Abstract
Objective:
Despite the recognized anti-inflammatory potential of heterocyclic antidepressants, the mechanisms concerning their modulating effects are not completely known. Thus, we evaluated the anti-inflammatory effect of amitriptyline, clomipramine, and maprotiline and the possible modulating properties of these drugs on neutrophil migration and mast cell degranulation.
Methods:
The hind paw edema and air-pouch models of inflammation were used. Male Wistar rats were treated with saline, amitriptyline, clomipramine or maprotiline (10, 30, or 90 mg/kg, per os [p.o.]) 1 h before the injection of carrageenan (300 μg/0.1 mL/paw) or dextran (500 μg/0.1 mL/paw). Then, edema formation was measured hourly. Neutrophil migration to carrageenan (500 μg/pouch) and N-formyl-methionyl-leucyl-phenylalanine (fMLP) (10-6 M/mL/pouch) was also investigated in 6-day-old air-pouch cavities. Compound 48/80-induced mast cell degranulation was assessed in the mesenteric tissues of antidepressant-treated rats.
Results:
All tested antidepressants prevented both carrageenan- and dextran-induced edema. The anti-inflammatory effect of these drugs partially depends on the modulation of neutrophil migration, since they significantly counteracted the chemotactic response of both carrageenan and fMLP (p < 0.01). Furthermore, amitriptyline, clomipramine and maprotiline inhibited compound 48/80-induced mast cell degranulation (p < 0.001).
Conclusions:
These results suggest an important anti-inflammatory role of heterocyclic antidepressants, which is dependent on the modulation of neutrophil migration and mast cell stabilization.
Antidepressant agents; inflammation; neutrophil; mast cells; rats
Introduction
Heterocyclic antidepressants are widely used to treat a number of medical disorders, such as depression, social phobia, generalized anxiety, panic, obsessive-compulsive, and eating disorders. In addition to their pharmacological action on the reuptake inhibition of serotonin and norepinephrine, variable interactions with receptors, such as H1 histamine receptors, muscarinic receptors, and α-adrenergic receptors, have been reported.11. Brunton L, Parker K, Blumenthal D, Buxton I. Goodman & Gilman's Manual of Pharmacology and Therapeutics. New York: McGraw Hill; 2008.
Several studies have suggested a potential analgesic activity of antidepressants independent of
their effects on mood.22. Mitra R, Jones S. Adjuvant analgesics in cancer pain: a review. Am J Hosp Palliat
Care. 2012;29:70-9.
3. Magni G. The use of antidepressants in the treatment of chronic pain. A review of
the current evidence. Drugs. 1991;42:730-48.
4. Bianchi M, Panerai AE. Antidepressant drugs and experimental inflammation.
Pharmacol Res. 1996;33:235-8.
5. Fishbain D. Evidence-based data on pain relief with antidepressants. Ann Med.
2000;32:305-16.-66. Vorobeychik Y, Gordin V, Mao J, Chen L. Combination therapy for neuropathic pain:
a review of current evidence. CNS Drugs. 2011;25:1023-34. Furthermore, it has been reported that heterocyclic antidepressants are able to modulate
the immune system.77. Littrell JL. Taking the Perspective that a Depressive State Reflects
Inflammation: Implications for the Use of Antidepressants. Front Psychol.
2012;3:297.
8. Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a
study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology.
2010;86:231-9.-99. Sacerdote P, Bianchi M, Panerai AE. Chlorimipramine and nortriptyline but not
fluoxetine and fluvoxamine inhibit human polymorphonuclear cell chemotaxis in vitro. Gen Pharmacol.
1994;25:409-12.
In addition, a clear reciprocal effect between inflammatory mediators and development of depression
is even more evident.1010. Capuron L, Hauser P, Hinze-Selch D, Miller AH, Neveu PJ. Treatment of
cytokine-induced depression. Brain Behav Immun. 2002;16:575-80.
11. Corcos M, Guilbaud O, Hjalmarsson L, Chambry J, Jeammet P. Cytokines and
depression: an analogic approach. Biomed Pharmacother. 2002;56:105-10.-1212. Kulmatycki KM, Jamali F. Drug disease interactions: role of inflammatory
mediators in depression and variability in antidepressant drug response. J Pharm Pharm Sci.
2006;9:292-306. Since these reports, there has been growing research interest in the acute and chronic
anti-inflammatory potential of these drugs.88. Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a
study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology.
2010;86:231-9.,1313. Bianchi M, Rossoni G, Sacerdote P, Panerai AE, Berti F. Effects of chlomipramine
and fluoxetine on subcutaneous carrageenin-induced inflammation in the rat. Inflamm Res.
1995;44:466-9.
14. Abdel-Salam OM, Nofal SM, El-Shenawy SM. Evaluation of the anti-inflammatory and
anti-nociceptive effects of different antidepressants in the rat. Pharmacol Res.
2003;48:157-65.
15. Hajhashemi V, Sadeghi H, Minaiyan M, Movahedian A, Talebi A. Central and
peripheral anti-inflammatory effects of maprotiline on carrageenan-induced paw edema in rats.
Inflamm Res. 2010;59:1053-9.-1616. Sadeghi H, Hajhashemi V, Minaiyan M, Movahedian A, Talebi A. A study on the
mechanisms involving the anti-inflammatory effect of amitriptyline in carrageenan-induced paw edema
in rats. Eur J Pharmacol. 2011;667:396-401.
Current studies on the anti-inflammatory effects of cyclic antidepressants are mainly based on
the model of carrageenan-induced paw edema,88. Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a
study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology.
2010;86:231-9.,1313. Bianchi M, Rossoni G, Sacerdote P, Panerai AE, Berti F. Effects of chlomipramine
and fluoxetine on subcutaneous carrageenin-induced inflammation in the rat. Inflamm Res.
1995;44:466-9.
14. Abdel-Salam OM, Nofal SM, El-Shenawy SM. Evaluation of the anti-inflammatory and
anti-nociceptive effects of different antidepressants in the rat. Pharmacol Res.
2003;48:157-65.
15. Hajhashemi V, Sadeghi H, Minaiyan M, Movahedian A, Talebi A. Central and
peripheral anti-inflammatory effects of maprotiline on carrageenan-induced paw edema in rats.
Inflamm Res. 2010;59:1053-9.-1616. Sadeghi H, Hajhashemi V, Minaiyan M, Movahedian A, Talebi A. A study on the
mechanisms involving the anti-inflammatory effect of amitriptyline in carrageenan-induced paw edema
in rats. Eur J Pharmacol. 2011;667:396-401. and considerable
progress has been achieved in this area of research. However, further investigation regarding the
mechanisms involved in the anti-inflammatory activity of heterocyclic antidepressants is still
needed. Therefore, we aimed to study the effect of amitriptyline, clomipramine, and maprotiline in
different animal models of inflammation and to investigate the modulating properties of these drugs
on neutrophil migration and mast cell degranulation.
Methods
Animals
Male Wistar rats (180-200 g) were obtained from the local animal breeding facility of the School of Medicine, Universidade Federal do Ceará (UFC), and divided into experimental groups (n=6/group). The animals were kept in a temperature-controlled room with free access to food and water, under 12/12h dark-light cycles, and were deprived of food 18 h previous to experiments. The local Ethics Committee for Animal Experimentation approved the study protocol, which strictly followed the NIH guidelines for care and use of laboratory animals.
Chemicals
Amitriptyline (PRODOME, São Paulo, Brazil, 25 mg tablet), clomipramine (Novartis, São Paulo, Brazil, 10 mg tablet), and maprotiline (Novartis, São Paulo, Brazil, 75 mg tablet) were used. Carrageenan, dextran 70, and N-formyl-methionyl-leucyl-phenylalanine (fMLP) were purchased from Sigma Chemicals (St. Louis, MO, USA). All drugs were dissolved in sterile saline solution.
Carrageenan- and dextran-induced paw edema
Animals were treated with saline (10 mL/kg), amitriptyline (10, 30, or 90 mg/kg, per os [p.o.]), clomipramine (10, 30, or 90 mg/kg, p.o.), or maprotiline (10, 30, or 90 mg/kg, p.o.) 1 h before the stimulus injection. Paw edema was induced by sub-plantar injection of carrageenan (300 μg/0.1 mL/paw) or dextran (500 μg/0.1 mL/paw). Control group animals received the same volume of sterile saline (0.1 mL/paw). Paw volume was measured by plethysmometry (Ugo Basile 7140 water plethysmometer) immediately before (basal volume) and at 1, 2, 3, and 4 h after carrageenan or dextran administration. Results were expressed as paw volume variation (mL), calculated by subtracting basal paw volume from the corresponding plethysmometer readings.
In vivo neutrophil migration induced by carrageenan or fMLP in air-pouch cavities
Six-day-old rat skin air pouches were produced as described by Ribeiro et al.1717. Ribeiro RA, Flores CA, Cunha FQ, Ferreira SH. IL-8 causes in vivo neutrophil migration by a cell-dependent mechanism. Immunology. 1991;73:472-7. Briefly, the backs of the rats were shaved and 20 mL of sterile air injected subcutaneously. Three days later, 10 mL of sterile air were again injected to maintain pouch patency. Six days after the initial air injection, the pouches were used. Vehicle (sterile saline, 1 mL/pouch), carrageenan (500 μg/pouch), or fMLP (10-6 M/mL/pouch) were injected into the 6-day-old air pouches of rats previously treated with saline (10 mL/kg), amitriptyline (90 mg/kg, p.o.), clomipramine (90 mg/kg, p.o.), or maprotiline (40 mg/kg, p.o.).
Collection of exudates
Six hours after injection of the chemotactic stimulus into the air pouches, the animals were killed and the air pouches were washed by injection of 5 or 10 mL of phosphate-buffered saline (PBS) containing 5 U/mL of heparin. Cell counting was performed as described by Ribeiro et al.1717. Ribeiro RA, Flores CA, Cunha FQ, Ferreira SH. IL-8 causes in vivo neutrophil migration by a cell-dependent mechanism. Immunology. 1991;73:472-7. The results were reported as the number of neutrophils x 106/mL exudate.
Mast cell degranulation in mesenteric tissue
Animals were given saline (10 mL/kg), amitriptyline (90 mg/kg, p.o.), clomipramine (90 mg/kg, p.o.), or maprotiline (40 mg/kg, p.o.) 1 h before euthanasia. After euthanasia, mesenteric tissues were carefully collected from the respective groups and placed into individual Petri dishes containing Ringer-Locke solution (10 mL). Mast cell degranulation was induced by tissue incubation with compound 48/80 (final concentration, 0.8 μg/mL) for 30 min. Hydrated tissue sections were immersed in a 0.1% toluidine blue solution (in 0.9% sodium chloride) for 60 s, followed by extensive rinsing in deionized water as described by Oliveira et al.1818. Oliveira FA, Lima-Junior RC, Cordeiro WM, Vieira-Júnior GM, Chaves MH, Almeida FR, et al. Pentacyclic triterpenoids, alpha,beta-amyrins, suppress the scratching behavior in a mouse model of pruritus. Pharmacol Biochem Behav. 2004;78:719-25. The percentage of degranulated mast cells per tissue section was then determined.
Statistical analysis
Data were analyzed by one-way or two-way ANOVA followed by Bonferroni's test as appropriate. Values were expressed as mean ± standard error of the mean. The level of significance was set at p < 0.05.
Results
Anti-inflammatory effect of different heterocyclic antidepressants in carrageenan and dextran-induced paw edema
As demonstrated in Figures 1 and 2 respectively, the intraplantar injection of carrageenan or dextran induced marked paw edema, which peaked 3 h (carrageenan) and 2 h (dextran) after the stimulus injection. Administration of amitriptyline (Figures 1A and 2A), clomipramine (Figures 1B and 2B), and maprotiline (Figures 1C and 2C) significantly prevented the development of edema (p < 0.01) at the highest doses tested (90 mg/kg). The most prominent effect was seen with clomipramine, which also inhibited edema formation at the dose of 30 mg/kg (p < 0.05). Two-way ANOVA revealed a significant main effect for treatment (amitriptyline: F3,60 = 2.99, p < 0.05; clomipramine: F3,60 = 25.57, p < 0.0001; maprotiline: F3,60 = 3.47, p = 0.0352) and time (amitriptyline: F3,60 = 43.25, p < 0.0001; clomipramine: F3,60 = 25.55, p < 0.0001; maprotiline: F3,60 = 40.96, p < 0.0001) in the carrageenan model. This was also observed for the dextran model of inflammation regarding treatment (amitriptyline: F3,60 = 3.082, p < 0.001; clomipramine: F3,54 = 7.69, p = 0.0016; maprotiline: F3,60 = 1.61, p = 0.1603) and time (amitriptyline: F3,60 = 13.70, p < 0.0001; clomipramine: F3,54 = 11.98, p < 0.0001; maprotiline: F3,60 = 2.67, p < 0.05).
Effect of heterocyclic antidepressants on carrageenan-induced paw edema in rats. Amitriptyline (A), clomipramine (B), and maprotiline (C) (10, 30, and 90 mg/kg, per os [p.o.]) and saline (10 mL/kg, p.o.) were administered 1 h before carrageenan (300 μg/0.1 mL/paw) injection. Edema formation (mL) was then measured hourly up to 4 h post-carrageenan injection and subtracted from basal paw volume. Data expressed as mean ± standard error of the mean (n=6, * p < 0.05 and † p < 0.01 vs. carrageenan group). AMT = amitriptyline; CMP = clomipramine; MPL = maprotiline.
Effect of heterocyclic antidepressants on dextran-induced paw edema in rats. Amitriptyline (A), clomipramine (B), and maprotiline (C) (10, 30 and 90 mg/kg, per os [p.o.]) and saline (10 mL/kg, p.o.) were administered 1 h before dextran (500 μg/0.1 mL/paw) injection. Edema formation (mL) was then measured hourly up to 4 h post-dextran injection and subtracted from basal paw volume. Data expressed as mean ± standard error of the mean (n=6, * p < 0.05 and † p < 0.01 vs. dextran group). AMT = amitriptyline; CMP = clomipramine; MPL = maprotiline.
Anti-inflammatory effect of heterocyclic antidepressants partially depends on the modulation of neutrophil migration
As shown in Figure 3, carrageenan (Figure 3A) and fMLP (Figure 3B) induced a conspicuous neutrophil migration when compared with the groups of rats that received only saline into the air pouch (p < 0.001). In addition, amitriptyline (90 mg/kg), clomipramine (90 mg/kg), and maprotiline (40 mg/kg) significantly counteracted the chemotactic response of both carrageenan and fMLP (p < 0.01) (Figures 3A and B).
Effect of heterocyclic antidepressants on neutrophil migration into 6-day-old air pouches. Amitriptyline (90 mg/kg), clomipramine (90 mg/kg), maprotiline (40 mg/kg), and saline (10 mL/kg, per os [p.o.]) were administered 1 h before carrageenan (500 μg/pouch [A]) or N-formyl-methionyl-leucyl-phenylalanine (fMLP) (10-6 M/mL/pouch [B]) injection. Neutrophil count in the exudates was determined 6 h after the stimulus injection. Data expressed as mean ± standard error of the mean (n=6, * p < 0.001 vs. saline, † p < 0.01 vs. carrageenan or fMLP). AMT = amitriptyline; CMP = clomipramine; MPL = maprotiline.
Mast cell degranulation is inhibited by heterocyclic antidepressants
As observed in Figures 4 and 5, in vitro incubation of mesenteric tissues with compound 48/80 significantly induced a notable mast cell degranulation (Figures 4B and C) when compared with tissues incubated with saline (Figures 4A and B, p < 0.001). Furthermore, this effect was prevented (p < 0.001) when animals were previously treated with amitriptyline (90 mg/kg, Figures 4E and F), clomipramine (90 mg/kg, Figures 4G and H), and maprotiline (40 mg/kg, Figures 4I and J). The percentage of degranulated cells is expressed in Figure 5.
Effect of heterocyclic antidepressants on mast cell degranulation. Animals were killed 1 h per os (p.o.) after treatment with amitriptyline (90 mg/kg), clomipramine (90 mg/kg), maprotiline (40 mg/kg), or saline (10 mL/kg, p.o.) and the mesenteric tissue was harvested. The tissue collected was incubated with compound 48/80 (0.8 μg/mL) and stained with 0.1% toluidine blue solution. A, C, E, G and I represent 100x magnification; B, D, F, H and J represent 400x magnification. Saline (A and B), compound 48/80 (C and D), amitriptyline + compound 48/80 (E and F), clomipramine + compound 48/80 (G and H), maprotiline + compound 48/80 (I and J).
Effect of heterocyclic antidepressants on mast cell degranulation. Animals were killed 1 h per os (p.o.) after treatment with amitriptyline (90 mg/kg), clomipramine (90 mg/kg), maprotiline (40 mg/kg), or saline (10 mL/kg, p.o.) and the mesenteric tissue was harvested. The tissue collected was incubated with compound 48/80 (0.8 μg/mL) and stained with 0.1% toluidine blue solution. Data represent the percentage of degranulated cells and were expressed as mean ± standard error of the mean (n=6, * p < 0.001 vs. saline, † p < 0.01 vs. compound 48/80). AMT = amitriptyline; CMP = clomipramine; MPL = maprotiline.
Discussion
In the present study, we demonstrated that the heterocyclic antidepressants amitriptyline, clomipramine, and maprotiline exert anti-inflammatory effects by a mast cell-dependent mechanism and by inhibition of neutrophil migration. These observations were achieved by the classic protocols of carrageenan and dextran-induced paw edema, neutrophil migration in the 6-day-old rat air pouch, and mast cell degranulation in the rat mesentery.
In previous studies, the doses of amitriptyline, maprotiline, and clomipramine used to test their
potential anti-inflammatory effects ranged from 5 to 80 mg/kg.44. Bianchi M, Panerai AE. Antidepressant drugs and experimental inflammation.
Pharmacol Res. 1996;33:235-8.,88. Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a
study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology.
2010;86:231-9.,1313. Bianchi M, Rossoni G, Sacerdote P, Panerai AE, Berti F. Effects of chlomipramine
and fluoxetine on subcutaneous carrageenin-induced inflammation in the rat. Inflamm Res.
1995;44:466-9.
14. Abdel-Salam OM, Nofal SM, El-Shenawy SM. Evaluation of the anti-inflammatory and
anti-nociceptive effects of different antidepressants in the rat. Pharmacol Res.
2003;48:157-65.
15. Hajhashemi V, Sadeghi H, Minaiyan M, Movahedian A, Talebi A. Central and
peripheral anti-inflammatory effects of maprotiline on carrageenan-induced paw edema in rats.
Inflamm Res. 2010;59:1053-9.-1616. Sadeghi H, Hajhashemi V, Minaiyan M, Movahedian A, Talebi A. A study on the
mechanisms involving the anti-inflammatory effect of amitriptyline in carrageenan-induced paw edema
in rats. Eur J Pharmacol. 2011;667:396-401. In all cases, these agents were given intraperitoneally, which
partially explains the lower doses injected. In general, long-term treatment of patients with
antidepressants involves oral administration. Therefore, in order to better mimic the clinical
settings, gavage was used in our study as the preferential route of administration for the
antidepressants tested. In addition, the oral route commonly requires higher doses of drugs due to
several reasons, including lower bioavailability and erratic absorption.
Several published articles report the inhibitory effect of antidepressants on edema formation due
to intraplantar injection of carrageenan.88. Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a
study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology.
2010;86:231-9.,1313. Bianchi M, Rossoni G, Sacerdote P, Panerai AE, Berti F. Effects of chlomipramine
and fluoxetine on subcutaneous carrageenin-induced inflammation in the rat. Inflamm Res.
1995;44:466-9.
14. Abdel-Salam OM, Nofal SM, El-Shenawy SM. Evaluation of the anti-inflammatory and
anti-nociceptive effects of different antidepressants in the rat. Pharmacol Res.
2003;48:157-65.
15. Hajhashemi V, Sadeghi H, Minaiyan M, Movahedian A, Talebi A. Central and
peripheral anti-inflammatory effects of maprotiline on carrageenan-induced paw edema in rats.
Inflamm Res. 2010;59:1053-9.-1616. Sadeghi H, Hajhashemi V, Minaiyan M, Movahedian A, Talebi A. A study on the
mechanisms involving the anti-inflammatory effect of amitriptyline in carrageenan-induced paw edema
in rats. Eur J Pharmacol. 2011;667:396-401. Despite progress
regarding the mechanisms involved in the anti-inflammatory effect of these drugs, some questions
remain to be answered. For instance, which inflammatory cells would be involved in the
anti-edematogenic effect of antidepressants? Do all antidepressant drugs share the same
anti-inflammatory mechanism?
It is well known that the edematogenic effects of carrageenan and dextran occur through different pathways.1919. Lo TN, Almeida AP, Beaven MA. Dextran and carrageenan evoke different inflammatory responses in rat with respect to composition of infiltrates and effect of indomethacin. J Pharmacol Exp Ther. 1982;221:261-7. A biphasic inflammatory response due to carrageenan injection has been suggested,2020. Vinegar R, Schreiber W, Hugo R. Biphasic development of carrageenin edema in rats. J Pharmacol Exp Ther. 1969;166:96-103. with the participation of several inflammatory mediators, including prostaglandins, bradykinin, and serotonin,2121. Morris CJ. Carrageenan-induced paw edema in the rat and mouse. Methods Mol Biol. 2003;225:115-21. cytokine production by resident macrophages, and neutrophil migration to the lesion site.2121. Morris CJ. Carrageenan-induced paw edema in the rat and mouse. Methods Mol Biol. 2003;225:115-21.,2222. Cunha TM, Verri WA Jr, Schivo IR, Napimoga MH, Parada CA, Poole S, et al. Crucial role of neutrophils in the development of mechanical inflammatory hypernociception. J Leukoc Biol. 2008;83:824-32. On the other hand, dextran-induced edema is chiefly a result of mast cell degranulation. Therefore, the use of various experimental approaches is essential to better determine the mechanism through which anti-inflammatory substances produce their effects.
In our study, we demonstrated the protective effect of different antidepressants on both the
carrageenan and dextran models of rat paw edema, suggesting that the function of both neutrophils
and mast cells might be modulated by these drugs. Regarding carrageenan, our findings are in
accordance with other studies.88. Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a
study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology.
2010;86:231-9.,1313. Bianchi M, Rossoni G, Sacerdote P, Panerai AE, Berti F. Effects of chlomipramine
and fluoxetine on subcutaneous carrageenin-induced inflammation in the rat. Inflamm Res.
1995;44:466-9.
14. Abdel-Salam OM, Nofal SM, El-Shenawy SM. Evaluation of the anti-inflammatory and
anti-nociceptive effects of different antidepressants in the rat. Pharmacol Res.
2003;48:157-65.
15. Hajhashemi V, Sadeghi H, Minaiyan M, Movahedian A, Talebi A. Central and
peripheral anti-inflammatory effects of maprotiline on carrageenan-induced paw edema in rats.
Inflamm Res. 2010;59:1053-9.-1616. Sadeghi H, Hajhashemi V, Minaiyan M, Movahedian A, Talebi A. A study on the
mechanisms involving the anti-inflammatory effect of amitriptyline in carrageenan-induced paw edema
in rats. Eur J Pharmacol. 2011;667:396-401. However, to the best of our knowledge,
this is the first report of a protective effect of the tested drugs against dextran-induced
edema.
It has been well established that polymorphonuclear (PMN) leukocyte infiltration plays an important role in the inflammation induced by carrageenan in the hind paw model. Additionally, taking into consideration that antidepressants are potent inhibitors of edema formation in that animal model, we decided to test the hypothesis of an effect of these drugs on neutrophil recruitment. For that purpose, we used the air-pouch model. The rat air pouch is a cavity that differs from others, such as the peritoneum, by its absence of mast cells.2323. Kowanko IC, Gordon TP, Rozenbilds MA, Brooks PM, Roberts-Thomson PJ. The subcutaneous air pouch model of synovium and the inflammatory response to heat aggregated gammaglobulin. Agents Actions. 1986;18:421-8. We intended to investigate whether the tested antidepressant drugs would still produce an anti-inflammatory response in the absence of these cells.
We demonstrated that the effects of both carrageenan and the direct chemotactic factor fMLP were markedly inhibited by amitriptyline, clomipramine, and maprotiline. Several other studies have already stated the anti-inflammatory effect of antidepressants. Sacerdote et al.99. Sacerdote P, Bianchi M, Panerai AE. Chlorimipramine and nortriptyline but not fluoxetine and fluvoxamine inhibit human polymorphonuclear cell chemotaxis in vitro. Gen Pharmacol. 1994;25:409-12. showed that clomipramine was able to block human neutrophil chemotaxis in vitro. The same authors also demonstrated a similar modulating effect on macrophages in vivo.2424. Sacerdote P, Bianchi M, Panerai AE. In vivo and in vitro clomipramine treatment decreases the migration of macrophages in the rat. Eur J Pharmacol. 1997;319:287-90. These authors attributed that activity over inflammatory cells to the cyclic chemical structure of clomipramine, noting that other non-cyclic antidepressant drugs, such as fluoxetine and fluvoxamine, do not modify cell migration. Sadeghi et al.1616. Sadeghi H, Hajhashemi V, Minaiyan M, Movahedian A, Talebi A. A study on the mechanisms involving the anti-inflammatory effect of amitriptyline in carrageenan-induced paw edema in rats. Eur J Pharmacol. 2011;667:396-401. further showed that both local and intracerebroventricular administration of amitriptyline elicits a marked reduction in the infiltration of PMN leukocytes into the carrageenan-treated paws, according to pathological examination and the activity of myeloperoxidase in the inflamed paw tissues. These findings were corroborated by Vismari et al.88. Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology. 2010;86:231-9. by intravital microscopy, further showing the involvement of α1-adrenoceptors in the anti-inflammatory effects of amitriptyline. In addition, Hajhashemi et al.2525. Hajhashemi V, Minaiyan M, Efthekhari M. Anti-Inflammatory activity of a selection of antidepressant drugs. IJPR. 2008;4:225-30. revealed that systemic administration of maprotiline reduces the development of carrageenan-induced paw edema in the rat. Maprotiline is also effective in decreasing edema when it is injected at the time of or after inducing inflammation.1515. Hajhashemi V, Sadeghi H, Minaiyan M, Movahedian A, Talebi A. Central and peripheral anti-inflammatory effects of maprotiline on carrageenan-induced paw edema in rats. Inflamm Res. 2010;59:1053-9.
The participation of preformed mast cell products, such as serotonin and histamine, is the main mechanism involved in the short-lived edematogenic response elicited by dextran injection.1919. Lo TN, Almeida AP, Beaven MA. Dextran and carrageenan evoke different inflammatory responses in rat with respect to composition of infiltrates and effect of indomethacin. J Pharmacol Exp Ther. 1982;221:261-7. In our study, all of the tested antidepressants had a protective effect against dextran-induced edema. Lo et al.1919. Lo TN, Almeida AP, Beaven MA. Dextran and carrageenan evoke different inflammatory responses in rat with respect to composition of infiltrates and effect of indomethacin. J Pharmacol Exp Ther. 1982;221:261-7. demonstrated that the accumulation of protein-free filtrates induced by dextran is not affected by treatment with indomethacin, whereas the infiltration of plasma protein and neutrophils in response to carrageenan is inhibited, suggesting the involvement of different mediators. Taking into consideration the participation of mast cells in dextran-induced edema, we assessed the possible effect of cyclic antidepressants on these cells. We observed a prominent effect of all drugs tested on preventing mast cell degranulation in the rat mesentery.
The mechanism through which tricyclic antidepressants can inhibit mast cell secretion was investigated by Clemons et al.2626. Clemons A, Vasiadi M, Kempuraj D, Kourelis T, Vandoros G, Theoharides TC. Amitriptyline and prochlorperazine inhibit proinflammatory mediator release from human mast cells: possible relevance to chronic fatigue syndrome. J Clin Psychopharmacol. 2011;31:385-7. These authors suggested a reduction of intracellular calcium ion levels due to amitriptyline and prochlorperazine treatment. However, the modulating effect of antidepressants on mast cells seems to vary depending on the drug.2727. Ferjan I, Erjavec F. Changes in histamine and serotonin secretion from rat peritoneal mast cells caused by antidepressants. Inflamm Res. 1996;45:141-4. As we showed in the present paper, an effect on mast cells might be a characteristic of most heterocyclic antidepressants.
In our opinion, some mechanistic aspects concerning the anti-inflammatory activity of antidepressants at the molecular level have yet to be elucidated. These aspects include their effects on cytokine release, the modulation of inflammatory pathways regulated by these mediators, and, further, how leukocyte trafficking is affected both in acute and in chronic inflammation.
In summary, the results of the present study provide evidence of the modulating effect of heterocyclic antidepressants on neutrophil migration and on mast cell stabilization. These findings might have an implication for the treatment of several inflammatory conditions, including allergic diseases.
We are grateful to Maria Silvandira Freire and Karina Felismino da Silva Santos for their technical assistance. This work was supported by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), and Fundação Cearense de Apoio ao Desenvolvimento Científico (FUNCAP). Gerly Anne Castro Brito and Ronaldo Albuquerque Ribeiro are recipients of CNPq fellowships.
References
-
1Brunton L, Parker K, Blumenthal D, Buxton I. Goodman & Gilman's Manual of Pharmacology and Therapeutics. New York: McGraw Hill; 2008.
-
2Mitra R, Jones S. Adjuvant analgesics in cancer pain: a review. Am J Hosp Palliat Care. 2012;29:70-9.
-
3Magni G. The use of antidepressants in the treatment of chronic pain. A review of the current evidence. Drugs. 1991;42:730-48.
-
4Bianchi M, Panerai AE. Antidepressant drugs and experimental inflammation. Pharmacol Res. 1996;33:235-8.
-
5Fishbain D. Evidence-based data on pain relief with antidepressants. Ann Med. 2000;32:305-16.
-
6Vorobeychik Y, Gordin V, Mao J, Chen L. Combination therapy for neuropathic pain: a review of current evidence. CNS Drugs. 2011;25:1023-34.
-
7Littrell JL. Taking the Perspective that a Depressive State Reflects Inflammation: Implications for the Use of Antidepressants. Front Psychol. 2012;3:297.
-
8Vismari L, Alves GJ, Palermo-Neto J. Amitriptyline and acute inflammation: a study using intravital microscopy and the carrageenan-induced paw edema model. Pharmacology. 2010;86:231-9.
-
9Sacerdote P, Bianchi M, Panerai AE. Chlorimipramine and nortriptyline but not fluoxetine and fluvoxamine inhibit human polymorphonuclear cell chemotaxis in vitro. Gen Pharmacol. 1994;25:409-12.
-
10Capuron L, Hauser P, Hinze-Selch D, Miller AH, Neveu PJ. Treatment of cytokine-induced depression. Brain Behav Immun. 2002;16:575-80.
-
11Corcos M, Guilbaud O, Hjalmarsson L, Chambry J, Jeammet P. Cytokines and depression: an analogic approach. Biomed Pharmacother. 2002;56:105-10.
-
12Kulmatycki KM, Jamali F. Drug disease interactions: role of inflammatory mediators in depression and variability in antidepressant drug response. J Pharm Pharm Sci. 2006;9:292-306.
-
13Bianchi M, Rossoni G, Sacerdote P, Panerai AE, Berti F. Effects of chlomipramine and fluoxetine on subcutaneous carrageenin-induced inflammation in the rat. Inflamm Res. 1995;44:466-9.
-
14Abdel-Salam OM, Nofal SM, El-Shenawy SM. Evaluation of the anti-inflammatory and anti-nociceptive effects of different antidepressants in the rat. Pharmacol Res. 2003;48:157-65.
-
15Hajhashemi V, Sadeghi H, Minaiyan M, Movahedian A, Talebi A. Central and peripheral anti-inflammatory effects of maprotiline on carrageenan-induced paw edema in rats. Inflamm Res. 2010;59:1053-9.
-
16Sadeghi H, Hajhashemi V, Minaiyan M, Movahedian A, Talebi A. A study on the mechanisms involving the anti-inflammatory effect of amitriptyline in carrageenan-induced paw edema in rats. Eur J Pharmacol. 2011;667:396-401.
-
17Ribeiro RA, Flores CA, Cunha FQ, Ferreira SH. IL-8 causes in vivo neutrophil migration by a cell-dependent mechanism. Immunology. 1991;73:472-7.
-
18Oliveira FA, Lima-Junior RC, Cordeiro WM, Vieira-Júnior GM, Chaves MH, Almeida FR, et al. Pentacyclic triterpenoids, alpha,beta-amyrins, suppress the scratching behavior in a mouse model of pruritus. Pharmacol Biochem Behav. 2004;78:719-25.
-
19Lo TN, Almeida AP, Beaven MA. Dextran and carrageenan evoke different inflammatory responses in rat with respect to composition of infiltrates and effect of indomethacin. J Pharmacol Exp Ther. 1982;221:261-7.
-
20Vinegar R, Schreiber W, Hugo R. Biphasic development of carrageenin edema in rats. J Pharmacol Exp Ther. 1969;166:96-103.
-
21Morris CJ. Carrageenan-induced paw edema in the rat and mouse. Methods Mol Biol. 2003;225:115-21.
-
22Cunha TM, Verri WA Jr, Schivo IR, Napimoga MH, Parada CA, Poole S, et al. Crucial role of neutrophils in the development of mechanical inflammatory hypernociception. J Leukoc Biol. 2008;83:824-32.
-
23Kowanko IC, Gordon TP, Rozenbilds MA, Brooks PM, Roberts-Thomson PJ. The subcutaneous air pouch model of synovium and the inflammatory response to heat aggregated gammaglobulin. Agents Actions. 1986;18:421-8.
-
24Sacerdote P, Bianchi M, Panerai AE. In vivo and in vitro clomipramine treatment decreases the migration of macrophages in the rat. Eur J Pharmacol. 1997;319:287-90.
-
25Hajhashemi V, Minaiyan M, Efthekhari M. Anti-Inflammatory activity of a selection of antidepressant drugs. IJPR. 2008;4:225-30.
-
26Clemons A, Vasiadi M, Kempuraj D, Kourelis T, Vandoros G, Theoharides TC. Amitriptyline and prochlorperazine inhibit proinflammatory mediator release from human mast cells: possible relevance to chronic fatigue syndrome. J Clin Psychopharmacol. 2011;31:385-7.
-
27Ferjan I, Erjavec F. Changes in histamine and serotonin secretion from rat peritoneal mast cells caused by antidepressants. Inflamm Res. 1996;45:141-4.
Publication Dates
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Publication in this collection
Dec 2013
History
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Received
27 Aug 2012 -
Accepted
7 Jan 2013