- Open Access
Morphine immunomodulation prolongs inflammatory and postoperative pain while the novel analgesic ZH853 accelerates recovery and protects against latent sensitization
Journal of Neuroinflammation volume 16, Article number: 100 (2019)
Numerous studies have identified the proinflammatory, pronociceptive effects of morphine which ultimately exacerbate pain. Our novel endomorphin analog ZH853 does not produce proinflammatory effects on its own and gives potent, long-lasting analgesia. This study investigates whether ZH853’s lack of interaction with the neuroimmune system reduces the risk of prolonged pain.
Adult male Sprague-Dawley rats were subjected to one of two treatment paradigms. Either (1) chronic pain followed by chronic treatment with morphine, ZH853 or vehicle, or (2) chronic drug administered prior to pain induction. Complete Freund’s adjuvant (CFA) was injected or paw incision surgery was performed on the left hind plantar foot pad. Drugs were administered through Alzet osmotic minipumps at a rate of 1 μl/h for 5 days at appropriate doses based on prior experiments. Animals were tested for mechanical allodynia and thermal hyperalgesia using von Frey filaments and the Hargreaves apparatus, respectively. Additionally, several gait parameters were measured using the CatWalk XT. When all animals had recovered from pain, 1 mg/kg of naltrexone was administered to test for development of latent sensitization (LS). A second set of animals was used to investigate dorsal horn inflammation following CFA and drug treatment. ANOVAs were used to assess differences between drug treatment groups.
As expected, morphine increased and prolonged pain in all experiments compared to vehicle treatment. However, ZH853 treatment reduced the overall time spent in pain and the severity of pain scores compared to morphine. ZH853 not only reduced inflammation versus morphine treatment but also, in some instances, acted as an anti-inflammatory drug compared to vehicle treatment. Finally, ZH853 prevented the development of LS while vehicle- and morphine-treated animals showed robust relapse to pain.
ZH853 has a favorable side effect profile versus morphine and provides superior analgesia in a number of pain states. We now know that chronic use of this compound reduces time spent in a chronic pain state, the opposite of common opioids like morphine, and reduces the risk of LS, making ZH853 an excellent candidate for clinical development in humans for inflammatory and postoperative pain.
In addition to the well-known negative side effects of currently used opioids, including abuse liability, respiratory depression, tolerance, and others, several recent studies have shown a lesser-known side effect; chronic exposure to morphine and other opioids can paradoxically exacerbate and prolong pain hypersensitivity. Known as the “two hit” hypothesis, it has been proposed that injury causes pro-inflammatory signaling in the central nervous system (CNS) which is exacerbated by morphine such that pain is ultimately more intense and longer-lasting [1, 2]. This exacerbation can occur with either order of stimulus (injury then drug or vice-versa) and can contribute to the transition from acute to chronic pain. The transition to chronic pain can also occur through another recently described mechanism known as “latent sensitization” (LS). LS is pathological pain following injury or inflammation that is “masked” during apparent recovery by endogenous opioid receptor function and “unmasked” by treatment with an opioid inverse agonist, such as naltrexone, or by stress [3,4,5,6,7,8,9,10]. In this study, we compare the effects of morphine and a novel opioid on both the paradoxical exacerbation of pain and on LS, with the goal of assessing the new analog for preventing the transition from acute to chronic pain.
We recently characterized a novel endomorphin  analog (ZH853) that shows antinociceptive effects equivalent to or greater than morphine, but with reduced abuse liability, respiratory depression, tolerance, hyperalgesia, impairment of motor coordination, and glial activation . We also characterized the effectiveness of acute administration of the analog in alleviating several forms of chronic pain, including neuropathic, inflammatory, postoperative, and visceral pain . This lead compound has been selected for development for clinical application and will be tested here for the effects of short term (3–5 days) chronic administration on the recovery from inflammatory and postoperative pain and the presence of LS.
In this study, drugs were chronically infused either before or after pain. Recovery from pain was measured to determine whether ZH853 causes detrimental effects on pain similar to those reported with morphine use in humans and animals [1, 2, 13].
The drug-then-pain paradigm has been studied by several groups in different pain states. Some chronic pain patients who use opioids therapeutically are known to experience worse pain following surgery than non-opioid users, and that pain cannot always be controlled satisfactorily [14, 15]. In rodent studies, Horvath et al.  showed that 7 or 14 days of chronic morphine infusion increased and prolonged both allodynia and thermal hyperalgesia, and the Watkins lab found that animals treated with morphine prior to chronic constriction injury or complete Freund’s adjuvant (CFA) had more intense and prolonged pain that correlated with a number of upregulated proinflammatory markers . The reverse paradigm (pain then drug) is perhaps more clinically relevant but has been explored to a lesser extent. Recently, Grace et al.  found that morphine given after the induction of neuropathic pain prolonged hypersensitivity versus vehicle treatment, and this result was consistent with the effects of morphine treatment on postoperative pain . Both studies found that morphine plus pain increased proinflammatory signaling in the spinal dorsal horn and that blocking inflammation pharmacologically blocks the effect of morphine on prolonged pain.
Comprehensively described by Taylor , Corder , and Marvizon [3, 6], LS and endogenous dependence are best thought of as two sides of the same coin; the phenomena are inextricably linked and cause a susceptibility to unmasking pain through either stress or chemical inactivation of Mu-opioid receptor (MOR) constitutive activity. The initial pain insult activates pain pathways (“accelerator”) and descending pathways induce constitutive activity at the MOR (MORCA) to counteract pain (“brake”). Over a long period of recovery from the injury, the body becomes dependent on MORCA, which causes increased sensitization of pain pathways (increasing the “brake” increases the “accelerator”). This interplay between increasing pain sensitization and increasing endogenous analgesia continues in a feed-forward cycle, establishing chronic, relapsing pain that is susceptible to stress [5, 9] or inverse agonists at the MOR [4, 6]. In fact, after an injury, descending pathways can be inhibited at the cervical spinal cord to induce a relapse to pain at the level of the lumbar spinal cord , indicating that descending modulation of opioid receptors and, to some extent, α2A adrenergic receptors is necessary to continually suppress pain . LS has been demonstrated in humans , a subset of whom appear to be more prone to developing LS. As with inflammation, LS plays a role in the transition from acute to chronic pain.
In the current study, we examined the effects of morphine and ZH853 on two pain models (CFA and paw incision) in two long-term paradigms (drug then pain, pain then drug) using both traditional test methods (e.g., von Frey, Hargreaves, Randall-Selitto) as well as a functional assay (CatWalk XT), which examine different aspects of pain . To assess inflammation, spinal cords were collected from a subgroup of animals and processed for immunohistochemistry when behavioral differences were most profound.
Finally, we tested the effects of morphine and ZH853 on LS induced by inflammatory (CFA) and postoperative (paw incision) pain. To do this, we used a standard 1 mg/kg injection of the MOR inverse agonist naltrexone (NTX) to shut off MOR constitutive activity, then measured mechanical allodynia, thermal hyperalgesia, and several CatWalk variables.
The results show that morphine exacerbated and prolonged chronic pain and had no effect on LS, while ZH853 accelerated time to recovery and blocked LS. These two findings in different paradigms indicate that ZH853 has a superior profile for reducing the transition from acute to chronic pain.
Male Sprague-Dawley rats (~ 59–67 days old and 250–300 g at the beginning of the experiments, Charles River, Wilmington, MA) were group housed in a 12-h light/dark cycle (6 am/6 pm) in a temperature- (68–72 °F) and humidity-controlled room with food and water provided ad libitum. All experiments were approved by the Tulane Institutional Animal Care and Use Committee and conducted according to the NIH Guide for the Care and Use of Laboratory Animals. All efforts were made to minimize animal suffering, and to reduce the number of animals used. No alternatives to in vivo techniques are available.
Drug injections for rats were given as described previously through intrathecal (i.t.) catheters [11, 12, 19]. Before drug dosing, rats with i.t. catheters underwent lidocaine testing to determine successful placement of the catheter. After a 10 μl injection of lidocaine followed by 12 μl of streptokinase (to maintain catheter patency), rats with properly placed catheters develop rapid but transient bilateral paralysis and recover in fewer than 5 min. Rats who did not recover or respond were immediately euthanized.
Osmotic minipumps (Alzet model 2001, Durect Corp, Cupertino, CA) filled with vehicle, morphine, or ZH853 and primed in 0.9% saline at 37 °C for 16 h, were implanted subcutaneously (s.c.), and connected to a PE-8 (0.008″ I.D.) i.t. catheter. In the pain-then-drug experiment, 80% of the Emax interpolated from dose response curves in  for CFA pain were given as a bolus dose (4.657 μg morphine, 0.06 μg ZH853) followed by infusion at a rate of 2.3285 μg/h of morphine and 0.02 μg/h of ZH853. Hourly dose was calculated as the bolus dose divided by the number of hours that the dose lasted. For ZH853, 0.06 μg lasted 3 h, so continual dosing was set at 0.02 μg/h. Then, 4.657 μg of morphine lasted 2 h, so 2.3285 μg/h was used as the hourly dose. Doses for postoperative pain were a bolus dose (1.932 μg morphine, 0.176 μg ZH853) followed by infusion at a rate of 1.932 μg/h of morphine and 0.07 μg/h of ZH853 for 3 days to comply with CDC guidelines for postoperative opioid use . Hourly dose was calculated as the bolus dose divided by the number of hours that the dose lasted. For ZH853, 0.176 μg lasted 2.5 h, so continual dosing was set at 0.07 μg/h. Then, 1.932 μg of morphine lasted 1 h, so this was also used as the hourly dose. For the drug-then-pain experiment, the pumps delivered 8× the ED50/h (2 μg/h morphine , and 0.056 μg/h ZH853) for 5 days as determined previously to be equianalgesic in the tail flick assay . Drug solutions were coded and the experimenter was blind to treatment.
Hind paws were swabbed with a sterile 70% alcohol pad. As previously described [12, 22], CFA (100 μl, s.c., Sigma, St. Louis, MO) was injected into the left hindpaw using a 27-gauge needle. As an internal control, the rat’s right hind paw was injected with 100 μl of sterile saline. Testing started 24 h after injection. Before testing, swelling in the left paw was measured with a Plethysmometer Paw Volume Meter (IITC Life Science Inc., Woodland Hills, CA). Animals were monitored for signs of infection or axotomy at the injection site.
Paw incision surgery
Hindpaws were swabbed with a sterile 70% alcohol pad. As previously described [12, 23], a 1-cm longitudinal incision was made with a No. 11 blade through the skin and fascia on the plantar aspect of the left hindpaw beginning 0.5 cm from the end of the heel. The flexor muscle was elevated with forceps and incised longitudinally several times. The skin was closed with two 5–0 surgical sutures (Ethicon, Somerville, NJ). Behavioral testing started 1 h after wound closure.
All animals were monitored for signs of axotomy, infection, or porphyrin staining which would indicate extreme stress and exclude them from behavioral testing. All tests were started in the morning, beginning with the least noxious (CatWalk and von Frey) and followed by Hargreaves and Randall-Selitto testing with at least 20 min of acclimation between tests. Animals were acclimated for at least 30 min prior to von Frey testing at the beginning of the test period. Baseline measurements were conducted after the i.t. catheter was implanted. Animals were randomized into drug groups by an experimenter blinded to drug treatment such that average baselines for each group were as similar as possible across all baseline tests. All animals were used only once to prevent drug or testing experience from confounding the study and were drug- and test-naïve when the study started.
Mechanical allodynia was assessed using nylon von Frey filaments (Stoelting, Wood Dale, IL) according to the “up-down” algorithm described by Chaplan . The apparatus and procedure are described elsewhere . Briefly, rats were placed on wire mesh platforms in plexiglass boxes for 30 min of acclimation. Fibers of increasing stiffness were applied dorsally just lateral to the paw incision, pressed upward to cause a slight bend in the fiber and left in place for 8 s . The experimenter was careful to avoid the toes and hairline of the paw. Withdrawal of the hind paw from the fiber was scored as a response. When no response was obtained, the next stiffest fiber in the series was applied to the same paw; if a response was obtained, a less stiff fiber was applied. Testing proceeded in this manner until four fibers had been applied after the first one causing a withdrawal response, allowing the estimation of the mechanical withdrawal threshold. Sensory thresholds were estimated as described previously . This assay can detect mechanical thresholds as low as 0.02 g.
Withdrawal latency to heat was evaluated using the IITC Plantar Analgesia Meter (IITC Life Science, Inc.) to assess thermal hyperalgesia [12, 26]. In this procedure, a radiant heat source was directed at the hind paws (intensity 70, cutoff 15 s) and latency to withdraw was recorded. A high intensity projector bulb (Osram 58–8007 8 V, 50 W) positioned 40 mm under a glass floor was projected through a 5 × 10 aperture in the top of a movable case. Once the rat withdrew the hindpaw, the heat source was turned off and latency to withdraw was recorded three times for each paw and averaged.
To measure functional impairment and recovery from inflammation, we used the CatWalk XT version 10.6 gait analysis system (Noldus Information Technology, Wagening, Netherlands), which has been described in detail elsewhere [27,28,29,30,31]. Briefly, paw prints are captured by a high-speed video camera positioned underneath a long narrow plexiglass-bottomed chamber. The rat is put in one end of the chamber and crosses it to reach a dark chamber that leads to the animal’s home cage. Contact with the plexiglass causes a distortion of light that the system then interprets to track and analyze paw prints. Three compliant runs were collected at each time point with a maximum run time of 5 s (average = 1.52 ± 0.03 s) and run variation of less than 60% (average = 28 ± 0.79%). These parameters were sufficient to produce smooth, consistent runs across the experiment. The CatWalk XT also has an automatic classification system to define all four paws. A researcher not involved in data analysis went through each compliant run to filter out false signals or errant classifications and exclude partial paw prints at the beginning and ending of each run. We investigated the following parameters:
Swing time is the duration of no contact with the glass plate per step cycle and has been shown to increase in pain conditions.
Swing speed is the rate in meters/second that a paw is not in contact with the glass plate.
Stand time is the duration of ground contact for a single paw. This variable will decrease with pain and is the counterpart to the swing phase.
Duty cycle expresses the stand as a percentage of a step cycle. Duty cycle = stand/(stand + swing) × 100%.
Single stance measures the amount of time that the left hind paw is contacting the glass in the absence of the right hind also touching the glass. This will decrease in pain conditions.
Paw print length which is the length from the center toe to the farthest central point of the print. Print length decreases in pain conditions.
Maximum contact intensity of a paw which is an indirect measure of how much weight the animal bears on that paw. Weight bearing, and therefore contact intensity, decrease in pain states.
Naltrexone-precipitated unmasking of pain
Regardless of the order of intervention or pain type, all animals recovered to baseline, but dysregulation of the endogenous opioid system by morphine, a pain state, or both has been documented to “mask” the actual pain state [5,6,7, 9, 32, 33]. By using naltrexone 1 mg/kg s.c., we probed whether drug, pain, or drug plus pain groups showed an unmasking of latent sensitization. Animals were given naltrexone and testing occurred 30–60 min after injection, at a time when naltrexone activity is stable. All testing techniques described in Marvizon 2015  were followed as closely as possible except that animals were not tested over a time course.
When behavioral scores were most different, 25 days after CFA injection in the first paradigm (pain then drug) and 21 days after CFA injection in paradigm 2 (drug then pain), a subset of animals were deeply anesthetized with ketamine/xylazine (85/10 mg/kg) and transcardially perfused with 0.1 M phosphate-buffered saline (PBS) followed by 4% paraformaldehyde. Spinal cords were collected and post-fixed overnight at 4 °C, cryoprotected in 30% sucrose/0.1 M PBS for 2 days, and sectioned in 50 μm slices using a cryostat. Spinal cord sections from L4-L5 were collected and every 6th section was developed with a different antibody stain or combination of two stains. After two washes in PBS and blocking with 5% normal horse serum/0.3% Triton X-100, sections were incubated in the following primary antibodies: calcitonin gene-related peptide (CGRP) (rabbit, T-4032, Peninsula Labs, San Carlos, CA), glial fibrillary acidic protein monoclonal (GFAP) (mouse, Astro6 MA5-12023, ThermoFisher, Carlsbad, CA), Anti-CD11b/c (OX42) (rabbit, CBL1512-100UG, Millipore Sigma, St. Louis, MO), purinergic receptor 7 (P2X7R) (rabbit, #APR-008, Alomone Labs, Jerusalem, Israel), phosphorylated-p38 MAP kinase (pp38) (rabbit, #4511, Cell Signaling Technology, Danvers, MA), or interleukin-1beta (IL-1β) (rabbit, ab9787, Abcam, Cambridge, MA) and were incubated for 24 h at 4 °C on a slow rocker. All tissue was washed twice, re-blocked with serum, and incubated in donkey anti-mouse secondary antibody conjugated to Alexa488 (A21202, ThermoFisher) or donkey anti-rabbit conjugated to Alexa594 (A21207, ThermoFisher) for 2 h at room temperature, washed, and slide mounted with VECTASHIELD Antifade mounting medium with DAPI (H-1200, Vector Laboratories, Burlingame, CA). For all negative controls, the same procedure was performed but the primary antibody was omitted to check for non-specific staining.
Imaging and analysis
All images were captured with a Nikon Ni-E microscope and Hammamatsu camera. ImageJ software was used to assess integrated density as previously described . Briefly, a blinded observer set thresholds on images with the default ImageJ algorithm and calculated the integrated density (area times mean gray value) in a specified region of interest. The gray value includes both the intensity and number of pixels above the set threshold in the region of interest. This controls for background staining variability. When counting stain-positive cells, a blinded observer used ImageJ to count cells from five randomly selected viewing fields within the region of interest, and a second blinded observer confirmed these counts. At least 4–6 rats per group, per endpoint were used for immunohistochemistry (IHC) experiments, and 4–6 slices per rat (right and left dorsal horns) were quantified for each experiment. There were no differences between right and left dorsal horns, so data was collapsed into one column.
Data sets were analyzed with Prism (GraphPad Software, La Jolla, CA) and are expressed as mean ± standard error of the mean (SEM). Animal numbers of 4–7 per group were used based on similar experiments in our lab and others’ for appropriate statistical analysis. For all time course data, two-way repeated measures analysis of variance (ANOVA)s followed by Newman-Keuls post-hoc testing were used to determine differences in drug group over time. In the recovery analysis, the same analysis was used to compare each point to the baseline. The time point when test scores are not significantly different from baseline was considered “recovery.” Areas under the curve (AUC) were calculated for each time course for each animal. Differences between group means were determined by one-way ANOVA with Newman-Keuls post-hoc test.
Paw volumes for the CFA experiment, reflecting inflammation-induced edema, were determined by plethysmometer, and left hind (LH)/right hind (RH) values were calculated for vehicle, morphine, and ZH853 groups prior to CFA and after injection. There were no significant differences between groups (Fig. 1). Despite the consistency of injury, morphine caused increased sensitivity in all tests compared to vehicle treatment while ZH853 did not.
CFA then drug
Mechanical allodynia and naltrexone unmasking
After treating CFA-induced mechanical allodynia with vehicle or equi-antinociceptive doses of morphine or ZH853, animals treated with morphine experienced greater allodynia than vehicle-treated animals at 25, 39, and 46 days after CFA injection (Fig. 2a). ZH853-treated animals, however, recovered to baseline by day 18 and experienced less allodynia than vehicle from day 18 to 32 and less than morphine-treated animals from day 18 to 46 (interaction F28, 266 = 4.681, p < 0.0001; time F14, 266 = 35.29, p < 0.0001; drug F2, 19 = 14.09; p = 0.0002). The AUC between day 11 and 60 shows that morphine-treated animals had significantly more allodynia than vehicle- and ZH853-treated groups, and that vehicle-treated animals had more overall pain than ZH853 animals (F2, 19 = 15.61, p < 0.0001). At day 53 and 60, all groups had returned to baseline allodynia, and a naltrexone injection was used to probe whether LS had developed. In both vehicle (p < 0.0001) and morphine (p < 0.0001) groups, significant allodynia developed after 30 min, but ZH853-treated animals showed no change in allodynia. Additionally, on the last day of drug dosing (D8, green box), ZH853 still produced some anti-allodynia which was not the case for morphine, indicating reduced tolerance caused by ZH853.
After the development of thermal hyperalgesia, drug dosing with either morphine or ZH853 reversed pain on the first day of drug dosing (D4, green box) (Fig. 2b). This effect diminished by day 8, but to a lesser extent in the ZH853 group. Although no specific time point was significantly different between groups during recovery, there were significant differences in the time by drug interaction (interaction F26, 247 = 2.223, p = 0.0009; time F13, 247 = 38.99, p < 0.0001; drug F2, 19 = 2.624, p = 0.0986). Additionally, the AUC indicates that morphine-treated animals experienced more sensitivity overall (F2, 19 = 4.763; p = 0.0211) (Fig. 2b).
In the analysis of seven CatWalk variables, changes in gait function were apparent following CFA injection but, because drug dosing occurred when most of these variables had nearly returned to baseline, there were no differences between groups due to drug treatment (swing time interaction F16, 152 = 0.3986, p = 0.9813; time F8, 152 = 19.04, p < 0.0001; drug F2, 19 = 0.7010, p = 0.5085) (Fig. 2c). Additionally, LH/RH values for each variable were stable around 1 from day 18 onward and did not change following naltrexone injections (data not shown).
By comparing the means at each time point with the group baseline using a two-way ANOVA, we determined the average length of time in pain by drug treatment groups from day 11 to the end of the study. Significance is listed in Table 1. Morphine significantly prolonged allodynia and thermal hyperalgesia versus both vehicle and ZH853. ZH853, on the other hand, shortened allodynia and thermal hyperalgesia versus both morphine and vehicle. Drug administration did not affect CatWalk variables, likely because animals had nearly returned to baseline by the onset of drug treatment.
Drug then CFA
Mechanical allodynia and naltrexone unmasking
After chronic drug dosing, the subsequent CFA injection induced mechanical allodynia over the first 7 days. Animals treated with morphine experienced greater allodynia than vehicle-treated animals at 21, 28, and 35 days after CFA injection (Fig. 3a). ZH853-treated animals, however, experienced less pain than the morphine group from day 14 to 35 (interaction F26, 234 = 2.399, p = 0.0003; time F13, 234 = 21.10, p < 0.0001; drug F2, 18 = 18.87, p < 0.0001). The AUC between day 1 and 49 shows that morphine animals had significantly greater allodynia than vehicle and ZH853 groups, and that vehicle animals had similar pain to ZH853 animals (F2, 18 = 12.22, p = 0.0004). At day 49, all groups had returned to baseline allodynia, and a naltrexone injection (1 mg/kg) was used to probe whether latent sensitization had developed. In both vehicle- and morphine-treated animals, significant allodynia developed after 30 min, but ZH853-treated animals showed no significant change in allodynia after either 1 or 5 mg/kg of naltrexone. After the 1 mg/kg injection of naltrexone, allodynia was slightly increased in morphine versus vehicle-treated animals, but at 5 mg/kg a floor effect made them equally sensitive (see graph for statistics).
After pre-treatment with drug, thermal hyperalgesia developed. Animals treated with morphine experienced greater hyperalgesia than vehicle-treated animals at 14, 21, and 49 days after CFA injection (Fig. 3b). ZH853-treated animals, however, experienced less pain than the morphine group from day 7–21 and on day 35 (interaction F22, 198 = 1.027 p = 0.4331; time F11, 198 = 53.68, p < 0.0001; drug F2, 18 = 10.75, p = 0.0008). The AUC between day 1 and 56 shows that morphine animals had significantly more pain than vehicle and ZH853 groups, and that vehicle animals had similar pain to ZH853 animals (F2, 18 = 10.42, p = 0.0010). Notably, morphine-treated animals were significantly more sensitive than vehicle and ZH853 groups when tested just prior to CFA injection 2 days after cessation of drug dosing, which is not unusual given morphine’s proinflammatory and pain sensitizing effects after chronic dosing (see figure for statistics).
In the analysis of seven CatWalk variables, changes in gait were apparent following CFA injection, and made worse by pre-treatment with morphine for the first few days (Fig. 3c). Morphine animals had greatly increased swing time, the amount of time that the paw is held in the air, for the first 3 days after CFA injection (interaction F16, 144 = 2.889, p < 0.0004; time F8, 144 = 40.6, p < 0.0001; drug F2, 18 = 4.061; p = 0.0350). Print length was shortened in the first few days after injury; even more so in morphine-treated animals (interaction F16, 144 = 2.426, p = 0.0029; time F8, 144 = 33.75; p < 0.0001; drug F2, 18 = 1.693, p = 0.2119). All animals had a decrease in swing speed after injury, the rate in meters/second that a paw is not in contact with the glass plate (interaction F16, 144 = 1.590, p = 0.0782; time F8, 144 = 81.14; p < 0.0001; drug F2, 18 = 1.099, p = 0.3545). Stand time, or duration of ground contact, was also decreased by injury (interaction F16, 144 = 1.253, p = 0.2354; time F8, 144 = 46.16; p < 0.0001; drug F2, 18 = 2.817, p = 0.0863). Duty cycle (interaction F16, 144 = 1.601, p = 0.0753; time F8, 144 = 64.26; p < 0.0001; drug F2, 18 = 2.277, p = 0.1314), single stance (interaction F16, 144 = 1.258, p = 0.2324; time F8, 144 = 76.66; p < 0.0001; drug F2, 18 = 1.383, p = 0.2762), and maximum contact area (interaction F16, 152 = 0.6678, p = 0.8220; time F8, 152 = 47.76; p < 0.0001; drug F2, 19 = 0.2218, p = 0.8031) were also decreased within the first few days. (LH/ RH values for each variable were back to baseline from day 14 onward and did not change following naltrexone injections of either 1 mg/kg or 5 mg/kg (data not shown). Data are summarized in Table 2.
Duration of allodynia and hyperalgesia
Means were compared between each time point and the group baseline using a two-way ANOVA to determine the average length of time in pain by drug treatment groups from day 1 to the end of the study. Significance is listed in Table 3. Morphine significantly prolonged allodynia versus both vehicle and ZH853. ZH853 shortened allodynia and thermal hyperalgesia versus both morphine and vehicle.
Paw incision then drug
After treating paw incision-induced mechanical allodynia with vehicle or equi-antinociceptive doses of morphine or ZH853, animals treated with morphine experienced greater allodynia overall than vehicle-treated animals (Fig. 4a). ZH853-treated animals, however, experienced less pain than vehicle on days 14 and 28, and less pain than morphine-treated animals from day 14 to 28 (interaction F20, 160 = 2.976, p < 0.0001; time F10, 160 = 32.82, p < 0.0001; drug F2, 16 = 12.64, p = 0.0005). The AUC between day 7 and 42 shows that morphine-treated animals had significantly more pain than vehicle- and ZH853-treated groups, and that vehicle-treated animals had more overall pain than ZH853-treated animals (F2, 16 = 9.293, p = 0.0021). At day 42, all groups had returned to baseline allodynia, and a naltrexone injection was used to probe whether latent sensitization had developed. In both vehicle- (p < 0.001) and morphine- (p < 0.001) treated animals, significant allodynia developed after 30 min, but ZH853-treated animals showed no change in allodynia. Additionally, on the last day of drug dosing (D3, green box), ZH853 still produced some anti-allodynia versus vehicle which was not the case for morphine.
Morphine and ZH853 were antinociceptive in the first hour of drug dosing (Fig. 4b: H1, green box), but morphine antinociception was greatly reduced at 3 and 5 h. By D1, morphine-treated animals had pain similar to vehicle-treated animals, but ZH853 was still providing some pain relief. By D3, all groups were similarly hyperalgesic. On days 21–28, morphine-treated animals were in more pain than ZH853-treated animals, and on day 28, vehicle-treated animals were also in more pain than ZH853-treated animals (interaction F26, 208 = 14.56, p < 0.0001; time F13, 208 = 47.27, p < 0.0001; drug F2, 16 = 60.74, p < 0.0001). After all groups were recovered at D42, naltrexone was administered and thermal hyperalgesia developed in vehicle- and morphine-treated animals but not ZH853-treated animals (p = 0.0001). Additionally, the AUC indicates differences in sensitivity over the recovery time course (F2, 16 = 5.970, p = 0.0116) with morphine-treated animals experiencing the most sensitivity followed by vehicle- then ZH853-treated animals.
In the analysis of seven CatWalk variables, changes in gait function were apparent following CFA injection, but there were no differences between drug treatment groups (swing time, interaction F10, 75 = 0.9907, p = 0.4591; time F5, 75 = 4.082, p = 0.0025; drug F2, 15 = 2.062, p = 0.1617) (Fig. 4c). It should be noted that the CatWalk only captures subtle changes in gait following paw incision surgery unlike the dramatic changes seen with CFA. The small dynamic range in these gait changes may make it more difficult to see differences in drug treatment groups.
Prolonged allodynia and hyperalgesia
By comparing the means at each time point with the group baseline using a two-way ANOVA, we determined the average length of time in pain by drug treatment groups from day 1 to the end of the study. Significance at each time point is listed in Table 4. Morphine significantly prolonged thermal hyperalgesia versus both vehicle and ZH853. ZH853, on the other hand, shortened allodynia and thermal hyperalgesia versus both morphine and vehicle. Drug administration did not affect CatWalk variables, likely because they had nearly returned to baseline by the onset of drug treatment.
Drug then paw incision
After exposure to tolerance-inducing doses of morphine or ZH853, animals treated with morphine experienced greater allodynia than vehicle-treated animals at 14 and 21 days after paw incision (Fig. 5a). ZH853-treated animals, however, showed improved pain sensitivity versus vehicle- and morphine-treated animals as early as D7, and experienced less pain than morphine-treated animals from D7 to 21 (interaction F18, 144 = 1.957, p = 0.0158; time F9, 144 = 57.06, p < 0.0001; drug F2, 16 = 2.540, p = 0.1102). The AUC between D1 and 42 shows that morphine animals had significantly greater allodynia than ZH853-treated animals (F2, 16 = 6.509, p = 0.0085). At day 28, all groups had returned to baseline, and a naltrexone injection was used to probe whether latent sensitization had developed. Unexpectedly, no allodynia was observed in any group at this time point.
After drug treatment, paw incision induced a strong thermal hypersensitivity in all animals. There were significant differences by the interaction of time and drug group (interaction F28, 224 = 2.697, p < 0.0001; time F14, 224 = 79.95, p < 0.0001; drug F2, 16 = 1.433, p = 0.2676) and a naltrexone challenge caused thermal hyperalgesia in vehicle- and morphine-treated groups but not ZH853-treated groups (p < 0.0001). The AUC indicates a lack of overall differences in sensitivity (F2, 16 = 1.324, p = 0.2937) (Fig. 5b).
In the analysis of seven CatWalk variables, changes in gait function were apparent following paw incision, but there were no differences between groups due to drug treatment (swing time: interaction F14, 112 = 0.7318, p = 0.7385; time F7, 112 = 19.82, p < 0.0001; drug F2, 16 = 0.5549, p = 0.5848) (Fig. 5c).
Prolonged allodynia and hyperalgesia
By comparing the means at each time point with the group baseline using a two-way ANOVA, we determined the average length of time in pain by drug treatment groups from D1 to the end of the study. Significance at each time point is listed in Table 5. Morphine significantly prolonged allodynia versus both vehicle and ZH853. ZH853, on the other hand, shortened allodynia vs morphine and thermal hyperalgesia versus both morphine and vehicle.
In order to determine whether morphine-exacerbated CFA pain is associated with potentiated pro-inflammatory signaling in the spinal dorsal horn, spinal cords were collected from animals perfused at 25 days (CFA then drug) and 21 days (drug then CFA) for IHC. These time points were chosen because of the profound differences in allodynia between drug treatment groups. Several measures of inflammation were assessed at the level of L4–L6 of the spinal cord. Overall, inflammatory markers were upregulated consistently among morphine-treated animals. In almost every instance, ZH853-treated animals had reduced inflammation when compared with morphine-treated animals, and vehicle-treated animals had variable inflammation in relation to morphine or ZH853.
In the CFA-then-drug paradigm (Fig. 6a), drug treatment impacted pp38 (F2,25 = 8.013; p = 0.0020), IL-1β (F2,24 = 6.358; p = 0.0061), CGRP (F2,25 = 11.12; p = 0.0004), astrocyte activation (GFAP) (F2,23 = 4.285; p = 0.0262), and P2X7Rs (F2,25 = 3.713; p = 0.0401). Microglial (OX42) differences were not apparent at this time point (F2,25 = 1.029; p = 0.3719).
In the drug-then-CFA paradigm (Fig. 6b), drug greatly impacted microglial activation (OX42) (F2,19 = 6.891; p < 0.0001), pp38 (F2,21 = 9.140; p = 0.0014), IL-1β (F2,21 = 10.86; p = 0.0006), CGRP (F2,21 = 10.35; p = 0.0007), astrocyte activation (GFAP) (F2,21 = 12.57; p = 0.0003), and P2X7Rs (F2,20 = 9.328; p = 0.0014). Representative images for this paradigm for all markers are included in Fig. 7.
The effect of CFA alone is represented by the vehicle-treated group. Except for OX42 in the CFA-then-drug model (Fig. 6a), morphine increased all inflammatory markers relative to ZH853. pp38 was reduced by ZH853 relative to vehicle; otherwise, ZH853 and vehicle groups were not significantly different. Morphine increased IL-1β and CGRP relative to vehicle. In the drug-then-CFA model, morphine increased all inflammatory markers relative to ZH853. ZH853 reduced IL-1β and GFAP versus vehicle, and morphine increased OX42, CGRP, and P2X7Rs versus vehicle.
A simple linear regression was calculated to determine whether a correlation existed between inflammatory markers and von Frey scores regardless of drug administered or paradigm (Fig. 8). A significant positive correlation with mechanical allodynia was found for pp38 (F1,24 = 12.87, p = 0.0015), with an R2 of .3490, and for P2X7R (F1,21 = 4.930, p = 0.0375), with an R2 of 0.1901. There were no significant correlations between allodynia and OX42, IL-1β, CGRP, or GFAP at these time points.
While we expected that morphine-treated animals would experience greater LS compared to vehicle-treated animals, there appears to have been a “bottoming out” effect after naltrexone administration, causing both groups to appear equally affected. However, ZH853-treated animals consistently did not experience LS unmasking regardless of type of pain or order of drug treatment.
Corder et al.  described the unmasking of LS following recovery from CFA in mice and showed that both mechanical allodynia (von Frey) and thermal hyperalgesia (Hargreaves) scores indicated a relapse to pain. We were surprised to find that in both paradigms of the CFA model, LS unmasking was apparent in von Frey testing (Figs. 2a and 3a) but not in the Hargreaves test, even with a 5 mg/kg naltrexone dose (Figs. 2b and 3b). After paw incision then drug treatment, allodynia was apparent in vehicle- and morphine-treated groups, but there was no relapse to allodynia in the reverse paradigm (Fig. 4b). However, relapse to thermal hyperalgesia was clearly present in both paradigms of paw incision (Fig. 5b). To see if there was any connection between the lengths of time in pain and whether or not LS developed, we plotted a summary of the total number of days in pain, charted according to pain type and sequence of drug and pain timing (Fig. 9). The total number of days in pain were calculated by two-way ANOVA as described in Tables 1, 2, 3, and 4. In addition, asterisks mark the instances where vehicle- or morphine-treated animals showed LS unmasking after naltrexone was administered. It is visually clear that LS occurred in instances where there was prolonged pain, but not if pain was under 21 days for allodynia (Fig. 9a) or under 11 days of thermal hyperalgesia (Fig. 9b). ZH853-treated animals consistently experienced less time in a hypersensitive state than other groups, which could be a major contributing factor to ZH853’s protective effect against LS.
The results of this study show that chronic use of ZH853 does not exacerbate the hyperalgesia and allodynia induced by inflammatory or post-operative pain while morphine does. Consistent with prior literature [1, 2, 16, 17], morphine exposure at moderately antinociceptive doses caused increased pain sensitivity. ZH853, which produced antinociception with less tolerance than morphine, caused no such increase in pain sensitivity across all pain tests. In fact, ZH853 diminished the amount of time in pain versus morphine in all tests and even versus vehicle treatment in several instances. This was an unexpected and unprecedented finding considering that opioids are known to increase and prolong many types of pain [1, 2, 16, 17]. Finally, ZH853 protected against the development or susceptibility to LS while morphine did not.
In addition to classical pain tests, we assessed operant behavior using the CatWalk and found that injury-induced deficits were transient and detectable at earlier time points than in the classical von Frey and Hargreaves tests. Significant impairment of gait by morphine, but not ZH853, was observed in several parameters during the drug-then-CFA paradigm. Gait analysis for pain monitoring is becoming increasingly developed for use in humans [34, 35] and, similarly to the animals in this study, pain-inducing inflammatory conditions of the human foot result in a loss of heel strike . Antalgic (pain-avoidance) gait is defined by a reduced stance phase relative to swing phase, which is observed in humans with pain as well as animals [28, 35, 36] and observed in both paradigms of this study following CFA (Figs. 2c and 3c). In the pain-then-drug paradigm (Fig. 2c), drug dosing began as functional impairments were nearly back to baseline, which was likely the reason that no differences were apparent between drug groups. In the drug-then-pain paradigm (Fig. 3c), animals exposed to morphine showed greater gait impairments across several parameters up to the 7th day after CFA injection, indicating a decreased use of the left hind foot (guarding) versus vehicle- and ZH853-treated animals. The drug-then-CFA paradigm was the only test that captured a drug-induced difference in sensitivity within the first few days. For the drug-then-paw incision test, a less robust hypersensitivity, and therefore smaller dynamic range of responses, may have masked differences. For both the CFA and paw incision then drug tests, recovery had occurred by the end of dosing. The fact that functional impairments were observed from day 1 after CFA until day 3 or day 7 but not after that suggests that this test is not measuring mechanical allodynia as some groups have proposed . The recovery timelines observed in this study mimicked those previously described in mice  and rats , showing short-term functional impairments (guarding, spontaneous pain) and long-term increases in allodynia and thermal hyperalgesia. In a comprehensive study by Djouhri et al. , spontaneous foot lifting (SFL) was used to measure spontaneous pain in comparison to von Frey and Hargreaves testing after CFA injections. In the first 2 days after injury, rats exhibited significant SFL which did not correlate with von Frey scores. However, they found that spontaneous C-fiber activity had greatly increased in these early time points. Although not directly compared in this study, it is not unreasonable to suggest that gait impairments are indicative of spontaneous pain, but many investigators have commented on the inability of painkillers to reverse these gait impairments acutely. Interestingly, some aspect of prior morphine, but not ZH853, managed to make these gait impairments worse, possibly through an increase in spontaneous activity at Aδ and/or C-fibers , which was not directly tested here. Finally, naltrexone was unable to provoke antalgic gait changes, which may differentiate this phase of pain from allodynia or thermal hyperalgesia that are susceptible to relapse (LS).
Rats treated with morphine generally showed signs of increased spinal inflammatory markers in immunohistochemical tests when compared to vehicle- and ZH853-treated animals. This supports findings from several other studies [1, 2, 11, 16, 17, 40]. While vehicle-treated animals usually had inflammatory expression somewhere between ZH853- and morphine-treated animals, ZH853-treated animals consistently showed the least amount of inflammation.
Previous reports from our lab and others have shown pro-inflammatory effects of morphine , and additive inflammatory effects of morphine in an animal in pain [1, 2, 16, 17]. Anti-inflammatory drugs like minocycline can block the development of tolerance, addiction, and dependence [41,42,43,44], but in humans it is not always possible or beneficial to treat with these drugs long-term. Several mechanisms by which morphine activates glia or enhances trauma-induced activation have been proposed (Fig. 10), including (1) induction of neuronal CGRP that activates microglial CGRP receptors , (2) binding at toll-like receptors (TLRs) alone or in concert with damage-associated molecular patterns (DAMPs) , and (3) activation of purinergic P2X receptors including by upregulation through MOR  (but see ). Each of these mechanisms causes phosphorylation of the mitogen-activated protein kinase (MAPK) p38, which activates nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) to increase transcription and translation of cytokines, including interleukin-1β (IL-1β , example shown), as well as IL-6, IL-18, and tumor necrosis factor-α (TNF-α). P2X7R activation also induces NOD-like receptor family, pyrin domain containing 3 (NLRP3) to become a complex (inflammasome)  that contains and releases active caspase-1 which cleaves pro-IL-1β into the active cytokine IL-1β . IL-1β activates IL-1 receptors on astrocytes and neurons, further increasing inflammation. Ultimately, this proinflammatory pathway causes dorsal horn plasticity that leads to central sensitization and increased pain . Pre- and/or postoperative inhibition of TLR4, phosphorylated p38 (pp38), NFκB, and IL-1β have been shown to reduce postoperative mechanical hyperalgesia [53,54,55,56].
While chronic morphine also activates all of these pathways in naïve rats, we recently showed the ZH853 activates none of them in a pain-naïve state . In pain states, preemptive use of EM-1 and EM-2 reduces inflammatory (CFA) pain for days, even though the analgesic actions of the EMs only last ~ 30 m . Through a number of pharmacological manipulations, Zhang et al. determined that p38 activation was significantly increased by pain but dramatically reduced by the EMs through a MOR-dependent mechanism . Additionally, they found EM-induced reductions in IL-1β, TNF-α, C-C motif chemokine ligand 2 and 3 (CCL2/3), with an increase in IL-10 mRNA.
Others have shown that chronic morphine upregulates CGRP [45, 58], but this is the first time that long-term upregulation of CGRP following morphine and pain has been observed. In both CFA paradigms, vehicle- and ZH853-treated animals had similar CGRP expression, but weeks after the cessation of drug administration and CFA, morphine-treated animals had significantly higher levels of CGRP. Although not a direct component of the immune system, CGRP has been identified as a key player in the neuro-immune axis  with a range of functions at T cells, dendritic cells, mast cells, and macrophages that modulate pro- or anti-inflammatory factors. In particular, CGRPRs on microglia are likely a site of immune cell priming by pain in the spinal cord  which is then exacerbated by morphine or vice versa.
Astrocytes have largely been neglected in the long-term pain and opioid studies mentioned here, but one study found that astrocyte activation, not microglia, is best correlated with allodynia over time after induction of neuropathic pain . After postoperative CFA plus morphine, neither astrocytes nor microglia appeared to be activated in staining, but other markers (pp38) indicated that they were activated . In the current study, reduced immunofluorescence of GFAP and other markers indicates an anti-inflammatory effect of ZH853 versus the morphine-treated group (Fig. 6a). In the drug-then-CFA paradigm, ZH853 is anti-inflammatory versus the vehicle-treated group (GFAP, IL-1β) and, to a greater degree, versus the morphine-treated group (all markers) (Fig. 6b). However, astrocyte activation does not correlate with CFA-induced pain scores (Fig. 8).
Despite the seemingly clear relationship between increased inflammation and prolonged pain, pp38 and P2X7R are the only markers whose upregulation actually correlates directly with pain scores (Fig. 8). These findings underscore the utility of the pp38 marker in assessing pain pathways after complex manipulations; it is a unifying factor regardless of whether microglia are activated by CGRP, TLR4, or P2XRs. In addition, the results indicate that P2X7R may be of particular importance in CFA-induced pain. Given that ZH853 reduced all inflammatory factors versus morphine, it is reasonable to use the novel peptide in place of morphine to avoid production of additional pro-inflammatory, pronociceptive agitation in the CNS.
LS has been demonstrated in a number of pain types and animals [6, 7, 32, 61]. LS develops as a homeostatic mechanism to combat ongoing pain, allowing an organism to function effectively in the face of pain that has outlasted utility. Chen et al. discovered that top-down initiation of MORCA is blocked by spinal lidocaine administration , indicating that initiation comes from the brain in response to long-lasting pain. It appears that ZH853, either prior to or after pain induction, acts to quiet pain signaling in a manner distinct from morphine, alleviating the need for development of a compensatory mechanism (MORCA). When the pain insult finally resolves, there is no underlying pathology in place that is susceptible to unmasking by naltrexone. Morphine, on the other hand, continues to exacerbate pro-inflammatory, pro-nociceptive signaling that ramps up the pain signal. This in turn ramps up the compensatory MORCA, allowing LS to manifest. Additionally, opioids like morphine induce LS in the absence of pain in an N-methyl-d-aspartate receptor (NMDA)-dependent manner , and one group has found that N2O can prevent the development of opioid-induced LS by acting as an NMDA antagonist . While some unpublished work in the lab has indicated that ZH853 does not bind significantly to NMDARs, no studies have been done to determine whether ZH853 acts as an NMDA allosteric modulator, but this is a possible explanation for the results described in this section.
As shown in Fig. 9, LS was produced in five of the eight paradigms tested. Those not producing LS were conditions in which the days in pain were generally shorter. This suggests that perhaps the severity and length of pain signaling has an influence on the development of LS and ZH853 might be protective against LS simply because ZH853-treated animals spent less time in pain overall. However, postoperative thermal hyperalgesia (Fig. 9b 3rd column) was the exception to this with ZH853-treated animals experiencing 21 days in pain with no sign of LS, indicating that factors other than time in pain contribute to both LS and its blockade by ZH853.
A drug that prevents the transition from acute to chronic relapsing pain would represent a true breakthrough in drug development for pain management. Not only have the mechanisms behind the shift from acute to chronic pain been elusive, but efforts to thwart this transition have been unsuccessful thus far. Two recognized markers of this transition are sustained glial activation [1, 2, 16, 43, 46, 63,64,65,66,67,68] and development of LS [4, 6, 8, 10, 62], which were both reduced by ZH853.
Chronic pain patients and their doctors often face the dilemma of whether to risk serious side effects to achieve needed pain relief with opioids. Here, we show that the novel opioid, ZH853, shortens recovery time from inflammatory and postoperative pain while morphine prolongs recovery. Further, morphine does not affect latent sensitization while ZH853 blocks it. These results indicate two mechanisms of reduced transition from acute to chronic pain after treatment with ZH853. In addition, previous studies showed significant reduction, relative to morphine, of respiratory depression, abuse liability, tolerance, inflammation, and impairment of motor coordination  and equal or greater relief of pain in multiple chronic pain models . Taken together, these results indicate that ZH853 could transform pain management.
Analysis of variance
Area under the curve
Chronic constriction injury
Complete Freund’s adjuvant
Calcitonin gene-related peptide
Central nervous system
Damage-associated molecular patterns
Glial fibrillary acidic protein
- MORCA :
Mu-opioid receptor constitutive activity
Nuclear factor kappa-light-chain-enhancer of activated B cells
Nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing 3 (inflammasome complex)
Anti-CD11b/c antibody (microglial marker)
Purinergic receptors- e.g., P2X4, P2X7
Phosphorylated-p38 MAP Kinase
Standard error of the mean
Spontaneous foot lifting
Grace PM, Strand KA, Galer EL, Urban DJ, Wang X, Baratta MV, Fabisiak TJ, Anderson ND, Cheng K, Greene LI, et al. Morphine paradoxically prolongs neuropathic pain in rats by amplifying spinal NLRP3 inflammasome activation. Proc Natl Acad Sci U S A. 2016;113(24):E3441–E50.
Loram LC, Grace PM, Strand KA, Taylor FR, Ellis A, Berkelhammer D, Bowlin M, Skarda B, Maier SF, Watkins LR. Prior exposure to repeated morphine potentiates mechanical allodynia induced by peripheral inflammation and neuropathy. Brain Behav Immun. 2012;26(8):1256–64.
Chen W, Tache Y, Marvizon JC. Corticotropin-releasing factor in the brain and blocking spinal descending signals induce hyperalgesia in the latent sensitization model of chronic pain. Neuroscience. 2018;381:149–58.
Corder G, Doolen S, Donahue RR, Winter MK, Jutras BL, He Y, Hu X, Wieskopf JS, Mogil JS, Storm DR, et al. Constitutive μ-opioid receptor activity leads to long-term endogenous analgesia and dependence. Science. 2013;341(6152):1394–9.
Rivat C, Laboureyras E, Laulin JP, Le Roy C, Richebe P, Simonnet G. Non-nociceptive environmental stress induces hyperalgesia, not analgesia, in pain and opioid-experienced rats. Neuropsychopharmacol. 2007;32(10):2217–28.
Walwyn WM, Chen W, Kim H, Minasyan A, Ennes HS, McRoberts JA, Marvizón JCG. Sustained suppression of hyperalgesia during latent sensitization by μ-, δ-, and κ-opioid receptors and α2A; adrenergic receptors: role of constitutive activity. J Neurosci. 2016;36(1):204.
Pereira MP, Donahue RR, Dahl JB, Werner M, Taylor BK, Werner MU. Endogenous opioid-masked latent pain sensitization: studies from mouse to human. PLoS One. 2015;10(8):e0134441.
Taylor BK, Corder G. Endogenous analgesia, dependence, and latent pain sensitization. Curr Top Behav Neurosci. 2014;20:283–325.
Le Roy C, Laboureyras E, Gavello-Baudy S, Chateauraynaud J, Laulin J-P, Simonnet G. Endogenous opioids released during non-nociceptive environmental stress induce latent pain sensitization via a nmda-dependent process. J Pain. 2011;12(10):1069–79.
Marvizon JC, Walwyn W, Minasyan A, Chen W, Taylor BK. Latent sensitization: a model for stress-sensitive chronic pain. Curr Protoc Neurosci. 2015;71:9 50 1–14.
Zadina JE, Nilges MR, Morgenweck J, Zhang X, Hackler L, Fasold MB. Endomorphin analog analgesics with reduced abuse liability, respiratory depression, motor impairment, tolerance, and glial activation relative to morphine. Neuropharmacology. 2016;105:215–27.
Feehan AK, Morgenweck J, Zhang X, Amgott-Kwan AT, Zadina JE. Novel endomorphin analogs are more potent and longer-lasting analgesics in neuropathic, inflammatory, postoperative, and visceral pain relative to morphine. J Pain. 2017;18(12):1526–41.
Hoffman EM, Watson JC, St Sauver J, NP S, Klein CJ. Association of long-term opioid therapy with functional status, adverse outcomes, and mortality among patients with polyneuropathy. JAMA Neurol. 2017;74(7):773–9.
Rapp SE, Ready LB, Nessly ML. Acute pain management in patients with prior opioid consumption: a case-controlled retrospective review. Pain. 1995;61(2):195–201.
de Leon-Casasola OA, Lema MJ. Epidural sufentanil for acute pain control in a patient with extreme opioid dependency. Anesthesiology. 1992;76(5):853–6.
Horvath RJ, Landry RP, Romero-Sandoval EA, DeLeo JA. Morphine tolerance attenuates the resolution of postoperative pain and enhances spinal microglial p38 and extracellular receptor kinase phosphorylation. Neuroscience. 2010;169(2):843–54.
Grace PM, Galer EL, Strand KA, Corrigan K, Berkelhammer D, Maier SF, Watkins LR. Repeated morphine prolongs postoperative pain in male rats. Anesth Analg. 2019;128(1):161–7.
Pitzer C, Kuner R, Tappe-Theodor A. Voluntary and evoked behavioral correlates in neuropathic pain states under different social housing conditions. Mol Pain. 2016;12. https://doi.org/10.1177/1744806916656635
Yaksh TL, Rudy TA. Chronic catheterization of the spinal subarachnoid space. Physiol Behav. 1976;17(6):1031–6.
Dowell D, Haegerich TM, Chou R. CDC guideline for prescribing opioids for chronic pain—United States, 2016. MMWR Recomm Rep. 2016;65(1):1–49.
Stevens CW, Yaksh TL. Potency of infused spinal antinociceptive agents is inversely related to magnitude of tolerance after continuous infusion. J Pharmacol Exp Ther. 1989;250(1):1–8.
Iadarola MJ, Douglass J, Civelli O, Naranjo JR. Differential activation of spinal cord dynorphin and enkephalin neurons during hyperalgesia: evidence using cDNA hybridization. Brain Res. 1988;455(2):205–12.
Xu J, Brennan TJ. Comparison of skin incision vs. skin plus deep tissue incision on ongoing pain and spontaneous activity in dorsal horn neurons. Pain. 2009;144(3):329–39.
Chaplan SR, Bach FW, Pogrel JW, Chung JM, Yaksh TL. Quantitative assessment of tactile allodynia in the rat paw. J Neurosci Methods. 1994;53(1):55–63.
Decosterd I, Woolf CJ. Spared nerve injury: an animal model of persistent peripheral neuropathic pain. Pain. 2000;87(2):149–58.
Hargreaves K, Dubner R, Brown F, Flores C, Joris J. A new and sensitive method for measuring thermal nociception in cutaneous hyperalgesia. Pain. 1988;32(1):77–88.
Sakuma T, Kamoda H, Miyagi M, Ishikawa T, Arai G, Eguchi Y, Suzuki M, Oikawa Y, Sakuma Y, Kubota G, et al. Comparison of CatWalk analysis and von Frey testing for pain assessment in a rat model of nerve crush plus inflammation. Spine. 2013;38(15):E919–24.
Parvathy SS, Masocha W. Gait analysis of C57BL/6 mice with complete Freund's adjuvant-induced arthritis using the CatWalk system. BMC Musculoskelet Disord. 2013;14(1):14.
Bozkurt A, Deumens R, Scheffel J, O'Dey DM, Weis J, Joosten EA, Fuhrmann T, Brook GA, Pallua N. CatWalk gait analysis in assessment of functional recovery after sciatic nerve injury. J Neurosci Methods. 2008;173(1):91–8.
Hamers FP, Koopmans GC, Joosten EA. CatWalk-assisted gait analysis in the assessment of spinal cord injury. J Neurotrauma. 2006;23(3–4):537–48.
Vrinten DH, Hamers FF. ‘CatWalk’ automated quantitative gait analysis as a novel method to assess mechanical allodynia in the rat; a comparison with von Frey testing. Pain. 2003;102(1–2):203–9.
Lian B, Vera-Portocarrero L, King T, Ossipov MH, Porreca F. Opioid-induced latent sensitization in a model of non-inflammatory viscerosomatic hypersensitivity. Brain Res. 2010;1358:64–70.
Celerier E, Laulin JP, Corcuff JB, Le Moal M, Simonnet G. Progressive enhancement of delayed hyperalgesia induced by repeated heroin administration: a sensitization process. J Neurosci. 2001;21(11):4074–80.
Paraschiv-Ionescu A, Perruchoud C, Buchser E, Aminian K. Barcoding human physical activity to assess chronic pain conditions. PLoS One. 2012;7(2):e32239.
DeLisa JA. Scientific USVHA, Section. TP: gait analysis in the science of rehabilitation. Washington, D.C: Dept. of Veterans Affairs, Veterans Health Administration, Rehabilitation Research and Development Service, Scientific and Technical Publications Section; 1998.
Piesla MJ, Leventhal L, Strassle BW, Harrison JE, Cummons TA, Lu P, Whiteside GT. Abnormal gait, due to inflammation but not nerve injury, reflects enhanced nociception in preclinical pain models. Brain Res. 2009;1295:89–98.
Gabriel AF, Marcus MA, Walenkamp GH, Joosten EA. The CatWalk method: assessment of mechanical allodynia in experimental chronic pain. Behav Brain Res. 2009;198(2):477–80.
Djouhri L, Koutsikou S, Fang X, McMullan S, Lawson SN. Spontaneous pain, both neuropathic and inflammatory, is related to frequency of spontaneous firing in intact C-fiber nociceptors. J Neurosci. 2006;26(4):1281–92.
Hogan D, Baker AL, Moron JA, Carlton SM. Systemic morphine treatment induces changes in firing patterns and responses of nociceptive afferent fibers in mouse glabrous skin. Pain. 2013;154(11):2297–309.
Doyle HH, Murphy AZ. Sex-dependent influences of morphine and its metabolites on pain sensitivity in the rat. Physiol Behav. 2018;187:32–41.
Hutchinson MR, Lewis SS, Coats BD, Skyba DA, Crysdale NY, Berkelhammer DL, Brzeski A, Northcutt A, Vietz CM, Judd CM, et al. Reduction of opioid withdrawal and potentiation of acute opioid analgesia by systemic AV411 (ibudilast). Brain Behav Immun. 2009;23(2):240–50.
Lau D, Harte SE, Morrow TJ, Wang S, Mata M, Fink DJ. Herpes simplex virus vector-mediated expression of interleukin-10 reduces below-level central neuropathic pain after spinal cord injury. Neurorehabil Neural Repair. 2012;26(7):889–97.
Raghavendra V, Rutkowski MD, DeLeo JA. The role of spinal neuroimmune activation in morphine tolerance/hyperalgesia in neuropathic and sham-operated rats. J Neurosci. 2002;22(22):9980–9.
Raghavendra V, Tanga FY, DeLeo JA. Attenuation of morphine tolerance, withdrawal-induced hyperalgesia, and associated spinal inflammatory immune responses by propentofylline in rats. Neuropsychopharmacol. 2004;29(2):327–34.
Wang Z, Ma W, Chabot JG, Quirion R. Morphological evidence for the involvement of microglial p38 activation in CGRP-associated development of morphine antinociceptive tolerance. Peptides. 2010;31(12):2179–84.
Watkins LR, Hutchinson MR, Rice KC, Maier SF. The “toll” of opioid-induced glial activation: improving the clinical efficacy of opioids by targeting glia. Trends Pharmacol Sci. 2009;30(11):581–91.
Ferrini F, Trang T, Mattioli TA, Laffray S, Del'Guidice T, Lorenzo LE, Castonguay A, Doyon N, Zhang W, Godin AG, et al. Morphine hyperalgesia gated through microglia-mediated disruption of neuronal Cl- homeostasis. Nat Neurosci. 2013;16(2):183–92.
Corder G, Tawfik VL, Wang D, Sypek EI, Low SA, Dickinson JR, Sotoudeh C, Clark JD, Barres BA, Bohlen CJ, et al. Loss of mu opioid receptor signaling in nociceptors, but not microglia, abrogates morphine tolerance without disrupting analgesia. Nat Med. 2017;23(2):164–73.
Kigerl KA, de Rivero Vaccari JP, Dietrich WD, Popovich PG, Keane RW. Pattern recognition receptors and central nervous system repair. Exp Neurol. 2014;258:5–16.
Franceschini A, Capece M, Chiozzi P, Falzoni S, Sanz JM, Sarti AC, Bonora M, Pinton P, Di Virgilio F. The P2X7 receptor directly interacts with the NLRP3 inflammasome scaffold protein. FASEB J. 2015;29(6):2450–61.
Dinarello CA. A clinical perspective of IL-1β as the gatekeeper of inflammation. Eur J Immunol. 2011;41(5):1203–17.
Yan XS, Yadav R, Gao M, Weng HR. Interleukin-1 beta enhances endocytosis of glial glutamate transporters in the spinal dorsal horn through activating protein kinase C. Glia. 2014;62(7):1093–109.
Chen H, Jiang YS, Sun Y, Xiong YC. p38 and interleukin-1 beta pathway via toll-like receptor 4 contributed to the skin and muscle incision and retraction-induced allodynia. J Surg Res. 2015;197(2):339–47.
Yang T, Yang P, Jiang LM, Zhou RY. Activation of spinal NF-κB mediates pain behavior induced by plantar incision. Int J Clin Exp Med. 2015;8(6):9149–55.
Huang LA, Wang CF, Serhan CN, Strichartz G. Enduring prevention and transient reduction of postoperative pain by intrathecal resolvin D1. Pain. 2011;152(3):557–65.
Sahbaie P, Li X, Shi X, Clark JD. Roles of Gr-1+ leukocytes in postincisional nociceptive sensitization and inflammation. Anesthesiology. 2012;117(3):602–12.
Zhang T, Zhang N, Zhang R, Zhao W, Chen Y, Wang Z, Xu B, Zhang M, Shi X, Zhang Q, et al. Preemptive intrathecal administration of endomorphins relieves inflammatory pain in male mice via inhibition of p38 MAPK signaling and regulation of inflammatory cytokines. J Neuroinflammation. 2018;15(1):320.
Menard DP, van Rossum D, Kar S, St Pierre S, Sutak M, Jhamandas K, Quirion R. A calcitonin gene-related peptide receptor antagonist prevents the development of tolerance to spinal morphine analgesia. J Neurosci. 1996;16(7):2342–51.
Assas BM, Pennock JI, Miyan JA. Calcitonin gene-related peptide is a key neurotransmitter in the neuro-immune axis. Front Neurosci. 2014;8:23.
Colburn RW, DeLeo JA, Rickman AJ, Yeager MP, Kwon P, Hickey WF. Dissociation of microglial activation and neuropathic pain behaviors following peripheral nerve injury in the rat. J Neuroimmunol. 1997;79(2):163–75.
Campillo A, Cabanero D, Romero A, Garcia-Nogales P, Puig MM. Delayed postoperative latent pain sensitization revealed by the systemic administration of opioid antagonists in mice. Eur J Pharmacol. 2011;657(1–3):89–96.
Bessiere B, Richebe P, Laboureyras E, Laulin JP, Contarino A, Simonnet G. Nitrous oxide (N2O) prevents latent pain sensitization and long-term anxiety-like behavior in pain and opioid-experienced rats. Neuropharmacology. 2007;53(6):733–40.
Yang Y, Li H, Li TT, Luo H, Gu XY, Lu N, Ji RR, Zhang YQ. Delayed activation of spinal microglia contributes to the maintenance of bone cancer pain in female Wistar rats via P2X7 receptor and IL-18. J Neurosci. 2015;35(20):7950–63.
Gao YJ, Ji RR. Light touch induces ERK activation in superficial dorsal horn neurons after inflammation: involvement of spinal astrocytes and JNK signaling in touch-evoked central sensitization and mechanical allodynia. J Neurochem. 2010;115(2):505–14.
Clark AK, Gentry C, Bradbury EJ, McMahon SB, Malcangio M. Role of spinal microglia in rat models of peripheral nerve injury and inflammation. Eur J Pain. 2007;11(2):223–30.
Obata H, Eisenach JC, Hussain H, Bynum T, Vincler M. Spinal glial activation contributes to postoperative mechanical hypersensitivity in the rat. J Pain. 2006;7(11):816–22.
Tawfik VL, LaCroix-Fralish ML, Nutile-McMenemy N, DeLeo JA. Transcriptional and translational regulation of glial activation by morphine in a rodent model of neuropathic pain. J Pharmacol Exp Ther. 2005;313(3):1239–47.
Raghavendra V, Tanga FY, DeLeo JA. Complete Freunds adjuvant-induced peripheral inflammation evokes glial activation and proinflammatory cytokine expression in the CNS. Eur J Neurosci. 2004;20(2):467–73.
The authors thank Xing Zhang for excellent technical work in drug preparation and perfusions, Melita Fasold for her kind and thorough help with editing, Kristy Dorsa and Devin Skoll for behavioral testing and Alea Zone for imaging.
This research was financially supported by grants from the Department of Veterans Affairs (I01Bx003776), and Louisiana Board of Regents (ITRS-015B) to JEZ, and a Board of Regents predoctoral fellowship to AKF (LEQSF(2014-19)-GF-09). The contents do not represent the views of the U.S. Department of Veterans Affairs or the United States Government.
Availability of data and materials
The datasets generated and/or analyzed during the current study are not publicly available due to patent and legal restrictions but are available from the corresponding author on reasonable request.
All experiments were approved by the Tulane Institutional Animal Care and Use Committee and conducted according to the NIH Guide for the Care and Use of Laboratory Animals. All efforts were made to minimize animal suffering, and to reduce the number of animals used. No alternatives to in vivo techniques are available.
Consent for publication
JEZ and AKF are inventors on patents covering the compounds characterized here. These are assigned under joint agreement to The Department of Veterans Affairs and Tulane University School of Medicine.
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