates to hallucinogenic agents. Thus, this study should afford a better understanding of certain classes of drugs of abuse and will also shed light on the functional role of a major neurotransmitter.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA001642-10
Application #
3206971
Study Section
Drug Abuse Biomedical Research Review Committee (DABR)
Project Start
1989-04-01
Project End
1992-03-31
Budget Start
1990-04-01
Budget End
1991-03-31
Support Year
10
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Type
Schools of Pharmacy
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Glennon, Richard A; Dukat, Ma?gorzata (2017) Synthetic Cathinones: A Brief Overview of Overviews with Applications to the Forensic Sciences. Ann Forensic Res Anal 4:
Glennon, Richard A; Dukat, Ma?gorzata (2017) Structure-Activity Relationships of Synthetic Cathinones. Curr Top Behav Neurosci 32:19-47
Glennon, Richard A (2017) The 2014 Philip S. Portoghese Medicinal Chemistry Lectureship: The ""Phenylalkylaminome"" with a Focus on Selected Drugs of Abuse. J Med Chem 60:2605-2628
Glennon, Richard A (2014) Bath salts, mephedrone, and methylenedioxypyrovalerone as emerging illicit drugs that will need targeted therapeutic intervention. Adv Pharmacol 69:581-620
Khorana, Nantaka; Young, Richard; Glennon, Richard A (2009) Effect of 8-hydroxy-2-(N,N-di-n-propylamino)tetralin and MDMA on the discriminative stimulus effects of the classical hallucinogen DOM in rats. Pharmacol Biochem Behav 91:385-92
Young, Richard; Glennon, Richard A (2009) S(-)Propranolol as a discriminative stimulus and its comparison to the stimulus effects of cocaine in rats. Psychopharmacology (Berl) 203:369-82
Young, Richard; Glennon, Richard A (2008) MDMA (N-methyl-3,4-methylenedioxyamphetamine) and its stereoisomers: Similarities and differences in behavioral effects in an automated activity apparatus in mice. Pharmacol Biochem Behav 88:318-31
Glennon, Richard A; Young, Richard; Dukat, Malgorzata et al. (2007) N-Methyl-1-(4-methoxyphenyl)-2-aminopropane (PMMA) and N-Methyl-1-(3,4-methylenedioxyphenyl)-2-aminopropane (MDMA) produce non-identical discriminative stimuli in rats. Pharmacol Biochem Behav 86:477-84
Glennon, Richard A; Bondareva, Tatiana; Young, Richard (2006) alpha-Ethyltryptamine (alpha-ET) as a discriminative stimulus in rats. Pharmacol Biochem Behav 85:448-53
(1994) Hallucinogenic agents: drugs of abuse as neurochemical tools. NIDA Res Monogr 140:94-8

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