The discovery of the endogenous opiate peptides (endorphins, dynorphin, methionine and leucine-enkephalin being among the most prominent) has led to a detailed search for a physiological function for these substances. It has been suggested that the enkephalins and endorphins may function as neurotransmitters or neuromodulators in the central and peripheral nervous system. Morphine interacts preferentially with mu receptors, whereas the enkephalins interact preferentially with delta receptors. Dynorphin interacts specifically with a third type of opiate receptor, the kappa receptor. Attempts to assign a physiological role to the opiates is complicated by the heterogeneity of receptors and at present the evidence available is not sufficient to assign different receptors to different physiological functions. In this proposal, we will test the effects of morphine, enkephalins, dynorphin, endorphins and other endogenous and synthetic opiate agonists and antagonists in perfused organ systems in which the nerve stimulation mediated release of norepinephrine can be evaluated. Changes in the release of norepinephrine following nerve stimulation will be determined in the isolated perfused cat and rat spleen and adrenal gland, guinea-pig and rat heart and the rat tail artery. These studies will help in elucidating events occurring at nerve endings in organs of different species and aid in determining physiological functions of various opiates. By comparing presynaptic and postsynaptic effects of these opiate agonists and antagonists in perfused organ systems, we hope to assign physiological functions to the various opiate receptors. Blood pressure and heart rate changes in conscious rats will be measured after administration of the opiate agonists and antagonists intraventricularly, and intravenously to attempt to correlate receptor function with physiological parameters. Opiates have extensive effects on behavior and mood and Beta-endorphin is being used clinically for the treatment of a variety of psychiatric illnesses on an experimental basis. A more complete understanding of the physiological roles of the various opiates will aid the treatment of mental illness.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
3R01DA003504-06S1
Application #
3207972
Study Section
Drug Abuse Biomedical Research Review Committee (DABR)
Project Start
1984-07-01
Project End
1990-07-31
Budget Start
1989-08-01
Budget End
1990-07-31
Support Year
6
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Kansas Lawrence
Department
Type
Schools of Pharmacy
DUNS #
072933393
City
Lawrence
State
KS
Country
United States
Zip Code
66045
Dixon, W R; Chang, P L (1990) Changes in cardiovascular responses of conscious rats to endogenous opioids following treatment with catecholamine-depleting agents. Ann N Y Acad Sci 604:152-68
Chang, A P; Dixon, W R (1990) Role of plasma catecholamines in eliciting cardiovascular changes seen during naloxone-precipitated withdrawal in conscious, unrestrained morphine-dependent rats. J Pharmacol Exp Ther 254:857-63
Chen, Y M; Dixon, W R (1990) The effect of etorphine on nicotine- and muscarine-induced catecholamine secretion from perfused rat adrenal glands. Life Sci 46:1167-73
Semafuko, W E; Rutledge, C O; Dixon, W R (1989) Modulation of adrenergic neurotransmission in the rat tail artery by dietary lipids. J Cardiovasc Pharmacol 13:138-45
Dixon, W R; Chang, A P; Machado, J et al. (1989) Effect of intravenous infusion and oral self-administration of cocaine on plasma and adrenal catecholamine levels and cardiovascular parameters in the conscious rat. NIDA Res Monogr 95:335-6
Chen, Y M; Dixon, W R; Wakade, A R (1989) The effect of etorphine on the secretion of endogenous catecholamines and total tritium evoked by nerve- and acetylcholine-stimulation in perfused rat adrenal glands. Life Sci 44:167-74
Dixon, W R; Lau, B; Chang, A P et al. (1989) Effect of oral self-administration of cocaine on adrenal catecholamine levels and cardiovascular parameters in the conscious rat. Proc West Pharmacol Soc 32:231-4
Chang, A P; Dillard, M; Dixon, W R (1989) Effect of naloxone on blood pressure responses and plasma catecholamine levels following clonidine injection in conscious, unrestrained rats. J Cardiovasc Pharmacol 13:277-82
Semafuko, W E; Follett, D L; Dixon, W R (1988) Effect of etorphine on adrenergic neurotransmission in the rat and guinea pig heart. Pharmacology 37:195-202
Dixon, W R; Chang, A P (1988) Effect of phentolamine on blood pressure, heart rate and plasma catecholamine levels in conscious, unrestrained morphine dependent rats during naloxone precipitated autonomic withdrawal responses. Proc West Pharmacol Soc 31:117-9

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