Effects of neuregulin-1 on autonomic nervous system remodeling post-myocardial infarction in a rat model

Xin Lai, Liang Zhong, Hai-xia Fu, Song Dang Xin Wang Ning Zhang Gao-ke Feng Zi-qiang Liu Xi Wang,Long Wang

1 Department of Cardiology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, China

2 Cardiovascular Research Institute, Wuhan University, Wuhan, Hubei Province, China

3 Hubei Key Laboratory of Cardiology, Wuhan, Hubei Province, China

4 Wuhan Medical & Healthcare Center for Women and Children, Wuhan, Hubei Province, China

5 Department of Cardiology, Henan Province People’s Hospital, Zhengzhou, Henan Province, China

How to cite this article:Lai X, Zhong L, Fu HX, Dang S, Wang X, Zhang N, Feng GK, Liu ZQ, Wang X, Wang L (2017) Effects of neuregulin-1 on autonomic nervous system remodeling post-myocardial infarction in a rat model Neural Regen Res 12(11):1905-1910.

Funding: This work was supported by a grant from the National Key Basic Research Development Program, the “973” Program, No.2012CB518604; the National Natural Science Foundation of China, No. 81260052; the Natural Science Foundation of Hubei Province, No.2014CKB497, 2014BKB075, and 2015BKA339; and the Natural Science Foundation of Henan Province of China, No. 201602262.

Introduction

Neuregulin-1 (NRG-1), a member of the epidermal growth factor family, plays an important regulatory role in the development and repair of the nervous system (Murphy et al.,2002; Lemmens et al., 2007; Melenhorst et al., 2008; Ding et al., 2014; Yamada et al., 2014). Moreover, some scholars believe that NRG-1 and its receptors (ErbB2, ErbB3, and ErbB4) are crucial in cardiac development (Mei and Xiong,2008; Pasca et al., 2014). NRG-1 has been found to be able to induce hypertrophy and inhibit cell apoptosis in rat ventricular myocytes (Zhao et al., 1998; Baliga et al., 1999;Rohrbach et al., 1999). Recent studies also found that NRG-1 activates tyrosine kinase, thus causing various cardiovascular biological effects, including regulating the structure and function of cardiomyocytes and its apoptosis and proliferation, and promoting angiogenesis (Odiete et al., 2012;Mendes-Ferreira et al., 2013). Experimental studiesin vivohave found that NRG-1 can significantly improve acute and chronic ischemic cardiomyopathy and myocarditis, and phase II clinical trials revealed that the short-term administration of recombinant human NRG-1 can improve chronic cardiac function in patients with heart failure (Gao et al.,2010; Jabbour et al., 2011). However, phase III clinical trials of recombinant human NRG-1 for heart failure are ongoing.Notably, in patients with breast cancer accepting anti-ErbB2 monoclonal antibody trastuzumab treatment, heart failure occurred partially (Feldman et al., 2000; Schneider et al.,2001). Therefore, NRG-1 and its receptors are being considered gradually for the cardiovascular system.

A large amount of norepinephrine is released from sympathetic nerves during acute myocardial ischemia, and sympathetic sprouting and sympathetic remodeling reach a peak at 1 week after myocardial infarction (MI) (Wu et al., 2012;Holmes et al., 2016; Prabhu and Frangogiannis, 2016). At the same time, sympathetic nerve reinnervated by budding results in sympathetic hyperinnervation, and this imbalanced innervation plays an important role in the occurrence of ventricular arrhythmias (Li et al., 2004; Zhou et al., 2004;Boogers et al., 2010; Alston et al., 2011). Meanwhile, vagus nerve injury, necrosis, regeneration, and reconstruction also occur post-MI (Suo et al., 2013).

Most studies focused on the roles of NRG-1 in nerve repair and neurohumoral regulation of heart injuries (Monje et al., 2006; Calvo et al., 2010; Cahill et al., 2013), but the effects of NRG-1 on the neural remodeling post-MI remain unclear. We hypothesized that NRG-1 might play a role in neural remodeling following MI. Thus, we prepared a rat model of MI to investigate how NRG-1 impacts cardiac function and neural remodeling after MI.

Materials and Methods

Animals

Forty-five adult male Sprague-Dawley rats aged 12 weeks and weighing 250–300 g were provided by the Animal Experiment Center of Wuhan University in China (No.42000500005679). Rats were housed in temperature-controlled and humidity-controlled large cages with sawdust bedding and given access to tap water and foodad libitumfor 7 days. All animal care and experimental procedures were performed in accordance with the United States National Institutes of Health Guide for the Care and Use of Laboratory Animals (publication no. 85-23, revised 1986).This research was approved by the Administration Committee of Experimental Animals, Hubei Province, China. Rats were randomized into three groups (n= 15 per group): sham operation group, MI group, and MI plus NRG-1 group.

Establishment of the MI model

The left anterior descending coronary artery of the rats in the MI and MI plus NRG-1 groups was ligated to establish the MI model, as previously described (Wang et al., 2014). In brief, after anesthesia with 3.6% chloral hydrate (1 mL/100 g, Sinopharm Chemical Reagent Co., Ltd, Shanghai, China)was administered, the rats were connected to the electrocardiograph and then disinfected. We cut the skin along the left side of the sternum; separated fascia and muscle with hemostatic forceps; performed thoracotomy at the third and fourth ribs to expose the mediastinum and pericardium;found the left atrial appendage, pulmonary artery cones,and veins; identified the left anterior descending coronary artery and ligated it using a 5-0 (or 6-0) suture; and closed the chest and skin layer by layer. A successful MI model was confirmed when the color of the ischemic area became pale and ST-segment elevation was detected in leads I, II,and aVL by electrocardiography. In the sham group, rats received the same procedures, except leftanterior descending coronary artery ligation.

Experimental interventions

Rats in the MI plus NRG-1 group were given an intraperitoneal injection of NRG-1 (10 µg/kg) after MI, once daily for 7 consecutive days (Lemmens et al., 2011). At 4 weeks after MI, echocardiography was performed to evaluate cardiac function, and myocardial tissues from the infarct border zone were collected to detect the levels of tyrosine hydroxylase (TH), growth associated protein-43 (GAP43), nerve growth factor (NGF), choline acetyltransferase (CHAT), and vesicular acetylcholine transporter (VACHT) in the assessment of neural remodeling (Ajijola et al., 2015).

Assessment of heart function

Heart function was tested using the Philips IE33 ultrasound system (GE Healthcare, Milwaukee, WI, USA) at 4 weeks post-MI. Each rat was measured under anesthesia,and the indexes included the left ventricular end-systolic inner diameter (LVESD), leftventricular diastolic diameter(LVEDD), leftventricular end-systolic volume (LVESV), leftventricular end-diastolic volume (LVEDV), leftventricular ejection fraction (LVEF%), and left ventricular fractional shortening (LVFS%) were recorded and measured. The following equation was used: LVEF% = (LVEDD3– LVESD3)/LVEDD3× 100% and LVFS% = (LVEDD – LVESD)/LVEDD × 100%.(1:500; Abcam), anti-CHAT (1:500; Bioss, Beijing, China),anti-VACHT (1:500; Abcam), or anti-GAPDH (1:10,000;Abcam) overnight at 4°C. After the membrane was washed three times, the blots were incubated with secondary HRP conjugated goat anti-rabbit antibody (1:10,000; Pierce,Rockford, IL, USA) for 30 minutes at room temperature.Membranes were detected by enhanced chemiluminescence(Beyotime Biotechnology, Jiangsu, China) and exposed to film in the dark. The optical density intensity of each band was measured using AlphaEaseFC so ft ware (Alpha Innotech

Table 1 Gene sequences

Measurements of the neural remodeling markers (TH,GAP43, NGF, CHAT, and VACHT)

Quantitative real-time polymerase chain reaction (qRT-PCR)Approximately 100 mg of myocardial tissues from the infarct border zone were collected at 4 weeks after MI. Total RNA was extracted by Trizol reagent (15596-026; Invitrogen, Carlsbad, CA, USA), cDNA was obtained with the First Strand cDNA Synthesis Kit (FSK-100; Toyobo, Kita-ku,Osaka, Japan), and then the fragments were amplified with the SYBR Green-based assays kit (Invitrogen) according to the manufacturer’s instructions. Next, qRT-PCR was conducted using the StepOne™ Real-Time PCR System(ABI, Life Technologies, Rockville, MD, USA). RT-PCR conditions were 42°C/30 minutes and 80°C/5 minutes for reverse transcription; 95°C/60 seconds for pre-denature; and 95°C/15 seconds, 58°C/20 seconds, and 72°C/20 seconds.All steps were performed for 40 cycles. The gene sequences are shown inTable 1. The mRNA expression levels of TH,GAP43, NGF, CHAT, VACHT, and GAPDH were detected,and GAPDH was used for normalization. The relative gene expression in the sample was calculated as 2-ΔΔCT. Experiments were performed in triplicate.

Western blot assay

Fifty µg of protein was extracted from the ischemic myocardial tissues at 4 weeks after MI. The tissues were lysed in radioimmunoprecipitation assay (AS1004, Aspen, Wuhan,China), and lysis buffer and protein concentrations were determined using the BCA kit (AS1086, Aspen). The proteins were used for sodium dodecyl sulfate-polyacrylamide gel electrophoresis and then transferred to nitrocellulose membranes. The membranes were blocked by incubation with 5%bovine serum albumin in a TBS-Tween buffer (10 mM Tris-HCl, 150 mM NaCl, and 0.5% Tween-20) for 1 hour at room temperature, and subsequently, incubated with different primary antibodies: rabbit anti-TH (Santa, Shanghai, China),anti-GAP43 (1:1,000; Abcam, Cambridge, UK), anti-NGF Corp., San Leandro, CA, USA). Results are shown as the optical density ratio to GAPDH.

Statistical analysis

All data were analyzed by SPSS 16.0 (SPSS Inc., Chicago, IL,USA). Values are presented as the mean ± SD. The statistical significance of differences was analyzed using one-way analysis of variance with the Student-Newman-Keulspost hoctest for comparisons among groups. Values ofP< 0.05 were considered statistically significant.

Results

Effect of NRG-1 on cardiac function

At 4 weeks after MI, echocardiography results showed significant differences in LVESD, LVEDD, LVESV, LVEDV,LVEF%, and LVFS% among groups. Compared with the sham group, the MI group showed a significant deterioration in cardiac function; that is, LVESD, LVEDD, LVESV,and LVEDV were significantly increased, and LVEF% and LVFS% were significantly decreased (P< 0.05). After NRG-1 injection, LVESD, LVEDD, LVESV, and LVEDV significantly decreased; whereas, LVEF%, and LVFS% significantly increased (P< 0.05), suggesting a significant improvement in cardiac function (Table 2).

Effect of NRG-1 on the mRNA levels of neural remodeling markers

The mRNA expression levels of TH, GAP43, NGF, CHAT,and VACHT were significantly increased in the MI and MI plus NRG-1 groups compared with the sham group (P<0.05). Compared with the MI group, there was a significant decrease in mRNA expression levels of TH, GAP43, and CHAT in the MI plus NRG-1 group (P< 0.05). Simultaneously, there was a decreasing trend in NGF and VACHT mRNA expression levels (P> 0.05;Table 3).

Effect of NRG-1 on the protein levels of neural remodeling markers

The protein expression levels of TH, GAP43, NGF, CHAT,and VACHT were significantly increased in the MI and MI plus NRG-1 groups compared with the sham group (P<0.05). The protein expression levels of TH and GAP43 in the ischemic myocardia in the MI plus NRG-1 group were significantly lower than those in the MI group (P< 0.05); the protein expression levels of NGF, CHAT, and VACHT were slightly lower in the MI plus NRG-1 group than those in the MI group (P> 0.05;Table 4andFigure 1).

Table 2 Effect of NRG-1 on cardiac function in rats after MI

Table 3 Effect of NRG-1 on relative mRNA levels (/GAPDH) of neural remodeling markers in rat ischemic myocardia

Table 4 Effect of NRG-1 on protein levels (/GAPDH) of neural remodeling markers in rat ischemic myocardia

Figure 1 NRG-1 injection regulated protein levels of neural remodeling markers in rat ischemic myocardia.Target protein expression was analyzed by western blot assay with antibodies against TH, GAP43, NGF, CHAT, and VACHT relative to GAPDH. MI: Myocardial infarction; N: neuregulin-1; TH: tyrosine hydroxylase; GAP43: growth associated protein-43; NGF: nerve growth factor; CHAT: choline acetyltransferase; VACHT: vesicular acetylcholine transporter; GAPDH: glyceraldehyde-3-phosphate dehydrogenase.

Discussion

Some studies have shown that in the NRG-1 knockout mouse model of MI, cardiac systolic function was significantly impaired, but it was improved significantly after NRG-1 intervention (McCormick et al., 2015; Vandekerckhove et al., 2016; Yasui et al., 2016; Zhang et al., 2016). In an MI model, mitochondrial dysfunction and apoptosis were obviously reduced after intravenous administration of NRG-1, thereby reducing leftventricular remodeling post-injury(Guo and Wang, 2012). Gu et al. (2010) found that NRG-1 significantly up-regulated cardiac myosin light chain kinase and myosin light chain phosphorylation post-MI; the values of LVEF%, LVFS%, LVEDD, and LVESD were significantly increased, and cardiac function was significantly improved.In the current study, we observed that NRG-1 improved cardiac function post-MI.

NRG-1 can promote the proliferation of Schwann cells and increase the density and area of dendritic spines of neurons (Limpert and Carter, 2010). For peripheral nerves,NRG-1 promotes myelination and plays a significant role in axonal degeneration, axonal regeneration, remyelination,and innervation (Gambarotta et al., 2013; Shin et al., 2014).It has been reported that sympathetic nerve hyperinnervation and denervation result in neural remodeling, but generally, sympathetic nerve remodeling is also accompanied with vagus nerve remodeling (Yu et al., 2010). Additionally, our study found sympathetic and vagus nerve remodeling after MI, which was expressed as a significantly increased GAP43 level, as well as increased CHAT and VACHT levels.

TH was generated by norepinephrine and located in the cytoplasm of adrenergic nerve fibers. GAP43, a kind of neuronal specific protein, exists in axons, which marks neuronal growth by neuronal synthesis. NGF can promote the growth of neuritis and induce cardiac sympathetic hyperinnervation (Lu et al., 2012). Chen et al. (2014) reported that TH,GAP43, and NGF significantly increased post-MI as confirmed by western blot analysis and immunohistochemistry,and aerobic exercise inhibited the cardiac sympathetic nerve sprouting and restored B1-AR/B3-AR balance. Our study’s results also showed that the expression levels of TH, GAP43,and NGF were significantly increased post-MI, but after the NRG-1 intervention, their expression levels decreased,suggesting that NRG-1 can inhibit sympathetic remodeling

post-MI. CHAT is a vagus nerve marker. Suo et al. (2013)found that CHAT-positive nerve fiber density and its mRNA expression level were higher post-MI. Besides, VACHT is a cardiac vagal nerve fiber marker. Xi et al. (2004) reported that vagal innervation density appeared to significantly increase after MI. In the current study, after the NRG-1 intervention, the expression levels of CHAT and VACHT were not significantly different when compared with those in the MI group post-MI, except the mRNA level of CHAT, implying that NRG-1 may not inhibit vagus nerve regeneration and repair following MI.

In summary, NRG-1 intervention effectively down-regulates sympathetic nerve mRNA and protein expression levels, thus inhibiting the sympathetic nerve remodeling post-MI, which reaches a new equilibrium of the autonomic nervous system to protect cardiac function by reducing sympathetic nerve tension. But the further mechanism of nerve remodeling is not involved in the current study, and we will explore the possible mechanisms in the further research.

Author contributions:XW, LW and XL participated in study conception and design. GKF, LZ and XL collected and analyzed data, and ensured the integrity of the data. HXF, SD and XL wrote the paper. XW,NZ, ZQL and XL served as principle investigators, and were in charge of paper authorization. All authors approved the final version of the paper.

Conflicts of interest:None declared.

Research ethics:The study protocol was approved by Administration Committee of Experimental Animals of Wuhan University of China. All animal care and animal surgeries were in accordance with the Guide for Care and Use of Laboratory Animals (Public Health Service, 1996, NIH Publication No. 85-23).

Data sharing statement:Datasets analyzed during the current study are available from the corresponding author on reasonable request.

Plagiarism check:Checked twice by iThenticate.

Peer review:Externally peer reviewed.

Open access statement:This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under identical terms.

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