Bidirectional effects of fentanyl on dendritic spines and AMPA receptors depend upon the internalization of mu opioid receptors

doi:10.1038/npp.2009.34

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Neuropsychopharmacology. Author manuscript; available in PMC 2009 October 1.

Published in final edited form as:

Neuropsychopharmacology. 2009 August; 34(9): 2097–2111.

Published online 2009 March 18. doi: 10.1038/npp.2009.34.

PMCID: PMC2731771

NIHMSID: NIHMS115273

Bidirectional effects of fentanyl on dendritic spines and AMPA receptors depend upon the internalization of mu opioid receptors

Hang Lin,^*^# Paul Higgins,^* Horace H. Loh,⁺ Ping-Yee Law,⁺ and Dezhi Liao^*

^*Department of Neuroscience, The University of Minnesota, 321 Church St S.E. Minneapolis, MN 55455

⁺Department of Pharmacology, The University of Minnesota, 321 Church St S.E. Minneapolis, MN 55455

^#Department of Neurology, Chengdu General Military Hospital, Chengdu City, 610083, China

Correspondence should be sent to: Dezhi Liao, Ph.D., Associate Professor, Department of Neuroscience, The University of Minnesota, 321 Church St S.E. Minneapolis, MN 55455, Tel: 612-626-3522, e-mail: liaox020/at/umn.edu

The publisher's final edited version of this article is available at Neuropsychopharmacology.

Abstract

Fentanyl is a frequently used and abused opioid analgesic and can cause internalization of mu opioid receptors (MORs). Receptor internalization modulates the signaling pathways of opioid receptors. Because changes in dendritic spines and synaptic AMPA receptors play important roles in addiction and memory loss, we investigated how fentanyl affects dendritic spines and synaptic AMPA receptors in cultured hippocampal neurons. Fentanyl at low concentrations (0.01 and 0.1 µM) caused collapse of dendritic spines and decreased the number of AMPA receptor clusters. In contrast, fentanyl at high concentrations (1 and 10 µM) had opposite effects, inducing the emergence of new spines and increasing the number of AMPA receptor clusters. These dose-dependent bidirectional effects of fentanyl were blocked by a selective MOR antagonist CTOP at 5 µM. In neurons that had been transfected with HA-tagged or GFP-tagged MORs, fentanyl at high concentrations induced persistent and robust internalization of MORs, whereas fentanyl at lower concentrations induced little or transient receptor internalization. The blockade of receptor internalization with the expression of dominant negative Dynamin I (the K44E mutant) reversed the effect of fentanyl at high concentrations, supporting a role of receptor internalization in modulating the dose-dependent effects of fentanyl. In contrast to morphine, the effects of fentanyl on dendritic spines are distinctively bidirectional and concentration-dependent, probably due to its ability to induce robust internalization of MORs at high concentrations. The characterization of the effects of fentanyl on spines and AMPA receptors may help us understand the roles of MOR internalization in addiction and cognitive deficits.

Keywords: Fentanyl, Dendritic Spines, AMPA receptors, Receptor Internalization, Cognitive Dysfunctions

INTRODUCTION

Behavioral sensitization to psychostimulants was prevented when NMDA receptor antagonist MK-801 was administered prior to injection of cocaine and amphetamine (Karler et al., 1989) or when MK-801 was microinjected into ventral tegmental area (VTA) or amygdala (Kalivas and Alesdatter 1993). The tolerance and sensitization of opiates were also inhibited by treatment of MK-801 before opiate exposure (Trujillo and Akil, 1991; Wolf and Jeziorski, 1993). NMDA receptors are required for synaptic plasticity and therefore opioid-induced plasticity of dendritic spines is likely to play some roles in drug addiction. These pioneer studies lead to the widely accepted hypothesis that drug addiction is a neural plasticity-dependent pathological form of learning and memory (Kauer and Malenka 2007; Kelley 2004; Nestler 2002; Williams et al., 2001; Wolf 2002).

A large amount of evidence shows that chronic opioid use or abuse leads to impairment of cognitive functions (Ersche et al., 2006; Bodnar 2007; Gruber et al., 2007; Mintzer et al., 2005). The pyramidal cell layer of the hippocampus is one of the regions that have the highest level of MOR proteins (Arvidsson et al., 1995) and MOR mRNA (Mansour et al., 1995). The pyramidal neurons are glutamatergic neurons with numerous dendritic spines that contain AMPA receptors and NMDA receptors (Hollmann and Heinemann, 1994; Kennedy 2000). Synaptic plasticity of dendritic spines has been proposed to be the cellular basis for experience-dependent learning and memory for decades (Bliss and Collingridge, 1993; Malenka 1994; Martin et al., 2000). Chronic administration with morphine profoundly decreases the density of dendritic spines in the hippocampus in rats that self-administered morphine (Robinson et al., 2002; this group of rats repeatedly took morphine, resulting in long-time continuous exposure of morphine). Chronic treatment with morphine also caused collapse of dendritic spines in cultured hippocampal neurons (Liao et al., 2005). Therefore, chronic opioid exposure may cause cognitive deficits via MOR-mediated aberrations in dendritic spines and synaptic AMPA receptors.

Fentanyl is one of the most popular opioid analgesics for patients undergoing surgery or suffering from chronic pain (Stanley 1992, 2005; Skaer 2004, 2006). Overdose of “killer fentanyl” in opioid addicts has caused grave concerns in public health and safety (Fodale et al., 2008). Despite the extensive use and abuse of fentanyl, it is still unknown whether synthetic opioids such as fentanyl have the same pharmacological effect on excitatory synapses as naturally derived opiates such as morphine. In the present study, unlike morphine, fentanyl at a low concentration decreases the density of spines and AMPA receptor clusters whereas at a high concentration it increases the density of spines and AMPA receptor clusters. In our previous studies, naloxone and genetic deletion of MORs in transgenic mice increased the density of dendritic spines, suggesting that MOR-mediated tonic inhibition of spinogenesis may play an important role in maintaining the normal morphology of dendritic spines in mature neurons (Liao et al., 2005). In the present study, we will test the hypothesis that fentanyl at a high concentration induces emergence of new spines by removing MOR-mediated tonic inhibition of spinogenesis via receptor internalization.

MATERIALS AND METHODS

High-density neuronal cultures and neuronal transfection

A 25-mm glass polylysine-coated coverslip (thickness, 0.08 mm) was glued to the bottom of a 35-mm culture dish with a 22-mm hole using silicone sealant as previously described (Lin et al., 2004; Wiens et al., 2005). Dissociated neuronal cultures from rat hippocampus at postnatal day 1–2 were prepared as previously described (Liao et al., 2001). Primary hippocampal cultures were used because the hippocampus is one of the regions that contain the highest level of MORs (Arvidsson et al., 1995) and has been implicated to be important for addiction (Vorel et al., 2001; Biala et al., 2005; Fan et al., 1999) as well as learning and memory (Malinow et al., 2000). Neurons were plated onto prepared 35-mm culture dishes at a density of 1× 10⁶ cells per dish. The age of cultured neurons was counted from the day of plating, one day in vitro (DIV). Neurons at 5–7 DIV were transfected with appropriate plasmids using the standard calcium phosphate precipitation method as previously described (Lin et al., 2004). After transfection, neurons were put back to a tissue culture incubator (37°C, 5% CO₂) and allowed to mature and develop dendritic spines until ~3 weeks in vitro for usage. In co-transfections, several different plasmids were mixed together with the phosphate buffer and CaCl₂ before being added to culture media.

Low-density neuronal cultures

In order to detect the distribution of endogenous synaptic proteins with high resolution, low-density neuronal cultures were prepared as previously described with some modifications (Liao et al., 1999). Dissociated neuronal cultures from rat hippocampus at postnatal day 1–2 were plated into 12-well culture plates at a density of 50,000 to 100,000 cells per well. Each well contained a polylysine-coated 12-mm glass coverslip on the bottom. In order to maintain the low-density cultures for a long time (> 1 month), the above 12-mm coverslips with low-density cultured neurons were transferred to 60 mm dishes (4 coverslips per dish; the coverslips faced up) that contained high-density neuronal cultures after 1 week in vitro. In previous studies, dishes with a glial feed layer were often used to support low-density cultures (Goslin and Banker, 1991). Recently, we found that high-density neuronal cultures were far better supporters than pure glial cells, suggesting that neurons probably also play some roles in the survival of nearby neurons.

Time-lapse live imaging method

To label dendrites, high-density neurons at 5–7 DIV were transfected with plasmids encoding enhanced green fluorescence (GFP) or GFP-tagged molecules. The 35-mm culture dishes fit tightly in a homemade holding chamber on a fixed platform above an inverted Nikon microscope sitting on an X-Y translation stage (Burleigh, Inc). The location of any neuron of interest was recorded by the reading of the X-Y translation stage. The culture dish was immediately put back into a tissue culture incubator after each observation. Neurons could be found again in the next observation using the X-Y translation stage (accuracy, 4 µm). In addition, this X-Y translation stage could also be used to find neurons after fixation and permeabilization (see the next paragraph for fixation method). In order to block the internalization of MORs, neurons were co-transfected with HA-tagged dominant negative Dynamin I (the K44E mutant, referred to as Dyn-; Chu et al., 1997; Zhao et al., 2006) and GFP-tagged proteins. In these experiments, the X-Y translation stage was particularly useful in locating neurons because the expression of HA-tagged Dynamin I in these neurons was detected using a mouse monoclonal anti-HA antibody (Covance, Richmond, CA) after fixation and permeabilization.

Immunocytochemistry in fixed tissues

A rabbit polyclonal antibody against the N-terminus of GluR1 subunits of AMPA receptors was used to detect the surface AMPA receptors (see next paragraph for surface staining). Cultured neurons were fixed and permeabilized successively with 4% paraformaldehyde, 100% methanol and 0.2% Triton X-100 (Liao et al., 1999). Commercial antibodies against synaptophysin (mouse monoclonal, Chemicon) and PSD95 (mouse monoclonal, Chemicon) were used as pre- and post-synaptic markers, respectively (Liao et al., 1999; 2001). Finally, FITC (green) or Rhodamine (red)-conjugated secondary antibodies (Jackson Immuno) were used to recognize these primary antibodies.

Live surface staining of N-GluR1 and HA-tag MOR-GFP

The live surface staining of GluR1 subunits of AMPA receptors has been previously described (Liao et al., 1999; O’brien et al., 1998). A polyclonal rabbit antibody was made against the N-terminus of GluR1 subunits of AMPA receptors. Neurons at 21 DIV were treated with fentanyl at a concentration of 0 (untreated control), 0.01, 0.1, 1 or 10 µM for 3 days and, thereafter, were incubated with culture media that contained the anti-N-GluR1 antibody at 37°C in a tissue culture incubator for 1 hour. These neurons were incubated with a rhodamine-conjugated antibody diluted in 10% donkey serum for another 1 hour in 37°C after fixation and permeabilization. These neurons were also co-stained with either the pre-synaptic marker synaptophysin or the post-synaptic marker PSD95. To measure fentanyl-induced internalization of MORs, neurons were transfected with plasmids encoding MORs with an HA tag at the N-terminus and a GFP tag at the C-terminus. Neurons at 21 DIV were treated with fentanyl at a concentration of 0, 0.01, 0.1, 1 or 10 µM for 1 hour. A mouse monoclonal anti-HA antibody (Covance, Richmond, CA) was added to culture media that contained fentanyl (concentration unchanged) at 37°C for another 1 hour (fentanyl treatment time = 2 hours). Rhodamine-linked secondary anti-mouse antibody was used to label the primary anti-HA antibody after the cultured neurons were fixed and permeabilized with 4% paraformaldehyde, methanol and triton (Liao et al., 2007b).

Image analysis

Time-lapse live images from the same neuron at 21 DIV were taken before and at various time points after drug treatments as previously described (Liao et al., 2005). All digital images were analyzed with MetaMorph Imaging System (Universal Imaging Co.). Unless stated otherwise, all images of live neurons were taken as stacks and were averaged into one image before further analysis. In addition to simple averaging, stacks of images were also processed by deconvolution analyses using the MetaMorph software with the nearest planes. A stack of deconvoluted images was further averaged into one single image. A dendritic protrusion with an expanded head that was 50% wider than its neck was defined as a spine. The number of spines from a dendrite was manually counted and normalized per 100 µm dendritic length. The intensity of fluorescence in the soma and individual dendrites was measured using the MetaMorph program (auto-threshold for bright objects) and further calibrated by nearby baseline area: calibrated fluorescence = (dendritic fluorescence – baseline)/baseline. To quantify the endocytosis in neurons expressing HA-MOR-GFP, the HA tag was sequentially stained with a primary anti-HA antibody and a Rhodamine-labeled (red) secondary antibody. The ratio of red to green fluorescence in the same region was used to estimate the ratio of surface MOR/total MOR. Using another method to quantify endocytosis, the coefficient of variation (CV) was used to estimate the aggregation of MOR-GFP in dendrites. The CV values were estimated from un-deconvoluted images. A line (width = 3 pixels; fluorescence intensities at the 3 pixels were averaged into one pixel) was manually drawn in the middle of a dendrite. The fluorescence intensities at all pixels of this line were read out using the “line scan” program and all pixels were pooled together to calculate the coefficient of variation (CV = standard deviation/mean). Because CV reflects how variable the data in a sample are, a dendrite with relatively uniform MOR-GFP distribution should yield a low CV value. In contrast, a dendrite with aggregates of MOR-GFP should yield a high CV value. Student t-tests were used for comparison between parameters from two groups whereas ANOVA tests were used for comparison between parameters from multiple groups (n - number of neurons; p <0.05, significant). All data are reported as Mean ± Standard Error. *, P<0.05; **, P<0.01; ***, P<0.001.

RESULTS

Fentanyl causes concentration-dependent bidirectional changes in dendritic spines

Chronic treatment with the MOR agonist morphine caused collapse of dendritic spines in cultured dissociated neurons (Liao et al., 2005). It is still unknown whether synthetic opioids such as fentanyl have the same pharmacological effect on excitatory synapses as naturally derived opiates such as morphine. To determine how chronic treatment with fentanyl affects the morphology of dendritic spines, cultured dissociated rat hippocampal neurons were transfected with plasmids encoding the enhanced green fluorescence protein (GFP). Fentanyl at four concentrations (0.01, 0.1, 1 and 10 µM) was applied to GFP-labeled neurons at 21 days in vitro (DIV; Figure 1B–E

) and untreated neurons were used as the control (Figure 1A

). Time-lapse images were taken on dendrites before, 1 day and 3 days after the application of fentanyl. Dendritic spines gradually shrunk and eventually disappeared in 1–3 days after treatment with fentanyl at low concentrations (0.01 or 0.1 µM; Figure 1B–C

). These low concentrations of fentanyl significantly decreased the density of dendritic protrusions and spines after 1–3 days of treatment (Figure 1F and 1G

; repeated measurement ANOVA test, comparing with before treatment; n = 8 neurons in each group). In contrast, fentanyl at high concentrations (1 or 10 µM) induced the emergence of new dendritic spines (Figure 1D–E

) and significantly increased the density of dendritic protrusions and spines after 1–3 days of treatment (Figure 1F and 1G

). These results demonstrate that fentanyl can cause bidirectional effects on dendritic spines depending upon the concentrations that are used.

Figure 1

Fentanyl at a low concentration decreased the density of dendritic spines whereas fentanyl at a high concentration had an opposite effect

To test whether fentanyl induces acute changes in dendritic spines, the density of dendritic spines were measured before, 2 hours and 4 hours after treatment of fentanyl at 0.01 and 10 µM whereas untreated neurons were used as the control (Figure 1H

). Although fentanyl at 0.01 µM causes obvious decreases in 4 out of 8 neurons after 4 hours of treatment, these effects of fentanyl were not yet significant within 4 hours (Figure 1H and 1I

). Consistent with our previous studies (Liao et al., 2005), this result confirms that the temporal dynamics of MOR-mediated spine loss is slow. In contrast, fentanyl at 10 µM significantly increased the density of dendritic spines after 4 hours of treatment (Figure 1H and 1I

Fentanyl-induced bidirectional changes require the participation of MORs

Fentanyl is an opioid agonist that primarily activates MORs but can also activate delta opioid receptors (DORs) with a much lower affinity (Rang et al., 1995). To determine whether the activation of MORs plays an important role in the fentanyl-induced bidirectional change in dendritic spines, a selective MOR antagonist, D-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr-NH2 (CTOP), at 5 µM was added to the media of cultured neurons and neurons were continuously treated with CTOP for 1 week. In the two testing groups, dynamic changes in dendritic protrusions and spines were monitored for 3 days after adding fentanyl at 0.01 and 10 µM, respectively, to the CTOP-containing neuronal media (Figure 2A–C

). In the control group, neurons were continuously treated with CTOP alone (Figure 2A

). The density of dendritic protrusions and spines was increased in all three experimental groups, suggesting that blockade of MORs by CTOP facilitates the emergence of new dendritic spines (Figure 2D and 2F

; consistent with Liao et al., 2005). In the presence of CTOP, fentanyl no longer induced dose-dependent bidirectional changes in dendritic spines as the density of dendritic spines was increased in all three experimental groups (Figure 2F–G

). The increase in dendritic spines is probably due to the removal of MOR-mediated tonic inhibition of spinogenesis by CTOP (Liao et al., 2005; also see the model in Figure 9

). The amount of increase in the densities of dendritic protrusions and spines in fentanyl-treated neurons was not significantly different from that in the control neurons, indicating that the effects of fentanyl were blocked in the presence of CTOP (Figure 2E and 2G

). These results support that fentanyl-induced bidirectional changes in dendritic spines are mainly mediated via MORs.

Figure 2

The bidirectional effects of fentanyl on the density of dendritic spines require the participation of MORs

Figure 9

A hypothetical model summarizing the relationship between the internalization of MORs and fentanyl-induced dose-dependent bidirectional changes in dendritic spines

Fentanyl causes bidirectional changes in synaptic AMPA receptors

To test whether fentanyl can alter the function of excitatory synapses by regulating AMPA receptor trafficking, a polyclonal rabbit antibody against the N-terminus of GluR1 subunits was used to recognize surface AMPA receptors (see Materials and Methods for details). Low-density cultured neurons were treated with fentanyl at 0 (control), 0.01, 0.1, 1 and 10 µM for 3 days and were co-stained with antibodies against N-GluR1 and the pre-synaptic marker synaptophysin (Figure 3

). In control neurons, intensely stained clusters of GluR1 subunits were distributed along dendrites and were co-localized with or adjacent to clusters of synaptophysin proteins (Figure 3A

). Treatment with fentanyl at low concentrations (0.01 and 0.1 µM) reduced the size and fluorescence intensity of GluR1 clusters (Figure 3B

) and significantly decreased the density of these clusters (Figure 3D

, n = 10–11 neurons in each group). In contrast, fentanyl at high concentrations (1 and 10 µM) had opposite effects, significantly increasing the density of GluR1 clusters (Figure 3C and 3D

). Treatment with fentanyl at all concentrations had no significant effects on the number of synaptophysin clusters (Figure 3D

, black bars). Consequently, fentanyl at a low concentration (0.01 µM) significantly decreased the proportion of synaptophysin clusters that co-localized with GluR1 clusters versus total number of synaptophysin clusters, whereas fentanyl at high concentrations (1 and 10 µM) increased this proportion. These results indicate that fentanyl causes no significant change in pre-synaptic elements but induces dose-dependent bidirectional changes in post-synaptic elements.

Figure 3

Effects of Fentanyl on surface synaptic AMPA receptors in low density cultured neurons

Post-synaptic density protein 95 (PSD95) is an NMDA receptor anchoring protein that is abundant in the post-synaptic density of dendritic spines (Kennedy 2000) and is widely used to label excitatory glutamatergic synapses. Low-density cultured neurons were treated with fentanyl at 0 (control), 0.01, 0.1, 1 and 10 µM for 3 days and were co-stained with antibodies against N-GluR1 and PSD95 (Figure 4

). Consistent with previous results in Figure 3

, treatment with fentanyl at low concentration (0.01 µM) significantly decreased the density of GluR1 clusters whereas fentanyl at high concentrations (1 and 10 µM) had opposite effects (Figure 4D

, n = 10–12 neurons in each group). Interestingly, in addition to altering the density of AMPA receptor clusters, treatment with fentanyl also changed the density of PSD95 clusters (Figure 4D

, black bars). Because PSD95 proteins were strongly enriched in the postsynaptic membrane of glutamatergic synapses (Kennedy 2000), most of these PSD95 clusters were probably dendritic spines. As previously shown in Figure 1

, fentanyl had bidirectional effects on the density of dendritic spines. Therefore, consistent with changes in spines, fentanyl at a low concentration (0.01 µM) significantly decreased the density of PSD95 clusters whereas fentanyl at high concentrations (1 and 10 µM) had opposite effects (Figure 4D

, right black bars). Furthermore, fentanyl at low concentrations (0.01 and 0.1 µM) changed the proportion of PSD95 clusters that were co-localized with GluR1 clusters versus total number of PSD95 clusters (Figure 4E

), confirming that fentanyl can alter AMPA receptor trafficking in excitatory synapses. The combined results in Figure 3

and Figure 4

indicate that chronic treatment with fentanyl can alter the function of excitatory synapses by at least two ways: (1) changing the density of dendritic spines; and (2) changing the amount of post-synaptic AMPA receptors per synapse.

Figure 4

Effects of Fentanyl on surface AMPA receptors and PSD95 in low density cultured neurons

Fentanyl can cause persistent and robust internalization of MORs at a high concentration but little internalization at a low concentration

To investigate the effects of fentanyl on MOR endocytosis in hippocampal neurons, neurons were transfected with plasmids encoding MOR with a HA tag in the N-terminus (extracellular, labeled as red by antibodies) and a GFP tag in the C-terminus (green, label both intracellular and extracellular receptors; Figure 5

). The ratio of red versus green fluorescence was used as an index to quantify the proportion of surface MORs versus total amount of MORs and a decrease of this ratio would indicate endocytosis (Figure 5F

). In control untreated neurons, MORs were brightly stained on the surface (middle panels, Anti-HA, Figure 5A and 5B

) and clustered on the surface of dendritic spines (see arrows in Figure 5A and 5B

). Treatment with fentanyl at low concentrations (0.01 and 0.1 µM) caused no significant internalization of MORs (Figure 5C

for an example; Figure 5F

, P > 0.05, n = 10 in each group) and did not remove MORs from dendritic spines (Figure 5G

). In contrast, treatment with fentanyl at high concentrations (1 and 10 µM) caused significant internalization of MORs (Figure 5D, 5E and 5F

) and removed MORs from dendritic spines (Figure 5G

). Whenever the ratio of red/green fluorescence was decreased, fentanyl-induced endocytosis also caused aggregation of MORs in the middle of dendrites (see triangles in Figure 5D and 5E

Figure 5

The effect of fentanyl on the internalization of MORs was concentration dependent

The aggregation of MORs has widely been used to reflect the internalization of MORs in previous studies (Sternini et al., 1996; Haberstock-Debic et al., 2003, 2005). We used this phenomenon as a tool to examine the temporal dynamics of receptor internalization in live neurons expressing MOR-GFP (Figure 6

). Normalized coefficient of variation (CV) of green fluorescence was used to quantify the aggregation of MOR in dendrites, which should reflect the degree of receptor internalization (see Image Analysis in Materials and Methods). Time-lapse images were taken on the dendrites of neurons expressing MOR-GFPs before, 1 hour and 1 day after the application of fentanyl at concentrations of 0 (control), 0.01, 0.1, 1 and 10 µM (Figure 6A–E

). In untreated control neurons, MORs were mostly smoothly distributed along dendrites (Figure 6A

) and no significant change occurred in normalized CV during the entire observation period (Figure 6F

, p>0.05, n = 8). Fentanyl at 0.01 µM did not induce obvious aggregation of MORs (Figure 6B

) and caused no significant change in CV (Figure 6F

, p>0.05, n = 8). After the concentration was increased to 0.1 µM, fentanyl caused MORs to aggregate in dendrites after 1 hour exposure (Figure 6C and 6F

, p < 0.05, n = 8). However, most of these aggregates had disappeared after 1 day, suggesting that most of the internalized and aggregated MORs might have been re-inserted into the cell surface (Figure 6D and 6F

). In contrast, fentanyl at high concentrations (1 or 10 µM) induced persistent aggregation of MORs in dendrites, which lasted more than 1 day (Figure 6E–F

, n=8). These results indicate that fentanyl at high concentrations can induce prolonged internalization of MORs and block the MOR-mediated signaling pathway by removing MORs from the cell surface. In our previous studies, the peptide MOR agonist DAMGO caused robust internalization of MORs and most of the internalized MORs were degraded after 1 day of DAMGO treatment (Liao et al., 2007b). Unlike DAMGO, prolonged treatment with fentanyl did not significantly alter the overall fluorescence of the dendrites in neurons expressing MOR-GFP (Figure 6G

), suggesting that fentanyl and DAMGO might induce endocytosis of MORs via two distinctly different pathways.

Figure 6

The temporal dynamics of fentanyl-induced MOR internalization was concentration dependent

Blockade of receptor internalization prevents the fentanyl-induced bidirectional changes

Based on previous data in Figure 1

–Figure 6

, we proposed the hypothesis that fentanyl at high concentrations increase the density of dendritic spines by blocking the MOR-mediated signaling pathway via receptor internalization. To test this hypothesis, we used a dominant negative Dynamin I (the K44E mutant, referred to as Dyn-; see Chu et al., 1997) to block the dynamin-mediated internalization of MORs (Figure 7

). High density cultured neurons (at 21 DIV) that had been co-transfected with the K44E Dynamin I mutant and MOR-GFP were treated with fentanyl at concentrations of 0, 0.01, 0.1, 1 and 10 µM. In contrast to neurons without the K44E Dynamin I mutant (see Figure 6

for comparison), treatment with fentanyl at 1 µM no longer caused obvious MOR aggregation and had no significant effect on the CV of MOR-GFP fluorescence in dendrites of neurons expressing this mutant (Figure 7B and 7F

, p>0.05, n=8). However, the expression of dominant negative Dynamin I could not completely block the internalization of MORs when the concentration of fentanyl reached as high as 10 µM (Figure 7C and 7D

for two different examples; 7F for quantification, p < 0.05 at 1 hour, n = 8). At such a high concentration (10 µM), fentanyl could still cause aggregation of MORs in 5 out of 8 neurons and all of these 8 neurons clearly expressed K44E Dynamin I proteins (Figure 7E

). These results suggest that fentanyl might be able to induce the internalization of MORs via other dynamin independent pathways if the concentration is very high (>10 µM).

Figure 7

The expression of dominant negative Dynamin I blocked the internalization of MORs

To further test the hypothesis that fentanyl at high concentrations increases the density of dendritic spines by blocking the MOR-mediated signaling pathway via receptor internalization, high density cultured neurons that expressed K44E Dynamin I mutant and GFP were treated with fentanyl at concentrations of 0, 0.01, 0.1, 1 and 10 µM (n=17 in the group treated with fentanyl at 10 µM; n=10–12 in all other groups). Similar to neurons without the transfection of K44E Dynamin I mutant (see Figure 1

for comparison), treatment with fentanyl at a low concentration (0.01 µM) caused collapse of dendritic spines (Figure 8B

) and fentanyl at 0.01 and 0.1 µM significantly decreased the density of protrusions and spines after 1–3 days of treatment (Figure 8F–G

). In contrast to neurons without the transfection of K44E Dynamin I mutant, treatment with fentanyl at high concentrations (1 and 10 µM) no longer induced the emergence of new dendritic protrusions and spines in neurons expressing this mutant (Figure 8F–G

). On the contrary, fentanyl at 1 µM caused collapse of spines (Figure 8C

) and significantly decreased the density of dendritic protrusions and spines (Figure 8F–G

). The effects of fetanyl on dendritic spines became very variable when the concentration of fentanyl reached as high as 10 µM (Figure 8F–G

). At such a high concentration (10 µM), fentanyl decreased the density of spines in 9 out of 17 neurons and increased this density in 8 out 17 neurons. Due to this mixed result, no significant change was found after the treatment (p > 0.05, last 3 bars in Figure 8F–G

). This mixed result caused by fentanyl at a very high concentration (>10µM) might be due to incomplete blockade of the internalization of MORs by K44E Dynamin I (see Figure 7F

) or a non-specific effect via a MOR independent pathway. Experiments using neurons expressing K44E Dynamin I proteins (Figure 7

–Figure 8

) support the hypothesis that the concentration-dependent bidirectional effects of fentanyl on dendritic spines rely upon the internalization of MORs.

Figure 8

The blockade of MOR internalization reversed the effect of fentanyl at high concentrations

DISCUSSION

Morphine, oxycodone, methadone and fentanyl are among the most commonly prescribed opioids for pain management (Hank and Reid, 2005). Fentanyl is frequently used as an opioid analgesic in surgery (Stanley 2005) and often used to treat chronic cancer and non-cancer pains (Skaer 2006; Trescot et al., 2008). Furthermore, addiction to fentanyl has emerged as a major issue due to the marked increase in the number of abusers in the past decade and the propensity of opiate addicts to mix fentanyl with heroin and to die from overdose (Compton and Volkow, 2005; Schumann et al., 2008; Kronstrand et al., 1997; Fodale et al., 2008). Due to the extensive use and abuse of fentanyl and potential importance of neural plasticity in addiction, characterizing the effects of this drug on dendritic spines and AMPA receptors should be of great interest to clinicians, neuroscientists and pharmacologists.

Dose-dependent bidirectional effects of fentanyl on dendritic spines and AMPA receptors

The present study demonstrates that fentanyl causes dose-dependent bidirectional changes in dendritic spines and AMPA receptors (Figure 1

, Figure 3

and Figure 4

). These bidirectional changes were blocked by the selective MOR antagonist CTOP, indicating that fentanyl-induced changes in dendritic spines are mainly mediated via MORs (Figure 2

). This biphasic response stands in contrast to previous studies showing that chronic treatment with morphine, which induces little internalization of MORs, caused collapse of dendritic spines and decreased the amplitude and frequency of miniature excitatory synaptic currents (mEPSCs) (Liao et al., 2005; 2007a; 2007b). The decrease in mEPSC frequency was probably due to the collapse of spines whereas the decrease in mEPSC amplitude was probably due to the removal of synaptic AMPA receptors (Liao et al., 2007a). In contrast, opioids such as DAMGO and etorphine, which induced robust internalization of MORs, increased the density of dendritic spines and the frequency of mEPSCs, causing effects that are opposite to those of morphine (Liao et al., 2005; 2007a, b). In the present study, we found that the same opioid drug could cause opposite effects on dendritic spines if different concentrations were applied. Fentanyl at different concentrations induced bidirectional changes on the density of dendritic spines and synaptic AMPA receptors (Figure 1

–Figure 4

). At low concentrations (0.01 and 0.1 µM), chronic treatment with fentanyl caused collapse of pre-existing dendritic spines whereas, high concentrations (1 µM and 10 µM) induced the emergence of new dendritic spines (Figure 1

). Furthermore, fentanyl at a low concentration (0.01 µM) caused the removal of AMPA receptors from synapses whereas fentanyl at high concentrations (1 and 10 µM) increased the number of synapses that contained AMPA receptors (Figure 3

and Figure 4

). Chronic treatment with morphine decreases the density of dendritic spines and the amount of synaptic AMPA receptors in hippocampal neurons (Liao et al., 2005). In contrast, chronic morphine administration increases the amount of GluR1 subunits of AMPA receptors in the ventral tegmental area (Lane et al., 2008). It will be interesting to further investigate the cellular mechanism underlying the differential effects of chronic opioid exposure on different parts of the brain.

Relationship between fentanyl-induced changes in spines and cognitive dysfunctions

Chronic exposure to MOR agonists heroin, morphine and methadone lead to many cognition dysfunctions including deficits in spatial learning and memory (Bodnar and Hadjimarkou 2003; Gruber et al., 2007). In contrast, MOR antagonists such as naloxone and naltrexone enhance learning and memory and block the adverse cognitive effects of electroconvulsive therapy (ECT) (Canli et al., 1990; Gallagher 1985; Prudic et al., 1999). In mice overexpressing human amyloid precursor protein (hAPP; a model of pre-clinical Alzheimer’s disease), the expression level of enkephalin is increased and memory deficits are reduced by beta-funaltrexamine, an irreversible blocker of MORs (Meilandt et al., 2008). Morphine significantly decreases the density of dendritic spines whereas MOR antagonist naloxone has an opposite effect (Liao et al., 2005). Therefore, it is tempting to use the severity of opioid-induced collapse of dendritic spines to speculate on the likelihood for a specific opioid to cause cognitive deficits. Fentanyl at 0.01 µM decreased the density of spines by 36% (Figure 1

), which is similar to the effect of morphine (decreased by 35%, Liao et al., 2005). However, fentanyl decreased the density of spines by 24% at 0.1 µM and started to increase the density of spines at 1 µM (Figure 1

). Therefore, at a concentration ranging from 0.01 to 1 µM, fentanyl is likely to cause far less damage to dendritic spines than morphine. Although it is difficult to know the concentration of fentanyl in the brain during various clinical applications, the unique bidirectional effects of fentanyl on dendritic spines probably contribute to the cellular basis of an interesting clinical puzzle: Treatment of chronic pain with fentanyl caused fewer incidents of cognitive deficits than treatment with morphine in elderly patients (McNamara 2002). In another clinical puzzle, anesthesiologists were surprised that high-dose fentanyl caused significantly fewer incidents of postoperative cognitive dysfunction than low-dose (Silbert et al., 2006). Based on the present study, fentanyl at a high concentration might be able to protect dendritic spines during anesthesia, providing a plausible explanation for the second puzzle.

The Effects of Fentanyl on the Internalization of MORs

The present study demonstrates that the ability of fentanyl to induce receptor internalization is concentration dependent (Figure 5

and Figure 6

). Fentanyl is one of the most potent opioid agonists used in clinic; it is a synthetic opioid in the phenylpiperidine series with a chemical structure different from morphine (Cometta-Morini et al., 1992; Rang et al., 1995). It is believed that fentanyl has a very high affinity for MORs, mediates very strong transduction downstream from the ligand-receptor complex, occupies a small number of binding sites and induces “weak” internalization of opioid receptors (Martini and Whistler 2007). The present study reveals that fentanyl can induce “strong” internalization of MORs if high concentrations are applied (1 to 10 µM) whereas it induces “weak” internalization if low concentrations are applied (0.01 to 0.1 µM).

The present study demonstrates that the RAVE (Relative Activity Versus Endocytosis) value of a specific opioid can be changed if different concentrations are applied. Morphine induces little receptor internalization in most cell types, whereas other opioids such as DAMGO, etorphine and methadone cause strong receptor internalization (Alvarez et al., 2002; Sternini et al., 1996; Whistler and von Zastrow, 1998). A “RAVE” hypothesis has been proposed to explain the roles of receptor internalization and desensitization in opioid addiction and tolerance (Finn and Whistler, 2001; He et al., 2002; Whistler et al., 1999). According to this hypothesis, chronic treatment with an opioid drug with a high RA (Relative Activity) / VE (Endocytosis) value would cause more severe tolerance and addiction (Alvarez et al., 2001). Fentanyl was previously proposed to have high RAVE value and thus high addictive liability (Martini and Whistler, 2007). The present study indicates that the RAVE value of fentanyl can be “high” or “low” depending upon concentrations applied. Fentanyl at a low concentration (0.01 µM) causes strong collapse of spines but induces no significant receptor internalization, yielding a high RAVE value. Fentanyl at a high concentration (10 µM) causes no collapse of spines (actually has the opposite effects) but induces robust receptor internalization, yielding a low RAVE value.

Relationship between receptor internalization and spine changes

K44E mutant of Dynamin I is a dominant negative inhibitor that can block the internalization of mu, delta and kappa opioid receptors (Zhao et al., 2006; Chu et al., 1997). The blockade of receptor internalization by dominant negative Dynamin I (K44E) reversed the effects of fentanyl at high concentrations (1 and 10 µM) on dendritic spines, preventing the bidirectional effects of fentanyl (Figure 7

and Figure 8

). These results indicate that the bidirectional changes induced by fentanyl are mainly caused by fentanyl-induced MOR internalization at high concentrations. However, the possibility that Dynamin I (K44E) might affect a cellular mechanism that is independent of MOR internalization cannot be excluded. As summarized in our model (Figure 9

), the present study provides a direct mechanistic link between the internalization of MOR and fentanyl-induced plasticity of dendritic spines, which might play important roles in drug addiction and cognition dysfunctions. An ideal opioid drug with minimal side effects should have properties that are similar to those of endogenous opioid peptides: strong signal transduction and robust endocytosis (Martini and Whistler 2007). It is conceivable that a novel opioid with “ideal” properties might aim to shift the bidirectional effects toward a lower concentration in the future.

Summary

The present study demonstrates that chronic treatment with fentanyl at low concentrations causes the collapse of dendritic spines and removal of synaptic AMPA receptors, whereas fentanyl at high concentrations has opposite effects. This bidirectional effect is prevented by the blockade of MOR internalization via the expression of a dominant negative Dynamin I (K44E), indicating an important role of receptor internalization in this cellular process. Characterizing the fentanyl-induced alterations in dendritic spines and AMPA receptor trafficking might shed new light on the cellular mechanism underlying the addiction, tolerance and cognitive deficits that are caused by the illicit abuse and/or clinical use of this drug.

Acknowledgements

We thank Drs. George Wilcox and Brian Hoover for their helpful comments, and Mr. Eric Nordstrom for his technical support. This study is supported by National Institute for Drug Abuse (NIDA) grants R01-DA020582 and K02-DA025048 to DL, grants from Chinese government (30570591 and 06MA147) to HL and NIDA grants P50-DA011806, R01-DA007339, R01-DA000564, R01-DA016674, K05-DA070554 and K05-DA000513 to HHL and PYL.

Footnotes

Disclosure/Conflict of Interest:

The author(s) declare that, except for income received from my primary employer, no financial support or compensation has been received from any individual or corporate entity over the past three years for research or professional service and there are no personal financial holdings that could be perceived as constituting a potential conflict of interest.

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