Changes in levels of angiotensin II and its receptors in a model of inverted stress-induced cardiomyopathy
European Journal of Medical Research volume 19, Article number: 54 (2014)
Stress-induced cardiomyopathy (SIC) has gained increasing attention worldwide and is characterized by extensive ventricular akinesis, Beta-blockers and angiotensin-converting enzyme inhibitors (ACEIs) are the main treatments for SIC patients. The pharmacological mechanism of action of beta-blockers results in the inhibition of the biological effects of catecholamines. However, the mechanism of action of ACEIs in the treatment of cardiomyopathy is not known. Our aim is to assess changes in levels of angiotensin II, angiotensin-II receptors and ACE responses to SIC.
A model of inverted SIC was established in rabbits by vagal electrical stimulation. The serum concentration of angiotensin II and angiotensin (1-7) was detected by enzyme-linked immunosorbent assay. Expression of angiotensin-II receptors was measured by Western blotting and real-time reverse transcription-polymerase chain reaction (RT-PCR), with localization detected by immunofluorescent staining. ACE-II expression in the myocardium was measured by Western blotting.
From one day after vagal stimulation, concentrations of angiotensin II were significantly higher in the experimental group than those in the control group (P <0.05). Stress induced a time-dependent decrease in angiotensin subtype-1 (AT1) expression and a time-dependent increase in AT2 expression only in the apical portion of the myocardium. From three days after vagal stimulation, angiotensin (1-7) levels were significantly lower in the experimental group compared with the control group (P <0.05). Expression of the ACE-II protein was significantly downregulated in the experimental group compared with the control group from three days after vagal stimulation (P <0.05).
Expression of angiotensin II, its receptors, ACE-II and angiotensin (1-7) was altered in response to SIC. The renin-angiotensin system could represent a therapeutic target in the prevention of SIC.
Stress-induced cardiomyopathy (SIC; also named Takotsubo cardiomyopathy) was first described in Japan in 1991 . Stress factors can be sudden psychological, physical or emotional. SIC has gained increasing attention worldwide and is a well-recognized cause of acute heart failure, lethal arrhythmias and ventricular rupture . SIC is characterized by extensive ventricular akinesis involving apical segments with preserved function in basal segments without significant lesions in coronary arteries.
Recently, evidence has shown that serum levels of catecholamines in SIC patients one to two days after presentation are higher than in patients with myocardial infarction with pulmonary edema, and that epinephrine levels return to those seen in those with myocardial infarction only after seven to nine days . Experimental studies reported the catecholamine intoxication is the main etiology of SIC , , but the mechanism of action is not clear.
SIC patients have an excellent prognosis as well as absent or minimal residual cardiac impairment, and left ventricular (LV) function recovers within two to four weeks of presentation . At present, beta-blockers and angiotensin-converting enzyme inhibitors (ACEIs) are the main treatments for SIC patients , , . The pharmacological mechanism of action of beta-blockers results in the inhibition of the biological effects of catecholamines . However, the mechanism of action of ACEIs in the treatment of cardiomyopathy is not known. The target of ACEIs is angiotensin-converting enzyme 1 (the main function of which is to convert angiotensinogen to angiotensin II). Angiotensin II contains peptides that are involved in the renin-angiotensin system (RAS) and which regulate cellular and physiological responses in the cardiovascular system. Angiotensin II is also implicated in the pathophysiological processes related to myocardial remodeling , . Angiotensin II activates several nuclear transcription factors (such as signal transducer and activator of transcription (STAT) and cyclic adenosine monophosphate (cAMP) response element-binding (CREB) protein) by promoting fibroblast proliferation that leads to myocardial remodeling ,.
Angiotensin II signals through seven transmembrane-spanning G protein-coupled receptors that are characterized into angiotensin subtype-1 (AT1) and angiotensin subtype-2 (AT2) based on their selective affinity for peptide and non-peptide ligand . Northern blotting and reverse transcription-polymerase chain reaction (RT-PCR) analyses have been used to identify AT1 and AT2 mRNA in many cells and tissues (including the human myocardium). Pharmacological studies have revealed that the AT1 subtype mediates responses to angiotensin II caused by the release of aldosterone and epinephrine . One study showed that expression of angiotensin-II receptors changes in response to stress . Nevertheless, few studies have focused on the association between angiotensin II and its receptors with SIC.
In the present study, we assessed changes in angiotensin II, angiotensin-II receptors, and angiotensin-converting enzyme (ACE) responses to SIC from in vivo studies using a rabbit model of SIC.
All studies conformed to the Guide for the Care and Use of Laboratory Animals (US National Institutes of Health, publication number 85-23, revised 1996; Additional file 1: Figure S1).
Anti-AT1 and anti-AT2 receptor antibodies were purchased from Santa Cruz Biotechnology (Santa Cruz, California, United States). A one-step RT-PCR kit was obtained from TaKaRa (TaKaRa, Shiga, Japan). Angiotensin II, angiotensin (1-7) and ACE-II enzyme-linked immunoassay (ELISA) kits (all from rabbits) were obtained from Blue Gene Chemical Company (Blue Gene Chemical Company, Shanghai, China). Tween 20, Nonidet 40 (NP-40), aprotinin, leupeptin, phenylmethylsulfonyl fluoride (PMSF) and dithiothreitol (DTT) were purchased from Sigma-Aldrich (Sigma, St. Louis, United States).
In vivo model of stress-induced cardiomyopathy
Experimental procedures were designed according to those of Takato et al. . Female rabbits (weighing approximately 2 kg; General Hospital of Chengdu Military Command, Kunming, China) were anesthetized (100 mg/kg ketamine, 5 mg/kg xylazine(Aibixin Chemical Company, Shanghai, Chin), intramuscular injection). Electrical stimulations of 50-Hz intensity and l-ms duration with stepwise increases in voltage from 0.1 to 1.0 V were applied to the right cervical intact vagus under electrocardiographic monitoring. Stimulation was maintained for 1 minute with a pause of 2 minutes between stimulations for approximately 1 hour. The sham group did not have electrical stimulations. At 1, 3, 7 and 14 days after vagal stimulation, animals were anesthetized and hearts removed.
Proteins were extracted as described . 100 ug of protein were separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (10% polyacrylamide gel (Xibao Chemical Company, Shanghai, China)). Proteins were transferred onto polyvinylidene difluoride membranes by electroblotting for 3 hours at 150 mA. Membranes were blocked in 5% non-fat milk solution in Tris-buffered saline with 0.5% Tween 20 (Sigma, St. Louis, United States). Membranes were allowed to react with primary antibodies (respectively AT1 and AT2 antibody). Detection of specific proteins was done by enhanced chemiluminescence following manufacturer instructions. Densitometric signals were quantified using Quantity One software (BioRad, Hercules, California, United States).
RNA isolation and real-time reverse transcription-polymerase chain reaction
Total RNA was isolated with TRIzol™ reagent according to manufacturer protocols (Sigma, St. Louis, United States). Total RNA was reverse-transcribed into cDNA. The resultant cDNA was amplified by SYBR Green 1 fluorescence real-time RT-PCR. The PCR reaction was monitored directly using the Bioer FQD-66A sequence detection system(Bioer Company, Hangzhou, China).
The primers for AT1 were 5’-TTTGGGAACAGCTTGGCGGT-3’ (forward) and 5’-GCCAGCCAGCAGCCAAATAA-3’ (reverse). The primers for AT2 were 5’-AGGTTTCCAGCATTTACATC-3’ (forward) and 5’-GTCACCAGCCAACGCTATC-3’ (reverse). The primers for β-actin were 5’-AGGAAGGAGGGCTGGAACA-3’ (forward) and 5’-CCCATCTACGAGGGCTACGC-3’ (reverse).
ug single-stranded cDNA was amplified by PCR using 35 cycles. The PCR profile used for AT1 amplification was 30 s of denaturation at 94°C, 30 seconds of annealing at 57°C, and 1.5 minutes of extension at 72°C. The PCR profile used for AT2 amplification was 30 seconds of denaturation at 94°C, 30 seconds of annealing at 60°C, and 1.5 minutes of extension at 72°C. The profile for β-actin amplification was: 30 s of denaturation at 94°C, 30 seconds of annealing at 57°C, and 1.5 minutes of extension at 72°C. Results were expressed as the mean ± SD for relative expression levels.
Apical tissue was removed and used for detection of AT1 and AT2 by immunofluorescence. For staining, sections were fixed in acetone for 10 minutes, air dried, and rehydrated with phosphate-buffered saline (PBS) before incubation in serum-free Protein Block (Dako, Glostrup, Denmark) for 30 minutes. Sections were stained with antibody diluted in 1% blocking reagent/0.3% Triton X-100 in PBS overnight before being washed in Tris-NaCl-Tween-Buffer (TNT) wash buffer (Tris-HCl, pH 7.5, 0.15 mol/L NaCl, and 0.05% Tween 20 (Sigma, St. Louis, United States). Sections incubated with an isotype-matched control antibody were used as the negative control. Subsequently, sections were incubated with fluorescein isothiocyanate-goat anti-mouse IgG(Zhongshan, Beijing, China) for 30 minutes before washing. Nuclei were stained with 4’,6-Diamidino-2-phenylindole dihydrochloride. Images were obtained using a Confocal Laser Scanning Microscope (TCS SP5; Leica, Wetzlar, Germany).
The concentration of angiotensin II and angiotensin (1-7) in serum samples was detected by ELISA according to specifications in the kit (Sigma, St. Louis, United States).
Results are the mean ± SEM. SPSS version 13.0 (SPSS, Chicago, Illinois, United States) was used for statistical analyses. The Student t-test was employed to compare two groups. Analysis of variance (ANOVA) was used with the Tukey multiple comparison test for multiple groups. A P value of <0.05 was considered significant.
Change in plasma levels of angiotensin II in response to stress
At 0, 1, 3, 7 and 14 days after vagal stimulation, the plasma of rabbits in control and experimental groups was extracted, and the concentration of angiotensin II measured by ELISA. From 1 day after vagal stimulation, the concentration of angiotensin II increased gradually in the experimental group. At seven days, the concentration of angiotensin II reached its peak (1.353 ± 0.003 ng/mL), and was significantly higher than that 0 days after vagal stimulation (P <0.05). Meanwhile, the concentrations of angiotensin II were significantly higher in experimental group than those in the control group from one day after vagal stimulation (P <0.05). Detailed data was listed in Figure 1.
Expression of AT1 and AT2 mRNA and protein in a model of acute cardiomyopathy
We next examined the effect of stress on angiotensin receptor mRNA and protein expression. From one day after vagal stimulation, stress induced a time-dependent decrease in the expression of AT1 mRNA and protein in the apical portion. Compared to that in basal portion, the expression of AT1 mRNA and protein significantly downregulated in the apical portion from three days after vagal stimulation (P <0.05). Expression of apical AT1 mRNA and protein in the experimental group was significantly lower than that in the control group (P <0.05) (Figure 2A). Conversely, expression of AT2 mRNA and protein in the apical portion was increased by stress from one day after vagal stimulation. Compared with that in the basal portion of the experimental group and the apical portion of the control group, expression of AT2 mRNA and protein was upregulated significantly in the apical portion of the experimental group (P <0.05) (Figure 2B).
Localization of AT1 and AT2 in basal and apical portions upon response to stress
Immunofluorescent staining was undertaken to determine the localization of AT1 and AT2 in basal and apical portions of the experimental group seven days after vagal stimulation. Clear immunoreactivity for AT1 and AT2 was detected in scattered cells of the myocardium in basal and apical portions. In addition, compared with those in the myocardium of the basal portion, an increased number of AT1-positive cells and a decreased number of AT2-positive cells was observed in the myocardium of the apical portion (Figure 3).
Change in plasma levels of angiotensin (1-7) and ACE-II protein in a model of acute cardiomyopathy
At 0, 1, 3, 7 and 14 days after vagal stimulation, the plasma of rabbits in control and experimental groups was extracted, and the concentration of angiotensin (1-7) measured by ELISA. From three days after vagal stimulation, angiotensin (1-7) levels were significantly lower in the experimental group compared with the control group (P <0.05). When compared with 0 days after vagal stimulation, the concentration of angiotensin (1-7) was significantly lower at 3, 7 and 14 days (P <0.05) (Figure 4A). Apical tissue of the control group and experimental group was collected, and levels of ACE-II protein measured by Western blotting. Compared with that in the control group, expression of ACE-II protein was downregulated significantly in the experimental group from three days after vagal stimulation (P <0.05) (Figure 4B).
The RAS has been shown (clinically and experimentally) to be associated with the progression and outcome of cardiovascular diseases such as atherosclerosis, acute coronary syndrome, cardiac hypertrophy and heart failure , . Angiotensin II has been implicated in the pathophysiological processes related to myocardial remodeling , . The link that connects SIC and RAS is not known.
In the context of former studies on cardiomyopathy and the rennin angiotensin system, our study elicited three main findings. Firstly, the concentration of angiotensin II increased gradually in the rabbit model of inverted SIC by vagal stimulation. Secondly, expression of apical AT1 mRNA and protein in the experimental group was decreased significantly, but expression of AT2 mRNA and protein was upregulated significantly. Finally, plasma levels of angiotensin (1-7) and ACE-II expression were decreased in the rabbit model of inverted SIC.
Recently, epinephrine-induced cardiotoxicity has been postulated to be involved in the pathogenesis of SIC , . It is well established that angiotensin II can stimulate epinephrine release from the adrenal glands , . The present study is the first to show that the plasma concentration of angiotensin II increases gradually in SIC. These data strongly suggest that angiotensin II and its signaling pathway may be involved in the pathogenesis of SIC. Nevertheless, the underlying mechanism of action merits further study.
Premer et al. revealed that the AT1 subtype mediates the release of aldosterone and epinephrine as well as pressor, dipsogenic and sodium-appetite responses to angiotensin II in the brain . We examined the effect of stress on the expression of mRNA and proteins from angiotensin receptors. The results showed that stress induced a time-dependent decrease in the expression of AT1 mRNA and protein in only the apical portion. Conversely, expression of AT2 mRNA and protein in the apical portion was increased by stress. Immunofluorescent staining showed AT1 and AT2 in scattered parts of the myocardium. Izumi et al. also reported that expression of AT1 mRNA was significantly reduced, and that of AT2 remarkably increased, in apical portions . Several lines of evidences suggest that catecholamine concentrations are increased by stress , . Downregulation of expression of AT1 and upregulation of expression of AT2 in the apical portion of the myocardium may be induced by excess epinephrine . Data have shown expression of AT1 and AT2 in the left ventricle to be decreased in human heart failure, which is different to the effect of stress on expression of AT1 and AT2 . AT2 mediates cardioprotection, so upregulation of expression of AT2 in the apical portion of the myocardium could (at least in part) influence the prognosis of patients with SIC.
ACE-II is a homolog of ACE compounds, and has been found to be present in the heart, kidney and other tissues . The bioactivity of ACE-II helps to catalyze angiotensin II to angiotensin (1-7). Angiotensin (1-7) is a cardiovascular-protective peptide with vasodilatory and antiproliferative effects. ACE-II can increase the degradation of angiotensin II, thereby reducing the adverse effects of angiotensin II ,. Our study is the first to show that angiotensin (1-7) levels were significantly lower in response to SIC. Expression of ACE-II proteins was also significantly downregulated in the apical myocardium in SIC, and is part of the cause of stress-induced heart failure.
Expression of angiotensin II, its receptors, ACE-II and angiotensin (1-7) was altered in response to SIC. The renin-angiotensin system could represent a therapeutic target in the prevention of SIC.
Y-yX and BL carried out the establishment of SIC model, participated in the Western blotting and real-time RT-PCR. L-xY carried out the extraction of protein and RNA and drafted the manuscript. C-wK carried out the immunofluorescence and ELISA. R-wG participated in the design of the study and performed the statistical analysis. All authors read and approved the final manuscript.
Angiotensin-converting enzyme inhibitors
Cyclic adenosine monophosphate
Enzyme-linked immunosorbent assay
Real-time reverse transcription-polymerase chain reaction
Signal transducer and activator of transcription
Dote K, Sato H, Tateishi H, Uchida T, Ishihara M: Myocardial stunning due to simultaneous multivessel coronary spasms: a review of 5 cases. J Cardiol 1991, 21: 203–214.
Spadotto V, Zorzi A, Elmaghawry M, Meggiolaro M, Pittoni GM: Heart failure due to ‘stress cardiomyopathy’: a severe manifestation of the opioid withdrawal syndrome. Eur Heart J Acute Cardiovasc Care 2013, 2: 84–87. 10.1177/2048872612474923
Nielsen LH, Munk K, Goetzsche O, Christiansen EH, Nørgaard BL: Takotsubo cardiomyopathy. An important differential diagnosis to acute myocardial infarction. Dan Med Bull 2009, 56: 165–168.
Paur H, Wright PT, Sikkel MB, Tranter MH, Mansfield C, O’Gara P, Stuckey DJ, Nikolaev VO, Diakonov I, Pannell L, Gong H, Sun H, Peters NS, Petrou M, Zheng Z, Gorelik J, Lyon AR, Harding SE: High levels of circulating epinephrine trigger apical cardiodepression in a β2-adrenergic receptor/Gi-dependent manner: a new model of Takotsubo cardiomyopathy. Circulation 2012, 126: 697–706. 10.1161/CIRCULATIONAHA.112.111591
Lyon AR, Rees PS, Prasad S, Poole-Wilson PA, Harding SE: Stress (Takotsubo) cardiomyopathy–a novel pathophysiological hypothesis to explain catecholamine-induced acute myocardial stunning. Nat Clin Pract Cardiovasc Med 2008, 5: 22–29. 10.1038/ncpcardio1066
Kurisu S, Kihara Y: Tako-tsubo cardiomyopathy: clinical presentation and underlying mechanism. J Cardiol 2012, 60: 429–437. 10.1016/j.jjcc.2012.06.015
Pullara A, Chinaglia A, Giammaria M, Bequaraj F, Orlando F, Coda L, Lucciola MT, Forno D, Ravera L, Cecchi E, Gaita F, Belli R: Takotsubo cardiomyopathy: real life management in the intensive coronary care unit. Minerva Med 2013, 104: 537–544.
Itoh H, Miyake Y, Hioki I, Tanaka S, Okabe M: Report of takotsubo cardiomyopathy occurring during cardiopulmonary bypass. J Extra Corpor Technol 2007, 39: 109–111.
Palla AR, Dande AS, Petrini J, Wasserman HS, Warshofsky MK: Pretreatment with low-dose β-adrenergic antagonist therapy does not affect severity of Takotsubo cardiomyopathy. Clin Cardiol 2012, 35: 478–481. 10.1002/clc.21983
Monge M, Lorthioir A, Bobrie G, Azizi M: New drug therapies interfering with the renin-angiotensin-aldosterone system for resistant hypertension. J Renin Angiotensin Aldosterone Syst 2013, 14: 285–289. 10.1177/1470320313513408
Nanayakkara G, Viswaprakash N, Zhong J, Kariharan T, Quindry J, Amin R: PPARγ activation improves the molecular and functional components of I(to) remodeling by angiotensin II. Curr Pharm Des 2013, 19: 4839–4847. 10.2174/1381612811319270006
Jiang L, Xu L, Song Y, Li J, Mao J, Zhao AZ, He W, Yang J, Dai C: Calmodulin-dependent protein kinase II/cAMP response element-binding protein/Wnt/β-catenin signaling cascade regulates angiotensin II-induced podocyte injury and albuminuria. J Biol Chem 2013, 288: 23368–23379. 10.1074/jbc.M113.460394
Chen D, Liu J, Rui B, Gao M, Zhao N, Sun S, Bi A, Yang T, Guo Y, Yin Z, Luo L: GSTpi protects against angiotensin II-induced proliferation and migration of vascular smooth muscle cells by preventing signal transducer and activator of transcription 3 activation. Biochim Biophys Acta 2014, 1843: 454–463. 10.1016/j.bbamcr.2013.11.024
Siragy HM: Angiotensin receptor blockers: how important is selectivity. Am J Hypertens 2002, 15: 1006–1014. 10.1016/S0895-7061(02)02280-X
Xu TB, Eppel GA, Head GA, Evans RG: Angiotensin II Type 1 Receptors and Systemic Hemodynamic and Renal Responses to Stress and Altered Blood Volume in Conscious Rabbits. Front Physiol 2011, 2: 40. 10.3389/fphys.2011.00040
Izumi Y, Okatani H, Shiota M, Nakao T, Ise R, Kito G, Miura K, Iwao H: Effects of metoprolol on epinephrine-induced takotsubo-like left ventricular dysfunction in non-human primates. Hypertens Res 2009, 32: 339–346. 10.1038/hr.2009.28
Takato T, Ashida T, Seko Y, Fujii J, Kawai S: Ventricular tachyarrhythmia-related basal cardiomyopathy in rabbits with vagal stimulation–a novel experimental model for inverted Takotsubo-like cardiomyopathy. J Cardiol 2010, 56: 85–90. 10.1016/j.jjcc.2010.03.002
Guo RW, Yang LX, Li MQ, Liu B, Wang XM: Angiotensin II induces NF-kappa B activation in HUVEC via the p38MAPK pathway. Peptides 2006, 27: 3269–3275. 10.1016/j.peptides.2006.08.014
Divchev D, Schieffer B: The secretory phospholipase A2 group IIA: a missing link between inflammation, activated renin-angiotensin system, and atherogenesis? Vasc Health Risk Manag 2008, 4: 597–604.
Bertagnolli M, Huyard F, Cloutier A, Anstey Z, Huot-Marchand JÉ, Fallaha C, Paradis P, Schiffrin EL, Deblois D, Nuyt AM: Transient neonatal high oxygen exposure leads to early adult cardiac dysfunction, remodeling, and activation of the Renin-Angiotensin system. Hypertension 2014, 63: 143–150. 10.1161/HYPERTENSIONAHA.113.01760
Kaireviciute D, Aidietis A, Lip GY: Pathophysiological insights into atrial fibrillation following cardiac surgery: implications for current pharmaceutical design. Curr Pharm Des 2009, 15: 3367–3383. 10.2174/138161209789105063
Amruthlal Jain SK, Larsen TR, Souqiyyeh A, David SW: Takotsubo cardiomyopathy: reversible stress-induced cardiac insult - a stress protective mechanism. Am J Cardiovasc Dis 2013, 3: 53–59.
Douglas SA, Stevenson KE, Knowles PJ, Bunn SJ: Characterization of catecholamine release from deer adrenal medullary chromaffin cells. Neurosci Lett 2008, 7: 126–129. 10.1016/j.neulet.2008.08.060
Premer C, Lamondin C, Mitzey A, Speth RC, Brownfield MS: Immunohistochemical localization of AT1a, AT1b, and AT2 angiotensin II receptor subtypes in the Rat adrenal, pituitary, and brain with a perspective commentary. Int J Hypertens 2013, 2013: 175428. 10.1155/2013/175428
Vargovic P, Ukropec J, Laukova M, Kurdiova T, Balaz M, Manz B, Ukropcova B, Kvetnansky R: Repeated immobilization stress induces catecholamine production in rat mesenteric adipocytes. Stress 2013, 16: 340–352. 10.3109/10253890.2012.736046
Kvetnansky R, Ukropec J, Laukova M, Manz B, Pacak K, Vargovic P: Stress stimulates production of catecholamines in rat adipocytes. Cell Mol Neurobiol 2012, 32: 801–813. 10.1007/s10571-012-9822-6
Tsutsumi Y, Matsubara H, Ohkubo N, Mori Y, Nozawa Y, Murasawa S, Kijima K, Maruyama K, Masaki H, Moriguchi Y, Shibasaki Y, Kamihata H, Inada M, Iwasaka T: Angiotensin II type 2 receptor is upregulated in human heart with interstitial fibrosis, and cardiac fibroblasts are the major cell type for its expression. Circ Res 1998, 83: 1035–1046. 10.1161/01.RES.83.10.1035
Chamsi-Pasha MA, Shao Z, Tang WH: Angiotensin-converting enzyme 2 as a therapeutic target for heart failure. Curr Heart Fail Rep 2014, 11: 58–63. 10.1007/s11897-013-0178-0
Bader M: ACE2, angiotensin-(1–7), and Mas: the other side of the coin. Pflugers Arch 2013, 465: 79–85. 10.1007/s00424-012-1120-0
Qi Y, Zhang J, Cole-Jeffrey CT, Shenoy V, Espejo A, Hanna M, Song C, Pepine CJ, Katovich MJ, Raizada MK: Diminazene aceturate enhances angiotensin-converting enzyme 2 activity and attenuates ischemia-induced cardiac pathophysiology. Hypertension 2013, 62: 746–752. 10.1161/HYPERTENSIONAHA.113.01337
This study was supported by postdoctoral financial grant (number 201104901916) from the China postdoctoral science foundation and grant (number C12046) from Chengdu Military Command. The authors thank Shiliang Huang for his technical assistance.
The authors declare that they have no competing interest.
Electronic supplementary material
Additional file 1: Figure S1.: A model of stress-induced cardiomyopathy was established in rabbits by vagal electrical stimulation according to the method of Takato et al. . Female rabbits (weighing approximately 2 kg; General Hospital of Chengdu Military Command, Kunming, China) were anesthetized (100 mg/kg ketamine, 5 mg/kg xylazine, intramuscular injection). The right cervical vagus was exposed (A). Electrical stimulations of 50-Hz intensity and l-ms duration with stepwise voltage increases from 0.1 to 1.0 V were applied to the right cervical vagus under electrocardiographic monitoring. Stimulation was maintained for 1 minute with a pause of 2 minutes between each stimulation for approximately 1 hour (B). (DOC 259 KB)
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Xi, Yy., Liu, B., Yang, Lx. et al. Changes in levels of angiotensin II and its receptors in a model of inverted stress-induced cardiomyopathy. Eur J Med Res 19, 54 (2014). https://doi.org/10.1186/s40001-014-0054-8