|Induction of chagasic-like arrhythmias in the isolated beating hearts of healthy rats perfused with Trypanosoma cruzi-conditioned medium.|
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|PMID: 23314340 Owner: NLM Status: Publisher|
|Chagas' myocardiopathy, caused by the intracellular protozoan Trypanosoma cruzi, is characterized by microvascular alterations, heart failure and arrhythmias. Ischemia and arrythmogenesis have been attributed to proteins shed by the parasite, although this has not been fully demonstrated. The aim of the present investigation was to study the effect of substances shed by T. cruzi on ischemia/reperfusion-induced arrhythmias. We performed a triple ischemia-reperfusion (I/R) protocol whereby the isolated beating rat hearts were perfused with either Vero-control or Vero T. cruzi-infected conditioned medium during the different stages of ischemia and subsequently reperfused with Tyrode's solution. ECG and heart rate were recorded during the entire experiment. We observed that triple I/R-induced bradycardia was associated with the generation of auricular-ventricular blockade during ischemia and non-sustained nodal and ventricular tachycardia during reperfusion. Interestingly, perfusion with Vero-infected medium produced a delay in the reperfusion-induced recovery of heart rate, increased the frequency of tachycardic events and induced ventricular fibrillation. These results suggest that the presence of parasite-shed substances in conditioned media enhances the arrhythmogenic effects that occur during the I/R protocol.|
|H Rodriguez-Angulo; J Toro-Mendoza; J Marques; R Bonfante-Cabarcas; A Mijares|
|Type: JOURNAL ARTICLE Date: 2013-1-11|
|Title: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas / Sociedade Brasileira de Biofisica ... [et al.] Volume: - ISSN: 1414-431X ISO Abbreviation: Braz. J. Med. Biol. Res. Publication Date: 2013 Jan|
|Created Date: 2013-1-14 Completed Date: - Revised Date: -|
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|Nlm Unique ID: 8112917 Medline TA: Braz J Med Biol Res Country: -|
|Languages: ENG Pagination: 1-7 Citation Subset: -|
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Journal ID (nlm-ta): Braz J Med Biol Res
Journal ID (iso-abbrev): Braz. J. Med. Biol. Res
Publisher: Associação Brasileira de Divulgação Científica
Received Day: 25 Month: 5 Year: 2012
Accepted Day: 3 Month: 9 Year: 2012
Electronic publication date: Day: 11 Month: 1 Year: 2013
collection publication date: Month: 1 Year: 2013
Volume: 46 Issue: 1
First Page: 58 Last Page: 64
PubMed Id: 23314340
|Induction of chagasic-like arrhythmias in the isolated beating hearts of healthy rats perfused with Trypanosoma cruzi-conditioned medium|
1Instituto Venezolano de Investigaciones Científicas, Centro de Biofísica y Bioquímica, Caracas, Venezuela
2Instituto Venezolano de Investigaciones Científicas, Centro de Estudios Interdisciplinarios de la Física, Caracas, Venezuela
3Instituto de Medicina Tropical, Universidad Central de Venezuela, Servicio de Cardiología, Caracas, Venezuela
4Universidad Centroccidental “Lisandro Alvarado”, Unidad de Investigación en Bioquímica, Decanato de Ciencias de la Salud, Barquisimeto, Venezuela
|Correspondence: Correspondence: J. Toro-Mendoza, Centro de Estudios Interdisciplinarios de la Física, Instituto Venezolano de Investigaciones Científicas, Caracas, 1020A, Venezuela, E-mail: firstname.lastname@example.org and/or email@example.com
Chagas' disease is a tropical disease, initially confined to Central and South America, caused by the intracellular protozoan Trypanosoma cruzi. This illness is characterized by an acute phase, which is generally asymptomatic or oligosymptomatic; an indeterminate phase, which may persist for several years, and a chronic phase, when dilated cardiomyopathy and arrhythmias are primarily observed. Chagasic cardiomyopathy has been attributed to an imbalance between adrenergic or cholinergic innervations, cellular and humoral autoimmunity, parasitic effects, or microischemic disturbances 1.
The phenomenon of microvascular alterations and the generation of microischemic foci have been studied extensively during the acute and chronic phases of Chagas' disease. Several researchers have described changes indicative of ischemia in the hearts of chagasic patients, mainly associated with platelet aggregation 2, thinning of the capillary basement membranes 3, and areas of focal vascular constriction, microaneurysms, and dilatation of vascular beds in murine hearts during the acute phase of this infection 4. These disturbances could generate or enhance arrhythmias that are observed during chronic Chagas' disease.
Cardiac arrhythmias are one of the most important disorders occurring during Chagas' disease. Traditionally, arrhythmias have been considered to be a consequence of cardiac structural changes that occur during the chronic phase. In this respect, the main alterations reported are atrial and ventricular extrasystoles, intraventricular and/or AV conduction disturbances, and primary ST-T wave changes 5. However, ST and T abnormalities, ventricular and supraventricular arrhythmias and low-voltage QRS have been reported in a recent acute oral outbreak characterized by high parasitemia 6, which suggest that the parasite may have a role in arrhythmia generation. The mechanisms associated with non-structural-related arrhythmias in Chagas' disease are poorly understood.
Soluble factors that are generated during ischemia have been linked to cardiac arrhythmias, which are observed in isolated beating chagasic hearts 7. Moreover, it is known that T. cruzi can release several substances into the extracellular milieu that produce alterations in microvascular 8 and intracellular calcium homeostasis B09, 9,10, thereby contributing to arrhythmogenesis. Nevertheless, the association between proteins that are secreted and/or shed by T. cruzi and the disturbances in heart conduction system and arrhythmias has not been fully elucidated. The aim of the present study was to determine whether perfusion of non-chagasic beating hearts with substances released by T. cruzi can potentiate arrhythmias under ischemic conditions. Therefore, we performed a triple ischemia/reperfusion (I/R) protocol to induce the ischemic and pro-arrhythmic conditions that are present in chronic chagasic hearts. To obtain quantitative information, the effects on heart rate (HR) were analyzed by fitting against a double-logistic model, and the results were compared to the changes observed in the ECG recordings during the different protocol stages.
Vero cells were plated in a 75-cm2 Easy Flask in 20-mL complete minimum essential medium (MEM) supplemented with 10% (v/v) fetal bovine serum (FBS), and were infected with 2 × 105 trypomastigotes/mL of the EP strain at a ratio of 2 parasites per cell. Noninvasive parasites were removed after 24 h and the initial medium was changed at this time. The conditioned media were collected on the 5th or 6th day post-infection. The criteria for medium collection were that a minimum of 75% Vero cells should have adhered and that at least 2.5 × 106 trypomastigotes/mL should be present in the supernatant. The medium was centrifuged at 1500 g for 10 min to separate the parasites, and the supernatant was subsequently filtered using a 0.2-µM membrane filter (Millipore®, USA) and stored at -20°C until use.
For the isolated beating heart experiments, hearts were removed from adult female Sprague Dawley rats weighing 300-400 g anesthetized ip with 40 mg/kg pentobarbital. The isolated hearts were placed in cold Tyrode's solution (25 mM sodium bicarbonate, 10 mM glucose, 116 mM sodium chloride, 3.3 mM potassium chloride, 2.5 mM calcium chloride, and 1 mM magnesium sulfate), cannulated through the aorta, and perfused in a retrograde manner with warm Tyrode's solution (37°C) for 30 min by using the isolated beating heart system (AD Instruments, Australia). The presence of sinus rhythm, HR greater than 180 bpm, perfusion pressure higher than 30 mmHg, and a flow rate of 8-10 mL/min were considered to be stable values for all experiments. All procedures were approved by the Institutional Committee of the Venezuelan Institute for Scientific Research.
After stabilization was achieved, a protocol consisting of three consecutive I/R cycles (10 and 20 min, respectively) was initiated. During each ischemic cycle, deoxygenated complete MEM (1.8 mM calcium chloride, 0.81 mM magnesium sulfate, 5.33 mM potassium chloride, 117.24 mM sodium chloride, 1.01 mM sodium phosphate monobasic, 5.56 mM D-glucose, plus L-glutamine, phenol red and essential amino acids) supplemented with 24 mM sodium bicarbonate was perfused at a low flow rate (2 mL/min) for 10 min, followed by reperfusion with oxygenated Tyrode's solution for 20 min (flow of 8 to 10 mL/min). During the ischemic periods, the hearts were perfused with medium that was conditioned with either control Vero cells (Vero-control medium, n = 12) or infected Vero cells (Vero-infected medium, n = 14). Both of these media contained 10% FBS (v/v).
For biochemical analysis of the I/R process, we determined aspartate aminotransferase (AST) activity by sampling the effusate to indicate cardiac damage. The samples were collected every 2 min for a period of 30 min. The samples were immediately frozen and stored at -20°C until further processing. The enzyme activity was measured with a commercially available ELISA kit (Invelab™, Venezuela) according to manufacturer specifications.
In this study, we used a double-logistic model 11
Data are reported as means ± SE. The Student t-test was used to determine statistical significance, and results with P < 0.05 were considered to be statistically significant. The χ2 test was used to compare the ventricular fibrillation rate between the groups. Data analysis was performed using the Prism5® software (GraphPad Software, Inc., USA).
To evaluate cardiac damage during the I/R cycles, we collected the media after heart reperfusion and measured AST activity (Figure 1). A rapid increase in enzymatic activity was observed during the three ischemic phases (0-10, 30-40 and 60-70 min; Figure 1, thick black lines), which returned to basal levels during reperfusion. The enzymatic activity was not found to be different between the different ischemic cycles; therefore, these results suggest that our protocol produced a transient damage to the isolated beating hearts. Similarly, no significant differences were observed between the hearts that were perfused with Vero-control or Vero-infected medium (Figure 1).
Figure 2 demonstrates the fitting of Equation 1 to HR kinetics during the I/R protocol for perfusion with Vero-control (A) or Vero-infected conditioned (B) medium (r2 = 0.94 and 0.92, respectively). The plot shows that HR recovery (P5) was significantly slower in hearts perfused with Vero-infected medium compared to Vero-control medium (0.53 ± 0.1422 vs 2.87 ± 0.36555, P = 0.0006). Interestingly, these results were associated with bradyarrhythmias, particularly sinus arrest during the reperfusion period (middle portion of Figure 3), and were not observed in hearts perfused with Vero-control (top portion of Figure 3) that showed AV blockade during the final phase of ischemia.
In addition, tachyarrhythmias and the low-voltage QRS complex generated during perfusion of Vero-infected medium are displayed in Figure 3A (Vero-infected “2”, bottom). Ventricular tachycardia was observed during the first reperfusion phase, whereas ventricular fibrillation was noted during the last reperfusion phase. Hearts perfused with Vero-infected medium demonstrated atrial flutter and nodal and ventricular tachycardia during the I/R stages, whereas in hearts perfused with Vero-control medium, nodal and ventricular tachycardia was observed in the reperfusion stage only. Overall, 1.5 ± 0.43 tachyarrhythmic events/record were recorded in hearts perfused with Vero-infected medium, whereas 0.25 ± 0.13 tachyarrhythmic events/record were recorded in hearts perfused with Vero-control medium (P = 0.0156). Ventricular fibrillation was detected in 4 of 14 hearts perfused with Vero-infected medium compared to 0 of 12 hearts perfused with Vero-control medium (P = 0.0441).
Ischemia-reperfusion can lead to arrhythmias and sudden death. In particular, ischemia can lead to ventricular tachycardia and, finally, ventricular fibrillation 12. These events correlate with a concomitant increase in the intracellular H+, Na+, and Ca2+ levels 12, affecting the cardiac action potential and thereby generating arrhythmias. Furthermore, microvascular alterations observed in Chagas' disease could produce transient ischemia 2, and this is probably due to parasite-shed proteins 13. However, their participation in arrythmogenesis, which is observed in Chagas' disease, are still unclear.
The fitting of a double-logistic equation (Equation 1) to model the I/R process is suitable to quantify and compare the different situations explained above. Despite the high complexity of the heart dynamics, the tendency shown allows us to use this tool to have an idea of the kinetics of the process with a reasonable degree of precision. However, a full mathematical description of the heart is far from being obtained and is out of the scope of the present study.
During our experiments, we observed an increase in the frequency of tachyarrhythmias during perfusion with Vero-infected medium; therefore, we suggest that proteins present in the conditioned medium have the ability to enhance arrhythmias, probably by increasing the intracellular calcium levels. During parasite-host cell interaction, several secreted or released proteins can bind to the host cell receptors and modify cellular signaling. The different mucins present on the surface of trypomastigotes have been associated with the process of invasion. The protein gp82, a surface mucin of T. cruzi, causes an increase in intracellular calcium in Hela cells infected with metacyclic trypomastigotes, an effect mediated by IP3, phospholipase C and protein tyrosine kinase B09, 9,14. Gp90 and gp35/50 proteins are involved in the modulation of calcium increase in the host cell and the invasiveness of the strain of the parasite in which they are present 15. On the other hand, it has been reported that protein members of the transialidase and mucin family attach to the host cells and increase the intracellular calcium levels 13. Similarly, parasite cysteine proteases can cleave extracellular precursors, such as kininogens, which in turn bind to the host cell BK2R receptors and increase the intracellular calcium concentration 16. These phenomena facilitate the entry of the parasite into its respective host cell.
Interestingly, the existence of calcium overload in the ventricular myocytes of chagasic patients was recently reported 17. It is well known that increases in the intracellular calcium levels are responsible for the extension of the plateau phase of the cardiac action potential. This phenomenon contributes to the generation of re-entry circuits and therefore the appearance of malignant ventricular arrhythmias 18. It is possible that the calcium overload that occurs during parasitic invasion of the cardiac cells can potentiate the proarrhythmogenic status produced by the ischemia due to microvascular alterations, which is observed in Chagas' disease.
Ventricular arrhythmias observed in the isolated beating chagasic hearts have been attributed to the activation of adenosine and adrenergic systems, both of which are present during ischemia 7. To our knowledge, this is the first report that demonstrates a causal link between trypomastigote-conditioned medium and arrythmogenesis in Chagas' disease.
Other ionic currents may be associated with electrical alterations produced by T. cruzi-conditioned medium. Pacioretty et al. 19 reported a reduction of transient outward potassium current in epicardial myocytes during the acute phase of Chagas' disease. This reduction was associated with the parasitemia peak, suggesting that a direct action of the parasite may be involved in this effect. Also, sera from chagasic patients with beta-adrenergic activity shortened the QT interval and the action potential duration and increased slow inward potassium current (IKs) and inward calcium current (Ica) 20.
On the other hand, parasite-cell interaction relies on specific signaling pathways in the host cells that facilitate the entry of the parasite, which could contribute to the physiopathology of the disease. Andrade et al. 21 reported that exogenous endothelin-1 (ET-1) potentiated T. cruzi uptake in vitro and was associated with interstitial edema elicited by extracellular trypomastigotes. ET-1 is a potent vasoconstrictor and is present in high levels in the serum of chagasic patients. ET-1 induces vasospasm in T. cruzi-infected mice, consequently contributing to the development of myocardial ischemia and myonecrosis 16. Additionally, other non-protein soluble mediators are secreted by the parasite and may be related to ischemic and electrical disturbances in chagasic hearts. T. cruzi-derived thromboxane A2 (TXA2) has been detected in the circulation of infected mice 22. Interestingly, TXA2 has been associated with reperfusion arrhythmias 23. Therefore, it could be involved in the arrythmogenesis observed in Chagas' disease.
Perfusion with conditioned media produced a delay in HR recovery during the early reperfusion phase (see Figures 2 and 3). This is particularly relevant because it has been widely reported that Chagas' disease is characterized by an alteration in the heart conduction pathways, which leads to AV block and sinus arrest among other complications 24. In addition, it has been reported that sera obtained from chronic chagasic patients who suffer from complex cardiac arrhythmias show depressed electrogenesis and conduction when used in different isolated beating heart preparations 25. It has been suggested that dampening of electrogenesis and bradyarrhythmias is due to the presence of autoantibodies against the second extracellular loop of cardiac M2 acetylcholine receptor and β2 adrenoceptor B26, 26,27. Interestingly, some investigators have reported a decrease in the expression of connexin 43, a gap junction protein, in the infected cardiac myocytes 28. This implies a causal relationship between parasitic infection and cardiac conduction disorders. However, to our knowledge, this is the first report that demonstrates the association of cardiac bradyarrhythmias with the perfusion of T. cruzi-conditioned medium.
We developed an experimental protocol to reproduce the ischemic and pro-arrhythmic conditions that exist in chronic chagasic hearts. The application of a double-logistic model allows the comparison of HR in the different media perfused. Our results suggest that substances present in the conditioned media have the ability to enhance I/R-induced arrhythmic and conduction disorders, which are similar to those observed in chagasic cardiomyopathy.
Research supported by IVIC, project #N-305, and by Misión Ciencia, Ministerio del Poder Popular para la Ciencia y Tecnología, Fondo Nacional de Ciencia y Tecnología (FONACIT), project #2007001425.
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[Figure ID: f01]
Average evolution of enzymatic activity (AST) in ischemia-reperfusion cycles. The graph shows the values of enzymatic activity measured every 2 min during the three ischemia-reperfusion cycles. Thick horizontal lines (top) indicate the different ischemia stages and are identified as I1 (ischemia 1), I2 (ischemia 2), and I3 (ischemia 3) and match the increased AST activity. The graph averages the data of Vero-control (n = 12) and Vero-infected hearts (n = 14).
[Figure ID: f02]
Average heart rate (HR) during the ischemia-reperfusion process. Dotted lines represent the mean ± SE HR in all ischemia-reperfusion cycles. Panel A shows the data of Vero-control-perfused hearts (n = 12), and Panel B shows data of Vero-infected-perfused hearts (n = 14). Continuous lines are the results of the fitting of Equation 1, and parameters are shown in the inset.
[Figure ID: f03]
Panel A shows representative ECG recordings of the ischemia-reperfusion process for different perfused media. The figure shows the ECG recordings during the different stages of ischemia-reperfusion processes, which were identified as I1, I2, I3 for the three ischemia stages and as R1, R2, and R3 for the reperfusion ones. The upper recording shows the ECG of an isolated beating heart perfused with Vero cell-conditioned medium (Vero-control), and the middle and bottom recordings show ECGs of two different isolated beating hearts perfused with Vero-infected-conditioned medium. Panel B shows a numerical comparison of tachyarrhythmia and ventricular fibrillation events between Vero-control and Vero-infected perfused hearts. The P value was 0.0138 in tachyarrhythmia comparison (Student t-test) and 0.0441 in ventricular fibrillation comparison (chi-square test).
Keywords: Chagas' disease, Arrhythmias, Ischemia.
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