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Isobolographic analysis of the opioid-opioid interactions in a tonic and a phasic mouse model of induced nociceptive pain
Journal of Biomedical Science volume 21, Article number: 62 (2014)
Opioids have been used for the management of pain and coadministration of two opioids may induce synergism. In a model of tonic pain, the acetic acid writhing test and in a phasic model, the hot plate, the antinociceptive interaction between fentanyl, methadone, morphine, and tramadol was evaluated.
The potency of opioids in the writhing test compared to the hot plate assay was from 2.5 (fentanyl) to 15.5 (morphine) times, respectively. The ED50 was used in a fixed ratio for each of the six pairs of opioid combinations, which, resulted in a synergistic antinociception except for methadone/tramadol and fentanyl/tramadol which were additive, in the hot plate. The opioid antagonists naltrexone, naltrindole and nor-binaltorphimine, suggests that the synergism of morphine combinations are due to the activation of MOR subtypes with partially contribution of DOR and KOR, however fentanyl and methadone combinations are partially due to the activation of MOR and DOR subtypes and KOR lack of participation. The antinociceptive effects of tramadol combinations, are partially due to the activation of MOR, DOR and KOR opioid subtypes.
These results suggets that effectiveness and magnitude of the interactions between opioids are dependent on pain stimulus intensity.
Opioids have been the main drugs used in the management of pain for several decades. However, repeated use of opioids, such as morphine and heroin, cause analgesic tolerance, physical dependence, and opioid addiction .Opioid effects are mediated by three major types of opioid receptors: μ-, δ-, and κ-opioid receptors (MORs, DORs, and KORs, respectively) . Previous studies have shown that majority of opioid effects, including analgesia, tolerance, and addiction, are primarily mediated by MORs, however the effects of the other two opioid receptors remain elusive ,. Several types of analgesic combinations are available for the treatment of pain, using drugs which differ in their mechanisms of action with the aim of maximize therapeutic efficacy while minimizing side effects. Also, fixed ratio drug combinations are widely used . Combinations between different non-steroidal anti-inflammatory drugs (NSAIDs) and opioids, have been evaluated either experimentally or clinically -. However, combinations of two opioid receptor agonists have been poorly explored experimentally ,. There is scarce information about clinical trials performed with opioid associations in patients affected by pain . From the theoretical point of view, the combination opioid-opioid could induce an adequate control of pain, with a reduced doses and less adverse effects.
In this study, a tonic model of induced pain, the writhing test was selected as a model of acute visceral pain, because it seems to be a model of clinical relevancy in intestinal pain in humans . The acetic acid is an easy and fast screening model to access the activity of analgesic drugs and their mechanisms. These models induce a characteristic and quantifiable overt pain-like behaviour described as a writhing response or abdominal contortion . A phasic model of induced pain was also utilized, the hot plate assay . In this assay, the latency to pain reflex behaviour is measured.
The purpose of this study was to evaluate the interaction between all possible combinations of the following opioids: morphine, methadone, tramadol and fentanyl, in both models of pain. The analysis of the interaction was carried out by isobolographic analysis with the calculations of the interactions indexes. Besides the role of the antagonists of different subtypes of opioid receptors in the interaction was evaluated.
In all experiments CF-1 male mice, weighing 28–30 g, housed in a 12-h light–dark cycle at 22 ± 1°C, with free access to food and water were used. The animals were acclimatized to the laboratory environment for at least 2 h before use. Experiments were carried out in accordance with the Guide for the Care and Use of Laboratory Animals issued by the National Institute of Health, and experimental procedures were approved by the Institutional Animal Care and Use Committee at the Universidad de Chile, Santiago, Chile. Each animal was used only once, and received only one dose of the drugs tested. All drugs were freshly prepared by dissolving them in normal saline, and administered intraperitoneally (i.p.). The authors performed all observations in a randomized and blind manner. Control saline animals were run interspersed concurrently with the drug-treated animals (at least two mice per group), which prevented all the controls being run on a single group of mice at one time during the course of the research.
Acetic acid writhing test
A modification of the method previously described was used . To perform the test, mice were injected i.p. with10 mL/kg of 0.6% acetic acid solution, 30 min after the i.p. administration of the drugs, a time at which preliminary experiments showed the occurrence of the maximum effect. A writhe is characterized by a wave of contractions of the abdominal musculature, followed by the extension of the hind limbs. The number of writhes in a 5 min period was counted, starting 5 min after the administration of acetic acid. Antinociceptive activity was expressed as the maximum possible effect (% MPE) of the percent inhibition of the usual number of writhes observed in control animals ( 20.4 ± 0.36, n = 12). The dose of the drug that produced 50% of MPE (ED50) was calculated from the linear regression analysis of the curve obtained by plotting log dose vs percentage of MPE.
Hot plate test
This thermal antinociceptive test was performed according with a modification to the method of Eddy and Leimbach . A commercial device (Ugo Basile, Italy) was calibrated at 50 ± 0.2°C and the cut-off time was set at 30 sec. Each mouse was placed on the heated surface and the time, in sec, between placement and licking or shaking the hind paw or jumping was recorded as response latency and is a sign of thermal nociception. Each animal was tested twice before (control latency = 15.50 ± 0.40) and after the drug administration and the antinociceptive activity and was expressed as the maximum possible effect (MPE) using the formula:
Writhing and hot plate test
Dose–response curves for i.p. administration of the following opioids: morphine, methadone, fentanyl and tramadol were obtained using eight animals with at least four doses for each. Linear regression analysis of the log dose–response curves allowed the calculation of the doses that produced 50% of antinociception (ED50), when each drug was administered alone. ED50 was used in the acetic acid writhing test or in the hot plate assay, as the equieffective dose for isobolographic analysis. Then a similar dose–response curve was also obtained and analysed after the coadministration of morphine with methadone, fentanyl and tramadol. Similarly, after the coadministration of methadone with fentanyl and tramadol, and finally, coadministration of fentanyl and tramadol. The dose–response curve was obtained by the intraperitoneal coadministration of each mixture of opioids in fixed ratio combinations of fractions of their respective ED50 values: 1/2, 1/4, 1/8, 1/16. In addition, the effect of the pretreatment on the mice with naltrexone (NTX), naltrindole (NTI) and nor-binaltorphimine (nor-BNI) in the antinociception induced by the coadministration of opioids was evaluated.
Isobolographic analysis was used to characterize drug interactions. The method of isobolographic analysis has been previously described in detail ,. The isobolograms were constructed by connecting the ED50 of one opioid plotted on the abscissa with the ED50 of other opioid plotted on the ordinate, to obtain the additive line. For each mixture of opioids, the ED50 and its associated 95% confidence intervals (CL) were determined by linear regression analysis of the log dose–response curve (eight animals at each with at least four doses), and compared by a t test to a theoretical additive ED50 that was obtained from: ED50 add = ED50 one opioid/(P1 + R X P2 ) where R is the potency ratio of one opioid alone compared to the other opioid alone, P1 is the proportion of one of the opioids and P2 is the proportion of the other opioid in the total mixture.
In this study, fixed ratio proportions were selected, first by combining the ED50 of each compound, and then constructing a dose–response curve in which ED50 fractions (1/2, 1/4, 1/8, and 1/16) of the one opioid and the other opioid combination were administered. In the equation above, ED50 add is the total dose and the variance of ED50 add was calculated from the fraction of the ED50s (i.e., 0.5) in the combination as:
From these variances, confidence limits were calculated and determined according to the ratio of the individual drugs in the combination. The ED50 for the drug combinations was obtained by linear regression analysis of the dose–response curves. Supra-additivity or synergistic effect is defined as the effect of a drug combination that is higher and statistically different (ED50 significantly lower) than the theoretically calculated equieffect of a drug combination with the same proportions. If the ED50s are not statistically different, the effect of the combination is additive, and additivity means that each constituent contributes with its own potency to the total effect.
Furthermore, the interaction index (I.I.), or the combination potency to additive potency ratio, indicates the magnitude and nature of the interaction. I.I. It was calculated as :I.I. = experimental ED50/theoretical ED50.
When the value is close to 1, the interaction is additive. Values lower than 1 are indications of the supra-additive or synergistic interactions magnitude, and values higher than 1 correspond to sub-additive or antagonisticinteractions ,.
All drugs were freshly dissolved in saline on a constant volume of 10 ml/kg and administered as mg/kg. Morphine hydrochloride, methadone hydrochloride, fentanyl citrate, tramadol hydrochloride, naltrexone hydrochloride, naltrindole hydrochloride and nor-BNI dihydrochloride were purchased from Sigma Chemical Co, USA. Doses were expressed on the basis of the salts.
Results are presented as a mean ± standard error of the mean (SEM) or as ED50 values with 95% confidence limits (95% CL). All calculations, including the statistical analysis of the isobolograms related to the difference between experimental ED50 and theoretical ED50 values by Student’s t test for independent means, were performed with the program Pharm Tools Pro (version 1.27; McCary Group Inc., PA, USA), and based on Tallarida . P values under 0.05 (P < 0.05) were considered significant.
The opioid treatments in this study did not affect the functional aspect of the mice, because no abnormality was observed in the motor function after the opioid treatments, even at the highest doses used in this study.
Antinociception induced by opioids
The i.p. administration of morphine (0.01, 0.03, 0.1 and 0.3 mg/kg), displayed a dose-dependent antinociceptive activity with different efficacy in the acetic acid writhing assay of the mice, and the ED50 resulted to be 0.124 ± 0.018 mg/kg. The administration of methadone (0.01, 0.03, 0.1 and 0.3 mg/kg), induced a dose–response curve, and the ED50 was 0.005 ± 0.018 mg/kg. After the administration of fentanyl (0.001, 0.003, 0.01 and 0.03 mg/kg) the ED50resulted in 0.016 ± 0.002 mg/kg. The administration of tramadol (1, 3, 10 and 30 mg/kg) with an ED50 of 3.904 ± 0.495 mg/kg. The ED50 demonstrated the following rank of efficacy: fentanyl > methadone > morphine > tramadol. All these results are summarized in Figure 1 and Table 1.
In the hot-plate test of mice, the same doses of opioids induced a dose-dependent antinociception with different efficacy. The ED50 values of fentanyl, methadone, morphine and tramadol were 0.040, 0.24, 1.94 and 30.53 mg/kg, respectively (see Table 2).
The rank of potency of opioids in the writhing test to hot plate assay was from 2.5 (fentanyl) to 15.5 (morphine) times, respectively.
Effect of naltrexone (NTX), naltrindole (NTI) and nor-BNI in the antinociception of opioids
In the writhing test, t he pretreatment with NTX, 1 mg/kg i.p. antagonized the antinociceptive activity of the ED50 of morphine, fentanyl and methadone, but partially reversed the effect of tramadol. The administration of 2 mg/kg i.p. of NTI, antagonized the antinociception induced by morphine and fentanyl, however, partially reversed the effect of methadone and tramadol. The administration of 3 mg/kg i.p. of nor-BNI, partially antagonized the antinociceptive activity of morphine and tramadol, but there was a lack of effect in the antinociception induced by fentanyl and methadone, all these results are summarized in Table 1. In the case of hot plate assay, NTX antagonized the antinociceptive activity of morphine, methadone, fentanyl and tramadol. The pretreatment with NTI antagonized the antinociceptive action of all opioids with the exception of tramadol. In addition, mice pretreated with nor-BNI lack of effect in the antinociception produced by all the opioids tested. These results are summarized in Table 2. The opioid antagonist doses were adapted or modified from previously published studies that showed the pharmacological activity of each individual receptor subtype -.
Interactions between opioids
The antinociceptive activity interactions of the i.p. coadministration on the basis of a fixed ratio of (1:1) combination of their ED50 values alone of the different opioids used in this work was evaluated by isobolographic analysis.
The isobolograms demonstrated that all the mixtures of opioids, in the writhing test of the mice, resulted in synergistic interaction of different magnitudes as can be seen in Figure 2 (panel A-F). Table 3 shows the theoretical additive and the experimental ED50 values for the combinations with their 95% CL and their interaction index values.
Furthermore, the interaction index values of the i.p. combinations on the writhing test, demonstrated the following rank of potencies: morphine with methadone > methadone with fentanyl > morphine with tramadol > morphine with fentanyl > methadone with tramadol > fentanyl with tramadol as it is shown in Table 3.
In the hot plate assay, the isobolographic analysis of the opioids coadministration on the basis of a fixed ratio of (1:1) combination of their ED50 values alone, resulted in a synergistic interaction between morphine with methadone, methadone with fentanyl, morphine with fentanyl and morphine with tramadol. The mixtures methadone with tramadol and fentanyl with tramadol resulted only additive, as can be seen in Figure 3 (panel A-F). In addition, Table 4 shows the theoretical additive and the experimental ED50 values for the different combinations with their 95% CL and their interaction index values. In this assay, the rank of potency of the interaction index was: morphine with methadone > methadone with fentanyl > morphine with fentanyl > morphine with tramadol > methadone with tramadol > fentanyl with tramadol as it is shown in Table 4.
The relation between the interaction index, in the opioid mixtures changes from 1.41 in morphine with fentanyl to 2.35 in morphine with methadone, respectively, to compare both assays. In addition, the ratio of experimental ED50 of the opioid combinations, in the writhing to hot plate tests, varied from 4 in methadone with fentanyl to 25 in morphine with methadone, respectively.
Effect of naltrexone (NTX), naltrindole (NTI) and nor-BNI in the interactions of opioids
Using the writhing test, NTX antagonized the antinociceptive activity of the coadministration of methadone with fentanyl, morphine with methadone, morphine with fentanyl, morphine with tramadol, methadone with tramadol, and fentanyl with tramadol. The pretreatment with NTI antagonized the antinociceptive action of the all mixture of opioids. In addition, mice pretreated with nor-BNI, the κ-opioid antagonist lack of effect in the antinociception produced by all the different combination of opioids. All these results are summarized in Table 5.
In the hot plate assay, NTX was able to antagonize the antinociception induced by the combinations of morphine with methadone, methadone with fentanyl, morphine with fentanyl and morphine with tramadol. NTX did not induced changes in the analgesic activity of methadone with tramadol and fentanyl with tramadol. The pretreatment of the mice with NTI, reply the antagonistic activity of NTX, however nor-BNI lack of blocking action in all the combinations of opioids. See all these results in Table 6.
Opioids are the foremost drugs in the pharmacological treatment of pain.
However, they have not been compared extensively in different animal pain models. The writhing test is a model of visceral acute pain, it is very useful when drawing up directions for the therapeutic administration of drugs in humans . This model was selected because it closely resembles clinical relevant acute post operatory pain in humans .
The results obtained in this work, demonstrate that the different opioids used in this work -- fentanyl the most potent and tramadol the least potent -- produced antinociceptive activity in the acetic acid writhing test and in the hot plate assay. The analysis of the ED50 values of four opioids reveal different efficacies depending on the selective opioid receptor ligands. Thus the binding potencies in nmol for MOR are 0.39 for fentanyl, 0.72 for methadone and 14 for morphine ,. In the case of the racemic tramadol, the (+) enantiomer had a binding potency value of only 1.33 and the (−) enantiomer had even lower affinity of 24.8 for MOR . Also, the degree of lipophilicity could help to correlate the difference between the ED50 of the opioids. Consequently, high-efficacy ligands, such as fentanyl and methadone possesses a higher ED50 compared to lower efficacy ligands such as morphine with a lower ED50,.
The findings of this study are in agreement with previous works. So, morphine induced analgesia in acetic acid writhing test, with a dose range from 0.12 – 2.67 mg/kg , and tramadol produced antinociceptive activity in the same test with doses between 3.9 to 14.73 mg/kg . Besides, the analgesic effect produced by fentanyl was reported at 0.016 – 0.03 mg/kg, by using the same assay utilized in this work ,. In addition, methadone at 0.085 to 0.467 mg/kg, produced antinociception in the acetic acid writhing test . Also, in the hot plate the findings are concordant with previous works. So, antinociceptive effects of morphine, fentanyl, tramadol and their combination it has been described , and also the methadone induced antinociception .
After i.p. administration of morphine with methadone or morphine with fentanyl or morphine with tramadol; methadone with fentanyl or methadone with tramadol, and fentanyl plus tramadol in the writhing test a synergic interaction was obtained. In the hot plate assay, the same combination of opioids resulted in a synergic interaction, except of the additivity interaction induced by tramadol with methadone or fentanyl. These results corroborate that this work supports the general premises of interactions between drugs with the same effect but acting through different mechanism of action. Therefore, one possibility in these interactions could be due to different types of the MOR receptor splice variant, where each one of them may use a different downstream signalling pathway, or it may be expressed in a different anatomical region to exhibit a distinctive pharmacological profile . Moreover, hetero dimerization of the MOR and other receptor may express another mechanisms in a characteristic opioid efficacy, since the intracellular signalling can be altered by receptor dimerization .
On the other hand, it is likely that the interactions observed when combining morphine, methadone, fentanyl and tramadol, could be related to multiple events that underlying in the mechanisms of the different efficacy among these opioids and dependent of pain stimulus.
The opioid interactions described, could occur at one or more levels of cell functions including receptors, ion channels, lipids and protein of the membrane, second messengers, protein kinases, gene induction, or others. These interaction events are dependent on the local concentration of opioids and on the nature of the nociceptive stimulus and its transduction mechanisms .
The administration of acetic acid solution induces nociception by increasing the levels of prostaglandins at the peritoneum . The inhibition induced by opioids in the number of writhes produced by the administration of an acetic acid solution in mice in this work, suggests the involvement of peripheral pain receptors. This also help explain the interactions obtained in this study, the fact that methadone is a mixed enantiomer with not only MOR agonist but also N-methyl-D-aspartate receptor antagonist and GABA antagonists, as morphine. This condition could increase the analgesic activity of other MOR agonists like morphine, fentanyl and tramadol .
Additionally, the nonopioid component of tramadol, the inhibition reuptake of norepinephrine and serotonin, could play an important role in the synergism obtained in this work.
The use of opioid antagonists help to understand the interactions induced by different combinations of opiods. Thus, morphine effects are due to the activation of MOR subtypes with partially contribution of DOR and KOR subtypes. However, the combinations of fentanyl and methadone are partially due to the activation of MOR and DOR subtypes and lack of participation of KOR subtypes. The analgesic effects of the combination of tramadol with the other opiods, are partially due to the activation of MOR, DOR and KOR opioid subtypes, beside their activity on noradrenaline and serotonin reuptake.
In conclusion the results from this work could be explained by the complex pharmacology of opioids, accompanied by a variation in the spectrum of opioids which could be dependent of the chemical structure, physicochemical properties, dose, receptor binding, distribution and metabolism. These results provide evidence that the effectiveness and magnitude of the interactions between opioids are dependent on the intensity of the pain stimulus in acute pain states. The use of lower doses of opioids in this work may have some utility in the clinical treatment of pain and reduce some of the adverse effects often associated with opioid administration.
Trescot AM, Datta S, Lee M, Hanssen H: Opioid pharmacology. Pain Pysician. 2008, 11: S133-S153.
Waldhoer M, Barlett SE, Whistler JL: Opioid receptors. Ann Rev Biochem. 2004, 73: 753-990. 10.1146/annurev.biochem.73.011303.073940.
Mao J, Gols MS, Backonja MM: Combination drug therapy for chronic pain: a call for more clinical studies. J Pain. 2011, 12: 157-166. 10.1016/j.jpain.2010.07.006.
Lashbrook JM, Ossipov MH, Hunter JC, Raffa RB, Tallarida RJ, Porreca F: Synergistic antiallodynic effects of spinal morphine with ketorolac and selective COX1- and COX2-inhibitors in nerve-injured rats. Pain. 1999, 82: 65-72. 10.1016/S0304-3959(99)00031-7.
Miranda HF, Puig MM, Prieto JC, Pinardi G: Synergism between paracetamol and nonsteroidal anti-inflammatory drugs in experimental acute pain. Pain. 2006, 121: 22-28. 10.1016/j.pain.2005.11.012.
Miranda HF, Puig MM, Romero MA, Prieto JC: Effect of tramadol and dexketoprofen on analgesia and gastrointestinal transit in mice. Fund Clin Pharmacol. 2009, 23: 81-88. 10.1111/j.1472-8206.2008.00636.x.
Silva-Moreno A, Gonzalez-Espinosa CM, Cruz SL: Synergistic antinociceptive actions and tolerance development produced by morphine-fentanyl coadministration: correlation with μ-opioid receptor internalization. Eur J Pharmacol. 2012, 674: 239-247. 10.1016/j.ejphar.2011.10.034.
Ramiro S, Radner H, Van der Heijde DM, Buchbinder R, Aletaha D, Landewé RB: Combination therapy for pain management in inflammatory arthritis: a Cochrane systematic review. J Rheumatol. 2012, 90: 47-55.
Kolesnikov YA, Oksman G, Pasternak GW: Topical methadone and meperidine analgesic synergy in the mouse. Eur J Pharmacol. 2010, 38: 61-64. 10.1016/j.ejphar.2010.04.020.
Miranda HF, Noriega V, Zepeda RJ, Sierralta F, Prieto JC: Synergism between fentanyl and tramadol in tonic inflammatory pain: the orofacial formalin test. Inflammation. 2012, 35: 1132-1137. 10.1007/s10753-011-9420-7.
Whittle SL, Richards BL, Husni E, Buchbinder R: Opioid therapy for treating rheumatoid arthritis pain. Cochrane Database Syst Rev. 2011, ᅟ (11): CD003113-doi:10.1002/14651858.CD003113.pub3
Kurihara T, Nonaka T, Tanabe T: Acetic acid conditioning stimulus induced long-lasting antinociception of somatic inflammatory pain. Pharmacol Biochem Behav. 2003, 74: 841-849. 10.1016/S0091-3057(03)00014-5.
Pavao-de-Souza G, Zarpelon F, Tedeschi AC, Mizokami GC, Sanson SS, Cunha TM, Ferreira SH, Cunha FQ, Casagrande R, Verri WA: Acetic acid- and phenyl-p-benzoquinone-induced overt pain-like behavior depends on spinal activation of MAP kinases, PI (3)K and microglia in mice. Pharmacol Biochem Behav. 2012, 101: 320-328. 10.1016/j.pbb.2012.01.018.
Le Bars D, Gozariu M, Cadden SW: Animal models of nociception. Pharmacol Rev. 2001, 53: 597-652.
Koster R, Anderson M, de Beer EJ: Acetic acid for analgesic screening. Fed Proc. 1959, 18: 412-414.
Eddy NB, Leimbach D: Synthetic analgesics: II dithienylbutenyl- and dithienylbutenylamines. J Pharmacol Exp Ther. 1953, 107: 385-393.
Tallarida RJ: Drug synergism and dose-effect data analysis. 2000, Chapman & Hall/CRC Press. USA, Boca Ratón
Takemori AE, Ho BY, Naeseth JS, Portoghese PS: Nor-binaltorphimine, a highly selective kappa-opioid antagonist in analgesic and receptor binding assays. J Pharmacol Exp Ther. 1988, 246: 255-258.
Suzuki T, Narita M, Takahashi Y, Misawa M, Nagase H: Effects of nor-binaltorphimine on the development of analgesic tolerance to and physical dependence on morphine. Eur J Pharmacol. 1992, 213: 91-97. 10.1016/0014-2999(92)90237-X.
Satyanarayana PSV, Jain NK, Singh A, Kulkarni SK: Isobolographic analysis of interaction between cyclooxygenase inhibitors and tramadol in acetic acid-induced writhing in mice. Prog Neuropsychopharmacol Biol Psychiatr. 2004, 28: 641-649. 10.1016/j.pnpbp.2004.01.015.
Naidu PS, Lichtman AH, Archer CC, May EL, Harris LS, Aceto MD: NIH 11082 produces anti-depressant-like activity in the mouse tail-suspension test through a delta-opioid receptor mechanism of action. Eur J Pharmacol. 2007, 566: 132-136. 10.1016/j.ejphar.2007.03.031.
Mary F, Divin MF, Holden Ko MC, Traynor JR: Comparison of the opioid receptor antagonist properties of naltrexone and 6β-naltrexol in morphine-naïve and morphine-dependent mice. Eur J Pharmacol. 2008, 583: 48-55. 10.1016/j.ejphar.2008.01.004.
Loscalzo LM, Wasowski C, Paladini AC, Marder M: Opioid receptors are involved in the sedative and antinociceptive effects of hesperidin as well as in its potentiation with benzodiazepines. Eur J Pharmacol. 2008, 580: 306-313. 10.1016/j.ejphar.2007.11.011.
Reichter A, Daughters RS, Rivard R, Simone DA: Peripheral and preemptive opioid antinociception in a mouse visceral pain model. Pain. 2001, 89: 221-227. 10.1016/S0304-3959(00)00365-1.
Raynor K, Kong H, Chen Y, Yasuda Y, Bell GI, Reisine T: Pharmacological characterization of cloned kappa-, delta-, and mu-opioid receptors. Mol Pharmacol. 1994, 45: 330-334.
Raffa RB, Friderichs E, Reimann W, Shank RP, Codd EE, Vaught JL, Jacoby HI, Selve N: Complementary and synergistic antinociceptive interaction between the enantiomers of tramadol. J Pharmacol Exper Ther. 1993, 267: 331-340.
McQuay HJ, Sullivan AF, Smallman K, Dickenson H: Intrathecal opioids, potency and lipophilicity. Pain. 1989, 36: 111-115. 10.1016/0304-3959(89)90118-8.
Miranda HF, Silva E, Pinardi G: Synergy between the antinociceptive effects of morphine and NSAIDs. Can J Physiol Pharmacol. 2004, 82: 331-338.
Romero A, Miranda HF, Puig MM: Antinociceptive effects of morphine, fentanyl, tramadol and their combination, in morphine-tolerant mice. Pharmacol Biochem Behav. 2010, 97: 363-369. 10.1016/j.pbb.2010.09.005.
Sirohi S, Dighe SV, Walker EA, Yoburn CB: The analgesic efficacy of fentanyl: relation to tolerance and μ-opioid receptor regulation. Pharmacol Biochem Behav. 2008, 91: 115-120. 10.1016/j.pbb.2008.06.019.
Collier HOJ, Dinneen LC, Johnson CA, Schneider C: The abdominal constriction response and its suppression by analgesic drugs in the mouse. Br J Pharmacol Chemother. 1968, 32: 295-310. 10.1111/j.1476-5381.1968.tb00973.x.
Neelakantan H, Walker EA: Temperature-dependent enhancement of the antinociceptive effects of opioids in combination with gabapentin in mice. Eur J Pharmacol. 2012, 686: 55-59. 10.1016/j.ejphar.2012.04.042.
Lemberg K, Kontinen VS, Viljakka K, Kylânlathi I, Yli-Kauhaluoma J, Kalso E: Morphine, oxycodone, methadone and its enantiomers in different models of nociception in the rat. Anesth Anal. 2006, 102: 1768-1774. 10.1213/01.ane.0000205751.88422.41.
Pan YX, Xu J, Bolan E, Moskowitz HS, Xu M, Pasternak GW: Identification of four novel exon 5 splice variants of the mouse mu-opioid receptor gene: functional consequences of C-terminal splicing. Mol Pharmacol. 2005, 68: 866-875.
Hojo M, Sudo Y, Ando Y, Minami K, Takada M, Matsubara T, Kanaide M, Taniyama K, Sumikawa K, Uezono Y: Mu-Opioid receptor forms a functional heterodimer with cannabinoid CB1 receptor: electrophysiological and FRET assay analysis. J Pharmacol Sci. 2008, 108: 308-319.
Barrera NP, Morales B, Torres S, Villalón M: Principles: mechanisms and modeling of synergism in cellular responses. Trends Pharmacol Sci. 2005, 26: 526-532. 10.1016/j.tips.2005.08.003.
Simmons DL, Botting RM, Timothy HLA: Cyclooxygenase isozymes: the biology of prostaglandin synthesis and inhibition. Pharmacol Rev. 2004, 56: 387-437. 10.1124/pr.56.3.3.
Zhang Z, Pan ZZ: Synaptic mechanism for functional synergism between δ- and μ- opioid receptors. J Neurosci. 2010, 30: 4735-4745. 10.1523/JNEUROSCI.5968-09.2010.
This work was partially supported by project DI-02-11/CB from Universidad Andres Bello.
The authors have declared that they have no competing interest.
All the authors participated in planning research, in performing experiments, and were responsible for data interpretation and collaborate in writing process of the manuscript. All authors read and approved the final manuscript.