The antioxidant N-acetyl cysteine suppresses lidocaine-induced intracellular reactive oxygen species production and cell death in neuronal SH-SY5Y cells
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The local anesthetic lidocaine can affect intra- and extra-cellular signaling pathways in both neuronal and non-neuronal cells, resulting in long-term modulation of biological functions, including cell growth and death. Indeed, lidocaine was shown to induce necrosis and apoptosis in vitro. While several studies have suggested that lidocaine-induced apoptosis is mitochondrial pathway-dependent, it remains unclear whether reactive oxygen species (ROS) are involved in this process and whether the observed cell death can be prevented by antioxidant treatment.
The effects of lidocaine and antioxidants on cell viability and death were evaluated using SH-SY5Y cells, HeLa cells, and HeLa cell derivatives. Cell viability was examined via MTS/PES ([3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt]/phenazine ethosulfate) assay. Meanwhile, cell apoptosis and necrosis were evaluated using a cell death detection assay with Annexin V-FITC and PI staining, as well as by assaying for caspase-3/7 and caspase-9 activity, and by measuring the release of lactate dehydrogenase, respectively. Mitochondrial transmembrane potential (ΔΨm) was assessed using the fluorescent probe tetramethylrhodamine ethyl ester.
Lidocaine treatment resulted in suppression of the mitochondrial electron transport chain and subsequent attenuation of mitochondrial membrane potential, as well as enhanced ROS production, activation of caspase-3/7 and caspase-9, and induction of apoptosis and necrosis in SH-SY5Y cells in a dose- and time-dependent manner. Likewise, the anesthetics mepivacaine and bupivacaine also induced apoptosis in SH-SY5Y cells. Notably, the antioxidants N-acetyl cysteine (NAC) and Trolox successfully scavenged the mitochondria-derived ROS and suppressed local lidocaine-induced cell death.
Our findings demonstrate that the local anesthetics lidocaine, mepivacaine, and bupivacaine inhibited the activity of mitochondria and induced apoptosis and necrosis in a dose-dependent manner. Furthermore, they demonstrate that treatment with the antioxidants NAC, Trolox, and GGA resulted in preservation of mitochondrial voltage and inhibition of apoptosis via suppression of caspase activation.
KeywordsLidocaine Mitochondria ROS Redox Apoptosis Necrosis Oxygen consumption
Oxygen consumption rate
Reactive oxygen species
There is an established consensus that local anesthetics exert nerve-blocking activity, primarily through the inhibition of voltage-gated sodium channels . However, these compounds can also affect the intra- and extra-cellular signaling pathways of both neuronal and non-neuronal cells, resulting in long-term modulation of biological functions, including cell growth and death . Lidocaine is a widely used local anesthetic and anti-arrhythmic agent. Notably, lidocaine was also shown to induce apoptosis and necrosis both in vitro [3, 4, 5] and in vivo , and to cause transient or permanent nerve injury, such as cauda equina syndrome, after spinal anesthesia in clinical settings [7, 8]. In addition, it was reported that lidocaine inhibits the invasive ability of cancer cells at concentrations used for surgical operations (5–20 mM).
Apoptosis is a form of programmed cell death that is characterized by a series of distinct morphological and biochemical changes, and is an important process in a wide variety of biological systems. There are two major signaling pathways by which apoptosis is induced: the intrinsic and extrinsic pathway. While the extrinsic pathway is dependent on cell-surface death receptors such as Fas (First apoptosis signal), the intrinsic pathway is initiated within mitochondria . Specifically, in the intrinsic pathway, the formation of a multimeric Apaf-1/cytochrome c complex results in activation of caspase-9, which in turn cleaves and activates the downstream caspases caspase-3, −6, and −7 [1, 10]. Notably, reactive oxygen species (ROS) are widely believed to play an essential role in apoptosis. Indeed, several studies indicate that ROS scavengers, including the synthetic compound N-acetyl cysteine (NAC) and the endogenous redox-active molecule thioredoxin (TRX), can be used to alleviate intracellular ROS and thereby prevent apoptosis and necrosis.
Previous studies demonstrated that lidocaine-induced cell death is dependent on the mitochondrial pathway; however, it is still largely unclear whether ROS are involved in this process. In this study, we demonstrate that in vitro lidocaine treatment resulted in attenuation of mitochondrial membrane potential and promoted caspase-dependent apoptosis in neuronal SH-SY5Y cells. Moreover, we show that the observed increases in cell death were mitochondria-derived ROS-dependent and could be blocked by treatment with several antioxidant compounds.
Lidocaine, mepivacaine, bupivacaine, NAC, and (±)-6-Hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid (Trolox) were obtained from Sigma-Aldrich (St. Louis, MO, USA), teprenone (geranylgeranylacetone, GGA) was obtained from Wako Pure Chemical Industries (Osaka, Japan), and recombinant human TRX (rhTRX) was obtained from Oriental Yeast Co., Ltd. (Tokyo, Japan). GGA and Trolox were dissolved in absolute ethanol, while bupivacaine and NAC were dissolved in H2O, and rhTRX was dissolved in citric acid. Rotenone, oligomycin and antimycin A were obtained from Abcam, Inc. (Cambridge, MA, USA).
All cell lines were obtained from American Type Culture Collection (ATCC; Manassas, VA, USA). The established cell lines derived from human neuroblastoma SH-SY5Y cells and cervical carcinoma HeLa cells were maintained in Roswell Park Memorial Institute (RPMI) 1640 medium supplemented with 10 % fetal bovine serum, 100 units/ml penicillin, and 0.1 mg/ml streptomycin. The characteristics of EB8 cells (HeLa cells lacking mtDNA) and HeEB1 cells (a hybrid clone of EB8 cells containing mtDNA from wild-type HeLa cells) have been described elsewhere [11, 12]. All cells were maintained at 37 °C in a humidified atmosphere containing 5 % CO2. Cells were grown in 100 mm dishes and were subcultured for experiments when they reached 85 % confluence.
Cell viability assay (MTS assay)
Cell viability was assessed using a CellTiter 96™ AQueous One Solution Cell Proliferation Assay (Promega, Madison, WI, USA). Briefly, SH-SY5Y cells were seeded into 96-well plates (2 × 104 cells/well) and cultivated overnight. The following day, cells were treated with the indicated concentrations of the appropriate drug(s) for varying lengths of time. After treatment, 20 μl of CellTiter 96 AQueous One Solution™ Reagent was added to each well, the plates were incubated at 37 °C for 1 h, and the absorbance of each sample was measured using an iMark™ Micropate Reader (BIO-RAD, Hercules, CA, USA) at a wavelength of 490 nm. Cell viability was then calculated by comparing the absorbance of treated cells with that of the control cells (incubated without drugs), which was defined as 100 % [13, 14]. All samples were tested in triplicate for each experiment.
Caspase-3/7 and caspase-9 activity assays
The levels of caspase-3/7 and caspase-9 activity were assessed using an Apo-ONE™ Homogeneous Caspase-3/7 Assay Kit (Promega) and a Caspase-Glo™ 9 Assays Kit (Promega), respectively, according to the manufacturer’s protocols. Briefly, SH-SY5Y cells were seeded into 96-well plates (2 × 104 cells/well) and incubated overnight. The following day, cells were treated with the indicated concentrations of the appropriate drug(s) for varying lengths of time. After treatment, 100 μl of Apo-ONE Caspase-3/7 Reagent™ or Caspase-Glo 9 reagent™ was added to each well, respectively. Cells were incubated at room temperature for 1 h and the luminescence of each well was measured using an EnSpire™ Multimode Plate Reader (PerkinElmer, Waltham, MA, USA). Caspase activity was then calculated by comparing the levels of luminescence of the treated cells with that of the control cell population (incubated without drugs), which was defined as 100 %. Assays were performed in triplicate at least twice. Data were expressed as means ± standard deviations (SD).
Whole cell lysates were prepared as described previously [15, 16]. Briefly, cells were lysed by suspension in ice-cold lysis buffer [0.1 % sodium dodecyl sulfate (SDS), 1 % NP40, 5 mM ethylene diamine tetraacetic acid (EDTA), 150 mM NaCl, 50 mM Tris-Cl (pH 8.0), 1 mM sodium orthovanadate, and Complete Protease Inhibitor™ (Roche Applied Science)] and centrifuged at 10,000 × g to pellet cell debris. Approximately 25 μg of each protein sample was then separated by SDS-polyacrylamide gel electrophoresis (SDS-PAGE) and subjected to immunoblot analysis using rabbit polyclonal antibodies specific to PARP [poly (ADP-ribose) polymerase; 1:1,000] or cleaved caspase-9 (Asp315; 1:1,000) (Cell Signaling Technology, Danvers, MA, USA) , β-actin (Sigma-Aldrich), and anti-rabbit IgG horseradish peroxidase-linked secondary antibodies (1:2000 dilution; Cell Signaling Technology). Immunolabeled proteins were then visualized using enhanced chemiluminescence (ECL™) reagents (Amersham Biosciences, Little Chalfont, UK).
Analysis of cell apoptosis
Levels of cell apoptosis were measured using an Annexin V-FITC Apoptosis Detection Kit™ (BioVision, Milpitas, CA, USA), according to the manufacturer’s instructions. For these analyses, SH-SY5Y cells were seeded into 6-well plates (3 × 105 cells/well) and incubated overnight. The following day, cells were treated with the indicated concentrations of the appropriate drug(s) for varying lengths of time and harvested by centrifugation at 1200 rpm for 3 min. The culture supernatants were discharged, and the resulting pellets were suspended in a mixture comprised of 500 μl binding buffer, 5 μl Annexing V-FITC, and 5 μl propidium iodide (PI; 50 μg/ml) for 5 min at room temperature in the dark and analyzed using a FACSCalibur flow cytometer (BD Biosciences, San Jose, CA, USA) equipped with CellQuest Pro™ software [4, 13]. Data were evaluated using FlowJo™ version 7.6.3 software (TreeStar, Ashland, OR, USA), exported to Excel spreadsheets, and subsequently analyzed using the statistical application R.
Lactate dehydrogenase (LDH)-based cytotoxic assay
Levels of cell cytotoxicity were evaluated using a CytoTox-ONE™ Kit (Promega). Briefly, SH-SY5Y cells were seeded into 96-well plates (2 × 104 cells/well) and incubated overnight. The following day, cells were treated with the indicated concentrations of the appropriate drug(s) for varying lengths of time. Twenty microliters of CytoTox-ONE™ reagent was added to each well, plates were incubated at 22 °C for 10 min, and then 50 μl of Stop Solution was added to each well. The resulting fluorescence was measured using an EnSpire™ Multimode Plate Reader (PerkinElmer) at an excitation wavelength of 560 nm and an emission wavelength of 590 nm. Percentages of cell death were calculated by comparing the level of LDH released (fluorescence value) from each treatment group with that of the positive control population (cells treated with Lysis solution), which was defined as 100 %. Meanwhile, the level of LDH released from the negative control population (untreated cells) was defined as 0 %. All samples were evaluated in triplicate for each experiment.
Determination of mitochondrial membrane potential (ΔΨm)
Mitochondrial membrane potential was determined by flow cytometry using a MitoPT™ JC-1 Assay Kit (ImmunoChemistry Technologies, Bloomington, MN, USA), according to the manufacturer’s instructions. For these analyses, SH-SY5Y cells were seeded into 6-well plates (3 × 105 cells/well) and cultivated overnight. The following day, cells were treated with the indicated concentrations of the appropriate drug(s) for varying lengths of time and then pelleted by centrifugation at 1200 rpm for 3 min. Supernatants were discharged, and cells were resuspended in JC-1, incubated at 37 °C for 15 min in the dark, and collected by centrifugation at 1200 rpm for 3 min. Supernatants were again discharged and the remaining cell residues were suspended in 500 μl assay buffer. Samples were subsequently analyzed using a FACSCalibur flow cytometer (BD Biosciences, San Jose, CA, USA) equipped with CellQuest Pro™ software [4, 13] for the detection of red JC-1 aggregates (590 nm emission) or green JC-1 monomers (527 nm emission). The resulting data were evaluated using FlowJo version 7.6.3 software (TreeStar, San Carlos, CA), exported to Excel spreadsheets, and subsequently analyzed using the statistical application R.
Measurement of total cellular O2 consumption rate (OCR)
Total OCR was measured as described previously [12, 16]. Briefly, SH-SY5Y cells were trypsinized and suspended at a concentration of 1 × 107 cells/ml in RPMI containing 10 % FBS and 25 mM HEPES buffer. For each experiment, equal numbers of cells (suspended in 1 ml) were pipetted into the chamber of an Oxytherm electrode unit (Hansatech Instruments, Norfolk, UK), which uses a Clark-type electrode to monitor the concentration of dissolved O2 in the sealed chamber over time. The test reagents including lidocaine, rotenone and FCCP were added into the chambers immediately before each measurement. The resulting data were exported to a computerized chart recorder (Oxygraph; Hansatech Instruments), which calculated the OCR values. The temperature was maintained at 25 °C during measurement. The concentrations of O2 in 1 ml of DMEM medium lacking cells was also measured over time and utilized as the background. O2 consumption experiments were repeated at least three times, and data were expressed as means ± SD .
Live cell ROS imaging
For evaluation of intracellular ROS generation, control and lidocaine-treated SH-SY5Y cells were treated with the ROS-sensitive dye 2', 7'-dichlorodihydrofluorescin diacetate (DCFH-DA) and analyzed using a BioStation IM live cell time-lapse imaging system (Nikon, Tokyo, Japan) at 37 °C and 5 % CO2; phase-contrast and fluorescence images were acquired at 15 min intervals [18, 19].
All experiments were repeated at least twice and each sample was evaluated in triplicate. Representative data, expressed as means ± SD, are shown. Differences between results were evaluated by one-way analysis of variance (ANOVA) or two-way ANOVA, followed by Dunnett’s test for multiple comparisons. All statistical analyses were performed using EZR (Saitama Medical Center, Jichi Medical University), which is a graphical user interface for R (The R Foundation for Statistical Computing, version 3.1.3) . More precisely, it is a modified version of R commander software (version 1.6–3) and includes statistical functions that are frequently used in biostatistics. P-values < 0.05 were considered statistically significant. All graphs were generated by the application Prism 6 for Mac OS X (GraphPad Software Inc., La Jolla, CA USA).
Lidocaine induces SH-SY5Y cell death in a dose- and time-dependent manner
To confirm these findings, SH-SY5Y cells were stained with PI and FITC-conjugated annexin V and evaluated by flow cytometry. Cells treated with 4 mM or 10 mM lidocaine exhibited significantly increased numbers of PI-positive or annexin V-positive cells after 12 h and 24 h of treatment (Fig. 1e and Additional file 1: Figure S1A–S1E). Additionally, treatment with 4 mM or 10 mM lidocaine resulted in significant reductions in mitochondrial voltage (Fig. 1f and Additional file 2: Figure S2A–S2D), while treatment with 10 mM lidocaine resulted in significant increases in SH-SY5Y cell death after 12 h, as indicated by the levels of LDH release (Fig. 1g).
Critical involvement of mitochondria in lidocaine-induced cell death
These findings are therefore consistent with those obtained by flow cytometry and indicate that lidocaine promotes cell death by targeting mitochondria.
Effect of synthetic antioxidants on lidocaine-induced cell death
Effects of an endogenous antioxidant on lidocaine-induced cell death
Effects of synthetic antioxidants on mepivacaine and bupivacaine-induced cell death
In this study, we demonstrated that the local anesthetic lidocaine suppresses the mitochondrial ETC in neuronal SH-SY5Y cells in a dose- and time-dependent manner, thereby attenuating mitochondrial membrane potential, inducing ROS production, and activating caspase-9- and caspase-3/7-mediated apoptosis and necrosis. Moreover, we observed similar effects in cells treated with mepivacaine and bupivacaine. Intriguingly treatment with the antioxidants NAC and Trolox successfully suppressed these effects by scavenging the ROS derived from mitochondria.
Lidocaine induces two types of cell death
Multiple studies have reported that clinically relevant concentrations (500 μM to 24 mM) of local anesthetics such as lidocaine are capable of inducing cell death in cells of neuronal origin as well as in established cell lines derived from cancerous tissues [23, 24]. Consistent with these findings, we demonstrated that 1 mM–10 mM lidocaine was sufficient to promote cell death in neuronal SH-SY5Y cells and HeLa cervical carcinoma cells (Figs. 1, 2, and Additional file 1: Figure S1).
Lidocaine induces apoptosis and necrosis in a dose-dependent manner
There are at least two modes of cell death: apoptosis and necrosis . Apoptosis is a strictly regulated (programmed) process involving the activation of specific cysteine proteases that is responsible for the ordered removal of superfluous, aged, or damaged cells. Notably, while this process plays critical roles in both health and disease, necrosis is solely the outcome of severe and acute injury. Apoptosis involves the regulated activity of catabolic enzymes (proteases and nucleases) within a near-to-intact plasma membrane, and is commonly accompanied by characteristic changes in nuclear morphology and chromatin biochemistry.
In this study, lidocaine treatment promoted caspase-3/7 and caspase-9 activation, as well as PARP cleavage, in SH-SY5Y cells (Fig. 1c and d). As such, these data indicate that lidocaine induces cell death via an authentic apoptosis pathway. Meanwhile, flow cytometry analyses demonstrated that treatment of cells with greater than 4 mM lidocaine especially 10 mM lidocaine also resulted in increased numbers of PI- and annexin V-positive cells (Additional file 1: Figure S1). These data strongly suggest that lidocaine elicits both types of cell death in a dose-dependent manner in vitro. Intriguingly, however, the observed increase in caspase 3/7 but not in cell death with LDH release, was significantly suppressed by treatment with NAC, Trolox and GGA. The evidence suggests that the antioxidants preferentially inhibit apoptosis rather than necrosis.
Functional mitochondria are necessary for lidocaine-induced apoptosis but not for necrosis
Local anesthetics have been found to inhibit mitochondrial ETC at several points along the respiratory chain, and to inhibit F1-ATPase activity and adenine-nucleotide transport . In this study, we also demonstrated the lidocaine inhibited oxygen consumption by mitochondria (Fig. 2c). Moreover, using ρ0 cells lacking mitochondrial DNA, we showed that functional mitochondria are required for lidocaine-induced cell death following caspase activation but not for lidocaine-induced necrosis with LDH release (Fig. 2b and e). These data strongly suggests that mitochondria comprise a critical target for lidocaine-induced cell death, particularly for apoptosis.
It was previously reported that dysfunction of the mitochondrial ETC due to mutations in OXPHOS subunits or treatment with chemical inhibitors is generally associated with increased production of mitochondrial ROS, including superoxide anions, hydroxyl radicals, and hydrogen peroxide . Specifically, inhibitor studies using isolated mitochondria demonstrated that complexes I and III of the ETC can act as relevant sources of mitochondrial ROS . Consistent with these findings, HEK293 cells treated with rotenone and antimycin A for inhibition of complexes I and III, respectively, exhibited increased ROS production and induction of oxidative stress . Meanwhile, ROS production was not observed in ρ0 cells in this study (data not shown).
ROS derived from mitochondria promote lidocaine-induced apoptosis
Another intriguing finding presented in this report was that both lidocaine-induced apoptosis and necrosis were ROS-dependent. The results presented in Fig. 3a clearly demonstrate that lidocaine treatment induced ROS generation. And while the precise origin of these ROS remains unclear, our findings strongly suggest that mitochondria play a critical role in this process (Fig. 2b and c). As such, these data imply that lidocaine-mediated cell death is dependent on mitochondria. Consistent with this conclusion, the mitochondrial DNA-deficient ρ0 cells were resistant to lidocaine treatment (Fig. 3b). Moreover, our data are consistent with a previous report demonstrating that tetracaine-induced apoptosis in rat cortical astrocytes is associated with increased ROS production .
Effect of antioxidants on lidocaine-induced cell apoptosis
Oxidative stress in response to various external stimuli has been implicated in the induction of apoptosis. Specifically, oxygen free radicals induce DNA sequence changes and rearrangements that may trigger apoptotic cell death of neuronal cells. In this study, we provided the first evidence that ROS scavengers such as NAC and Trolox can significantly suppress lidocaine-induced cell death in vitro. Conversely, while treatment with rhTRX had no affect on apoptosis or necrosis, GGA, which is known to induce TRX expression and is itself an antioxidant, exerted a protective effect against lidocaine-induced cell death. Although the molecular mechanisms underlying these discrepancies are unclear, it is possible that extracellular administration of rhTRX is an ineffective method for modulating intracellular redox status [22, 29, 30]. Also, GGA has been shown to promote the expression of heat shock protein 70, which was reported to alleviate cellular stress and exert cytoprotective effects [31, 32]. As such, the observed beneficial effects of GGA on cell survival may be dependent on induction of HSP70 and not TRX. In any case, future studies using cells that overexpress TRX may better elucidate whether this protein can inhibit anesthetic-induced cell death.
There are several limitations to the present study. First, the established SH-SY5Y and HeLa cell lines were used exclusively for all experiments. Although SH-SY5Y cells are derived from neuronal tissue and exhibit several characteristics similar to neurons, our experimental results and conclusions cannot necessarily by extrapolated to neuronal injuries induced by local anesthetics in an in vivo setting. Furthermore, although we evaluated the effects of lidocaine on ρ0 cells, which lack mitochondrial DNA, the majority of the data were obtained using HeLa cells, primarily due to technical issues. Lastly, the results presented in this study demonstrate that local anesthetics negatively affect mitochondrial activity, thereby inducing apoptosis; however, the specific molecular targets have yet to be identified. As such, the identification of such targets comprises a critical goal for future studies.
In this study, we demonstrated that the local anesthetics lidocaine, mepivacaine, and bupivacaine induce two types of cell death in neuronal cells in vitro. In particular, treatment with 1–4 mM lidocaine promoted apoptosis, while treatment with 10 mM lidocaine induced cell death with LDH release. Moreover, our data demonstrate that these compounds specifically target mitochondria, and that the ROS produced by mitochondria play an integral role in the observed induction of apoptosis. Lastly, we demonstrated that scavenging of ROS with antioxidants such as NAC, Trolox, and GGA preserved mitochondrial voltage and prevented apoptosis by suppressing caspase activation.
We would like to Editage (http://www.editage.jp) for English language editing.
This work was supported by grants from the Japan Society for the Promotion of Science (KAKENHI; Grant #26670693 and #24592336 to K.H., and #25462457 to K.N.) and by the research grant D2 from Kansai Medical University.
Availability of data and materials
The datasets analysed in the current study available from the corresponding author on reasonable request.
AO, KS, and KH designed the study, performed the data analyses, and wrote the manuscript. CS and KN collected and analyzed the data. MT, KO, and YM analyzed the data. KT provided experimental materials. All authors read and approved the final version of the manuscript.
The authors declare that they have no competing interest.
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