In our initial study we hypothesized that the combination of an intravenous anesthetic with an opioid might give different outcomes for different components of anesthesia. We confirmed this assumption with the most striking results being observed when using the diazepam-morphine combination which produced synergism with respect to the hypnotic action but antagonism with regard to the antinociceptive action. In this renewal application we propose investigations that will be devoted to a comprehensive analysis of the mechanisms of the benzodiazepine-opioid interactions. We hypothesize that the synergistic midazolam-morphine hypnotic interaction is pharmacodynamic in nature and that it is based on the interaction of opioid and benzodiazepine receptor systems in the mediation of the hypnotic effect, possibly to the degree when the hypnotic action of benzodiazepines has an underlying mechanism involving opioid receptors and vice versa for the hypnotic action of morphine. It is also hypothesized that the wide individual variability in response to the hypnotic action of benzodiazepines is largely due to pharmacodynamic factors and that it may be reduced by the addition of morphine. Finally, our hypothesis also considers that the antagonistic effect of midazolam on morphine analgesia is mediated by benzodiazepine receptors and associated with a benzodiazepine-induced depression of an inhibitory descending pain control system activated by morphine. To analyze the interactions between benzodiazepines (midazolam) and opioids (morphine) we will perform experiments in rats using the following basis tests: loss of the righting reflex, suppression of spontaneous locomotor activity, and increase in reaction threshold to noxious stimulation. Quantal dose-response curves for midazolam, morphine and their combinations concerned with the above test will be determined and the effects of various specific receptor antagonists on these curves will be investigated. Algebraic and isobolographic methods for analysis of agent interactions will be used. These experiments will test our hypotheses and produce new and detailed quantitative analysis of the mechanisms involved in hypnotic and analgesic interactions of benzodiazepines and opioids which are commonly used now in anesthesiological practice.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM035135-05
Application #
3287305
Study Section
Surgery, Anesthesiology and Trauma Study Section (SAT)
Project Start
1985-09-01
Project End
1994-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
5
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Alabama Birmingham
Department
Type
Schools of Medicine
DUNS #
004514360
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Kissin, I; Brown, P T; Bradley Jr, E L (1992) Locomotor activity after recovery from hypnosis: midazolam-morphine versus midazolam. Anesth Analg 75:929-31
Kissin, I; Brown, P T; Bradley Jr, E L (1990) Morphine and fentanyl anesthetic interactions with diazepam: relative antagonism in rats. Anesth Analg 71:236-41
Kissin, I; Brown, P T; Bradley Jr, E L (1990) Sedative and hypnotic midazolam-morphine interactions in rats. Anesth Analg 71:137-43
Kissin, I; Vinik, H R; Castillo, R et al. (1990) Alfentanil potentiates midazolam-induced unconsciousness in subanalgesic doses. Anesth Analg 71:65-9
Kissin, I; Brown, P T; Bradley Jr, E L et al. (1989) Diazepam--morphine hypnotic synergism in rats. Anesthesiology 70:689-94
Kissin, I; Mason 3rd, J O; Bradley Jr, E L (1987) Morphine and fentanyl hypnotic interactions with thiopental. Anesthesiology 67:331-5
Kissin, I; Mason 3rd, J O; Bradley Jr, E L (1986) Morphine and fentanyl interactions with thiopental in relation to movement response to noxious stimulation. Anesth Analg 65:1149-54