1. Introduction
Doxorubicin, an anticancer drug extracted from
Streptomyces peucetius var Caesius, has been shown to be highly effective against various human malignancies [
1]. However, its successful use in clinical cancer treatment has been limited due to its association with cardiotoxicity. Doxorubicin is known to induce cardiotoxicity in a dose-dependent manner, while it exerts different effects across individuals based on gender, age and time of cardiotoxicity onset [
1]. Complex mechanisms underlie doxorubicin-induced cardiotoxicity, one of which is associated with reactive oxygen species (ROS)-induced apoptosis in mitochondria, which leads to congestive heart failure [
2,
3,
4]. Many reports have shown that doxorubicin accumulates in cardiomyocyte mitochondria at a concentration one hundred times higher than that in the extracellular space [
5,
6]. Lipid emulsion, which was originally developed for parenteral nutrition, is now also used clinically as drug delivery vehicles (for example, propofol and etomidate) that do not induce severe side effects [
7]. In addition, lipid emulsion is effective at treating systemic toxicity induced by local anesthetics and other drugs with high lipid solubility [
8]. Lipid nanoemulsion with doxorubicin and oleic acid reduces the doxorubicin concentration in the heart and increases the blood concentration of doxorubicin [
9]. Furthermore, α-linolenic acid, a long-chain fatty acid present in Intralipid
®, inhibits the cardiotoxicity induced by doxorubicin [
10]. However, as intravenously administered fats do not pass through the gastrointestinal tract, these fats do not undergo pancreatic lipase-induced hydrolysis, bile-induced emulsification or transformation into chylomicron [
11]. Thus, in contrast to fatty acids, lipid emulsions for intravenous administration are prepared to be similar to the structure of chylomicron delivered into a hydrophilic environment, and lipid emulsions contain triglycerides (one glycerol plus three fatty acids), phospholipids (an emulsifier), and glycerin (an osmotic agent) [
11]. The mechanisms underlying lipid emulsion treatment include the scavenging effect, the inotropic effect, fatty acid supply, reversal of mitochondrial dysfunction, glycogen synthase kinase (GSK)-3β phosphorylation, inhibition of nitric oxide release, and attenuation of a cardiac sodium channel blockade [
8]. Moreover, lipid emulsion attenuates lung injury induced by acute malathion toxicity via reducing oxidative stress [
12]. Based on these previous reports, we tested the hypothesis that lipid emulsion attenuates doxorubicin-induced apoptosis by inhibiting oxidative stress [
2,
3,
4,
8,
10,
12]. The goal of this in vitro study was to examine the effect of lipid emulsion (Intralipid
® 20%) on the apoptosis induced by doxorubicin in H9c2 rat cardiomyoblasts and to elucidate the associated cellular mechanism.
2. Materials and Methods
All experimental methods and protocols were performed in accordance with the Regulation for the Care and Use of Laboratory Animals stipulated by Gyeongsang National University.
2.1. Cell Culture
H9c2 rat cardiomyoblasts obtained from the American Type Culture Collection (Manassas, VA, USA) were cultured in Dulbecco’s modified Eagle’s medium (DMEM, HyClone, GE Healthcare, Salt Lake City, UT, USA) supplemented with 10% fetal bovine serum, 100 U/mL penicillin, and 100 mg/mL streptomycin as described previously [
13,
14]. Cells were cultured in 100-mm dishes at 37 °C in 5% CO
2 and sub-cultured in 1:4 ratios upon reaching 90% confluence. All subsequent experiments were conducted using cells of at least passage 3.
2.2. Cell Viability Assay
Cell viability was estimated colorimetrically using the 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay as previously reported [
13,
14]. Cells were seeded on a 24-well plate at a density of 10
5 cells/well and were treated with doxorubicin (10
−6, 3 × 10
−6 and 10
−5 M) alone for 24 h, treated with lipid emulsion (0.125, 0.25, 0.75 and 2%) alone for 25 h, or pretreated with lipid emulsion (0.125, 0.25, 0.75 and 2%) for 1 h followed by doxorubicin (10
−5 M) for 24 h. After incubation, the cells were washed twice with phosphate buffered saline (PBS, pH 7.4), treated with MTT in PBS (0.5 mg/well), and then incubated for 4 h at 37 °C in the dark. After incubation, the MTT solution was removed, and the formazan crystals formed in each well were dissolved in 200 μL of dimethyl sulfoxide for 20 min at 37 °C under gentle shaking. The absorbance was measured spectrophotometrically using VersaMax
® (Molecular Devices, Sunnyvale, CA, USA) at 570 nm. Untreated cells were used as controls. Intralipid
® (20%), used in this study, is composed of 20% soya bean oil, 1.2% egg yolk phospholipid, 2.25% glycerin and water for injection [
15]. The fatty acid composition of Intralipid
® includes linoleic, oleic, palmitic, linolenic and stearic acid [
15].
2.3. Apoptosis Assay
2.3.1. Annexin V-FITC-PI Staining
To detect the apoptosis induced by doxorubicin in H9c2 cells, a FITC Annexin V Apoptosis Detection Kit (Invitrogen-Life Technologies, Carlsbad, CA, USA) was used, and a flow cytometric analysis was performed. Briefly, cells were cultured in 6-well plates at 3 × 105 cells/well and were then treated with doxorubicin (10−5 M) alone for 6 h, treated with lipid emulsion (0.25%) alone for 7 h, or pretreated with lipid emulsion (0.25%) for 1 h followed by doxorubicin (10−5 M) for 6 h. Following the treatment, the cells were washed three times with cold PBS (pH 7.4), resuspended in 1× binding buffer and stained with Annexin V-FITC and propidium iodide (PI) for 10 min at room temperature in the dark. Finally, the cells were resuspended in 400 μL of 1× binding buffer and immediately analyzed by flow cytometry. The cell viability and apoptosis rates were measured on a FC-500 flow cytometer (Beckman Coulter, Pasadena, CA, USA) using 488-nm laser excitation and fluorescence emission at 530 nm (FL1) and >575 nm (FL3). A total of 20,000 cells per treatment condition were acquired from three independent experiments and analyzed using Beckman Coulter CPX software (Beckman Coulter, CXP 2.2, Mervue Business Park, Mervue, Galway, Ireland). For forward and side scatter measurements, linear amplification was applied, and logarithmic amplification was used for all fluorescence measurements. Quadrant analysis was performed on the gated fluorescence dot plot to quantify the percentages of live, necrotic and apoptotic cell populations.
2.3.2. TUNEL Assay for Late Apoptosis Detection
To detect whether doxorubicin induces late apoptosis in H9c2 cells, a terminal deoxynucleotidyl transferase dUTP nick end-labeling (TUNEL) assay was conducted as previously reported [
16,
17]. Briefly, 10
5 cells/well were cultured on coverslips in a 24-well plate and then treated with doxorubicin (10
−5 M) alone for 6 h, treated with lipid emulsion (0.25%) alone for 7 h, or pretreated with lipid emulsion (0.25%) for 1 h followed by doxorubicin (10
−5 M) for 6 h. After treatment, a TUNEL assay was performed using a TUNEL kit (Roche, Indianapolis, IN, USA) according to the manufacturer’s instructions, and cells were counterstained with 4′,6-diamidino-2-phenylindole (Sigma Chemical Company, St. Louis, MO, USA). TUNEL-positive cells emitting fluorescence were visualized under a Fluoview 500 fluorescence microscope (Olympus, Tokyo, Japan). Three nonoverlapping fields per coverslip were counted per treatment, and the number of TUNEL-positive cells was calculated.
2.4. Estimation of ROS Generation
ROS generation was measured using the fluorescent dye 2,7-dichlorodihydrofluorescein diacetate (DCFH-DA) after treatment with doxorubicin. Briefly, H9c2 cells (106 cells/well) were cultured in a 24-well plate and then treated with doxorubicin (10−5 M) alone for 1 h, pretreated with lipid emulsion (0.25%) or α-linolenic acid (10−6 M) for 1 h followed by doxorubicin (10−5 M) for 1 h, or treated with lipid emulsion (0.25%) or α-linolenic acid (10−6 M) alone for 2 h. After the treatment, the cells were washed three times with PBS and stained with 5 μM DCFH-DA in PBS for 30 min at room temperature in the dark. The fluorescence intensity was measured using a FC-500 flow cytometer, and the results were analyzed using Beckman Coulter CPX software (Beckman Coulter).
2.5. Measurement of Antioxidants
The malondialdehyde (MDA) level, superoxide dismutase (SOD) activity, and catalase activity were evaluated using commercial detection kits for the respective assays. Briefly, H9c2 cells were grown to 70% confluence and then incubated in starvation media (DMEM without FBS) overnight. Next, the cells were treated with doxorubicin (10−5 M) alone for 24 h, pretreated with lipid emulsion (0.25%) for 1 h, followed by doxorubicin (10−5 M) for 24 h, or treated with lipid emulsion (0.25%) alone for 25 h. After treatment, the cells were washed with cold PBS, adherent cells were removed, and protein was extracted according to the manufacturer’s protocol using the respective kits. The protein concentration was estimated using the Bradford method. Lipid peroxidation (MDA) was estimated using a kit (Abcam, Cambridge, United Kingdom) according to the manufacturer’s protocol, and the optical density (OD) was measured at 532 nm using a VersaMax® microplate reader (Molecular Devices). The MDA concentrations in the treated samples were calculated using the formula described in the kit. Both SOD and catalase activity was detected using kits (Abcam) according to the manufacturer’s instructions. The OD was measured at 450 nm using the VersaMax® microplate reader (Molecular Devices), and the activity was calculated from the assay results.
2.6. Western Blot Analysis
Following treatment, proteins were extracted, and the total protein concentrations were determined using the Bradford method as previously reported [
13]. The sample protein from the cell lysate was mixed with 5× sodium dodecyl sulfate sample buffer (0.1 M Tris-HCl, 20% glycerol, 4% sodium dodecyl sulfate and 0.01% bromophenol blue). Aliquots of proteins (50 µg) were separated by 10% or 12% sodium dodecyl sulfate-polyacrylamide gel electrophoresis for 150 min at 80 V, and the separated proteins were electrophoretically transferred to polyvinylidene difluoride membranes at 190 mA for 2 h. The membranes were then blocked with 5%
w/
v nonfat dried milk or 5% bovine serum albumin in Tris-buffered saline containing Tween-20 (TBST) for 1 h at room temperature and incubated with specific primary antibodies (anti-Bax [1:500], anti-Bcl-XL [1:500], anti-cleaved caspase-3 [1:1000], anti-cleaved caspase-8 [1:1000], anti-GSK-3β [1:1000], anti-phospho-GSK-3β [1:1000], and anti-β-actin [1:2500]), which were diluted in TBST containing 5%
w/
v skim milk or 5% bovine serum albumin, overnight at 4 °C. After incubation, the membranes were washed 3 times with TBST and incubated with a horseradish peroxidase-conjugated anti-rabbit or anti-mouse IgG secondary antibody diluted 1:5000 in TBST containing 5%
w/
v skim milk for 1 h at room temperature. The membranes were washed in TBST, and the immunoreactive signals were detected using enhanced chemiluminescence (SuperSignal
® West Pico Chemiluminescent Substrate, Thermo Scientific, Rockford, IL, USA) and transferred onto an X-ray film (SuperRX-N Fuji Medical X-ray Film, Tokyo, Japan). The band intensity was measured using densitometry.
2.7. Determination of Mitochondrial Membrane Potential
JC-1 staining was employed to assess the mitochondrial membrane potential (MMP) according to the manufacturer’s protocol (Biotium, Hayward, CA, USA). Briefly, H9c2 cells (4 × 103 cells/100 μL) were cultured on glass coverslips coated with poly-l-lysine and in 96-well black plates for fluorescence microscopy and fluorescence ratio detection, respectively. The cells were treated with doxorubicin (10−5 M) for up to 6 h or with lipid emulsion (0.25%) for 1 h followed by doxorubicin for 6 h. In addition, cells were treated with lipid emulsion alone for 7 h. The chemically treated cells were stained with 1× MMP-sensitive JC-1 reagent at 37 °C for 15 min and washed with 1× PBS. The changes in MMP were measured using a confocal laser scanning microscope equipped with a fluorescence system (IX70 Fluoview, Olympus, Tokyo, Japan). Green JC-1 monomers and red aggregates were detected with 488 nm and 529 nm lasers, respectively. The JC-1 ratio was measured using a GloMax explorer (Promega, Madison, WI, USA), and the ratio was obtained by dividing the red fluorescence value by the green fluorescence value.
2.8. Chemicals and Media
All chemicals, the anti-β-actin antibody and DCFH-DA were obtained from Sigma Chemical Company. Intralipid® 20% was purchased from Fresenius Kabi Korea (Seoul, Korea). The anti-Bax and anti-Bcl-XL antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA, USA). The anti-cleaved caspase-3, anti-cleaved caspase-8, anti-GSK-3β, and anti-phospho-GSK-3β antibodies were obtained from Cell Signaling Technology (Beverly, MA, USA). Media, serum and buffers were obtained from Gibco (Invitrogen, Burlington, ON, Canada).
2.9. Statistical Analysis
Data are shown as the mean ± SD. The effects of lipid emulsion on the decreased cell viability, apoptosis, expression of cleaved caspase-3 and cleaved caspase-8, Bax/Bcl-XL ratio, and GSK-3β phosphorylation induced by doxorubicin were analyzed by one-way analysis of variance (ANOVA) followed by Bonferroni’s multiple comparison test. The effects of lipid emulsion on DCFH-DA, MDA, SOD, catalase and MMP induced by doxorubicin were analyzed by one-way ANOVA followed by Bonferroni’s multiple comparison test or Tukey’s multiple comparison test. A p value less than 0.05 was considered statistically significant.
4. Discussion
This is the first study to suggest that lipid emulsion attenuates the doxorubicin-induced late apoptosis of rat cardiomyoblasts, and this effect appears to be associated with the inhibition of oxidative stress (
Figure 7). The major findings of this in vitro study are as follows: (1) Lipid emulsion inhibited the cell viability reduction induced by doxorubicin; (2) lipid emulsion inhibited the late apoptosis induced by doxorubicin; and (3) lipid emulsion inhibited the increased ROS and MDA induced by doxorubicin, whereas lipid emulsion pretreatment reversed the decreased SOD and catalase activity and the reduced MMP induced by doxorubicin.
Extensive efforts have been dedicated to reducing doxorubicin-induced cardiotoxicity to improve the therapeutic potential of doxorubicin; however, due to the complex molecular mechanism underlying doxorubicin-induced cardiotoxicity, limited success in reducing its toxicity to cardiomyocytes has been achieved [
18,
19,
20,
21]. The two main mechanisms considered to be important in doxorubicin-induced cardiotoxicity are oxidative stress and cardiomyocyte apoptosis [
2,
22,
23], the latter of which contributes to heart failure [
24,
25]. The mechanism associated with the apoptosis observed in doxorubicin-induced cardiotoxicity has been extensively investigated, and multiple pathways are known to be involved in apoptotic cell death [
16,
26]. Lipid emulsion reversed the cell viability decrease induced by bupivacaine or verapamil in H9c2 cells [
13,
14]. Similar to these previous reports, the results presented herein demonstrated that lipid emulsion attenuated the decreased cell viability induced by doxorubicin, as determined by the MTT assay (
Figure 1B) [
13,
14]. α- and γ-linolenic acid, which are long-chain fatty acids, counteract the cardiotoxicity of doxorubicin [
10,
27]. However, this is the first study to employ lipid emulsion as a whole to counterbalance doxorubicin-induced cardiotoxicity in H9c2 cells. The long-chain fatty acids present in Intralipid
® (with 100% long-chain fatty acids) include 53% linoleic acid, 24% oleic acid, 11% palmitic acid, 8% α-linolenic acid and 4% stearic acid, but which long-chain fatty acid is mainly involved in the lipid emulsion-mediated attenuation of doxorubicin-induced decreased cell viability in H9c2 rat cardiomyoblasts remains to be determined [
7].
Lipid emulsion attenuates the increased expression of caspase-8 and/or Bax induced by verapamil, bupivacaine and malathion in rat cardiomyoblasts and lung tissue [
12,
13,
14]. In addition, lipid emulsion attenuates apoptosis induced by toxic doses of bupivacaine and verapamil in H9c2 rat cardiomyoblasts [
13,
14,
28,
29]. Similar to previous reports, Annexin-V-FITC/PI staining revealed that doxorubicin alone induced late apoptosis in H9c2 cells, and pretreatment with lipid emulsion decreased the late apoptosis induced by doxorubicin, which was further confirmed by the TUNEL assay [
13,
14,
28,
29]. Thus, our current results demonstrate that lipid emulsion have a protective effect on the late apoptosis induced by doxorubicin in H9c2 rat cardiomyoblasts. An in-depth evaluation of the apoptotic signaling pathway revealed that doxorubicin initiates apoptosis by increasing the expression of the intrinsic proapoptotic protein Bax and the extrinsic proapoptotic protein cleaved caspase-8, which stimulates the caspase cascade, ultimately activating cleaved caspase-3 and inducing cell death [
30]. In contrast to the effects of doxorubicin alone, lipid emulsion pretreatment activates the anti-apoptotic protein Bcl-XL and inhibits the expression of the proapoptotic protein Bax, thereby suppressing apoptosis and rescuing the cell from programmed cell death, as evidenced in our present findings. GSK-3β activates the proapoptotic protein Bax and capsase-3 in mitochondria, which leads to apoptosis [
31]. However, GSK-3β phosphorylation attenuates mitochondrial apoptosis via attenuation of cytochrome c release [
31]. Pretreatment with the GSK-3β inhibitor SB216763 followed by doxorubicin partially reversed the decreased cell viability induced by doxorubicin alone (
Figure 1D). Furthermore, the combined treatment with lipid emulsion and doxorubicin had no significantly different effects on the cell viability, as compared with the combined treatment with SB216763, lipid emulsion and doxorubicin (
Figure 1D). These results suggest that doxorubicin-induced decreased cell viability is partially mediated by GSK-3β activation. Consistent with the cell viability results of the current study, lipid emulsion reversed the decreased GSK-3β phosphorylation induced by doxorubicin (
Figure 3E), which is associated with GSK-3β inactivation and may subsequently lead to anti-apoptosis. Considering a previous report, the lipid emulsion-mediated reversal of the decreased GSK-3β phosphorylation induced by doxorubicin may partially contribute to lipid emulsion-mediated anti-apoptosis via decreasing the Bax/Bcl-XL ratio [
31].
Doxorubicin is known to cause oxidative stress-mediated cardiotoxicity via the formation of ROS and induction of cardiac dysfunction [
32]. Doxorubicin is one hundred times more concentrated in mitochondria than in plasma. Redox cycling of doxorubicin in mitochondria generates high levels of ROS, including superoxide anions and hydrogen peroxide, causing oxidative stress in cardiomyocytes and leading to cell damage [
6,
32]. Oxidative stress is associated with the imbalance induced by excessive oxygen free radicals that exceed the antioxidant response [
33]. Cell membranes are composed of polar lipids and their peroxidation, which is due to the attack of excessive ROS on polyunsaturated fatty acids, results in cell damage and death [
34]. Oxidative stress in the cell causes high lipid peroxidation, resulting in the release of MDA, the product of lipid peroxidation by free radicles [
34]. Excessive ROS production induces apoptosis via interacting with critical signaling molecules, including apoptosis signal-regulated kinase [
33]. Consistent with a previous report, doxorubicin increased ROS production, as shown in
Figure 4A,B, whereas lipid emulsion attenuated the increased production of ROS induced by doxorubicin (
Figure 4A,B) [
35]. MDA was increased by doxorubicin (
Figure 5A), whereas lipid emulsion pretreatment inhibited the increased MDA induced by doxorubicin (
Figure 5A). Lipid emulsion attenuates the increased MDA concentration and ROS production induced by bupivacaine, which leads to attenuation of apoptosis [
29]. Similar to this previous report, the results presented herein suggest that lipid emulsion attenuates the oxidative stress induced by doxorubicin, which appears to contribute to the inhibition of apoptosis induced by doxorubicin in H9c2 rat cardiomyoblasts [
29]. In addition, similar to this result, α-linolenic acid—a long-chain fatty acid found in Intralipid
®—inhibits cardiotoxicity by decreasing oxidative stress and apoptosis [
10]. As α-linolenic acid partially inhibited the increased amount of ROS evoked by doxorubicin (
Figure 4C), the lipid emulsion-mediated inhibition of ROS increased by doxorubicin may be partially due to the α-linolenic acid contained in Intralipid
® [
7]. ROS induced by doxorubicin-induced oxidative stress in cardiomyocytes are controlled by antioxidant enzymes, including SOD, catalase, and glutathione peroxidase [
36,
37]. SOD and catalase inhibit apoptosis by removing superoxide anions and hydrogen peroxide, respectively [
38]. Lipid emulsion was reported to reverse the inhibited activity of SOD or catalase induced by bupivacaine and malathion, leading to anti-apoptosis and decreased lung injury [
12,
29]. Consistent with these previous reports, the lipid emulsion-mediated reversal of the decreased activity of SOD and catalase induced by a toxic dose of doxorubicin observed in the current study appears to contribute to the anti-apoptosis of rat cardiomyoblasts [
12,
29].
Intrinsic mitochondrial apoptosis leads to mitochondrial membrane depolarization and mitochondrial outer membrane permeabilization, and doxorubicin reduces the MMP and calcium retention capacity [
39,
40]. Combined treatment with lipid emulsion and bupivacaine increases the MMP more than bupivacaine alone [
29]. In addition, the mitochondrial respiratory function in the cardiac depression induced by bupivacaine is enhanced by lipid emulsion [
41]. Consistent with these previous reports, doxorubicin decreased the MMP in H9c2 rat cardiomyoblasts, whereas lipid emulsion reversed the attenuated MMP induced by doxorubicin (
Figure 6) [
29,
40].
As lipid emulsion has been clinically used for parenteral nutrition, lipid-soluble drug delivery, and the treatment of drug toxicity without inducing severe side effects, lipid emulsion may be able to be clinically used to attenuate the cardiotoxicity induced by doxorubicin [
7,
11]. However, extrapolation of the results of this in vitro study to clinical applications has some limitations. First, the median plasma concentration of doxorubicin and the steady-state plasma concentration of doxorubicin in patients treated with doxorubicin are approximately 10
−7 and 4.3 × 10
−7 M doxorubicin, respectively [
32,
42]. The supraclinical concentration (10
−5 M) of doxorubicin used in the current study, which induced apoptosis in rat cardiomyoblasts, may be encountered in cardiac mitochondria because doxorubicin-induced cardiac toxicity is associated with a cumulative dose of doxorubicin, and the doxorubicin concentration in cardiac mitochondria is one hundred times more than that in extracellular fluid [
6,
43]. However, lipid emulsion may also inhibit the therapeutic effect (for example, apoptosis) of doxorubicin on cancer cells. As the effect of lipid emulsion on doxorubicin-induced apoptosis may be dependent on the type of cell, organ and concentration of doxorubicin, further study to examine whether lipid emulsion interferes with the antitumor activity of doxorubicin in cancer cells is needed. Second, pretreatment with lipid emulsion attenuated the doxorubicin-induced apoptosis of cardiomyoblasts in the current study, whereas posttreatment with lipid emulsion is clinically used to alleviate cardiotoxicity followed by toxic doses of local anesthetic or other drugs. Third, this study used H9c2 rat cardiomyoblasts instead of human cardiac myocytes.