Therapeutic concentration of morphine reduces oxidative stress in glioma cell line

Abstract

Morphine is a potent analgesic opioid used extensively for pain treatment. During the last decade, global consumption grew more than 4-fold. However, molecular mechanisms elicited by morphine are not totally understood. Thus, a growing literature indicates that there are additional actions to the analgesic effect. Previous studies about morphine and oxidative stress are controversial and used concentrations outside the range of clinical practice. Therefore, in this study, we hypothesized that a therapeutic concentration of morphine (1 μM) would show a protective effect in a traditional model of oxidative stress. We exposed the C6 glioma cell line to hydrogen peroxide (H₂O₂) and/or morphine for 24 h and evaluated cell viability, lipid peroxidation, and levels of sulfhydryl groups (an indicator of the redox state of the cell). Morphine did not prevent the decrease in cell viability provoked by H₂O₂ but partially prevented lipid peroxidation caused by 0.0025% H₂O₂ (a concentration allowing more than 90% cell viability). Interestingly, this opioid did not alter the increased levels of sulfhydryl groups produced by exposure to 0.0025% H₂O₂, opening the possibility that alternative molecular mechanisms (a direct scavenging activity or the inhibition of NAPDH oxidase) may explain the protective effect registered in the lipid peroxidation assay. Our results demonstrate, for the first time, that morphine in usual analgesic doses may contribute to minimizing oxidative stress in cells of glial origin. This study supports the importance of employing concentrations similar to those used in clinical practice for a better approximation between experimental models and the clinical setting.

Morphine; Glia; Oxidative stress; Hydrogen peroxide; Lipid peroxidation; Opiod

Introduction

Morphine is a potent analgesic opioid extensively used for pain treatment in diverse pathologies and clinical situations (cancer, neuropathic myalgia, emergencies, assisted ventilation, and anesthesia, among others). Although chronic treatment with opioid drugs leads to tolerance and dependence, morphine has proven to be one of the most potent and efficient analgesic drugs in clinical practice, becoming a major option for the treatment of moderately severe to severe pain. Thus, according to the most recent report of the International Narcotics Control Board of the United Nations (¹), global consumption of morphine for medical and scientific purposes rose considerably during the period from 1992 to 2011. During that time, morphine consumption grew more than 4-fold (from 10 to 42 tons) throughout the world. In Brazil, the consumption of this opioid also increased during the same period, reaching 106 defined daily doses for statistical purposes consumed per million inhabitants per day in 2009-2011 (¹).

However, the molecular mechanisms elicited by morphine are not totally understood. This molecule is able to activate a family of metabotropic receptors (μ-, δ-, and κ-type opioid receptors). Endogenous opioids are found in many structures of the central nervous system (CNS) and spinal cord (reviewed in Ref. 2). Classically, the analgesic effect of morphine is mainly attributed to μ-receptor activation, leading to an inhibition of calcium influx in presynaptic neurons and an increase in potassium conductance in postsynaptic neurons, among other effects. Additionally, opioid receptors are also localized in cells of glial origin, especially microglia and astrocytes (a feature preserved even in gliomas like the C6 cell line) where they may be involved in neurotrophism during development and under pathological conditions (³).

Interestingly, there is a growing literature supporting additional actions for morphine, as in the case of the role played by the opioid in oxidative stress (⁴-¹³). Oxidative stress is the disequilibrium between free radical generation and elimination (a free radical is a very reactive molecule with an unpaired electron). This excess of free radicals [usually reactive oxygen species (ROS)] reacts with macromolecules (DNA, proteins, and lipids) as a molecular mechanism underlying many pathologies and physiological processes. Interaction with lipids is especially deleterious for the membranes, triggering the self-propagated process of lipid peroxidation. To prevent the damage caused by ROS, cells rely on enzymatic [e.g., superoxide dismutase (SOD) or glutathione peroxidase (GPx)] and nonenzymatic antioxidant systems. Among the latter, glutathione stands out as a major scavenger molecule, representing the most common low molecular weight compound containing sulfhydryl groups in mammalian cells (with levels as high as millimolar for the majority of cells) (¹⁴). Thus, the content of sulfhydryl groups can be considered an indicator of the redox state of the cell.

Previous studies of the relationship between morphine and oxidative stress are not very abundant, and the results describing the pro-oxidant or antioxidant roles of the opioid are contradictory (⁴-¹³).

In addition to that controversy, all of those studies used doses of morphine outside the therapeutic range used in clinical practice (i.e., plasma levels of 16-364 ng/mL) (¹⁵) and, to date, no investigations have analyzed the effects of therapeutic concentrations of morphine in oxidative stress.

Therefore, in this study, we hypothesized that a therapeutic concentration of morphine (1 μM) would show a protective effect in a traditional model of oxidative stress [exposure to hydrogen peroxide (H₂O₂)] in the C6 glioma cell line.

Material and Methods

Cell culture

The rat glioma C6 cell line was purchased from American Type Culture Collection (ATCC, USA) and maintained at 37°C and 5% CO₂ in Dulbecco's modified Eagle's medium (DMEM) with 10% fetal bovine serum, 100 U/mL penicillin, and 100 μg/mL streptomycin. Approximately 1.5×10⁵ cells were seeded and maintained at 37°C for 24 h before exposure to H₂O₂ and/or morphine.

Treatment

H₂O₂ (30%) was diluted in DMEM to final concentrations of 0 to 0.005%. Morphine sulfate (10 mg/mL), kindly donated by Cristália (Brazil), was also diluted in DMEM to 1 μM (285.34 ng/mL). The C6 cell line was then incubated with H₂O₂ and/or morphine for 24 h.

Cell viability

Cell viability was assessed as previously described by Mosmann (¹⁶). After the treatment, cells were washed twice with phosphate-buffered saline (PBS) and incubated for 2 h with 5 mg/mL 4,5-dimethylthiazol bromide diphenyltetrazolium (MTT). Absorbance of the samples was measured at 570 nm and cell viability is reported as the percentage of reduced MTT compared to that of the control group.

Assay of lipid peroxidation

Lipid peroxidation was evaluated by measuring malondialdehyde (MDA) levels as described elsewhere (¹⁷). Briefly, after treatment, cells were homogenized in a solution containing 0.1% thiobarbituric acid, 0.25 M HCl, and 15% trichloroacetic acid. Samples were then incubated for 15 min at 70°C. Finally, absorbance was measured at 535 mm and compared to that of standard concentrations of MDA.

Assay of sulfhydryl groups

Levels of compounds containing sulfhydryl groups were assayed by the method described by Ellman (¹⁸) using the selective reaction of these groups with 5,5′-dithio-bis(2-nitrobenzoic acid (DTNB or Ellman's reagent). Treated cells were homogenized in ice-cold PBS with 1 mM EDTA and 0.1% sodium dodecyl sulfate and centrifuged for 5 min at 750 g. Supernatants were treated for 5 min with 5 mM DTNB and absorbance was evaluated at 412 nm.

Assay of protein content

Protein quantities in the samples were assayed using the method described by Bradford in 1976 (¹⁹). Thus, after correcting for protein concentration, the results of lipid peroxidation and sulfhydryl groups are reported as percentages of the control group values.

Assay of direct scavenging activity of H₂O₂molecules

To evaluate the possibility of direct scavenging of H₂O₂ by morphine, the protocol described by Gülçin et al. (⁵) was carried out. Briefly, morphine (1-100 µM) was added to a solution of 4 mM H₂O₂ in PBS. After 10 min, absorbance was measured at 230 nm and the percentage of scavenged H₂O₂ was calculated according to the following formula: percent scavenged H₂O₂=[(A₀-A₁)/A₀]×100, where A₀ is the absorbance of the control group and A₁ is the absorbance in the presence of morphine.

Statistical analysis

Statistical analysis was performed using the BIOESTAT 5.0 software (Brazil;http://www.mamiraua.org.br/pt-br/downloads/programas/). Initially, the Gaussian distribution of the data was tested by the Kolmorov-Smirnoff method with P<0.05 considered to be significant. Subsequently, all groups were analyzed with ANOVA and the Tukey post hoc test, when appropriate. Values of P<0.05 were considered to be statistically significant.

Results

Cell viability

Exposure to increasing concentrations of H₂O₂ reduced cell viability of the C6 cell line in a concentration-dependent manner (Figure 1). No significant changes in C6 cultures were detected when cells were incubated with 1 to 10 μM morphine (data not shown). Cotreatment with 1 µM morphine did not show significant differences in viability when compared with that of cells incubated only with H₂O₂. For subsequent experiments, a concentration of 0.0025% H₂O₂ (approximately 735 μM) was chosen, allowing more than 90% cell viability.

Figure 1
Cell viability of C6 cell line exposed to increasing concentrations of hydrogen peroxide (H₂O₂) and/or 1 µM morphine for 24 h. Data are reported as means±SE. No significant differences were detected in groups incubated with the same concentration of H₂O₂ (ANOVA).

Lipid peroxidation

Incubation of cells with 0.0025% H₂O₂ raised the level of lipid peroxidation more than three times that of the control group (Figure 2). Interestingly, morphine partially protected the cells, avoiding 44% of this increase.

Figure 2
Lipid peroxidation of C6 cell line exposed to 0.0025% hydrogen peroxide (H₂O₂) and/or 1 µM morphine for 24 h. Data are reported as means±SE. *P<0.05 vscontrol and morphine groups; ^#P<0.05 vsperoxide group (ANOVA and Tukey test).

Levels of sulfhydryl groups

In all cases, exposure to 0.0025% H₂O₂ enhanced the levels of compounds containing sulfhydryl groups in the C6 cells by about 20% (Figure 3). However, cotreatment with morphine did not prevent this increase, and no significant differences were detected between cells treated with H₂O₂ and those cotreated with morphine.

Figure 3
Content of sulfhydryl groups in the C6 cell line exposed to 0.0025% hydrogen peroxide (H₂O₂) and/or 1 µM morphine for 24 h. The insert shows levels of scavenged H₂O₂ in vitro in the presence of 1-100 µM morphine. Data are reported as means±SE. *P<0.05 vs all groups (ANOVA and Tukey test).

Scavenging activity of H₂O₂ molecules

Morphine at 1 and 10 µM concentrations did not change the levels of H₂O₂ (Figure 3, insert). Interestingly, 100 µM morphine was able to significantly scavenge (about 26.5%) these molecules in vitro.

Discussion

This study showed, for the first time, that a therapeutic concentration of morphine significantly reduced oxidative stress in cells of glial origin exposed to H₂O₂ (Figures 1 and2).

The concentration of the opioid used in the present study (1 µM or 285.34 ng/mL) is near the upper limit of human therapeutic concentrations. For example, patients with chronic treatment for pain management usually show plasma levels of morphine ranging from 16 to 364 ng/mL (¹⁵). The relatively high liposolubility of morphine allows it to easily cross the blood-brain barrier, making the levels of the opioid in nervous tissue very similar to those found in the blood.

In addition, this concentration (or 10 times higher) did not affect the viability of the C6 cells (data not shown). This fact was in agreement with results previously described, in which human fetal astrocytes exposed to 1 µM morphine did not develop apoptotic processes such as those found in neurons and microglia exposed to the same concentration of the opioid (²⁰).

Exposure to H₂O₂ is a traditional model of oxidative stress for cells of CNS origin. In our study, the concentration-response curve fitted to a sigmoid curve was designed to calculate the 50% lethal concentration value (0.0032%) characterizing the toxicity of H₂O₂ for the C6 cell line (Figure 1). Taking into account the cell viability data, a concentration of H₂O₂ (0.0025%) allowing more than 90% viable cells after 24 h of incubation was selected for all subsequent experiments.

This latter concentration of H₂O₂ did not affect cell viability when compared with that of the control group (Figure 1), but provoked a significant increase in levels of lipid peroxidation (Figure 2). Treatment with morphine reduced this increase by 44%, showing a significant antioxidant activity with a therapeutic dose.

Previous studies with morphine that have analyzed markers of oxidative stress are not very common, and the role attributed to the opioid remains, at the very least, controversial.

Studies indicating a pro-oxidant activity of morphine used high doses and/or evaluated oxidative stress as a mechanism associated with tolerance and/or dependence on the opioid (⁷,⁹,¹¹-¹³). Exposure to increased concentrations of morphine (as high as 6 mM) has already been used as a model of neuronal damage by oxidative stress in both in vivo and in vitro studies (including the C6 cell line) (⁷,¹¹-¹³). Morphine intoxication decreased the activity of antioxidant enzymes (SOD and GPx, among others) and induced apoptosis and glial activation. Glial activation closely associated with oxidative stress was also observed in opioid tolerance/dependence (⁹) with increased levels of lipid peroxidation and reduced levels of glutathione. Nevertheless, the doses of morphine included in those studies were much higher than those usually used in humans for therapeutic treatment of pain.

On the other hand, a number of studies using lower concentrations of morphine (but still outside the therapeutic range) show a possible antioxidant role for the opioid (⁴-⁶,⁸,¹⁰). Indeed, primary cultures (neurons and/or glial cells) and cell lines such as SHSY5Y (derived from a human neuroblastoma cell line) and C6 were protected by the opioid in models of neurotoxicity produced by peroxynitrite donors, glutamate, lipopolysaccharide (LPS), and 1-methyl-4-phenylpyridinium incubation (⁴,⁶,⁸).

Therefore, our hypothesis is that high doses of morphine may be pro-oxidative, but therapeutic doses, such as that used in this study, would have a significant antioxidant effect (especially in glia).

One interesting observation is that the antioxidant effects of morphine in previous studies were registered in isolated structures (mitochondria), in the presence of antagonists of opioid receptors or also for the synthetic enantiomerd-morphine (which does not bind to the μ-opioid receptor), demonstrating that the antioxidant activity of morphine is independent of opioid receptors (⁴,⁶,⁸). Reinforcing this idea, selective ligands for μ-, δ-, and κ-type opioid receptors did not show any of the neuroprotective effects of morphine (⁴,⁶).

In those studies, morphine reduced DNA fragmentation, stabilized mitochondrial permeability and function, inhibited microglial activation, and recovered glutathione levels (⁴,⁶,⁸,¹⁰). Detection of alterations in glutathione levels with morphine treatment is frequent even at higher concentrations of the opioid (⁷,⁹,¹²,¹³) and can be evaluated by the quantitation of levels of sulfhydryl groups. Reduced glutathione is the major intracellular compound containing these groups.

Surprisingly, our results about possible molecular mechanisms of this antioxidant effect of morphine showed that protection against lipid peroxidation (Figure 2) was independent of both a possible influence of the levels of sulfhydryl groups (morphine did not reduce the levels increased by H₂O₂) and a significant scavenger effect of H₂O₂ molecules with a 1 µM concentration of the opioid (Figure 3). Although no scavenging activity by morphine was shown with a 1 µM concentration, a significant decrease in H₂O₂ molecules was detected with higher concentrations of the opioid, similar to that reported previously (⁵). Additionally, a strong scavenging activity of morphine with compounds other than H₂O₂ has already been reported (⁴,⁵). Thus, an alternative molecular mechanism to explain the protection exerted by the opioid could be that of a direct scavenger effect of free radicals other than H₂O₂ molecules.

Nevertheless, other mechanisms must not be discarded. The research of Qian et al. (⁸) showed that morphine was not capable of protecting primary cultures (neurons and glial cells) from mice deficient in the catalytic subunit of NADPH oxidase (a key enzyme required for the production of ROS) against LPS incubation, demonstrating the importance of this enzyme in the protective effect of the opioid. Also, morphine attenuated the translocation of a cytosolic component of NADPH oxidase (p47^phox) to the cell membrane, a process necessary for assembling into an ative enzyme. Considering these results, the authors pointed to inhibition of NADPH oxidase as an essential molecular mechanism for the effect of morphine (⁸). Thus, reduced activity of this enzyme could be another possible explanation for the antioxidant effect of morphine found in our study. Additional studies must be carried out to elucidate the exact molecular mechanism underlying these effects.

This is the first study to analyze the effects of a therapeutic concentration of morphine in an in vitro model of oxidative stress. Our results demonstrated that morphine, in usual analgesic doses, may contribute to minimizing oxidative stress in glial cells. More studies employing concentrations similar to those used in clinical practice are necessary for a better understanding of the applicability of experimental models to the clinical setting.

Acknowledgments

The authors thank Cristália (Brazil) for the kind donation of morphine. Research supported by CNPq (#303110/2010-4 and #478580/2012-6). A. Costa-Malaquias thanks FAPESPA for his grant. J.L.M. Nascimento, A.M. Herculano, and M.E. Crespo-López thank CNPq for their grants. The authors also thank Pró-Reitoria de Pesquisa/Universidade Federal do Pará (PROPESP/UFPA) for support.

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• First published online April 11, 2014.

Publication Dates

• Publication in this collection
  11 Apr 2014
• Date of issue
  May 2014

History

• Received
  19 Nov 2013
• Accepted
  10 Feb 2014