Circulating microRNAs indicate cardioprotection by sevoflurane inhalation in patients undergoing off-pump coronary artery bypass surgery

Abstract

In patients undergoing off-pump coronary artery bypass surgery (OPCAB), it is important to attenuate myocardium injury during the surgery. The present study aimed to observe the cardioprotection induced by sevoflurane induction and maintenance compared with propofol intravenous anesthesia, and to detect its potential protection against acute myocardial injury with sensitive biomarkers. In total, 36 patients undergoing OPCAB were randomly assigned into two groups, receiving sevoflurane (n=18) or propofol (n=18) as the induction and maintenance anesthetic agent. The depth of anesthesia in the two groups was kept at a bispectral index value of 40–50. Physiological and hemodynamic parameters were recorded during the surgery. Cardiac troponin-I (cTnI), creatine kinase-MB (CK-MB), lactate dehydrogenase (LDH) and two microRNAs (miR-499 and miR-208b) were also measured during and subsequent to surgery. Nno statistically significant differences were observed in the physiological and hemodynamic parameters between the two groups prior to surgery. Following surgery, the cardiac output and stroke volume improved significantly in the sevoflurane group (P<0.05). In addition, patients in the sevoflurane group had lower miR-499 (P<0.05) and miR-208b (P<0.01) levels at 12 h after surgery when compared with the propofol group. However, no significant differences in cTnI, CK-MB and LDH levels were observed following surgery between the two groups. In conclusion, volatile induction and maintenance with sevoflurane resulted in some extent of cardiac function improvement in patients undergoing OPCAB. Cardioprotection by sevoflurane is suggested by reduced cardiac injury compared with propofol, and indicated by the sensitive biomarkers, circulating miR-499 and miR-208b.

Introduction

Coronary artery bypass (CAB) grafting is the main surgical treatment for coronary heart disease, which increases oxygen supply by coronary revascularization. Novel surgical techniques have been developed, such as off-pump CAB (OPCAB) surgery, which is currently widely used. OPCAB has a reduced effect on the physiological circulation (1); however, myocardial ischemia-reperfusion injury (MIRI) remains inevitable. Local and systemic inflammatory responses are considered to serve an important role in MIRI, but its development is also associated with the release of free radicals, calcium overload and ATP reduction. MIRI leads to decreased myocardial contractility, apoptosis of myocytes, subendocardial hemorrhage and myocardial infarction (2,3). Therefore, it is important to mitigate MIRI and protect the myocardium during the CAB surgery.

Sevoflurane is an inhaled anesthetic frequently used in cardiac surgery, since it has been reported to provide cardiac protection against MIRI by pre- or post-conditioning (4–9). Pre-conditioning by sevoflurane may improve the long-term outcomes of patients, decrease their mortality and morbidity rates, and prolong their survival (10,11). A previous meta-analysis included 22 studies on sevoflurane, involving 1,922 patients undergoing cardiac surgery (12). The study showed that desflurane and sevoflurane have cardioprotective effects that result in decreased morbidity and mortality. It was also shown that the selection of an anesthetic regimen based on halogenated anesthetics was associated with an improved outcome subsequent to cardiac surgery (12). The majority of previous clinical studies have selected to use inhaled anesthetics in combination with intravenous administration of propofol (12).

Cardiac troponins have been introduced as cardiac markers (13,14). Cardiac troponin I (cTnI) determination has been shown to have a potentially high diagnostic efficacy for cardiac ischemic injury (13). In addition, the nonspecific marker lactate dehydrogenase (LDH) and the cardiac-specific enzyme creatine kinase-MB (CK-MB) are frequently-used markers of cardiac infarction (15). However, these biomarkers are not consistently sensitive following ischemia onset, requiring repetitive measurements (16).

MicroRNAs (miRNAs) are short, non-coding small RNAs that regulate the expression of proteins by translational repression or degradation of mRNAs (17). In the last decade, studies revealed that miRNAs serve a crucial role in cardiac development and homeostasis, and that their expression is altered in the patients with heart diseases (18,19). It was also demonstrated that circulating miRNAs may be potential novel early biomarkers of cardiac injury and may help improve the management of suspected acute coronary syndrome (ACS) patients (20). In particular, miR-208b and miR-499 levels can provide a reasonable prognosis of left ventricular dysfunction (21).

In the present study, sevoflurane inhalation was used to perform volatile induction and maintenance of anesthesia (VIMA), and its effect was compared with that of total intravenous anesthesia (TIVA) with propofol. In addition, the cardioprotection induced by sevoflurane compared with propofol in off-pump CABG was evaluated using miR-208b and miR-499 as diagnostic biomarkers.

Patients and methods

Patient selection

In the present single-center randomized controlled study, 36 patients diagnosed with coronary artery disease and scheduled to undergo OPCAB were enrolled between January 2010 and December 2012. The patient characteristics were as follows: Age, 34–70 years; American Society of Anesthesiology physical status classification II–III; New York Heart Association (NYHA) functional classification II–III; and a body-mass index (BMI) of <30 kg/m². The study was approved by the Ethical Committee of Xiangya Hospital, Central South University (Changsha, China). All ongoing and associated trials for this intervention were registered. Written informed consent was obtained from all the patients. The exclusion criteria included emergency surgery, left ventricular ejection fraction of <40%, diabetes, previous administration of K-ATP channel antagonists or agonists, previous myocardial infarction, history of allergy to anesthetics and abnormal coagulate function. All patients were administered 25–100 mg metoprolol (AstraZeneca plc, London, UK) and 10–20 mg lovastatin (Yangzijiang Pharmaceutical Group, Wuhan, China) per day as preoperative medications. Coronary artery revascularization by OPCAB grafting was performed by one surgeon using two or three coronary vessel grafts per patient and the Octopus 4.3 Tissue Stabilizer (Medtronic, Inc, Minneapolis, MN, USA).

Anesthetic technique

The 36 patients undergoing OPCAB were randomly divided into two groups, namely the sevoflurane and propofol groups (n=18 each). For the random allocation of patients into the groups, a computer-generated list of random numbers was used. Two additional participants were excluded from each group due to a change to the surgical method. In total, 10 mg morphine (Renfu Pharmaceutical Co., Ltd., Yichang, China) and 0.3 mg scopolamine (Hefeng Pharmaceutical, Co., Ltd., Shanghai, China) were administrated 30 min before the anesthesia. The electrocardiogram (ECG), blood pressure (BP), heart rate (HR) and pulse oxygen saturation were continuously monitored using the CARESCAPE Monitor B850 (GE Healthcare, Dallas, TX, USA), and the bispectral index (BIS) value (BIS VISTA™ monitoring system; Aspect Medical Systems, Inc., Norwood, MA, US) was continuously recorded. Invasive monitoring lines, including a radial artery catheter (Edwards Lifesciences Corp., Irvine, CA, USA), a jugular vein catheter (B. Braun Melsungen AG, Melsungen, Germany) and a Swan-Ganz catheter (Edwards Lifesciences Corp.), were inserted under local anesthesia. Anesthesia was induced with 1–8% sevoflurane inhalation (Maruishi Pharmaceutical Co., Ltd., Osaka, Japan) in the sevoflurane group, or with 2–4 mg/kg propofol injection (AstraZeneca plc) in the propofol group, until the BIS reached 45. Subsequent to administration of 1.0 µg/kg sufentanil (Renfu Pharmaceutical Co., Ltd.) and 0.15 mg/kg vecuronium (Enhua Pharmaceutical Group Co., Ltd., Xuzhou, China), the patient was intubated and mechanically ventilated, and the ventilator parameters were adjusted to maintain the end-tidal CO₂ level at 40–45 mmHg. All patients received an intravenous infusion of 10–15 ng/kg/min sufentanil and 1.0 µg/kg/min vecuronium during the surgery. In addition, anesthesia was maintained with a 0.6–1.5 minimum alveolar concentration (MAC) of sevoflurane in the sevoflurane group or 4–8 mg/kg/h propofol in the propofol group, in order to maintain a BIS value of 40–50. Patients received routine monitoring for OPCAB using the Vigilance II Monitor (Edwards Lifesciences Corp.) to monitor the mean arterial pressure (MAP), pulmonary artery mean pressure (PAMP), pulmonary artery wedge pressure (PAWP), central vein pressure and core temperature. Nitroglycerin (Yimin Pharmaceutical Co., Ltd., Beijing, China), esmolol (Qilu Pharmaceutical Co., Ltd., Jinan, China) and phenylephrine (Hefeng Pharmaceutical, Co., Ltd.) were administered, according to hemodynamic parameters.

Hemodynamic parameters, including systolic BP, diastolic BP, MAP and PAMP, were monitored automatically and recorded prior to anesthesia, intraoperatively and postoperatively. In addition, the central venous pressure (CVP), cardiac output (CO) and stroke volume (SV) were recorded using pulmonary artery catheters. Furthermore, blood samples were obtained subsequent to anesthesia induction and surgery, and were immediately centrifuged at 3,000 × g for 10 min at 4°C. The serum was stored at −70°C for measurement of cTnI, CK-MB, LDH, miR-499 and miR-208b expression levels. Laboratory technicians were blinded to the sample groups.

Determination of quantitative cTnI, CK-MB and LDH cardiac marker expression levels using enzyme-linked immunosorbent assay (ELISA)

The details of the series were unknown to any of the investigators who performed the laboratory tests. Circulating cTnI protein concentration was measured by an ELISA. The method was based on a single-step sandwich principle (22), performed according to the instructions of the human cTnI ELISA kit (cat. no. GWB-83A61F; GenWay Biotech Inc., San Diego, CA, US). cTnI measurements were performed in duplicate and recorded by a batch ELISA analyzer (iMark 680 microplate absorbance reader; Bio-Rad Laboratories, Inc., Richmond, CA, US). In addition, the cardiac isoenzymes CK-MB and LDH were detected using commercially available kits (cat. nos. 04525299190 and 11644793001, respectively; Roche Diagnostics, Indianapolis, IN, USA) using an autoanalyzer system (Cobas 4000; Roche Diagnostics).

Determination of miR-208b and miR-499 cardiac marker expression levels using reverse transcription-quantitative polymerase chain reaction (RT-qPCR)

The serum, which had been stored at −70°C in RNAse-free tubes, was processed for miRNA analysis by RT-qPCR. Total RNA was isolated using TRIzol LS reagent (cat. no. 15596-026; Thermo Fisher Scientific Inc., Carlsbad, CA, USA). Genomic DNA contamination was eliminated using a DNAse I kit (cat. no. 89836; Fermentas; Thermo Fisher Scientific Inc., Vilnius, Lithuania) and RNA concentration was quantified with a spectrophotometer (NanoDrop ND-1000; Thermo Fisher Scientific Inc., Wilmington, DE, USA). The RNA integrity of small RNAs was determined using small RNA Chip analysis kit (cat. no. 5067-1548) along with an Agilent 2100 Bioanalyzer (Agilent Technologies Inc., Santa Clara, CA, US). A total of 2 µg DNA-free RNA was reverse transcribed into cDNA using the TaqMan miRNA Reverse Transcription kit (cat. no. 4366596; Thermo Fisher Scientific Inc., Carlsbad, CA, USA). qPCR was performed on a QuantStudio™ 7 Flex Real Time PCR System (Applied Biosystems; Thermo Fisher Scientific, Inc.) using the TaqMan Fast Advanced Master Mix (cat. no. 4444556; Thermo Fisher Scientific, Inc.) and miRNA-specific primers as follows: miR-208b forward, 5′-CCATAAGACGAACAAAAGGT-3′, and reverse, 5′-GTGCAGGGTCCGAGGT-3′; miR-499 forward, 5′-ACAGACTTGCTGTGATG-3′, and reverse, 5′-GTGCAGGGTCCGAGGT-3′; and RNU6 forward, 5′-CTCGCTTCGGCAGCACA-3′, and reverse, 5′-AACGCTTCACGAATTTGCGT-3′ (Applied Biosystems; Thermo Fisher Scientific Inc.). The PCR conditions were as follows: 95°C for 15 min, followed by 35 cycles at 94°C for 15 sec, 55°C for 30 sec and 72°C for 30 sec. RT-qPCR amplification was performed in duplicate using 1:5 diluted RT products for miR-208b and miR-499. All RT-qPCR data were normalized to RNU6, and the RNU6 levels did not differ between the two groups. After normalization for RNU6, the relative gene expression was calculated by the 2^−∆∆Cq method (23).

Statistical analysis

All data for variables are expressed as the mean ± standard deviation. For comparison between the two groups, the Mann-Whitney test was used, while categorical data were analyzed using χ2-test. The hemodynamic and serological data were analyzed using repeated measures analysis of variance (ANOVA), followed by a Bonferroni post-hoc correction or non-parametric test in cases where the ANOVA prerequisite was not met. A P-value of <0.05 was considered to indicate statistically significant differences. GraphPad Prism-5 statistical software (GraphPad Software, Inc., La Jolla, CA, USA) was used for data analysis.

Results

Patient characteristics

The basic characteristics of the patients in the two groups, including gender, age, BMI, NYHA level, the number of grafts and surgery duration, showed no significant differences between the two groups (P>0.05; Table I). In addition, the dosages of sufentanil, vecuronium, nitroglycerin, esmolol, and phenylephrine used in surgery were not significantly different between the two groups (P>0.05). None of these patients required further surgery.

Table I.

Patient characteristics.

Parameter	Sevoflurane group (n=18)	Propofol group (n=18)
Gender, male/female	11/7	13/5
Age (year)	63.3±7.2	61.8±10.8
Body mass index (kg/m2)	26.5±3.2	25.8±2.7
NYHA level, II/III	7/11	8/10
Number of grafts, 2/3	8/10	8/10
Surgery duration (min)	247.8±31.5	253.3±33.7

Data are presented as the mean ± standard deviation or absolute numbers. No statistically significant differences were observed between the two groups (P>0.05).

Hemodynamic and cardiac function measurements

Table II lists the preoperative and postoperative values of various hemodynamic and cardiac function measurements in the two groups. The results demonstrated no statistically significant differences in the preoperative hemodynamic variables, including HR, MAP, CVP, PAWP and PAMP, between the sevoflurane and propofol groups (P>0.05). By contrast, the CO and SV measured by pulmonary artery catheters showed a significant difference between the levels prior to surgery and subsequent to surgery in the sevoflurane group (P<0.05).

Table II.

Intraoperative hemodynamic and cardiac function measurements.

	Sevoflurane group			Propofol group
Measurement	Preoperative	Postoperative	P-value	Preoperative	Postoperative	P-value
HR (beats/min)	71.7±12.5	77.3±10.4	0.163	69.3±11.5	75.6±10.5	0.106
MAP (mmHg)	95.3±14.3	84.1±12.5	0.027	92.1±17.6	78.8±13.4	0.029
CVP (mmHg)	11.4±3.4	12.5±2.7	0.381	10.8±3.0	12.4±2.5	0.067
PAMP (mmHg)	23.0±5.6	25.0±5.7	0.288	22.8±5.1	26.2±6.3	0.092
PAWP (mmHg)	15.7±3.7	16.2±3.4	0.588	15.6±3.1	16.5±3.9	0.482
CO (l/min)	4.5±0.9	5.5±0.7	0.002	4.6±1.1	5.1±1.1	0.121
SV (ml)	62.8±10.7	72.3±12.7	0.034	66.8±12.9	69.1±11.6	0.476

Data are presented as the mean ± standard deviation. No statistically significant differences were observed between the two groups at the same time points (P>0.05). HR, heart rate; MAP, mean arterial pressure; CVP, central venous pressure; PAMP, pulmonary arterial mean pressure; PAWP, pulmonary artery wedge pressure; CO, cardiac output; SV, stroke volume.

Cardiac marker expression

The expression of cTnI, CK-MB and LDH cardiac markers was determined using ELISA. As shown in Fig. 1, the protein expression of cTnI at 12 h after surgery was significantly increased in both groups, when compared with the corresponding preoperative values (P<0.01). The CK-MB levels were found to be significantly increased at 12 h after surgery in the propofol group only (P<0.01; Fig. 2A), whereas significantly increased levels of LDH were observed at 12 h after surgery in both groups (P<0.01; Fig. 2B). However, no significant differences were detected between the two groups in the expression of these variables (Figs. 1 and 2).

Figure 1.

cTnI expression levels preoperatively (T1), and at 6 h (T2), 12 h (T3) and 24 h (T4) after surgery. **P<0.01 vs. the preoperative level in the sevoflurane group; ^##P<0.01 vs. the preoperative level in the propofol group. No significant difference was observed between the two groups at T3 and T4. Data are presented as the mean ± standard deviation. cTnI, cardiac troponin I; NS, not significant.

Figure 2.

CK-MB and LDH expression levels prior to surgery and at 12 h after surgery. (A) CK-MB: ^##P<0.01 vs. prior to surgery. (B) LDH: **P<0.01 vs. prior to surgery in the sevoflurane group; ^##P<0.01 vs. prior to surgery in the propofol group. No significant difference was observed between the two groups at 12 h after surgery. Data are presented as the mean ± standard deviation. CK-MB, creatine kinase-MB; LDH, lactate dehydrogenase; NS, not significant.

The expression levels of miR-499 and miR-208b were detected using RT-qPCR, and were found to be increased following surgery in both anesthesia groups, although the difference was only significant in the propofol group (P<0.05; Fig. 3). There was no significant difference between the two groups prior to surgery (P>0.05; Fig. 3). However, at 12 h after surgery, the levels of the two miRNA markers were significantly reduced in the sevoflurane group when compared with the propofol group (P<0.05; Fig. 3).

Figure 3.

Relative expression levels of (A) miR-499 and (B) miR-208b. miR-499 and miR-208b were significantly increased from preoperative baseline to 12 h after surgery in the propofol group (^##P<0.01 and ^#P<0.05). The level of miR-499 was significantly lower in the sevofluorane group when compared with the propofol group at 12 h after surgery (P<0.05). The level of miR-208b was also significantly lower in the sevoflurane group at 12 h after surgery (P<0.01). Data are presented as the mean ± standard deviation.

Discussion

Previous studies have suggested that sevoflurane exerts a cardioprotective effect, mitigating myocardial damage, reducing the levels of CK-MB and cTnI, reducing the infarction area, and decreasing the incidence of arrhythmia and cardiac dysfunction (6–9). A recent study demonstrated that rat heart infarct size was significantly reduced in the sevoflurane preconditioned group compared with that in the ischemia/reperfusion group (24). The underlying mechanisms may include nuclear factor-κB activation, upregulation of autophagy, and the attenuation of tumor necrosis factor-α, interleukin-1β and caspase-3 expression (25–27). Another study found that sevoflurane preconditioning mediates against MIRI via caveolin-3-dependent cyclooxygenase-2 inhibition and antioxidative effects (28). In addition, sevoflurane postconditioning for 5 min was sufficient to activate protein kinase B and exert maximal cardioprotection against MIRI in isolated rat hearts (29). However, these studies used sevoflurane pre- or post-conditioning, along with propofol for induction and maintenance. Zaugg et al (30) found that propofol was able to cancel the cardioprotective effect of sevoflurane in a concentration-dependent manner. By contrast, certain other studies suggested the same protective effect for propofol (31,32). Therefore, it is not certain which of the two drugs is mainly responsible for cardioprotection. The results of Jovic et al (33) indicated that sevoflurane and propofol led to cardiac protection via different mitochondrially-associated molecular mechanisms. It appears that sevoflurane acts by regulating cytochrome c oxidase and ATP synthase, while the effects of propofol occur through regulation of cytochrome c, connexin 43, mtDNA transcription and uncoupling protein 2 (33). Other studies also showed the superiority of sevoflurane over propofol anesthesia. For instance, Ballester et al (34) compared the influence of sevoflurane and propofol on the levels of myocardial oxidative stress markers (F2-isoprostanes and nitrates/nitrites) in coronary sinus blood samples from patients undergoing OPCAB. Their data suggested that sevoflurane showed improved antioxidative properties compared with propofol (34).

In the present study, sevoflurane inhalation for VIMA without propofol was used to observe its clinical effect in comparison with propofol TIVA. Our data showed that there was no significant difference between the sevoflurane group and propofol group in hemodynamic variables and cardiac function, which is similar to the results of previous studies (35). The CO and SV of patients were higher subsequent to surgery in the sevoflurane group. Although the difference between the two group following surgery was not significant, sevoflurane may potentially benefit the clinical outcome.

Myocardial damage leads to the release of specific enzymes from myocardial cells into the blood. The most common enzymes include cTnI, CK-MB and LDH. cTnI has a high degree of myocardial specificity and sensitivity and is considered as a ‘gold marker’ of myocardial infarction (36). Numerous previous studies have investigated the influence of sevoflurane on myocardial enzyme levels in patients undergoing CABG, and the results have been contradictory (37–40). Law-Koune et al (37) and Hemmerling et al (38) found no difference between sevoflurane and propofol in their effects on cTnI and CK-MB in patients undergoing OPCAB (37,38). However, two other studies showed the advantage of sevoflurane over propofol by reducing the levels of cardiac markers (39,40). In the current study, the increase in the levels of cTnI following surgery was less in the sevoflurane group compared with the propofol group; however, the difference was not statistically significant. The influence of sevoflurane on cTnI may be associated with its inhaled concentration. Exposure to 2.8 vol% sevoflurane provides a better functional return and a lower percentage of infarction on reperfusion compared with 1.4 vol% sevoflurane (40). In the current study, the depth of anesthesia was adjusted by BIS (value, 40–50), so that only a low inhaled concentration of sevoflurane (1.35±0.79 vol%) was required for the majority of time, with the exception of the induction period (8 vol%). Piriou et al (41) also found that inhaled sevoflurane at 1MAC for 15 min had limited impact on cTnI. The CK-MB levels significantly increased in the sevoflurane and propofol groups following surgery. However, compared with the propofol group, CK-MB expression was significantly lower in the sevoflurane group after the surgery. Vikenes et al (42) identified that CK-MB was superior to the cardiac troponins in predicting long-term event-free survival subsequent to elective cardiac surgery in low-risk patients with stable symptoms undergoing CAB grafting. Furthermore, LDH is a nonspecific marker of myocardial injury, and LDH activity in the serum can be released from various types of damaged cells (43). In the present study, LDH expression increased following surgery in both groups; however, this was not significantly different between the two groups.

miRNAs are short non-coding RNAs, approximately 18–25 nucleotides long, which act as negative or positive regulators, primarily post-transcriptionally. Besides their intracellular function, recent studies have demonstrated that miRNAs can be exported or released by cells and circulate within the blood in a remarkably stable form (44,45). The circulating miRNA patterns may be used as biomarkers for cardiovascular diseases. miR-499 and miR-208b are specifically expressed in myocardial tissue (46,47). Recent animal experiments and clinical studies revealed that miR-499 and miR-208b increased subsequent to myocardial injury, and the degree of increase was positively correlated with the increase in cTnI levels (48,49). Their diagnostic accuracy was found to be superior to other traditional biomarkers. Gidlof et al (50) collected plasma samples from 424 patients with suspected ACS treated in a coronary care unit, in order to measure cardio-enriched miRNAs. The authors found that miR-208b and miR-499 expression levels were higher in myocardial infarction patients, and established the association of increased miRNA levels with reduced systolic function subsequent to myocardial infarction and the risk of mortality or heart failure (50). The level of miR-499 in the plasma is very low in healthy individuals. Within 1–3 h after myocardial damage, this level begins to increase and reaches a peak at 3–12 h, and then decreases after 12–24 h (51). By contrast, miR-208b cannot be detected in healthy individuals, but appears in the plasma 1 h after myocardial injury, reaching a peak level at 3 and then decreasing after 12 h (46). A study by Ishikawa et al (52) showed that anesthetics cause numerous miRNA expression changes, and that the miRNA expression pattern was particular for each anesthetic, such as sevoflurane or propofol. Tanaka et al (53) found dynamic changes in miRNA expression caused by sevoflurane anesthesia on rats suffering from lung diseases.

The results of the present study showed that miR-499 and miR-208b were higher subsequent to surgery compared with those prior to surgery in both anesthesia groups. In addition, the two miRNA biomarkers were much lower in the sevoflurane group compared with the propofol group subsequent to surgery. This confirmed that the cardioprotective effect of sevoflurane on patients undergoing OPCAB is superior to that of propofol. Furthermore, the current study established an association between sevoflurane and miRNAs in patients undergoing OPCAB for the first time. The small number of patients included in the study limits our conclusion, and thus larger numbers should be used to further assess the cardioprotective effect of sevoflurane. Whether the results can be extended to other cardiac patients requires further research.

In conclusion, the present study demonstrated that VIMA with sevoflurane in patients undergoing OPCAB resulted in improved cardiac protection compared with propofol TIVA, and this effect was indicated based on the levels of two sensitive biomarkers, circulating miR-499 and miR-208b.