This research proposal is concerned with our earlier findings that either morphine or codeine administered intraventricularly to pentobarbital-anesthetized rabbits and/or rats exerted an analeptic effect which was potentiated by naloxone or naltrexone pretreatment. Codeine, but not morphine, also exerted its analeptic effect when given intravenously, even without prior treatment with an opiate antagonist. The analeptic effect was abolished by atropine pretreatment, suggesting involvement of a cholinergic mechanism. We propose to fully characterize the dose-response, time-effect and phramacological profile of this opiate arousal effect in the rat, and then proceed to determine by stereotaxic microinjection techniques their sites(s) of action in the brain. Upon establishing these properties we plan to determine whether other opiates of different analgesic potencies and chemical structures possess analeptic activity. They will be ranked according to their analeptic potencies, and possible correlations made between this property and any of their other known actions. Similar studies will be carried out with the various endogenous opioids and opiate antagonists. We shall then attempt to establish whether specific opiate receptor subtypes are involved in this action. Because the data thus far suggest possible relationships between opiate-induced arousal and cholinergic mechanisms, we plan to focus much of our neuroanatomical and neurochemical studies on central cholinergic pathways. Central cholinergic activity will be assessed by measuring high affinity choline uptake into synaptosomes from various regions of the brain, and levels of ACh and choline will be monitored. The main objective of this proposal is to understand the nature of this previously unknown property of the opiates and to determine whether it contributes to the overall pharmacology of those agents. Recent reports suggest that the arousal property of codeine may be useful in the treatment of narcolepsy, while that same property of morphine in chronic pain management may lead to sleep disorders. These studies may help establish the pharmacological bases of such clinical observations.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
1R01DA003824-01
Application #
3208539
Study Section
(DABA)
Project Start
1985-07-01
Project End
1988-12-31
Budget Start
1985-07-01
Budget End
1985-12-31
Support Year
1
Fiscal Year
1985
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
Schools of Medicine
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Horita, A; Carino, M A; Chinn, C (1989) Fentanyl produces cholinergically-mediated analeptic and EEG arousal effects in rats. Neuropharmacology 28:481-6
Horita, A; Carino, M A; Chinn, C (1988) Codeine produces a cholinergically mediated analeptic effect in rats and rabbits. Pharmacol Biochem Behav 30:115-8
Chinn, C; Horita, A (1988) Sites of action of morphine in generation of hippocampal theta rhythm in the rat. Proc West Pharmacol Soc 31:215-6
Yabase, M; Chinn, C; Horita, A (1988) Clonidine activates a cholinergic hippocampal theta rhythm in the rat. Proc West Pharmacol Soc 31:213-4
Horita, A; Carino, M A (1988) Intraseptal microinjection of adrenocorticotropic hormone1-24 antagonizes pentobarbital-induced narcosis and depression of hippocampal cholinergic activity. J Pharmacol Exp Ther 247:863-6
Chinn, C; Horita, A (1987) Activation of hippocampal theta rhythm by opiates in the rat. Proc West Pharmacol Soc 30:41-3