Skip Navigation LinksHome > October 2005 - Volume 103 - Issue 4 > Morphine Inhibits Acetylcholine Release in Rat Prefrontal Co...
Anesthesiology:
Laboratory Investigations

Morphine Inhibits Acetylcholine Release in Rat Prefrontal Cortex When Delivered Systemically or by Microdialysis to Basal Forebrain

Osman, Nadir I. M.D.*; Baghdoyan, Helen A. Ph.D.†; Lydic, Ralph Ph.D.†

Free Access
Article Outline
Collapse Box

Author Information

Collapse Box

Abstract

Background: Cortical acetylcholine originates in the basal forebrain and is essential for maintaining normal cognition and arousal. Morphine impairs these cholinergically mediated cortical functions. The current study tested the hypothesis that morphine decreases prefrontal cortical acetylcholine release by acting at the level of the basal forebrain.
Methods: Adult male Sprague-Dawley rats (n = 18) were anesthetized with isoflurane. One microdialysis probe was placed in the substantia innominata region of the basal forebrain and perfused with Ringer’s solution (control) followed by one concentration of morphine (1, 10, 100, or 1,000 μm) or morphine (1,000 μm) plus naloxone (100 μm). A second microdialysis probe was placed in the prefrontal cortex for measuring acetylcholine. In a second series of experiments, rats (n = 6) were implanted with electrodes for recording states of arousal, a guide cannula positioned above the prefrontal cortex for inserting a microdialysis probe, and an indwelling jugular vein catheter. The effects of administering intravenous morphine (30 mg/kg) versus normal saline (0.9%) on prefrontal cortical acetylcholine release, cortical electroencephalographic power, and behavior were quantified.
Results: Dialysis delivery of morphine to the substantia innominata caused a concentration-dependent, naloxone-sensitive decrease in acetylcholine release within the prefrontal cortex. The maximal decrease in acetylcholine was 36.3 ± 11.5%. Intravenous morphine administration significantly decreased cortical acetylcholine release, increased electroencephalographic power in the 0.5- to 5-Hz range, and eliminated normal wakefulness.
Conclusion: Morphine causes obtundation of arousal and may cause cognitive impairment by acting at the level of the substantia innominata to disrupt cortical cholinergic neurotransmission.
OPIOIDS are the main antinociceptive agents used for treating chronic and acute pain.1 The therapeutic potential of opioids must be balanced against unwanted side effects such as respiratory depression, diminished arousal, impaired cognition, and delirium. Among intensive care unit patients2 and nondemented elderly patients,3,4 delirium is common and is associated with delayed recovery and increased morbidity.2,5 The neuronal mechanisms by which opioids impair arousal and mental status remain poorly understood but are likely to involve cortical acetylcholine.
The prefrontal cortex comprises the most anterior cortical region and in humans represents approximately one third of the entire cortex.6,7 There is good agreement that major functions of the prefrontal cortex include regulation of attention,8,9 working memory,10 cardiopulmonary control,11 and sleep.12,13 Cortical acetylcholine also is essential for normal cognition and arousal,14–16 and anticholinergic drugs can contribute to delirium.2,5 The substantia innominata region of the basal forebrain contains cholinergic neurons that project to cortex.17 Opioids decrease acetylcholine release in regions of the pontine reticular formation regulating arousal.18,19 No studies have localized neurons through which morphine might alter acetylcholine in the prefrontal cortex. Therefore, this study was designed to evaluate the hypothesis that morphine decreases acetylcholine release in prefrontal cortex and slows cortical activity by disrupting cholinergic neurotransmission from basal forebrain. Portions of these data have been presented in abstract form.20
Back to Top | Article Outline

Materials and Methods

Chemicals and Drug Solutions
Chemicals used for Ringer’s solution, mobile phase, acetylcholine standards, and histology were purchased from Sigma-Aldrich (St. Louis, MO). Morphine sulfate was obtained from Sigma-Aldrich. Naloxone hydrochloride came from Mallinckrodt, Inc. (St. Louis, MO). Sterile saline (0.9%) was purchased from Abbott Laboratories (North Chicago, IL). Drug solutions used for microdialysis or for systemic administration were made immediately before use.
Back to Top | Article Outline
Experimental Procedures and Design
All experiments were approved by the University of Michigan Committee on Use and Care of Animals and conducted in accordance with the Public Health Service Policy on Humane Use and Care of Laboratory Animals (NIH Publication 80-23, National Academy of Sciences Press, Washington, DC, 1996). The two sets of experiments reported here used adult male Crl:CD®(SD)IGS BR (Sprague-Dawley) rats (n = 24) purchased from Charles River Laboratories (Wilmington, MA). The first set of studies measured acetylcholine release from prefrontal cortex of isoflurane anesthetized rat before and after dialysis delivery of morphine to basal forebrain. In the second set of experiments, prefrontal cortical acetylcholine release was measured from intact, unanesthetized rats before and after administering morphine or saline (control) via a permanently implanted jugular cannula.
Back to Top | Article Outline
Studies during Isoflurane Anesthesia
Rats (n = 18) were anesthetized with isoflurane in 100% O2 and placed in a Kopf Model 962 stereotaxic frame (David Kopf Instruments, Tujunga, CA) equipped with a Kopf Model 920 rat adaptor, anesthesia mask, and ear bars. A Cardiocap/5 monitor (Datex-Ohmeda, Madison, WI) was used to measure delivered isoflurane concentration, which was held at 1.5%. An isoflurane concentration of 1.38% ± 0.02 corresponds to a minimum alveolar concentration of 1 for rats.21 Spontaneous ventilation was maintained throughout the experiment, and continuous monitoring ensured that there was no depression of respiration. Core body temperature was measured by a rectal thermometer (YSI 400 Series; Harvard Apparatus, Holliston, MA) and maintained at 36°–37.5°C by a T/Pump Heat Therapy System (TP-500 model; Gaymar, Orchard Park, NY). A midline longitudinal scalp incision was made to expose the skull, and a drill (Dremel, Racine, WI) was used to make two small craniotomies for placing the microdialysis probes according to the rat brain atlas.22 Microdialysis probes (CMA/11; CMA Microdialysis, North Chelmsford, MA) had a membrane of 1 mm in length, 0.24 mm in diameter, and a molecular weight cutoff of 6,000 Da. One probe was aimed for the substantia innominata (stereotaxic coordinates: 1.6 mm posterior to bregma, 2.5 mm lateral to the midline, and 8.7 mm below bregma). A second microdialysis probe was aimed for the ipsilateral prefrontal cortex (stereotaxic coordinates: 3.0 mm anterior to bregma, 0.5 mm lateral to the midline, and 5.0 mm below bregma). Dialysis probes were perfused continuously with Ringer’s solution (147 mm NaCl, 2.4 mm CaCl2, 4.0 mm KCl, pH 5.8–6.2) at a flow rate of 2 μl/min using CMA/100 syringe pumps. The Ringer’s solution used to perfuse the prefrontal cortex probe also contained neostigmine bromide (10 μm) to prevent enzymatic degradation of acetylcholine. Dialysis probes were placed in the prefrontal cortex and after 45–60 min six dialysis samples (25 μl/sample) were collected from the prefrontal cortex while the substantia innominata probe was perfused with Ringer’s (control). A CMA/110 liquid switch was then used to deliver Ringer’s containing one concentration of morphine (1, 10, 100, or 1,000 μm) or a mixture of morphine (1,000 μm) and naloxone (100 μm) to the substantia innominata dialysis probe. The concentrations of morphine were based on previous studies.18,19 Six dialysis samples were collected from the prefrontal cortex during drug delivery to the substantia innominata. Only one concentration of morphine was tested per experiment, and separate experiments were performed for combined administration of morphine and naloxone. Morphine interferes with the electrochemical detection of acetylcholine by producing a large peak in the chromatogram that occludes the acetylcholine peak. Therefore, it was not possible to measure acetylcholine in the substantia innominata while delivering morphine to the substantia innominata.
Back to Top | Article Outline
Studies of Unanesthetized, Behaving Animals
Rats (n = 6) were implanted with CMA/11 guide cannula (Plastics One, Roanoke, VA) stereotaxically positioned 1 mm above the prefrontal cortex (guide tube coordinates: 3.0 mm anterior to bregma, 0.5 mm lateral to the midline, and 4.0 mm below bregma).22 Three skull electrodes were implanted for recording the cortical electroencephalogram. Electrodes were positioned 1 mm anterior and 1.5 mm lateral to bregma, 2 mm posterior and 1.27 mm lateral to bregma, and 2 mm posterior and 1.5 mm lateral to bregma. Additional recording electrodes were implanted in the dorsal neck muscles for measuring the electromyogram. Electrode pins were inserted into an electrical connector (Plastics One). Two stainless steel anchor screws (Small Parts Inc., Miami Lakes, FL) were placed in the skull, and dental acrylic was used to secure the dialysis guide tube, electrodes, and electrical connector to the skull.
This group of six rats also was implanted to permit jugular vein access for systemic injections during quiet wakefulness. The jugular vein was exposed and catheterized with a 12-cm length of Micro-Renathane tubing (MRE-040; Braintree Scientific, Braintree, MA). The tube was tunneled subcutaneously and led through the skin between the scapulas. This exposed end of the tube was fitted with a back-mounted flange guide cannula (C315GFL45UPB; Plastics One) and removable cap (C313CAC; Plastics One) and secured to be accessible for subsequent intravenous delivery of saline or morphine without handling the animal.
After postsurgical recovery, rats were conditioned to a Plexiglas recording chamber (Bioanalytical Systems, Inc. [BAS], West Lafayette, IN). This enclosure permitted recording of the electroencephalogram and electromyogram, in vivo microdialysis, and drug administration via a cannula connected to a syringe outside the chamber. The implanted electrodes were attached via a cable (Plastics One) to the digital polygraph. While in the recording chamber, rats could ambulate freely and had free access to bedding, food, and water. During the conditioning interval, rats spent 6–8 h/day in the recording chamber and then were returned to their home cages. Electroencephalographic recordings were amplified and filtered at 0.3 and 30 Hz. Signals were digitally captured using a Grass model 15LT digital polygraph (Astro-Med., Inc., Quincy, MA).
After at least 5 days of conditioning, experiments were initiated to measure acetylcholine release in prefrontal cortex of awake animals before and after systemic administration of either morphine or saline (control). A microdialysis probe was placed in the prefrontal cortex via the implanted guide tube. A syringe containing either morphine (30 mg/kg) or saline (0.9%) was connected by a 55.5 cm length of Micro-Renathane tubing (MRE-040; Braintree Scientific, Braintree, MA) to the jugular vein catheter. Tubing from the dialysis probe and the injection cannula were led out of the recording chamber. This made it possible to record the electroencephalogram, the electromyogram, and acetylcholine release before and after systemic drug delivery via the jugular cannula. States of arousal were scored in 10-s epochs based on the electroencephalogram, the electromyogram, and behavior. The dialysis probe was perfused continuously with Ringer’s solution at a flow rate of 2 μl/min using a CMA/100 syringe pump.
One hour after microdialysis probe insertion, six control dialysis samples (25 μl/sample) were collected during quiet wakefulness. At the end of the sixth sample, 1 ml of either morphine or saline was injected over a 4-min period via the jugular vein catheter. After these injections, another six microdialysis samples were collected from the prefrontal cortex. The prefrontal cortex probe was perfused with Ringer’s solution throughout the experiment. Preexperimental and postexperimental in vitro probe recoveries were performed and compared using a t test. These measures of probe recovery ensured that alterations in measured acetylcholine were not an artifact of changes in the dialysis membrane.
Back to Top | Article Outline
Acetylcholine Measurement Using Microdialysis and High-performance Liquid Chromatography with Electrochemical Detection
For quantification of acetylcholine, each dialysis sample was injected into a high-performance liquid chromatography system (CC-5 electrochemical detector; BAS). As previously described,23 samples were carried through the system by a 50 mm Na2HPO4 mobile phase (pH 8.5) at a flow rate of 1.0 ml/min and a pressure of 3,000–3,500 psi. An analytical column (MF-6150; 2.1 mm diameter, 100 mm length; BAS) separated choline and acetylcholine, and an immobilized enzyme reactor column (MF-6151; BAS) containing acetylcholinesterase converted acetylcholine into hydrogen peroxide. The hydrogen peroxide produced from this reaction was proportional to the amount of acetylcholine in the dialysis sample and was measured at a 500-mV applied potential on a platinum electrode referenced to a Ag+/AgCl electrode. Chromatograms were digitized using ChromGraph software (BAS), and the area under the chromatographic peak was referenced to the standard curve to express acetylcholine as pmol/12.5 min. The limit of detection for acetylcholine was 0.05 pmol/25 μl.
Back to Top | Article Outline
Histologic Analyses
All microdialysis sites were identified histologically according to the following procedure. Animals were deeply anesthetized and decapitated. Brains were immediately frozen and serially sectioned at 40 μm using a Leica cryostat (CM 3050S; Leica Microsystems, Nussloch, Germany). Coronal slide-mounted sections were dried, fixed in hot (80°C) paraformaldehyde vapor, and stained with cresyl violet. All tissue sections containing glial scars caused by microdialysis probes were compared to the rat brain atlas22 to localize probe placement. The deepest point of each probe site was assigned stereotaxic coordinates in millimeters relative to bregma. Histologically confirmed placement of dialysis probes in substantia innominata and prefrontal cortex was required for inclusion of acetylcholine measures in the results.
Back to Top | Article Outline
Statistical Analyses
Measures of acetylcholine were evaluated using descriptive statistics, one-way repeated-measures analysis of variance, and the Dunnett post hoc multiple comparisons test. Power calculations were used to confirm the appropriate sample size. A probability (P) value of 0.05 or less was considered statistically significant. Analyses of the cortical electroencephalogram using fast Fourier transformation quantified the dominant frequencies from 0.5 to 25 Hz. The total power for each frequency interval of cortical electroencephalogram was computed before and after intravenous injection of saline or morphine. Two-way analysis of variance for repeated measures and the Tukey-Kramer multiple comparisons test were used to evaluate the contributions of injection condition and electroencephalographic frequency to total electroencephalographic power.
Back to Top | Article Outline

Results

Histologic Analyses Confirmed Correct Dialysis Probe Placement
Fig. 1
Fig. 1
Image Tools
Figure 1 summarizes the histologically localized dialysis sites in prefrontal cortex and basal forebrain. Figure 1A schematically illustrates the relation between the two dialysis probes. Dialysis membranes are indicated by hatched lines at the end of the probe and are drawn to scale relative to the brain schematic. A distance of 7.3 mm separated the average microdialysis sites localized within the substantia innominata and prefrontal cortex. Figure 1B plots the deepest point of the cortical probe sites, confirming that all measures of acetylcholine were obtained from the prefrontal cortex. Figure 1C plots the deepest point of probes used for drug delivery, confirming that morphine and morphine plus naloxone were delivered to the substantia innominata region of the basal forebrain.
Back to Top | Article Outline
Acetylcholine in Prefrontal Cortex Was Decreased by Morphine in Substantia Innominata
Fig. 2
Fig. 2
Image Tools
Fig. 3
Fig. 3
Image Tools
Acetylcholine measured in prefrontal cortex during one representative experiment is plotted in figure 2 as function of time and drug delivery to the substantia innominata. Prefrontal cortex acetylcholine was quantified every 12.5 min. Thus, the raw data for each experiment was comprised of six acetylcholine measures (75 min) obtained during perfusion of the substantia innominata dialysis probe with Ringer’s (control) and six acetylcholine measures obtained during dialysis delivery of morphine (75 min). The data acquisition plan illustrated by figure 2 made it possible for a within-subjects design to quantify acetylcholine in the prefrontal cortex before and after dialysis delivery of morphine to the substantia innominata. Figure 3 summarizes the time course of acetylcholine release from prefrontal cortex of 12 rats during dialysis delivery of morphine to substantia innominata. Two-way analysis of variance indicated a significant effect of morphine concentration on cortical acetylcholine (F = 10.6; df = 3,71; P < 0.0001), no significant effect due to time alone, and no concentration by time interaction.
Fig. 4
Fig. 4
Image Tools
Figure 4 summarizes group data showing that morphine delivered to the substantia innominata caused a concentration-dependent decrease in prefrontal cortex acetylcholine. Regression analyses revealed that the concentration of morphine delivered to the substantia innominata accounted for 85% of the variance in acetylcholine measured from the prefrontal cortex. The mean (± SD) percent decreases in acetylcholine release caused by the different concentrations of morphine were −16.1 (± 14.06) for 10 μm, −19.53 (± 2.37) for 100 μm, and −36.28 (± 11.51) for 1,000 μm.
Fig. 5
Fig. 5
Image Tools
The uptake and distribution properties of isoflurane predict that partial pressure of isoflurane in rat brain would be constant within 10–15 min of isoflurane delivery. Given that isoflurane has been shown to decrease cortical acetylcholine release relative to waking levels of acetylcholine,24,25 additional experiments in three rats were performed to insure that the observed decreases in acetylcholine could be attributed only to morphine. For these experiments, 75 min of prefrontal cortex dialysis with Ringer’s was followed by an additional 75 min of dialysis with Ringer’s. Figure 5 results show that acetylcholine release in prefrontal cortex was not altered by 150 min of isoflurane anesthesia.
Fig. 6
Fig. 6
Image Tools
The next set of experiments was designed to test the hypothesis that the morphine-induced decrease in acetylcholine (figs. 3 and 4) could be blocked by coadministration of the μ-opioid antagonist naloxone. Dialysis delivery of morphine to the substantia innominata was followed by dialysis delivery of morphine and naloxone to the substantia innominata. Figure 6 shows that acetylcholine levels in prefrontal cortex during dialysis delivery of morphine and naloxone were not significantly different from acetylcholine levels during dialysis with Ringer’s.
Fig. 7
Fig. 7
Image Tools
The data summarized by figures 1–6 show that morphine significantly decreases prefrontal cortical acetylcholine release by actions on basal forebrain neurons that project to cortex. These results obtained during isoflurane anesthesia encouraged the second set of experiments using intact, unanesthetized rats to quantify the effect of systemically administered morphine on acetylcholine release and electroencephalographic power (fig. 7). Comparison of figures 7A and C show that intravenously administered morphine, but not saline, significantly decreased acetylcholine release in the prefrontal cortex of unanesthetized rats. During these microdialysis studies, simultaneous recordings were obtained of the electroencephalogram. Figures 7B and D show that morphine, but not saline, altered the electroencephalogram by significantly increasing power in the 0.5- to 4-Hz range. During the morphine-induced decrease in electroencephalographic activation, rats stopped all movements and displayed a frozen posture. The eyes remained open, and muscle tone was pronounced.
Back to Top | Article Outline

Discussion

The results are discussed in relation to the arousal-related role of cholinergic neurotransmission in the basal forebrain and prefrontal cortex. Opioid-induced delirium is a clinically significant problem defined by cognitive dysfunction, fluctuating levels of consciousness, and inability to maintain focused attention.2,5,26 The prefrontal cortex is involved in regulating all of the foregoing functions.
Back to Top | Article Outline
Morphine in Basal Forebrain Decreases Acetylcholine in Prefrontal Cortex
Neuroanatomical data demonstrate that basal forebrain neurons synthesize acetylcholine and send cholinergic projections to the cortex.17 These structural details encouraged the present use of microdialysis for site-directed opioid delivery to the basal forebrain. A major advantage of drug delivery by microdialysis is the potential to identify the role of restricted neuronal networks. Drug diffusion is not likely to account for the current finding of morphine-induced decrease in cortical acetylcholine. Dialysis delivery of morphine restricted to the substantia innominata region of the basal forebrain was more than 7 mm from the prefrontal cortex, where acetylcholine was measured (fig. 1). The large distance separating the two dialysis probes, and the finding that cortical acetylcholine was decreased with the onset of morphine delivery to the substantia innominata (fig. 2), are consistent with the interpretation that the effects of morphine were synaptically mediated.
Compared with waking levels of acetylcholine, isoflurane is known to decrease acetylcholine release in cat pontine reticular formation27 and in cerebral cortex and striatum of rat.24,25 Four lines of evidence indicate that in the current study, decreased acetylcholine release in prefrontal cortex was caused by morphine, independent of the effects of isoflurane. First, isoflurane was present in the control (Ringer’s-alone) condition, and the decrease in cortical acetylcholine release was always caused by onset of morphine administration. Second, time course data (fig. 3) show that acetylcholine release during dialysis delivery of the lowest concentration of morphine was not significantly different from acetylcholine release during Ringer’s control. In contrast, the highest concentration of morphine caused a significant decrease in cortical acetylcholine release (figs. 3 and 4). Third, in a series of positive control experiments, 75 min of dialysis with Ringer’s was followed by a second 75-min interval of dialysis with Ringer’s alone rather than with Ringer’s containing morphine. The results (fig. 5) showed that there was no progressive decrease in cortical acetylcholine release caused by isoflurane. Fourth, the results obtained from isoflurane-anesthetized rats (figs. 2–6) were corroborated by studies conducted without isoflurane anesthesia (fig. 7). The foregoing results and interpretation also are consistent with data showing that 150 min of isoflurane anesthesia did not cause a progressive decrease in acetylcholine release from prefrontal cortex of C57BL/6J mouse.28 Therefore, the current results do not contradict the fact that isoflurane decreases acetylcholine release relative to waking levels of acetylcholine.24,25,27 The current results demonstrate that morphine alone decreases acetylcholine release in prefrontal cortex.
The effects of opioids on cholinergic neurotransmission and states of arousal are site specific within the brain. Opioids disrupt sleep29–31 and, when delivered by microdialysis to the pontine reticular formation, inhibit acetylcholine release in the pontine reticular formation.18,19 In contrast, morphine increases acetylcholine release in rostral ventrolateral regions of the medulla32 and in the hippocampus,33 and morphine enhances slow wave sleep when microinjected into the nucleus of the solitary tract.34 The discrete actions of opioids within the central nervous system1 require site-specific studies to make inferences about the effects of morphine on cholinergic neurotransmission. Electrophysiologic data have shown that systemic administration of morphine causes a naloxone-reversible inhibition of the majority of neurons in the medial prefrontal cortex.35 In view of the fact that cholinergic input to the prefrontal cortex arises from the basal forebrain, the current results extend these previous findings by the discovery that morphine delivered to the basal forebrain causes a naloxone-reversible inhibition of acetylcholine release in the prefrontal cortex (figs. 4 and 6).
Back to Top | Article Outline
Prefrontal Cortical Functions Relevant to Anesthesia
Orientation to person, place, and time requires intact cholinergic neurotransmission at the level of the cortex.15,16 The prefrontal cortex has particular significance for regulation of arousal, autonomic control, and cognitive processing.6,11,13 The primate prefrontal cortex is commonly divided into dorsolateral and orbitomedial regions.11 The orbitomedial prefrontal cortex receives viscerosensory information.36 The dorsolateral prefrontal cortex receives information from all five senses, consistent with its role in integrating spatial and object information.6 Together, these two major divisions integrate somatosensory and visceral-sensory input with short- and long-term memories. This integration contributes to arousal state control and to behavioral planning that links past experiences with changing behavioral objectives.37
There is good agreement between preclinical and clinical data showing that opioids obtund wakefulness and disrupt sleep.38,39 Sleep deprivation impairs working memory,40 and prefrontal cortical function is disrupted by sleep deprivation.12,41 The current finding that morphine delivered to the substantia innominata caused a concentration-dependent (fig. 4), naloxone-reversible (fig. 6) decrease in prefrontal cortical acetylcholine encouraged studies using intact animals without anesthesia. Systemic delivery of morphine to these behaving rats also significantly decreased acetylcholine release in prefrontal cortex (fig. 7A) and significantly increased low-frequency electroencephalographic power (fig. 7B). Slow wave activity in the cortical electroencephalogram is unique to the postmorphine state and is accompanied by behavioral stupor and muscle rigidity.42 The figure 7 data also fit well with clinical studies showing that opioid anesthesia increases electroencephalographic power in the δ (0.35–3.5 Hz) and θ (3.5–8 Hz) frequency range.43,44 In the current control experiments, systemically administered saline had no effect on acetylcholine release (fig. 7C), electroencephalographic power (fig. 7D), or behavior. Considered together, these data demonstrate that morphine-induced changes in prefrontal cortical acetylcholine release caused functionally significant changes in the electroencephalogram and behavior. These preclinical findings support the hypothesis that in susceptible patients, opioids may induce delirium by disrupting cholinergic neurotransmission in prefrontal cortex. This speculation is supported by data showing that cholinergic neurotransmission is particularly relevant for activating the electroencephalogram45 and for regulating behavioral states of sleep,46 anesthesia,47 and sedation.48
Back to Top | Article Outline
Limitations and Conclusions
Much of the information about the prefrontal cortex has come from studies of primates, and the homology between rodent and primate prefrontal cortex has been questioned.49 The prefrontal cortex in rats is not as differentiated as it is in primates, but the homology between rodent and primate prefrontal cortex is supported by both structural and functional evidence.50 The finding that cholinergic mechanisms also modulate cortical excitability in prefrontal cortex of mice23,51,52 suggest that the current results are generalizable, rather than species specific.
Acetylcholine release in the cortex53 and in the substantia innominata region of the basal forebrain54 varies significantly as a function of arousal state. Therefore, the first set of studies was designed to limit fluctuations in levels of arousal by holding arousal state constant with isoflurane anesthesia. The current results cannot discount the possibility that additional neurotransmitters and neuromodulators also contribute to the opioid-induced decrease in acetylcholine. In some brain regions, morphine increases dopamine,55 and dopaminergic mechanisms contribute to decreasing acetylcholine.33 In cat basal forebrain, there are approximately twice as many γ-aminobutyric acid–containing neurons as there are cholinergic neurons, and γ-aminobutyric acid significantly modulates acetylcholine release.56
Although microdialysis has revolutionized neurochemistry, it has a number of limitations. The biophysical interface between microdialysis probe and brain tissue can vary as a function of brain region, time, analyte being measured, dialysis fluid composition, dialysis flow rate, temperature, anesthesia, and dialysis membrane.57 These potential confounding variables emphasize the power of the present within-subjects experimental design. Rather that assuming that all of the foregoing variables were normal, the within-subjects design distributes any potential effect of these variables across both control (Ringer’s-alone) and experimental (Ringer’s-plus-drug) conditions. The finding that morphine caused a statistically significant decrease in acetylcholine release (figs. 3, 4, and 7) means that the drug effect was large relative to all other potential sources of variability. These effects of morphine on cortical acetylcholine release agree with microdialysis studies in pons18,19 and with the established view58 that these microdialysis measures accurately reflect relative extracellular fluid levels of acetylcholine in the prefrontal cortex.
In contrast to studies that microinject nanoliter volumes of drug directly into the brain, microdialysis studies typically are unable to quantify the amount of drug delivered. The selectivity of dialysis probe membranes means that only a fraction of endogenous analyte is recovered and, during dialysis drug delivery, only a fraction of the drug is delivered. The recovery of analyte standards can provide a useful index of the percent of a drug concentration delivered. In the current experiments, dialysis probe recoveries ranged from 3 to 5%. Therefore, although the morphine concentrations were high, it is likely that only a small fraction (< 5%) of the morphine was transferred across the dialysis probe membrane into the brain.
Even with the foregoing limitations, the results support the conclusion that morphine significantly decreases acetylcholine release in prefrontal cortex. The decreased acetylcholine release was functionally significant because it was accompanied by significant changes in electroencephalographic power (fig. 7) and elimination of normal waking behaviors. The effects of morphine on acetylcholine release were concentration dependent and blocked by naloxone, consistent with the interpretation that morphine activates μ-opioid receptors in the basal forebrain.59,60 μ-Receptor activation would be expected to hyperpolarize cholinergic projection neurons,61 leading to decreased acetylcholine release in prefrontal cortex. The decreased acetylcholine release caused by dialysis delivery of morphine to the basal forebrain was replicated by systemic administration of morphine. This finding implies, for the first time, that some of the undesirable side effects of systemically administered morphine result from actions on basal forebrain cholinergic neurons projecting to prefrontal cortex. Diminished transmission in this cholinergic pathway may contribute to opioid-induced delirium and to delayed anesthetic recovery associated with the central anticholinergic syndrome.62 Even in the absence of neurodegenerative disorders,63 these unwanted opioid side effects are especially problematic in older patients.3,5 The need to understand basic mechanisms through which opioids alter cortical function is emphasized by the anticipated increase in the number of patients with cognitive dysfunction.64
The authors thank Adam Hill, B.S. (Research Assistant, Department of Anesthesiology), Sha Jiang, B.S. (Research Assistant, Department of Anesthesiology), Fang Liu, M.D. (Research Associate, Department of Anesthesiology), Mary A. Norat, B.S. (Senior Research Associate, Department of Anesthesiology), and Kathy B. Welch, M.S., M.P.H. (Computer Systems Consultant, Department of Biostatistics), all from the University of Michigan, Ann Arbor, Michigan, for their assistance.
Back to Top | Article Outline

References

1. Yaksh TL: Pharmacology and mechanisms of opioid analgesic activity. Acta Anaesthesiol Scand 1997; 41:94–111

2. Ely EW, Stephens RK, Jackson JC, Thomason JWW, Truman B, Gordon S, Dittus RS, Bernard GR: Current opinions regarding the importance, diagnosis, and management of delirium in the intensive care unit: A survey of 912 healthcare professionals. Crit Care Med 2004; 32:106–12

3. Parikh SS, Chung F: Postoperative delirium in the elderly. Anesth Analg 1995; 80:1223–32

4. Stone DJ, Bogdonoff DL, Leisure GS, Spiekermann BS, Mathes DD: Perioperative Care: Anesthesia, Medicine, and Surgery. St. Louis, Mosby, 1998, pp 455–6

5. Roche V: Etiology and management of delirium. Am J Med Sci 2003; 325:20–30

6. Fuster JM: The Prefrontal Cortex: Anatomy, Physiology and Neuropsychology of the Frontal Lobe, 3rd edition. New York, Lippincott–Raven, 1997, pp 1–333

7. Uylings H, Van Eden C, De Bruin M, Feenstra M, Pennartz C: Cognition, emotion and autonomic responses: The Integrative role of the prefrontal cortex and limbic structures, Progress in Brain Research. Amsterdam, Elsevier, 2000, pp 1–479

8. Arnold H, Burk J, Hodgson E, Sarter M, Bruno J: Differential increases in cortical acetylcholine release in rats performing a sustained attention task versus behavioral control tasks that do not explicitly tax attention. Neuroscience 2002; 114:451–60

9. Gill T, Sarter M, Givens B: Sustained visual attention performance-associated prefrontal neuronal activity: Evidence for cholinergic modulation. J Neurosci 2000; 12:4745–57

10. Goldman-Rakic PS. The prefrontal landscape: Implications of functional architecture for understanding human mentation and the central executive. Philos Trans Roy Soc London B Biol Sci 1996; 351:1445–53

11. Groenewegen H, Uylings H: The prefrontal cortex and the integration of sensory, limbic and autonomic information. Prog Brain Res 2000; 126:3–28

12. Horne JA: Human sleep, sleep loss and behaviour: Implications for the prefrontal cortex and psychiatric disorder. Br J Psychiatry 1993; 162:413–9

13. Muzur A, Pace-Schott EF, Hobson JA: The prefrontal cortex in sleep. Trends Cogn Sci 2002; 6:475–81

14. McGaughy J, Everitt BJ, Robbins TW, Sarter M: The role of cortical cholinergic afferent projections in cognition: impact of new selective immunotoxins. Behav Brain Res 2000; 115:251–63

15. Sarter M, Bruno JP, Turchi J: Basal forebrain afferent projections modulating cortical acetylcholine, attention, and implications for neuropsychiatric disorders. Ann N Y Acad Sci 1999; 877:368–82

16. Sarter M, Bruno JP: Cognitive functions of cortical acetylcholine: Toward a unifying hypothesis. Brain Res Rev 1997; 23:28–46

17. Wainer BH, Mesulam M-M: Ascending cholinergic pathways in the rat, Brain Cholinergic Systems. Edited by Steriade M, Biesold D. Oxford, Oxford University Press, 1990, pp 65–119

18. Lydic R, Keifer JC, Baghdoyan HA, Becker L: Microdialysis of the pontine reticular formation reveals inhibition of acetylcholine release by morphine. Anesthesiology 1993; 79:1003–12

19. Mortazavi S, Thompson J, Baghdoyan HA, Lydic R: Fentanyl and morphine, but not remifentanil, inhibit acetylcholine release in pontine regions modulating arousal. Anesthesiology 1999; 90:1070–7

20. Osman NI, Hill AT, Baghdoyan HA, Lydic R: Microdialysis delivery of morphine sulfate to the substantia innominata decreases acetylcholine release in the prefrontal cortex of rat. Soc Neurosci Abstr 2004; 30:546.1

21. White PF, Johnston RR, Eger EI: Determination of anesthetic requirement in rats. Anesthesiology 1974; 40:52–57

22. Paxinos G, Watson C: The Rat Brain in Stereotaxic Coordinates, 4th edition. New York, Academic Press, 1998, pp 1–474

23. Douglas CL, Baghdoyan HA, Lydic R: Postsynaptic muscarinic M1 receptors activate prefrontal cortical EEG of C576BL/6J mouse. J Neurophysiol 2002; 88:3003–9

24. Shichino T, Murakawa M, Adachi T, Arai T, Miyazaki Y, Mori K: Effects of inhalation anaesthetics on the release of acetylcholine in the rat cerebral cortex in vivo. Br J Anaesth 1998; 80:365–70

25. Shichino T, Murakawa M, Adachi T, Nakao S, Shinomura T, Kurata J, Mori K: Effects of isoflurane on in vivo release of acetylcholine in the rat cerebral cortex and striatum. Acta Anaesthesiol Scand 1997; 41:1335–40

26. Slatkin N, Rhiner M: Treatment of opioid-induced delirium with acetylcholinesterase inhibitors: A case report. J Pain Symptom Manage 2004; 27:268–73

27. Keifer JC, Baghdoyan HA, Becker L, Lydic R: Halothane anesthesia causes decreased acetylcholine release in the pontine reticular formation and increased EEG spindles. Neuroreport 1994; 5:577–80

28. DeMarco GJ, Baghdoyan HA, Lydic R: Carbachol in the pontine reticular formation of C57BL/6J mouse decreases acetylcholine release in prefrontal cortex. Neuroscience 2004; 123:17–29

29. Keifer JC, Baghdoyan HA, Lydic R: Sleep disruption and increased apneas after pontine microinjection of morphine. Anesthesiology 1992; 77:973–82

30. Cronin A, Keifer JC, Baghdoyan HA, Lydic R: Opioid inhibition of rapid eye movement sleep by a specific mu receptor agonist. Br J Anaesth 1995; 74:188–92

31. Cronin A, Keifer JC, Davies MF, King TS, Bixler EO: Postoperative sleep disturbances: influence of opioids and pain in humans. Sleep 2001; 24:39–44

32. Taguchi K, Kato M, Kikuta J, Abe K, Chikuma T, Utsunomiya I, Miyatate T: The effects of morphine-induced increases in extracellular acetylcholine levels in the rostral ventrolateral medulla of rat. J Pharmacol Exp Ther 1999; 289:1539–44

33. Imperato A, Obinu MC, Casu MA, Mascia MS, Carta G, Gessa GL: Chronic morphine increases hippocampal acetylcholine release: Possible relevance for drug dependence. Eur J Pharmacol 1996; 302:21–6

34. Reinoso-Barbero F, de Andres I: Effects of opioid microinjection in the nucleus of the solitary tract on the sleep–wakefulness cycle in cats. Anesthesiology 1995; 82:144–52

35. Giacchino JL, Henriksen SJ: Systemic morphine and local opioid effects on neuronal activity in the medial prefrontal cortex. Neuroscience 1996; 70:941–9

36. Carmichael ST, Price JL: Architectonic subdivision of the orbital and medial prefrontal cortex in the macaque monkey. J Comp Neurol 1994; 346:366–402

37. Dehaene S, Changeux JP: Reward-dependent learning in neuronal networks for planning and decision making. Prog Brain Res 2000; 126:217–29

38. Menefee LA, Cohen MJA, Anderson WR, Doghramji K, Frank ED, Lee H: Sleep disturbance and nonmalignant chronic pain: A comprehensive review of the literature. Pain Med 2000; 1:156–72

39. Moore P, Dimsdale JE: Opioids, sleep, and cancer-related fatigue. Med Hypotheses 2002; 58:77–82

40. Drummond SPA, Brown GG, Stricker JL, Buxton RB, Wong EC, Gillin JC: Sleep deprivation-induced reduction in cortical functional response to serial subtraction. Neuroreport 1999; 10:3745–8

41. Harrison Y, Horne JA, Rothwell A: Prefrontal neuropsychological effects of sleep deprivation in young adults: A model for healthy aging? Sleep 2000; 23:1–7

42. Mayo-Michelson L, Young GA: Genetic profiles of morphine-induced EEG, EEG power spectra, and behavior in two inbred rat strains. Brain Res Bull 1993; 30:79–84

43. Sebel PS, Bovill JG, Wauquier A, Rog P: Effects of high-dose fentanyl anesthesia on the electroencephalogram. Anesthesiology 1981; 55:203–11

44. Scott JC, Cooke JE, Stanski DR: Electroencephalographic quantification of opioid effects: Comparative pharmacokinetics of fentanyl and sufentanil. Anesthesiology 1991; 74:83–90

45. Hudetz AG, Wood JD, Kampine JP: Cholinergic reversal of isoflurane anesthesia in rats as measured by cross-approximate entropy of the electroencephalogram. Anesthesiology 2003; 99:1125–31

46. Lydic R, Baghdoyan HA: Neurochemical evidence for the cholinergic modulation of sleep and breathing, Sleep Related Breathing Disorders: Experimental Models and Therapeutic Potential. Edited by Carley D, Radulovacki M. New York, Marcel Dekker, 2003, pp 57–91

47. Lydic R, Baghdoyan HA: Cholinergic contributions to the control of consciousness, Anesthesia: Biologic Foundations. Edited by Yaksh T, Lynch C, Zapol WM, Maze M, Biebuyck JF, Saidman LJ. New York, Lippincott–Raven, 1998, pp 433–50

48. Meuret P, Backman SB, Bonhomme V, Plourde G, Fiset P: Physostigmine reverses propofol-induced unconsciousness and attenuation of the auditory steady state response and Bispectral Index in human volunteers. Anesthesiology 2000; 93:708–17

49. Preuss TM: Do rats have prefrontal cortex? The Rose-Woolsey-Akert program reconsidered. J Cogn Neurosci 1995; 7:1–24

50. Uylings HBM, Groenewegen HJ, Kolb B: Do rats have a prefrontal cortex? Behav Brain Res 2003; 146:3–17

51. Douglas CL, Baghdoyan HA, Lydic R: M2 muscarinic autoreceptors modulate acetylcholine release in prefrontal cortex of C57BL/6J mouse. J Pharmacol Exp Ther 2001; 299:960–6

52. Douglas CL, Baghdoyan HA, Lydic R: Prefrontal cortex acetylcholine release, EEG slow-waves, and spindles are modulated by M2 autoreceptors in C57BL/6J mouse. J Neurophysiol 2002; 87:2817–22

53. Morrosu F, Portas C, Mascia M, Casu M, Fa M, Giagheddu M, Imperato A, Gessa G: Microdialysis measurement of cortical and hippocampal acetylcholine release during sleep-wake cycle in freely moving cats. Brain Res 1995; 671:329–32

54. Vazquez J, Baghdoyan HA: Basal forebrain acetylcholine release during REM sleep is significantly greater than during waking. Am J Physiol 2001; 280:R598–601

55. Rada P, Mark GP, Pothos E, Hoebel BG: Systemic morphine simultaneously decreases extracellular acetylcholine and increases dopamine in the nucleus accumbens of freely moving rats. Neuropharmacology 1991; 30:1133–6

56. Vazquez J, Baghdoyan HA: Muscarinic and GABAA receptors modulate acetylcholine release in feline basal forebrain. Eur J Neurosci 2003; 17:249–59

57. Beneveniste H, Huttemeier PC: Microdialysis-theory and application. Prog Brain Res 1990; 35:195–215

58. Khan SH, Shuaib A: The technique of intracerebral microdialysis. Methods 2001; 23:3–9

59. Daunais JB, Letchworth SR, Sim-Selley LJ, Smith HR, Childers SR, Porrino LJ: Functional and anatomical localization of mu opioid receptors in the striatum, amygdala, and extended amygdala of the nonhuman primate. J Comp Neurol 2001; 433:471–85

60. Wamsley JK, Zarbin MA, Young III WS, Kuhar MJ: Distribution of opiate receptors in the monkey brain: An autoradiographic study. Neuroscience 1982; 7:595–613

61. Nicoll RA, Madison DV: General anesthetics hyperpolarize neurons in the vertebrate central nervous system. Science 1982; 217:1055–7

62. Link J, Papadopoulos G, Dopjans G, Guggenmoos-Holzmann I, Eyrich K: Distinct central anticholinergic syndrome following general anesthesia. Eur J Anaesthesiol 1997; 14:15–23

63. Scarpini E, Scheltens P, Feldman H: Treatment of Alzheimer’s disease: Current status and new perspectives. Lancet Neurol 2003; 2:539–47

64. Buccafusco JJ, Terry AV: Multiple central nervous system targets for eliciting beneficial effects on memory and cognition. J Pharmacol Exp Ther 2000; 295:438–46

Cited By:

This article has been cited 17 time(s).

Journal of Chemical Neuroanatomy
G proteins in rat prefrontal cortex (PFC) are differentially activated as a function of oxygen status and PFC region
Hambrecht, VS; Vlisides, PE; Row, BW; Gozal, D; Baghdoyan, HA; Lydic, R
Journal of Chemical Neuroanatomy, 37(2): 112-117.
10.1016/j.jchemneu.2008.12.002
CrossRef
Sleep
Benzodiazepine Receptor Agonists Cause Drug-Specific and State-Specific Alterations in EEG Power and Acetylcholine Release in Rat Pontine Reticular Formation
Hambrecht-Wiedbusch, VS; Gauthier, EA; Baghdoyan, HA; Lydic, R
Sleep, 33(7): 909-918.

Sleep
Microdialysis delivery of morphine to the hypoglossal nucleus of Wistar rat increases hypoglossal acetylcholine release
Skulsky, EM; Osman, NI; Baghdoyan, HA; Lydic, R
Sleep, 30(5): 566-573.

Peptides
Endogenous opiates and behavior: 2005
Bodnar, RJ; Klein, GE
Peptides, 27(): 3391-3478.
10.1016/j.peptides.2006.07.011
CrossRef
Sleep
Morphine Increases Acetylcholine Release in the Trigeminal Nuclear Complex
Zhu, Z; Bowman, HR; Baghdoyan, HA; Lydic, R
Sleep, 31(): 1629-1637.

Suppressing the Mind: Anesthetic Modulation of Memory and Consciousness
A Neurochemical Perspective on States of Consciousness
Watson, CJ; Baghdoyan, HA; Lydic, R
Suppressing the Mind: Anesthetic Modulation of Memory and Consciousness, (): 33-80.
10.1007/978-1-60761-462-3_3
CrossRef
Sleep
Hyperalgesia induced by REM sleep loss: A phenomenon in search of a mechanism
Baghdoyan, HA
Sleep, 29(2): 137-139.

Pharmacology Biochemistry and Behavior
Interactions between morphine, scopolamine and nicotine: Schedule-controlled responding in rats
Li, XW; Li, JX; France, CP
Pharmacology Biochemistry and Behavior, 96(1): 91-95.
10.1016/j.pbb.2010.04.011
CrossRef
European Journal of Pharmacology
Morphine-nicotine interaction in conditioned place preference in mice after chronic nicotine exposure
Vihavainen, T; Piltonen, M; Tuominen, RK; Korpi, ER; Ahtee, L
European Journal of Pharmacology, 587(): 169-174.
10.1016/j.ejphar.2008.03.028
CrossRef
Addiction Biology
Effect of chronic morphine exposure on response properties of rat barrel cortex neurons
Afarinesh, MR; Sheibani, V; Arabzadeh, S; Shamsizadeh, A
Addiction Biology, 13(1): 31-39.
10.1111/j.1369-1600.2007.00087.x
CrossRef
Neuroscience
Sleep and GABA levels in the oral part of rat pontine reticular formation are decreased by local and systemic administration of morphine
Watson, CJ; Lydic, R; Baghboyan, HA
Neuroscience, 144(1): 375-386.
10.1016/j.neuroscience.2006.09.007
CrossRef
Sleep
Pontine reticular formation (PnO) administration of hypocretin-1 increases PnO GABA levels and wakefulness
Watson, CJ; Soto-Calderon, H; Lydic, R; Baghdoyan, HA
Sleep, 31(4): 453-464.

Anesthesiology
γ-Aminobutyric Acid–mediated Neurotransmission in the Pontine Reticular Formation Modulates Hypnosis, Immobility, and Breathing during Isoflurane Anesthesia
Vanini, G; Watson, CJ; Lydic, R; Baghdoyan, HA
Anesthesiology, 109(6): 978-988.
10.1097/ALN.0b013e31818e3b1b
PDF (1249) | CrossRef
Anesthesiology
Opiates, Sleep, and Pain: The Adenosinergic Link
Moore, JT; Kelz, MB
Anesthesiology, 111(6): 1175-1176.
10.1097/ALN.0b013e3181bdfa2e
PDF (245) | CrossRef
Anesthesiology
Remifentanil Inhibits Rapid Eye Movement Sleep but Not the Nocturnal Melatonin Surge in Humans
Bonafide, CP; Aucutt-Walter, N; Divittore, N; King, T; Bixler, EO; Cronin, AJ
Anesthesiology, 108(4): 627-633.
10.1097/ALN.0b013e3181684bc3
PDF (1116) | CrossRef
Anesthesiology
Sleep, Anesthesiology, and the Neurobiology of Arousal State Control
Lydic, R; Baghdoyan, HA
Anesthesiology, 103(6): 1268-1295.

PDF (2526)
Anesthesiology
Opioid-induced Decreases in Rat Brain Adenosine Levels Are Reversed by Inhibiting Adenosine Deaminase
Nelson, AM; Battersby, AS; Baghdoyan, HA; Lydic, R
Anesthesiology, 111(6): 1327-1333.
10.1097/ALN.0b013e3181bdf894
PDF (840) | CrossRef
Back to Top | Article Outline

© 2005 American Society of Anesthesiologists, Inc.

Publication of an advertisement in Anesthesiology Online does not constitute endorsement by the American Society of Anesthesiologists, Inc. or Lippincott Williams & Wilkins, Inc. of the product or service being advertised.
Login

Article Tools

Images

Share