The protective effect of activating Nrf2 / HO-1 signaling pathway on cardiomyocyte apoptosis after coronary microembolization in rats
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Myocardial apoptosis is closely related to myocardial injury caused by coronary microembolization (CME).Nuclear factor erythroid 2-like (Nrf2) has been taken into account as an inhibitor of apoptosis in various tissues. Thus, this research aims to investigate which part Nrf2/HO-1 signaling pathway plays in myocardial apoptosis process following the effect of CME on rats.
Separate 40 rats then form them into a group of shame, a group of CME, a group of CME plus AAV-Nrf2(AAV-Nrf2 (CME) group) and a group of CME plus AAV-control (AAV-control (CME) group) stochastically and averagely. Rat CME was established by injecting into the left ventricular chamber, with or without pretreatment of adeno-associated virus Nrf2 (AAV-Nrf2). Echocardiological measurements, using Terminal-deoxynucleoitidyl Transferase Mediated Nick End Labeling (TUNEL) to stain, conducting Quantitative PCR in real time (RT-PCR) as well as Western blotting to evaluate the impacts of them functionally, morphologically and molecularly in CME.
Nrf2 decreased in cardiomyocytes after CME. Upregulation of Nrf2 inside an organism through AAV connect to improving the function of heart as well as attenuating myocardial apoptosis, following the restrain of proapoptotic mRNAs and proteins like caspase-3, caspase-9 and bax expressing as well as the increase of antiapoptotic mRNA and proteins like HO-1 and bcl-2 expressing.
Activation of Nrf2/HO-1 pathway can improve CME-induced cardiac dysfunction effectively and also reduce the myocardial apoptosis.
KeywordsNuclear factor erythroid 2-like Heme oxygenase-1 Coronary microembolization Apoptosis
Analysis of variance
Nuclear factor erythroid 2-like
Reverse Transcription-Polymerase Chain Reaction
Tris-buffered saline tween
TdT-mediated dUTP Nick-End labeling
Coronary microembolization (CME) is among those vital causes of dysfunctional heart without atherosclerotic obstacle inside the epicardial coronary artery. Tens of years ago, CME was discovered at postmortem for the first time in patients who died as a result of a unexpected cardiac events . Nevertheless, CME, following thrombolytic treatment and coronary disturbances for patients suffering a coronary thrombus, is becoming more regularly , or a remote arteriole thrombus in a spontaneous lysis. CME may cause myocardial perfusion-contraction mismatch, arrhythmias, inflammation and micro-infarction and so on, which can possibly result in harmful or fatal consequences [3, 4, 5, 6, 7, 8]. CME is a fundamental reason of non-blocked coronary artery illness. Numerous investigations have evidenced the underlying mechanisms of CME-induced myocardial damage as well as relieve the deleterious effects of CME. A considerable amount of studies demonstrated that cardiomyocyte apoptosis was a vital part of the mechanism of CME-induced myocardial damage [9, 10, 11], and extra modulatory mechanisms still need to be explained because of the overall complexity of myocardial injury.
Heme oxygenase-1(HO-1) is a phaseIIdefense enzyme which has potent antiapoptotic as well as antioxidative stress effects. In those HT22 cells, HO-1 is over expressed which confer antiapoptotic protective effects against H/R . Nuclear factor erythroid 2-like (Nrf2) is a primary element of transcription. It adjusts numerous ways of apoptosis in a cell . Recent studies have paid more attention to the Nrf2/HO-1 approach that is a key part in the apoptosis and that regulates and lowers the cardiomyocyte apoptosis .
The purpose of the current research was in order to determine the part of Nrf2/HO-1 in CME-induced myocardial apoptosis. Here, we focused on the interactions of Nrf2/HO-1 pathway with the bcl-2, bax, caspase3 and caspase9 in CME-induced myocardial apoptosis. The study suggested that Nrf2/HO-1 was a major part in CME-induced myocardial apoptosis and activation of Nrf2/HO-1 pathway could remarkably restrain apoptosis in CME-induced myocardial as well as enhance the function of heart. We supplied a possible CME-induced myocardial apoptosis mechanism.
Sprague-Dawley rats (250-300 g) were gained from the Animal Center of the Guangxi Medical Collage which is in Nanning, China. During every phase of this experiment, the rats were raised with manipulated light status, moisture, with clean water and feed provided unlimited. All the procedures were authorized and supervised by the Animal Experiment Ethics Committees of Guangxi Medical Collage.
Design, synthesis as well as transfection of AAV-Nrf2
The adeno-associated virus Nrf2(AAV-Nrf2) gene sequence was located in GeneBank (Gene ID: 83619) and compounded by Hanbio Biotechnology Co (Shanghai, China). Control AAV was also bought from this company. A dose of 10╳11E in all injected by tail veins was mixed with saline for each rat.
Creation of a CME model and grouping
CME model was generated as described by Li L et al. previously . Forty rats were separated then formed into 4 groups, containing a sham group, CME group, CME plus AAV-Nrf2 group (AAV-Nrf2(CME) group) and CME plus AAV-control group (AAV-control (CME) group), with 10 rats in each one of them. AAV-Nrf2(CME) group and AAV-control (CME) group both received 2-week transfection of AAV-Nrf2 or AAV-control virus. And then, the two groups received the following operation: put simply, a sternotomy in the middle the second and third intercostal was undertaken. The pericardium was unfolded and the increasing aorta was totally revealed. The plastic microspheres (3000 microspheres per rat, diameter of 42 μm, Biosphere Medical Inc., Rockland, USA) dissolved in 0.1 mL NS were injected into the ventricular (LV) chamber on the left and meanwhile clamping the ascending aorta with the use of the hemostatic forceps during the 10 s. Rats in the control group received 0.1 ml normal saline (PubChem CID: 5234) merely as the sham group did.
The left ventricle was detected applying echocardiography which was used to examine the left ventricle of rats, which were lightly anesthetized by injecting 10% chloral hydrate (1-2 ml/kg) into an enterocoelia. In a word, an S12 transducer was used to be put on the left side and anterior position of chest wall to gain the left ventricle end-diastolic dimension (LVEDd), left ventricle ejection fraction (LVEF), cardiac output (CO) as well as fractional shortening (FS). A Philips Sonos 7500 system (Philips, Andover, USA) was used then all echocardiography was carried on by a veteran physician. Evaluating cardiac function three times, and the average values of the three figures were taken.
Myocardial micro-infarct size measurement
HBFP stain was applied to detect myocardial ischemia in an early stage or infarct area. The dyed yellow or brown myocardial tissue was normal while the red tissue was ischemia or necrotic. A DMR-Q550 pathological picture analyzer (Lei, Germany) analyzed The HBFP-stained sections before. In short, 10 optical areas in the microscope (magnification, ×100) were casually selected from every part and Leica Qwin analysis software was used to observe. The formula- ischemic area/total area × 100% was used to calculate the relative ischemic area .
Using TUNEL assay to examining myocardial apoptosis
This process was grimly conformed to the instructions of Kit specification. Apoptotic nuclei showed yellow-brown while the normal colour is light blue (TUNEL positive), and a whole amount of 10 non-overlapping areas (magnification,×400) from every slice which was observed stochastically . The myocardial apoptotic ratio = apoptotic number/entire cell number × 100% was to be used.
Quantitative Polymerase Chain Reaction in real time (RT-PCR)
We extracted the entire RNA from the cardiac tissue of rats with TRIzol® Reagent (Takara, Japan) 6 h after CME operation. Reverse transcription RNA (1 μg) was performed applying a reverse transcriptase kit (Takara, Japan) referring to the instructions provided by the manufacturer. Reactions involved 2 μL cDNA, 2 μL primers and 12.5 μL SYBR Premix Ex Taq II, and put into a ultimate volume of 20 μL of water. Real time-PCR was undertaken the next phase situations: ten-min initial denaturation at 95 C following 15-s 40 phases of amplification with 95 C as well as 1-min 60 °C. PCR in real time was applied with the following primers: 5′-GCTGCCATTAGTCAGTCGCTCTC -3′ and 5′- ACCGTGCCTTCAGTGTGCTTC-3′ for the rat nuclear relative factor 2-like (Nrf2), 5′- TTAAGCTGGTGATGGCCTCC -3′ and 5′- GTGGGGCATAGACTGGGTTC-3′ for the rat heme oxygenase1(HO-1), and 5′-ACTGCTTCCCAGACCCACA-3′ and 5′-CGAGACCTTGGAACACAGAGAA-3′ for caspase9, and 5′-GCAGCAGCCTCAAATTGTTGAC-3′ and 5′-TGCTCCGGCTCAAACCATC-3′ for caspase3, and 5′-AGACACCTGACCTTGGA-3 and 5′-TTGAAGTTGCCATCAGCAAACA-3 for bax, and 5′-AGACACCTGACCTTGGA-3 and 5′-TTGAAGTTGCCATCAGCAAACA-3 for bcl-2, and 5′-GAGATTACTGCCCTGGCTCCTA-3′ and 5′-CATCGTACTCCTGCTTGCTGAT-3′ for β-actin. The dissociation curve was analyzed to confirm specific amplification. The amplification of the overall cDNA samples were divided into 3 portions and standardized compared to a triplicate of β-actin in this dish. The expression of the data was 2–∆∆Ct.
Proteins were extracted from tissue samples from 6 h after CME operation. Subsequently, the protein (50 μg) was quantified using a BCA assay (Solarbio, Beijing, China) and was loaded onto a 10% SDS-PAGE gel for electrophoresis and then transferred into a PVDF membrane (Millipore). Blocking with 5 % non-fat milk in TBS at the temperature in a room for 1 h, following the incubation of the membranes with a 1:500-10,000 dilution of primary antibody (anti-Nrf2, anti-HO-1, anti-caspase-3, anti-caspase-9, anti-bax, as well as anti-bcl-2; Abcam, UK) in buffer overnight at 4 °C, after washing 3 times in TBS, the incubation happened with a 1:10,000 dilution of fluorescent anti-rabbit secondary antibody (Abcam, UK) in buffer at the temperature in the room for 2 h. The immunoreactive bands were observed by exposing the blots in an Odyssey infrared imaging system (LI-COR).
To measure the expression of cTnI in serum, blood samples from each rat were collected for ELISA 6 h after CME operation based on the instructions provided by the manufacturer.
Preparation of the tissue samples
Ten rats per group were killed under anesthesia 6 h after CME operation. Blood samples were collected and used for enzyme linked immunoassay (ELISA). Heart tissue was harvested. Four tissue samples were fixed in 4% paraformaldehyde (PubChem CID: 62081) for 24 h for preparation of paraffin sections and the myocardial infarct size was detected by HE staining and hematoxylin-red complex picric acid (HBFP) staining. The apoptosis of myocardium was detected by TUNEL staining. Three hearts were preparation for Real time-PCR. The remaining heart tissue was used for the preparation of Western blotting. All tissue samples were prepared in an identical manner.
Data was analyzed by SPSS v18.0 (Chicago, Illinois, USA). Continuous variables are the mean ± SD. We applied one-way ANOVA (Analysis of Variance) to contrast differences among groups. Categorical variables were reported as frequencies and percentages (%), and differences between groups were examined by Fisher exact examination or chi-square examination. P < 0.05 was considered statistically remarkable.
Groups of animal
The weights and heart rates of four groups before operation. There were not any statistically significant differences among four groups
251.2 ± 10.3
253.2 ± 12.2
249.9 ± 11.3
250.8 ± 9.3
Heart rate (bpm)
463 ± 20
460 ± 27
458 ± 32
462 ± 24
HBFP staining and HE staining
AAV-Nrf2 pretreatment improved the function of heart following CME
Coefficient of the function of heart in rats in every group 6 h following CME modeling: the echocardiologic measurement conclusions
89.25 ± 2.52
42.33 ± 2.56
5.67 ± 2.12
0.232 ± 0.018
52.63 ± 1.78a
36.25 ± 3.22a
6.51 ± 3.33a
0.192 ± 0.033a
70.44 ± 3.21ab
44.74 ± 1.58ab
5.79 ± 1.66ab
0.255 ± 0.025ab
52.87 ± 2.12a
34.55 ± 2.24a
6.48 ± 1.85a
0.201 ± 0.011a
AAV-Nrf2 pretreatment attenuated myocardial damage following CME
Six hours following CME modeling, serum levels of cTnI in rats from the sham group (0.32 ± 0.015 μg/L vs 0.05 ± 0.002 μg/L, P < 0.05) were lower than the CME group or the AAV-control (CME) group. What’s more, AAV-Nrf2 pretreatment was involved with reducing cTnI levels (0.19 ± 0.014 μg/L) when contrasted with CME group as well (P < 0.05).
AAV-Nrf2 pretreatment decreased myocardial apoptosis following CME
The mRNA levels of Nrf2, HO-1, bax, bcl-2, caspase3 and caspase9
AAV-Nrf2 pretreatment activated myocardial HO-1 signaling in CME
In our research, we testified that transfecting Nrf2 attenuated myocardial apoptosis and partially reversed CME, and that Nrf2/HO-1 signaling pathway was concluded in the pathogenesis of CME-induced myocardial apoptosis was saw. The results of this research emphasized the significant part that Nrf2/HO-1 plays in the pathogenesis of CME-connected myocardial dysfunction as well as in the apoptosis. We initially illuminate the part of Nrf2/HO-1 pathway plays in the CME model. These findings could enable us to illustrate the mechanisms by which Nrf2/HO-1 mediates myocardial injury supports our hypothesis that Nrf2 might represent a potential target for therapy.
In the present study, transfection of AAV-Nrf2 can deduce TUNEL-positive cells significantly. TUNEL assay data suggested that the upregulation of Nrf2 could inhibit CME-induced myocardial apoptosis clearly. LVEF, FS and CO of the AAV-Nrf2(CME) group were markedly increased, whereas LVEDd was reduced as contrasted with that of the CME group or AAV-control (CME) group significantly (Table 2). In comparison, the AAV-Nrf2(CME) group had a significant attenuation of levels of cTnI. It was also supported by a significant improvement in cardiac function of AAV-Nrf2(CME) rats.
Apoptosis is a major role in coronary microembolization . The expression Bcl-2 and Bax, which belong to the Bcl-2 family members, is a key part in the cell apoptosis process. It reported that Bcl-2 is an anti-apoptotic protein and then Bax is a pro-apoptotic protein. The proportion of Bcl-2 to Bax is considered as a crucial factor for ensuring the threshold of apoptosis . In addition, it has been found caspase-3 is excited by the apoptotic approach and next processed into excited fragments like cleaved-caspase-3. It’s thought to be an apoptotic coefficient . Caspase-9 has the function to catalyze the activation of caspase-3 [27, 28], whereas caspase-9 is necessary in the cases of apoptotic cell mostly. A large number of studies have suggested that caspase-9  and caspase-3  are involved in the succession of myocardial infarction, also restriction of caspase-9  and caspase-3  can remarkably alleviate ischemia-induced myocardial apoptosis with heart function improvement. In this study, the expression of caspase3, caspase9 and Bax/Bcl-2 significantly increased in CME and AAV-control (CME) groups, and was dramatically reduced in AAV-Nrf2 (CME) group (Figs. 4 and 5). These results indicated that transfection of Nrf2 could decrease the apoptosis of myocardial cells, and improve the cardiac function.
Nrf2 is a gene which has been identified as the especially vital part of Nrf2. The factor of Nrf2 can adjust regular evolving procedures, such as migration, cell growth, apoptosis  as well as invasion. Moreover, Nrf2/HO-1 signaling approach is a vital part in the process of apoptosis in the recent studies [34, 35]. Actually, Nrf2 is a crucial modulator of the expression of HO-1 .HO is a stress-responsive enzyme which could reduce highly deleterious free heme and produce anti-oxidants, anti-inflammatories, and regulators of apoptosis as well as multiplication, therefore maintaining homeostasis under pathological conditions [37, 38]. There are two distinct mammalian HO isoforms: HO-1 and HO-2. HO-1 is upregulated in the myocardium of rats in response to ischemia-reperfusion injury. HO-1 can also protect cells from apoptosis induced by light . Some researches have clarified that HO-1 expressing is adjusted primarily by Nrf2. Activated Nrf2 has been considered to be a crucial contributor to the expression of HO-1 . Meanwhile, Ning et al. found that down-regulation of miR-142-5p attenuated ischemia/reperfusion injury in hippocampal neurons by promoting Nrf2/HO-1 signaling approach . Liu et al. found that apoptosis was negatively correlated with the Nrf2 and HO-1 expressing, and ultimately affected the expression of cleaved caspase-3 . In our study, mRNA and protein levels (Figs. 4 and 5) of Nrf2 and HO-1 upregulated in AAV-Nrf2(CME) rats and the Nrf2 could reduce the expression of caspase-3 as well as caspase-9 and a ratio of bax/bcl-2 and apoptosis of myocardial cells (Fig. 3), and decrease levels of cTnI, demonstrating activation of Nrf2/HO-1 signaling can improve cardiac function in CME rats. The apoptotic pathways mainly include intrinsic and extrinsic pathways . Some studies have confirmed that Nrf2/HO-1 mainly regulated apoptosis through intrinsic pathway, but relative studies about extrinsic pathway of Nrf2/HO-1 were few [44, 45].In our study, Nrf2/HO-1 could suppress the expression of caspase-9 and caspase-3, and caspase-9 is the key factor of intrinsic pathway and active caspase-3 to induce apoptosis. Nrf2/HO-1 is probably concluded in the process of myocardial apoptosis after CME through the intrinsic pathway. Whether Nrf2/HO-1 can regulate apoptosis through extrinsic pathway, further studies are still needed.
There are likewise some limitations in the current study: Firstly, the conclusions were drawn from the model of rat CME and it was prepared by the injection of the plastic microspheres into the LV. Thus, the present outcome might not be straightforward compared to the results achieved in the patient. Secondly, we only studied the short-term protection of Nrf2. Therefore, how long this protective effect lasts is uncertain. With this in mind, future research needs to be explored in more CME models.
These findings showed that activating Nrf2/HO-1 signaling can inhibit apoptosis to attenuate coronary microembolization, and also improve the cardiac function. Nrf2/HO-1 signaling pathway is possibly a potential medical goal for treatment associated and it has a chance to be worthy for sick people who are undergone acute coronary syndrome or PCI and improve the long-term prognosis.
We would like to thank Yuanxi Lu and Wenqin Guo for their technical support. In addition, we would like to thank all colleagues for contributing the experiments.
This research received support from National Natural Science Foundation of China (Grant No.81600283) and Guangxi Natural Science Foundation (Grant No. 2016GXNSFBA380022).
Availability of data and materials
The unprocessed data from the current study can be obtained from the corresponding author.
JL, LL and YS conceived the idea of the project. JL, XW, and QS conducted the experiments of real time-PCR and Western blotting and analyzed data. WH and YL collected samples. JL and LL wrote the manuscript. QS and YS participated in the revision of the important part of the manuscript. JL, XW and WG worked together to produce the tables and figures. All contributive authors of this original manuscript authorized the ultimate manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
This experiment got the Ethics Committee of Guangxi Medical University, China permission and was carried out according with the Norms on the Animal Experiments. The animals were sampled and managed under the National Institute of Health (NIH Publication NO. 85-23, revised 1996).
Consent for publication
All authors reach a consensus to consent for coming out in the journal. This paper has not been published elsewhere in whole or in part, which are no conflicts involved in the article.
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