Remifentanil induces autophagy and prevents hydrogen peroxide-induced apoptosis in Cos-7 cells

Ji-Young Yoon; Chul-Woo Baek; Mi-Na Woo; Eun-Jung Kim; Ji-Uk Yoon; Chang-Hoon Park

doi:10.17245/jdapm.2016.16.3.175

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Yoon, Baek, Woo, Kim, Yoon, and Park: Remifentanil induces autophagy and prevents hydrogen peroxide-induced apoptosis in Cos-7 cells

Original Article

Journal of Dental Anesthesia and Pain Medicine 2016; 16(3): 175-184.

Published online: 30 September 2016

DOI: https://doi.org/10.17245/jdapm.2016.16.3.175

Remifentanil induces autophagy and prevents hydrogen peroxide-induced apoptosis in Cos-7 cells

Ji-Young Yoon¹, Chul-Woo Baek¹, Mi-Na Woo¹, Eun-Jung Kim¹, Ji-Uk Yoon², Chang-Hoon Park¹

¹Department of Dental Anesthesia and Pain Medicine, Pusan National University Dental Hospital, Yangsan, Korea.

²Department of Anesthesia and Pain Medicine, Pusan National University Yangsan Hospital, Yangsan, Korea.

Corresponding Author: Chang-Hoon Park, Department of Dental Anesthesia and Pain Medicine, Pusan National University Dental Hospital, Yangsan, Korea. Tel: +82-55-360-5370, Fax: +82-55-360-5369, wjdental@hanmail.net

Received 16 August 2016 Revised 1 September 2016 Accepted 2 September 2016

(open-access, http://creativecommons.org/licenses/by-nc/3.0/):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

This study investigated the effect of remifentanil pretreatment on Cos-7 cells exposed to oxidative stress, and the influence of remifentanil on intracellular autophagy and apoptotic cell death.

Methods

Cells were divided into 4 groups: (1) Control: non-pretreated cells were incubated in normoxia (5% CO₂, 21% O₂, and 74% N₂). (2) H₂O₂: non-pretreated cells were exposed to H₂O₂ for 24 h. (3) RPC+H₂O₂: cells pretreated with remifentanil were exposed to H₂O₂ for 24 h. (4) 3-MA+RPC+H₂O₂: cells pretreated with 3-Methyladenine (3-MA) and remifentanil were exposed to H₂O₂ for 24 h. We determined the cell viability of each group using an MTT assay. Hoechst staining and FACS analysis of Cos-7 cells were performed to observe the effect of remifentanil on apoptosis. Autophagy activation was determined by fluorescence microscopy, MDC staining, and AO staining. The expression of autophagy-related proteins was observed using western blotting.

Results

Remifentanil pretreatment increased the viability of Cos-7 cells exposed to oxidative stress. Hoechst staining and FACS analysis revealed that oxidative stress-dependent apoptosis was suppressed by the pretreatment. Additionally, fluorescence microscopy showed that remifentanil pretreatment led to autophagy-induction in Cos-7 cells, and the expression of autophagy-related proteins was increased in the RPC+H₂O₂ group.

Conclusions

The study showed that remifentanil pretreatment stimulated autophagy and increased viability in an oxidative stress model of Cos-7 cells. Therefore, we suggest that apoptosis was activated upon oxidative stress, and remifentanil preconditioning increased the survival rate of the cells by activating autophagy.

Keywords: Apoptosis, Autophagy, Cos-7 cells, Oxidative stress, Remifentanil

INTRODUCTION

Oxidative stress is an imbalance between oxidant molecules and antioxidant species that protect cells from harmful effects of oxidants. The major molecules that are produced as a result of oxidative stress are reactive free radicals [1]. Reactive oxygen species (ROS), one of the major classes of reactive free radicals, are produced during aerobic metabolism in all oxygenic organisms. Cells also generate ROS as signaling molecules through the activation of various oxidases and peroxidases [2 3]. However, when ROS are present in excess, they have a direct oxidizing effect on crucial cell components needed for survival, such as lipids, proteins, and DNA, therefore ROS are involved in cell injury, necrosis, and apoptosis, which are often associated with human diseases [4 5 6 7]. ROS can be produced in the lung or other organs as a consequence of high oxygen therapy or hypoxia-reperfusion, and they can stimulate cell death pathways associated with tissue damage [8].

Autophagy is a degradation system within cells resulting in the reuse of intracellular proteins or other damaged organelles by nonselective, bulky engulfment, and digestion of cellular components into reusable molecules [9 10]. In general, autophagy is thought to be induced under stressful circumstances such as oxidative stress, starvation, and hypoxia-reoxygenation [11]. ROS accumulation induces autophagy, which then serves to reduce ROS levels [12].

Remifentanil is an ultra-short-acting, selective muopioid receptor agonist that has attracted attention because of its esterase-based metabolism, minimal accumulation, and very rapid onset and offset of clinical action [13 14 15 16]. Like several other anesthetics, remifentanil has been reported to protect various organs against ischemia-reperfusion injury (IRI) such as myocardium, brain, kidney and liver, possibly by inhibiting oxidative stress responses [17 18 19 20]. Autophagy is induced earlier than apoptosis so it can protect cells against damage in situations such as IRI [10]. However, the effects of remifentanil on Cos-7 cell survival and autophagy during oxidative stress has not been examined. Therefore, this study investigated whether remifentanil pretreatment has a protective effect on Cos-7 cells exposed to oxidative stress, and we determined the influence of this compound on intracellular autophagy and apoptotic cell death.

MATERIALS AND METHODS

1. Reagents

Remifentanil (Ultiva™ inj., 1 mg vial, GlaxoSmithKline, Belgium) was diluted in dimethyl sulfoxide (DMSO). Hoechst 33342 was purchased from Sigma. 3-[4,5-dimethylthiazol-2-yl]2,5-diphenyl tetrazolium bromide (MTT), acridine orange (AO), monodansylcadaverine (MDC), and 3-methyladenine (3-MA, class III PI3K inhibitor) were obtained from Calbiochem (La Jolla, CA, USA). Antibodies used in the study were as follows: LC3-II (microtubule-associated protein 1 light chain 3 form II) (1:3,000) and Beclin-1 (1:1,000) were obtained from Abcam, p62 (1:1,000) and Atg5 (1:500) from Santa Cruz. Secondary antibodies against rabbit (1:3,000), and mouse (1:3,000), immunoglobulins were purchased from Bio-Rad.

2. Cell culture

Cos-7 cells were obtained from the American Type Culture Collection (ATCC, Manassas, USA). Cells were cultured in Dulbecco's modified Eagle medium (DMEM, GIBCO) supplemented with 10% inactivated fetal bovine serum (FBS, GIBCO) containing 500 µg/ml penicillin and 500 µg/ml streptomycin (GIBCO), and cells were incubated at 37℃ in a humidified atmosphere with 5% CO₂. Media were changed every 3 days.

3. Remifentanil treatment

Remifentanil solutions in DMSO were kept frozen at −4℃ until use. The stock was diluted to the appropriate concentration in DMEM when needed. Prior to remifentanil treatment, cells were grown to about 80% confluence and then exposed to remifentanil at different concentrations (0, 0.1, 0.5, 1, 2 ng/ml) for 24 h. Cells grown in medium containing an equivalent amount of DMSO without remifentanil served as a control. Cells were randomly divided into the following groups: (1) Control: cells were incubated in normoxia (5% CO₂, 21% O₂, and 74% N₂) without remifentanil treatment. (2) H₂O₂: cells were exposed to H₂O₂ (0, 50, 100, 200, or 400 concentrations of H₂O₂) without remifentanil treatment for 24 h. (3) RPC + H₂O₂: cells pretreated with remifentanil were exposed to H₂O₂ for 24 h. (4) 3-MA + RPC + H₂O₂: cells pretreated with 3-MA and remifentanil were exposed to H₂O₂ for 24 h.

4. MTT assay

Cell viability was measured using a quantitative colorimetric assay with thiazolyl blue tetrazolium bromide (MTT, AMRESCO), which shows the mitochondrial activity of living cells. Cos-7 cells were seeded in 96-well plates. After drug treatment as indicated, cells were incubated with 300 µl MTT reagent (final concentration 0.5 mg/ml) for 1.5 h at 37℃. The reaction was terminated by adding 200 µl DMSO. Cell viability was measured by an ELISA reader (Tecan, Mannedorf, Switzerland) at 570 nm excitatory emission wavelength.

5. Hoechst staining (with 1 ng/ml remifentanil treatment)

After remifentanil treatment, the cells were transferred onto a clean, fat-free glass slide using a cytocentrifuge. They were stained with 4 µg/ml Hoechst 33342 for 10 min at 37℃ in darkness and washed twice in PBS. The slides were mounted with glycerol. The samples were observed and photographed using epifluorescence microscopy (Carl Zeiss, Göettingen, Germany). The number of cells with condensed or fragmented nuclei was determined by a blinded observer from a random sampling of 3 × 10² cells per experiment. Three independent experiments were conducted.

6. Fluorescence microscopy

Cells were grown on coverslips and treated with remifentanil. After 24 h, cells were stained with 0.05 mM MDC, a selective fluorescent marker for autophagic vacuoles, at 37℃ for 1 h. Changes in cellular fluorescence were observed using a fluorescence microscope (Axioskop, Carl Zeiss, Germany). For further detection of the acidic cellular compartment, we used acridine orange (AO), which emits bright red fluorescence in acidic vesicles but green fluorescence in the cytoplasm and nucleus. Cells were stained with 1 µg/ml AO for 15 min and washed with PBS. Autophagic vacuole organelle (AVO) formation was determined using a confocal microscope LSM 700 (Carl Zeiss, Germany).

7. Western blot analysis

Cells (2 × 10⁶) were washed twice in ice-cold PBS, resuspended in 200 µl ice-cold solubilizing buffer (300 mM NaCl, 50 mM Tris-Cl [pH 7.6], 0.5% Triton X-100, 2 mM PMSF, 2 µl/ml aprotinin and 2 µl/ml leupeptin) and incubated at 4℃ for 30 min. The lysates were centrifuged at 14,000 rpm for 15 min at 4℃. Cell lysate protein concentrations were determined with a Bradford protein assay (Bio-Rad, Richmond, CA, USA) and 20 µg of total proteins were resolved by 10% SDS-PAGE. Proteins were transferred to polyvinylidene fluoride (PVDF) membranes (Millipore, Billerica, MA, USA) and reacted with the appropriate primary antibody. Immunostaining with secondary antibodies was detected using SuperSignal West Femto (Pierce, Rockford, IL, USA) enhanced chemiluminescence substrate and observed with an Alpha Imager HP (Alpha Innotech, Santa Clara, USA).

8. Statistical analysis

Three independent experiments were performed for each experimental group and each experiment was performed in triplicate. The significance of differences between experimental and control groups were determined (p < 0.01 and 0.05) using a paired Student's t-test using SPSS for Win 12.0. Fluorescence activated cell sorting (FACS) analysis of Cos-7 cells was also performed for control, H₂O₂, RPC + H₂O₂, and 3-MA + RPC + H₂O₂ groups to determine apoptotic cell populations of each group.

RESULTS

1. Remifentanil pretreatment increased the viability of Cos-7 cells after oxidative stress

The effect of remifentanil on Cos-7 cells was investigated over a wide concentration range (0–2 ng/ml). Remifentanil and 3-MA treatment did not result in any significant effect on the viability of Cos-7 cells (Fig. 1A), while the cell viability in H₂O₂-treated groups decreased in a concentration-dependent manner (Fig. 1B). The viability of cells in the RPC + H₂O₂ group was 92.1% relative to the control cells (100%), while in the H₂O₂ group, viability was 67.2% (Fig. 2). In addition, the 3-MA + RPC + H₂O₂ group showed 75.8% cell viability, which was lower than cells pretreated with remifentanil before oxidative stress, but higher than cells treated with H₂O₂ alone (Fig. 2).

2. Oxidative stress-dependent apoptosis was suppressed by remifentanil

The effect of remifentanil on apoptosis was examined by Hoechst 33342 staining of Cos-7 cells exposed to normoxia (control), H₂O₂, RPC + H₂O₂, and 3-MA + RPC + H₂O₂ (Fig. 3). Cells were examined under a fluorescence microscope (400 ×). The majority of Cos-7 cells in the control and RPC + H₂O₂ groups showed normal morphology with round, regular nuclei. On the other hand, apoptotic bodies were seen in the H₂O₂ group and the 3-MA + RPC + H₂O₂ group. Pretreating with remifentanil effectively reduced Cos-7 cell apoptosis as observed by their normal morphology. In addition, FACS analysis of Cos-7 cells showed that the percentage of apoptotic cells in the remifentanil-preconditioned group was 6.4%, while in oxidative stressed group the percentage of apoptotic cells was 10.3% (Fig. 4).

3. Remifentanil pretreatment leads to autophagy induction in Cos-7 cells

A remarkable accumulation of autophagy-specific staining by MDC was observed around the nuclei in the RPC + H₂O₂ group of Cos-7 cells (Fig. 5A). Similarly, AO staining indicated by red fluorescent spots appeared in the RPC + H₂O₂ group cells, while the control, H₂O₂, and 3-MA + RPC + H₂O₂ groups showed mainly green cytoplasmic fluorescence (Fig. 5B). We clarified the role of remifentanil-induced autophagy in Cos-7 cells by investigating the consequences of treating with 3-MA, a selective autophagy inhibitor. The inhibitory effects on AVO formation by 3-MA was confirmed by quantitatively measuring the red fluorescence ratio after AO staining. We examined the activation of autophagy related proteins in each group of cells by western blotting. The recruitment of LC3-II to the membrane occurs via an Atg5-dependent mechanism, and thus Atg5 is essential for autophagosome formation in vivo. The levels of Atg5 and Beclin-1, LC3-II, and p62 were decreased or similar in the oxidative stressed group compared to the control group, but were increased in the RPC + H₂O₂ group (Fig. 6). In addition, the levels of Atg5, Beclin-1, LC3-II, and p62 were lowest in the 3-MA + RPC + H₂O₂ group. Levels of these autophagy-related proteins were increased when autophagy was induced by remifentanil, and they were decreased when autophagy was suppressed by 3-MA.

DISCUSSION

The purpose of this study was to determine whether remifentanil pretreatment exhibits protective effects on Cos-7 cells undergoing oxidative stress, and to determine the influence of this compound on intracellular autophagy and apoptotic cell death. The present study showed several principal findings. First, we found that remifentanil pretreatment increased the viability of cells exposed to oxidative stress (Fig. 2). Importantly, remifentanil pretreatment did not affect cell viability under normal conditions, nor did treatment with 3-MA (Fig. 1A). Second, oxidative stress-dependent apoptosis was suppressed by remifentanil pretreatment. We found that the number of apoptotic bodies was reduced in remifentanil-preconditioned cells (Fig. 3), and the apoptotic cell percentage in remifentanil-preconditioned Cos-7 cells under oxidative stress was lowered by 6.4% compared to cells exposed to oxidative stress without remifentanil pretreatment (Fig. 4). Third, remifentanil pretreatment protected Cos-7 cells against oxidative stress by activating intracellular autophagy, which was likely the anti-apoptotic mechanism. Western blot analysis showed that remifentanil pretreatment upregulated protein levels of ATG5, Beclin-1, LC3-II, and p62, which are autophagy-related proteins (Fig. 6) [21]. Lastly, as seen by autophagy-specific staining using MDC and AO, the RPC + H₂O₂ group showed the presence of autophagosomes by the observation of blue dots (MDC) or red spots (AO), and the autophagy pathway-specific inhibitor 3-MA blocked autophagosome formation (Fig. 5). These results regarding autophagy might be related with the cell viability finding (Fig. 2) that cells exposed to oxidative stress alone showed 67.2% cell viability, while cells under oxidative stress with remifentanil preconditioning showed 92.1% cell viability. These results show that remifentanil preconditioning has a protective effect on cells exposed to oxidative stress. The activation of autophagy is the mechanism by which remifentanil protects cells undergoing oxidative stress. Remifentanil preconditioning induced the autophagy response and it resulted in decreased cell death upon exposure to oxidative stress.

Autophagy is a cellular process used to deliver cytoplasmic organelles to the lysosome for degradation. It is most often implicated in cell survival by cleaning up damaged organelles and harmful substances inside the cell, but also by providing building blocks and nutrients to the cell [22 23]. However, autophagy has also been related to cell death [22 23 24 25]. Recent studies suggest that autophagy has a great effect on determining cell fate toward survival or death, depending on the stimulus, cell type, and context [9 24 26]. In this study, we assumed that cell survival would be promoted if autophagy is activated in the early period of cellular oxidative stress by preconditioning with remifentanil.

Oxidative stress can lead to cell death through the production of ROS, one of the major reactive free radical species induced by oxidative stress [1 27]. ROS can cause cell death by necrotic or apoptotic pathways due to its direct oxidizing effects on macromolecules such as lipids, proteins, and DNA [1 4 8 28], and ROS are involved in many diseases including cardiovascular diseases, nephropathy, neurodegenerative diseases, and aging [1 6 7 28 29]. Previous studies demonstrate an essential role for ROS in the activation of autophagy, which, in turn, leads to reduced ROS levels [30 31]. The results of this study indicate that remifentanil preconditioning suppresses cell damage and apoptosis due to oxidative stress, and increases cell viability by upregulating autophagy.

There have been various studies regarding the protective effect of remifentanil and its mechanisms against oxidative stress, similar to the effects of other types of anesthetics. Ge Zhao et al. (2013) showed that remifentanil may protect hepatocytes against IRI by reducing hepatic cell apoptosis [32]. T.Z. Zhang et al. (2014) showed that high-dosage remifentanil preconditioning played a protective role on brain cells, possibly by inhibiting the oxidative stress response [20]. In addition, Zhang Y et al. (2005) concluded that cardiac delta and kappa opioid receptors, but not mu opioid receptors, mediate cardioprotection by remifentanil preconditioning on ischemia-reperfused rat hearts [18 33 34], and H.S. Kim et al. (2009) suggested that the cardioprotective effect of remifentanil resulted from preserving anti-apoptotic pathways in ischemia-reperfused rat hearts, regardless of the administration period [19]. Cho SS et al. (2013) showed that preconditioning with remifentanil altered intestinal IRI and systemic inflammatory responses in mice, therefore they concluded that prophylaxis with remifentanil may be valuable in various clinical conditions of human IRI [17]. Recent mechanistic studies revealed a protective effect of opioids against oxidative stress, with opioid receptors as the major contributors to this effect [33 34 35]. However, it was not known if the protective effect of remifentanil was related to autophagy in cells under oxidative stress; hence, we sought to examine this possibility in the current study.

There are several limitations in present study. First, this study was performed in vitro. Further studies are needed to determine if the protective effect of remifentanil occurs through activation of autophagy in human cells and organs under oxidative stress. Secondly, the protective effect of remifentanil seemed to be through other pathways as well as activation of autophagy. When autophagy activation was suppressed by treating with 3-MA in the remifentanil-preconditioned Cos-7 cells under oxidative stress, cell viability was 75.8%, which was lower than the cell viability of 92.1% observed in the RPC + H₂O₂ group, but still higher than the H₂O₂ group (Fig. 2). There might be other remifentanil-mediated pathways affecting cell viability under oxidative stress, and further studies regarding this are needed. Third, further studies should be conducted to determine the mechanisms by which remifentanil increases autophagy activity in cells exposed to oxidative stress.

The current study showed that remifentanil preconditioning stimulated autophagy and increased cell viability in the oxidative stressed model of Cos-7 cells. In addition, remifentanil did not affect cell viability in cells not exposed to oxidative stress. Therefore, we suggest that cell autophagy in was activated only under oxidative stress conditions, and remifentanil preconditioning increased cell survival by activating autophagy.

Figures and Tables

Fig. 1

Cell viability of Cos-7 cells assessed by MTT assay.

(A) The effect of remifentanil and 3-MA + remifentanil preconditioning on Cos-7 cell viability at various concentrations (0, 0.1, 0.5, 1, 2 ng/ml) without exposure to H₂O₂, (B) Cell viability of Cos-7 cells upon exposure to various concentrations (0, 50, 100, 200, 400) of H₂O₂.

Fig. 2

The effect of remifentanil pretreatment on Cos-7 cell viability with or without autophagy inhibition, as examined by MTT assay.

^*P < 0.05 as compared with control group.

Control: no H₂O₂, remifentanil treatment group, H₂O₂: hydrogen peroxide exposure only, RPC + H₂O₂: remifentanil pretreatment group plus hydrogen peroxide exposure, 3-MA + RPC + H₂O₂: pretreatment with 3-MA and remifentanil plus hydrogen peroxide exposure.

Fig. 3

Hoechst staining: Morphological changes in Cos-7 cells upon pretreatment with remifentanil alone or in combination with 3-MA before exposure to oxidative stress. Cos-7 cells were pretreated with remifentanil or remifentanil and 3-MA, then exposed to oxidative stress. Cells were stained with Hoechst stain and observed by fluorescence microscopy. Apoptotic bodies were seen in H₂O₂ and 3-MA + RPC + H₂O₂ group cells. In contrast, they were remarkably reduced in RPC + H₂O₂ group cells. Control: no H₂O₂, remifentanil treatment group, H₂O₂: hydrogen peroxide exposure only, RPC + H₂O₂: remifentanil pretreatment group plus hydrogen peroxide exposure, 3-MA + RPC + H₂O₂: pretreatment with 3-MA and remifentanil plus hydrogen peroxide exposure.

Fig. 4

Fluorescence activated cell sorting (FACS) analysis of Cos-7 cells to determine apoptotic cell populations of each experimental group. Control: no H₂O₂, remifentanil treatment group, H₂O₂: hydrogen peroxide exposure only, RPC + H₂O₂: remifentanil pretreatment group plus hydrogen peroxide exposure, 3-MA + RPC + H₂O₂: pretreatment with 3-MA and remifentanil plus hydrogen peroxide exposure.

Fig. 5

Fluorescence microscopic analysis of autophagosomes in Cos-7 cells under oxidative stress to observe autophagy activation upon different pretreatment conditions.

(A) MDC staining of cytoplasmic vacuoles after preconditioning with remifentanil in Cos-7 cells followed by exposure to oxidative stress. Cellular oxidative stress resulted in greater accumulation of autophagosomes containing partially digested cytoplasmic contents compared to the control group. The remifentanil pretreatment group showed increased formation of autophagosomes. Compared with the RPC + H₂O₂ group, the autophagy pathway inhibitor, 3-MA, blocked formation of autophagosomes. Magnification: 400 ×, (B) AO staining of autophagosomes after remifentanil pretreatment in Cos-7 cells followed by exposure to oxidative stress. AO staining indicated by red fluorescent spots appeared in RPC + H₂O₂ group cells, while the control, H₂O₂, and 3-MA + RPC + H₂O₂ groups showed mainly green cytoplasmic fluorescence. The green shows where the dye has stained the nucleus and the red indicates autophagosome formation. Magnification: 400 ×. Control: no H₂O₂, remifentanil treatment group, H₂O₂: hydrogen peroxide exposure only, RPC + H₂O₂: remifentanil pretreatment group plus hydrogen peroxide exposure, 3-MA + RPC + H₂O₂: pretreatment with 3-MA and remifentanil plus hydrogen peroxide exposure.

Fig. 6

Western blot analysis and densitometry to determine the effects of remifentanil treatment ATG5, Beclin-1, LC3-II, and p62 protein levels in each experimental group of Cos-7 cells. In RPC + H₂O₂ groups, cellular expression of ATG5, Beclin-1, LC3-II and p62 were upregulated, while these proteins were downregulated in 3-MA+RPC+H₂O₂ groups. Control: no H₂O₂, remifentanil treatment group, H₂O₂: hydrogen peroxide exposure only, RPC+H₂O₂: remifentanil pretreatment group plus hydrogen peroxide exposure, 3-MA+RPC+H₂O₂: pretreatment with 3-MA and remifentanil plus hydrogen peroxide exposure.

^*P < 0.05 as compared with the control group.

Notes

^Note Thesis for the degree of Doctor of Philosophy.

References

1. Elahi MM, Kong YX, Matata BM. Oxidative stress as a mediator of cardiovascular disease. Oxid Med Cell Longev. 2009; 2:259–269.

2. Droge W. Free radicals in the physiological control of cell function. Physiol Rev. 2002; 82:47–95.

3. Halliwell B. Reactive species and antioxidants. Redox biology is a fundamental theme of aerobic life. Plant Physiol. 2006; 141:312–322.

4. Valko M, Rhodes C, Moncol J, Izakovic M, Mazur M. Free radicals, metals and antioxidants in oxidative stress-induced cancer. Chem Biol Interact. 2006; 160:1–40.

5. Zhao Y, Zhao B. Oxidative stress and the pathogenesis of alzheimer's disease. Oxid Med Cell Longev. 2013; 2013:316523.

6. Singh DK, Winocour P, Farrington K. Oxidative stress in early diabetic nephropathy: fueling the fire. Nat Rev Endocrinol. 2011; 7:176–184.

7. Giordano FJ. Oxygen, oxidative stress, hypoxia, and heart failure. J Clin Invest. 2005; 115:500–508.

8. Ryter SW, Kim HP, Hoetzel A, Park JW, Nakahira K, Wang X, et al. Mechanisms of cell death in oxidative stress. Antioxid Redox Signal. 2007; 9:49–89.

9. Mizushima N. The pleiotropic role of autophagy: From protein metabolism to bactericide. Cell Death Differ. 2005; 12:1535–1541.

10. Guan X, Qian Y, Shen Y, Zhang L, Du Y, Dai H, et al. Autophagy protects renal tubular cells against ischemia/reperfusion injury in a time-dependent manner. Cell Physiol Biochem. 2015; 36:285–298.

11. Kim YH, Kang JM, Kim IR, Lee BY, Yoon JY, Kim CH, et al. Protective effect of propofol against hypoxia-reoxygenation injury in HaCaT human keratinocytes. Int J Oral Biol. 2014; 39:97–105.

12. Scherz-Shouval R, Elazar Z. Regulation of autophagy by ROS: Physiology and pathology. Trends Biochem Sci. 2011; 36:30–38.

13. Kwon JY, Park BS, Kim YH, Kim YD, Kim CH, Yoon JY, et al. Remifentanil protects human keratinocytes against hypoxia-reoxygenation injury through activation of autophagy. PloS One. 2015; 10:e0116982.

14. Scott LJ, Perry CM. Spotlight on remifentanil for general anaesthesia. CNS drugs. 2005; 19:1069–1074.

15. Komatsu R, Turan A, Orhan-Sungur M, McGuire J, Radke O, Apfel C. Remifentanil for general anaesthesia: A systematic review. Anaesthesia. 2007; 62:1266–1280.

16. Marsh D, Hodkinson B. Remifentanil in paediatric anaesthetic practice. Anaesthesia. 2009; 64:301–308.

17. Cho SS, Rudloff I, Berger PJ, Irwin MG, Nold MF, Cheng W, et al. Remifentanil ameliorates intestinal ischemia-reperfusion injury. BMC Gastroenterol. 2013; 13:69.

18. Zhang Y, Irwin MG, Wong TM, Chen M, Cao CM. Remifentanil preconditioning confers cardioprotection via cardiac kappa- and delta-opioid receptors. Anesthesiology. 2005; 102:371–378.

19. Kim H, Cho J, Hong S, Kim S, Shim J, Kwak Y. Remifentanil protects myocardium through activation of anti-apoptotic pathways of survival in ischemia-reperfused rat heart. Physiol Res. 2010; 59:347–356.

20. Zhang TZ, Zhou J, Jin Q, Sun YJ, Diao YG, Zhang YN, et al. Protective effects of remifentanil preconditioning on cerebral injury during pump-assisted coronary artery bypass graft. Genet Mol Res. 2014; 13:7658–7665.

21. Chang C, Chen P, Lu S, Hsieh M, Lin C, Lee H, et al. Propofol-enhanced autophagy increases motility and angiogenic capacity of cultured human umbilical vascular endothelial cells. Life Sci. 2015; 142:49–59.

22. Anding AL, Baehrecke EH. Chapter three-autophagy in cell life and cell death. Curr Top Dev Biol. 2015; 114:67–91.

23. Baehrecke EH. Autophagy: Dual roles in life and death? Nat Rev Mol Cell Biol. 2005; 6:505–510.

24. Fitzwalter BE, Thorburn A. Recent insights into cell death and autophagy. FEBS J. 2015; 282:4279–4288.

25. Levine B, Yuan J. Autophagy in cell death: An innocent convict? J Clin Invest. 2005; 115:2679–2688.

26. Huang C, Lee C, Lin H, Chen M, Lin C, Chang J. Autophagy-regulated ROS from xanthine oxidase acts as an early effector for triggering late mitochondria-dependent apoptosis in cathepsin S-targeted tumor cells. PloS one. 2015; 10:e0128045.

27. Elahi M, Matata B. Free radicals in blood: Evolving concepts in the mechanism of ischemic heart disease. Arch Biochem Biophys. 2006; 450:78–88.

28. Finkel T, Holbrook NJ. Oxidants, oxidative stress and the biology of ageing. Nature. 2000; 408:239–247.

29. Yue Z, Friedman L, Komatsu M, Tanaka K. The cellular pathways of neuronal autophagy and their implication in neurodegenerative diseases. Biochim Biophys Acta. 2009; 1793:1496–1507.

30. Yan L, Sadoshima J, Vatner DE, Vatner SF. Autophagy: A novel protective mechanism in chronic ischemia. Cell Cycle. 2006; 5:1175–1177.

31. Scherz-Shouval R, Elazar Z. Regulation of autophagy by ROS: Physiology and pathology. Trends Biochem Sci. 2011; 36:30–38.

32. Zhao G, Shen X, Nan H, Yan L, Zhao H, Yu J, et al. Remifentanil protects liver against ischemia/reperfusion injury through activation of anti-apoptotic pathways. J Surg Res. 2013; 183:827–834.

33. Peart JN, Gross ER, Gross GJ. Opioid-induced preconditioning: Recent advances and future perspectives. Vascul Pharmacol. 2005; 42:211–218.

34. Headrick JP, See Hoe LE, Du Toit EF, Peart JN. Opioid receptors and cardioprotection–'opioidergic conditioning' of the heart. Br J Pharmacol. 2015; 172:2026–2050.

35. Costa-Malaquias A, Almeida MB, Monteiro JRS, de Matos Macchi B, do Nascimento JLM, Crespo-Lopez ME. Morphine protects against methylmercury intoxication: A role for opioid receptors in oxidative stress? PloS One. 2014; 9:e110815.

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