Until a shorttime ago, studies of neurotransmitter receptors in the brain have relied primarily upon neurophysiological techniques. Recently, however biochemical methods for the direct measurement of receptors have become available. We have demonstrated the specific binding of muscarinic receptors using QNB and CD, nicotinic receptors using Naja naja, GABAergic receptors using muscimol, dopamine receptors using spiroperidol and benzodiazepine receptors using flunitrazepam. We have used these ligands as tools in solving some of the problems in neuropharmacology. We have found biochemical receptor alterations in discrete brain regions from postmortem brain samples of persons dying from Huntington's, Parkinson's, Alzeheimer's Disease and found Schizophrenic brain samples. I am interested in finding new ligands in the future so that novel neurotransmitter and drug receptors can be labeled. We are currently identifying the barbiturate and nonbenzodiazepine receptors in brain. An important area of the research involves the mechanism of coupling between the receptor and the effector (perhaps the guanine nucleotide binding site or adenylate cyclase). Other important areas involve receptor regulation and receptor heterogeneity. Neurotransmitter receptors appear to be regulated in an up or down direction depending upon neuronal activity. We are interested in determining the exact mechanism of this regulation. Neurotransmitter receptors for the opiate, alpha- and beta-adrenergic, dopamine, histamine and muscarinic cholinergic systems exist as subtypes. Receptor binding studies have complimented classical pharmacological studies in this respect. We are interested in determining the mechanism of receptor heterogeneity. We have clues which indicate that ions, and guanine nucleotides are important agents in illustrating receptor homogeneity.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Scientist Development Award - Research (K02)
Project #
5K02MH000095-10
Application #
3069578
Study Section
Research Scientist Development Review Committee (MHK)
Project Start
1976-07-01
Project End
1986-06-30
Budget Start
1985-07-01
Budget End
1986-06-30
Support Year
10
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Arizona
Department
Type
Schools of Medicine
DUNS #
City
Tucson
State
AZ
Country
United States
Zip Code
85722
Lee, Royce; Meyerhoff, Jonah; Coccaro, Emil F (2014) Intermittent Explosive Disorder and aversive parental care. Psychiatry Res 220:477-82
Coccaro, Emil F; Boparai, Anjiwan; Lee, Royce (2013) Cerebrospinal fluid 5-hydroxyindolacetic acid correlates directly with negative affective intensity, but not affective lability, in human subjects. Int J Neuropsychopharmacol 16:261-9
Coccaro, Emil F; Lee, Royce; Liu, Tianmin et al. (2012) Cerebrospinal fluid neuropeptide Y-like immunoreactivity correlates with impulsive aggression in human subjects. Biol Psychiatry 72:997-1003
Coccaro, Emil F; Nayyer, Habiba; McCloskey, Michael S (2012) Personality disorder--not otherwise specified evidence of validity and consideration for DSM-5. Compr Psychiatry 53:907-14
Coccaro, Emil F; Lee, Royce; Owens, Michael J et al. (2012) Cerebrospinal fluid substance P-like immunoreactivity correlates with aggression in personality disordered subjects. Biol Psychiatry 72:238-43
Coccaro, Emil F; Kavoussi, Richard J (2010) GH response to intravenous clonidine challenge: absence of relationship with behavioral irritability, aggression, or impulsivity in human subjects. Psychiatry Res 178:443-5
Coccaro, Emil F; Lee, Royce (2010) Cerebrospinal fluid 5-hydroxyindolacetic acid and homovanillic acid: reciprocal relationships with impulsive aggression in human subjects. J Neural Transm (Vienna) 117:241-8
Lee, Royce; Petty, Frederick; Coccaro, Emil F (2009) Cerebrospinal fluid GABA concentration: relationship with impulsivity and history of suicidal behavior, but not aggression, in human subjects. J Psychiatr Res 43:353-9
Kavoussi, R J; Hauger, R L; Coccaro, E F (1999) Prolactin response to d-fenfluramine in major depression before and after treatment with serotonin reuptake inhibitors. Biol Psychiatry 45:295-9
Coccaro, E F; Kavoussi, R J; Cooper, T B et al. (1998) Acute tryptophan depletion attenuates the prolactin response to d-fenfluramine challenge in healthy human subjects. Psychopharmacology (Berl) 138:9-15

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