The pathological conse-quences of ischemic heart disease involve signaling through the autonomic nervous system. Although early activation may serve to maintain hemodynamic stability, persistent aberrant sympathoexcitation contributes to the development of lethal arrhythmias and heart failure. We hypothesized that as the myocardium reacts and remodels to ischemic injury over time, there is an analogous sequence of gene expression changes in the thoracic spinal cord dorsal horn, the processing center for incoming afferent fibers from the heart to the central nervous system. Acute and chronic myocardial ischemia (MI) was induced in a large animal model of Yorkshire pigs, and the thoracic dorsal horn of treated pigs, along with control nonischemic pigs, was harvested for transcriptome analysis. We identified 32 differentially expressed genes between healthy and acute ischemia cohorts and 46 differentially expressed genes between healthy and chronic ischemia cohorts. The canonical immediate-early gene c-fos was upregulated after acute MI, along with fosB, dual specificity phosphatase 1 and 2 (dusp1 and dusp2), and early growth response 2 (egr2). After chronic MI, there was a persistent yet unique activation of immediate-early genes, including fosB, nuclear receptor subfamily 4 group A members 1±3 (nr4a1, nr4a2, and nr4a3), egr3, and TNF-β-induced protein 3 (tnfaip3). In addition, differentially expressed genes from the chronic MI signature were enriched in pathways linked to apoptosis, immune regulation, and the stress response. These findings support a dynamic progression of gene expression changes in the dorsal horn with maturation of myocardial injury, and they may explain how early adaptive autonomic nervous system responses can maintain hemodynamic stability, whereas prolonged maladaptive signals can predispose patients to arrhythmias and heart failure. NEW & NOTEWORTHY Activation of the autonomic nervous system after myocardial injury can provide early cardiovascular support or prolonged aberrant sympathoexcitation. The later response can lead to lethal arrhythmias and heart failure. This study provides evidence of ongoing changes in the gene expression signature of the spinal cord dorsal horn as myocardial injury progresses over time. These changes could help explain how an adaptive nervous system response can become maladaptive over time.

Background Autonomic regulation therapy involving either vagus nerve stimulation (VNS) or spinal cord stimulation (SCS) represents emerging bioelectronic therapies for heart disease. The objective of this study was to determine if VNS and/or SCS modulate primary cardiac afferent sensory transduction of the ischemic myocardium. Methods Using extracellular recordings in 19 anesthetized canines, of 88 neurons evaluated, 36 ventricular-related nodose ganglia sensory neurons were identified by their functional activity responses to epicardial touch, chemical activation of their sensory neurites (epicardial veratridine) and great vessel (descending aorta or inferior vena cava) occlusion. Neural responses to 1 min left anterior descending (LAD) coronary artery occlusion (CAO) were then evaluated. These interventions were then studied following either: i) SCS [T1-T3 spinal level; 50 Hz, 90% motor threshold] or ii) cervical VNS [15–20 Hz; 1.2 × threshold]. Results LAD occlusion activated 66% of identified nodose ventricular sensory neurons (0.33 ± 0.08–0.79 ± 0.20 Hz; baseline to CAO; p < 0.002). Basal activity of cardiac-related nodose neurons was differentially reduced by VNS (0.31 ± 0.11 to 0.05 ± 0.02 Hz; p < 0.05) as compared to SCS (0.36 ± 0.12 to 0.28 ± 0.14, p = 0.59), with their activity response to transient LAD CAO being suppressed by either SCS (0.85 ± 0.39–0.11 ± 0.04 Hz; p < 0.03) or VNS (0.75 ± 0.27–0.12 ± 0.05 Hz; p < 0.04). VNS did not alter evoked neural responses of cardiac-related nodose neurons to great vessel occlusion. Conclusions Both VNS and SCS obtund ventricular ischemia induced enhancement of nodose afferent neuronal inputs to the medulla.

Miniswine underwent procedures to evaluate treating chronic ischemia with the implantation of autologous satellite cells and laser transmyocardial revascularization (TMR). The objective was to combine two therapies to restore cardiac function. This experiment involved three surgical procedures: (1) placing a constrictor on the coronary artery; (2) producing channels and implanting cells; (3) obtaining samples. The swine were divided into groups: Group 1, Ischemia; Group 2, Ischemia + Laser TMR; Group 3, Ischemia + Laser TMR+ Cells; Group 4, Ischemia + Cells. Sonomicrometry and Millar pressure transducers were used to determine contractility, left ventricular pressure, and pressure-volume loops. There were no significant differences (p<0.05)among the hemodynamic data except for Group 4, which produced significantly lower output values. Morphological evaluation revealed a significantly reduced scar area in Group 3. Although there was a significant difference in scar area, the phenomena behind this improvement as compared to the unimproved hemodynamic function is not understood.

No description available.

<p>Worldwide, more than 2 million patients die within 30 days after noncardiac surgery anually. Postoperative ischemic myocardial injury is frequent, however, no consensus exists about its definition.</p> <p><strong>Objective: </strong>to develop a term Myocardial Injury after Noncardiac Surgery (MINS) caused by myocardial ischemia, requiring at least, troponin T (TnT) elevation, and with prognostic relevance at 30 days after surgery.</p> <p><strong>Methods: </strong>we performed a prospective study including 15,167 patients ³45 years-old undergoing noncardiac surgery, who had fourth-generation TnT measurements during the first 3 postoperative days. We undertook Cox regression analyses with 30-day mortality after surgery as the dependent variable, using different TnT thresholds, clinical features and several perioperative variables. Non-ischemic etiologies were excluded. Furthermore, we developed a scoring system to predict risk in MINS patients.</p> <p><strong>Results:</strong> MINS was defined as TnT ≥0.03 ng/mL with or without clinical features, and it was an independent predictor of 30-day mortality (adjusted HR 3.82, CI 95% 2.84-5.10). We determined that MINS incidence was 8%, its population attributable risk 33.7%, and 30-days mortality rate 9.6%. Patients did not experience ischemic symptoms in 84% of MINS cases. Additionally, we developed a scoring system in patients suffering MINS with 3 independent predictors of death (age ≥75 years, new ST elevation or left bundle branch block, and anterior location of ECG changes),</p> <p><strong>Conclusion: </strong>Among patients undergoing noncardiac surgery, we defined MINS based on a TnT threshold ≥0.03 ng/mL. Mostly, MINS patients were asymptomatic. Therefore, this strongly suggests the importance of a troponin monitoring during the first few days after surgery.</p> / Master of Health Sciences (MSc)

No description available.

Introduction : La prévention de la mort de cellules cardiaques contractiles suite à un épisode d'infarctus du myocarde représente le plus grand défi dans la récupération de la fonction cardiaque. On a démontré à maintes reprises que l'ocytocine (OT), l'hormone bien connue pour ses rôles dans le comportement social et reproductif et couramment utilisée dans l’induction de l’accouchement, diminue la taille de l'infarctus et améliore la récupération fonctionnelle du myocarde blessé. Les mécanismes de cette protection ne sont pas totalement compris. Objectif : Étudier les effets d'un traitement avec de l'ocytocine sur des cardiomyocytes isolés en utilisant un modèle in vitro qui simule les conditions d'un infarctus du myocarde. Méthodes : La lignée cellulaire myoblastique H9c2 a été utilisée comme modèle de cardiomyocyte. Pour simuler le dommage d'ischémie-reperfusion (IR), les cellules ont été placées dans un tampon ischémique et incubées dans une chambre anoxique pendant 2 heures. La reperfusion a été accomplie par la restauration du milieu de culture régulier dans des conditions normales d'oxygène. L'OT a été administrée en présence ou en absence d'inhibiteurs de kinases connues pour être impliquées dans la cardioprotection. La mortalité cellulaire a été évaluée par TUNEL et l'activité mitochondriale par la production de formazan pendant 1 à 4 heures de reperfusion. La microscopie confocale a servie pour localiser les structures cellulaires. Résultats : Le modèle expérimental de l'IR dans les cellules H9c2 a été caractérisé par une diminution dans la production de formazan (aux alentours de 50 à 70 % du groupe témoin, p < 0.001) et par l'augmentation du nombre de noyaux TUNEL-positif (11.7 ± 4.5% contre 1.3 ± 0.7% pour le contrôle). L'addition de l'OT (10-7 a 10-9 M) au commencement de la reperfusion a inversé les effets de l'IR jusqu'aux niveaux du contrôle (p < 0.001). L'effet protecteur de l'OT a été abrogé par : i) un antagoniste de l'OT ; ii) le knockdown de l'expression du récepteur à l'OT induit par le siRNA ; iii) la wortmannin, l'inhibiteur de phosphatidylinositol 3-kinases ; iv) KT5823, l'inhibiteur de la protéine kinase dépendante du cGMP (PKG); v) l'ODQ, un inhibiteur du guanylate cyclase (GC) soluble, et A71915, un antagoniste du GC membranaire. L'analyse confocale des cellules traitées avec OT a révélé la translocation du récepteur à l'OT et la forme phosphorylée de l'Akt (Thr 308, p-Akt) dans le noyau et dans les mitochondries. Conclusions : L'OT protège directement la viabilité des cardiomyocytes, lorsqu'elle est administrée au début de la reperfusion, par le déclenchement de la signalisation du PI3K, la phosphorylation de l'Akt et son trafic cellulaire. La cytoprotection médiée par l'OT implique la production de cGMP par les deux formes de GC. / Introduction: The prevention of the death of contractile cardiac cells following an episode of myocardial infarction represents the largest challenge in the recovery of myocardial function. Oxytocin, the hormone best known for its roles in reproduction and social behaviour and used commonly for the induction of parturition, has been repeatedly demonstrated to decrease the infarct size and to ameliorate the functional recovery of the injured myocardium. The mechanisms for this protection are incompletely understood. Objective: To study the effects of oxytocin treatment on isolated cardiomyocytes using an in vitro model simulating the conditions of a myocardial infarction. Methods: The cardiomyoblastic cell line H9c2 was used as a model of cardiomyocyte. For IR injury, the cells were placed in ischemic buffer and incubated in an anoxic chamber for 2 hours. Reperfusion was achieved by restoring cell media under normoxic conditions. OT was administered in the presence or absence of enzyme inhibitors. Cell death was evaluated by TUNEL and mitochondrial activity by formazan production during 1-4 hours of reperfusion. Confocal microscopy served for localization of cell structures. Results. The experimental model of IR in H9c2 cells was characterized by decreased formazan production (at the range of 50-70% of normoxic control, p < 0.001) and by the increased number of TUNEL-positive nuclei (11.7±4.5 vs. 1.3±0.7% in normoxic control). The addition of OT (10-7 to 10-9 M) at the onset of reperfusion reversed the effects of IR to the control levels (p < 0.001). The protective effect of OT was abrogated by: i) an OT antagonist, OTA and siRNA-mediated OT receptor knockout; ii) the phosphatidylinositol 3-kinases inhibitor wortmannin; iii) the cGMP-dependent protein kinase (PKG) inhibitor, KT5823. Soluble guanylate cyclase (GC) inhibitor ODQ and particulate GC antagonist A71915 only partially blocked the protective effects of OT. Confocal analysis of OT-treated cells revealed translocation of OT receptor and the phosphorylated form of Akt (Thr 308, p-Akt) into the nucleus and mitochondria. Conclusions: OT directly protects cardiomyocyte viability if administered at the onset of reperfusion by triggering signaling of Pi3K, Akt phosphorylation and its cellular trafficking. OT-mediated cytoprotection involves cGMP production by both forms of GC.

Os Hormônios Tiroideanos (HT) representam um fenótipo de cardioproteção e influenciam no estado trófico do tecido cardíaco através de diversos mecanismos, dentre eles a modulação dos componentes do Sistema Renina Angiotensina- a Angiotensina II e seus receptores (AT1 e AT2). Este estudo teve como objetivos avaliar o papel do receptor AT2 na cardioproteção induzida pelo HT e a participação da proteína quinase ativada por AMP (AMPK) nesse processo. O modelo de isquemia e reperfusão (I/R) foi desenvolvido em corações de ratos submetidos ao hipertiroidismo experimental na presença ou ausêcia do antagonista do receptor AT2 (PD123319), utilizando-se o aparto de Langendorff. Os resultados mostraram que o HT exerce efeito cardioprotetor com aumento na expressão protéica do receptor AT2 e da AMPK fosforilada, que foi prevenido com a administração do PD, seguido de piora da função cardíaca. Estes dados sugerem que parte da cardioproteção induzida pelo HT é mediada pelo receptor AT2, e que a AMPK também está envolvida proteção do miocárdio após injúria por I/R. / Thyroid Hormones (TH) is a phenotype of cardioprotection and may influence the trophic state of cardiac tissue through several mechanisms, including the modulation of the components of renin-angiotensin system - angiotensin II and its receptors (AT1 and AT2). The present study aimed to evaluate the role of AT2 receptor in cardioprotection mediated by the TH and the involvement of AMP-activated protein kinase (AMPK) in this context. A model of Ischemia and Reperfusion (I/R) was performed in isolated hearts of rats subjected to experimental hyperthyroidism, in the presence or absence of the AT2 receptor antagonist (PD123319), using the Langendorff system. The results showed that TH exerts cardioprotective effect with increased levels of AT2 and phosphorylated AMP protein expression, which was prevented by the administration of PD, with a loss in cardiac function. These data suggest that part of the TH-induced cardioprotection is mediated by the AT2 receptor with the involvement of AMPK in protection of the myocardium after I/R injury.

A angiotomografia de múltiplos detectores (TC) é um exame útil no diagnóstico de doença arterial coronariana (DAC). Recentemente, a TC foi associada à perfusão miocárdica com estresse (PTC) para detectar DAC. O objetivo é comparar a perfusão miocárdica da TC, após estresse com dipiridamol, com a cintilografia miocárdica (SPECT) na detecção de estenose coronariana significativa (>70%), usando o cateterismo (CATE) como método de referência. Trinta e seis pacientes (62±8,0 anos, 20 homens) com suspeita de DAC e com SPECT positivo em menos de 2 meses foram submetidos a um protocolo de TC para avaliação da PTC e angiografia pela tomografia computadorizada (ATC). TC foi realizada em um equipamento de 64 detectores (Aquillion 64, Toshiba), com uma primeira aquisição com os seguintes parâmetros:100mA,120Kv, 32x1mm colimação e 60ml de contraste a 3ml/s, após estresse com dipiridamol (0,56mg/Kg/4min), seguida de uma aquisição de repouso/ATC após aminofilina e metoprolol (270-400mA, 120Kv,64x0,5mm e 80 ml de contraste a 5ml/s). Observadores cegos e independentes, sem conhecimento prévio dos dados clínicos ou dos exames, realizaram análise visual e quantitativa da perfusão e angiotomografia, além de análise angiográfica quantitativa (QCA) para avaliação do CATE. Todos os pacientes completaram o protocolo sem efeitos adversos com dose de radiação média de 14,7 ± 3,0 mSv e exames interpretáveis. PTC foi positiva em 27 de 36 pacientes (75%). Dos nove casos (25%) com discordâncias (PTC negativa e SPECT positivo), 6 pacientes tinham ATC ou CATE normal e 2 tinham estenose coronariana menor que 50%. Um apresentava stent pérvio e o outro um ramo diagonal com redução luminal de 50%.O terceiro paciente apresentava uma oclusão do ramo ventricular posterior da artéria coronária direita com circulação colateral detectado pela ATC e confirmado pelo CATE. A comparação entre a PTC e o SPECT em uma análise por paciente mostrou boa concordância (Kappa =0,53;p<0,001). Em 26 pacientes com CATE, como referência, os valores diagnósticos foram sensibilidade, especificidade, valor preditivo positivo, valor preditivo negativo e acurácia para a PTC 88,0; 79,3; 66,7; 93,3; 82,1% e para o SPECT 68,8; 76,1; 66,7; 77,8 e 73,1%, respectivamente. A perfusão miocárdica de repouso e estresse após dipiridamol na avaliação de doença aterosclerótica coronariana, associada à angiografia pela tomografia é factível e os resultados foram similares ao do SPECT. A combinação da informação anatômica e perfusional permite identificar os casos positivos do SPECT, sem estenose coronariana significativa. / Multidetector computed tomography is a useful method for the diagnosis of coronary artery disease. Recently, myocardial stress CT perfusion (CTP) was shown to detect myocardial ischemia. Our main objective was to evaluate the feasibility of dipyridamole stress CTP and compare to SPECT perfusion to detect significant coronary stenosis using conventional angiography (CCA) (stenosis >70%) as reference method. Thirty-six patients (62.0±8.0 years old, 20 males) with suspected CAD and < 2 months prior positive SPECT underwent a customized multidetector-row computed tomography (MDCT) protocol with rest/stress myocardial perfusion evaluation and CTA. MDCT was performed in a 64 scanner (Aquillion 64, Toshiba) with stress perfusion after 0.56mg/kg/4min of dipyridamole (100mA, 120 kV, collimation-32 x 1 mm and 60 ml of iodinated contrast) followed by aminophyline and metoprolol infusion prior to a second rest perfusion/CTA acquisition (270-400mA, 120 kV, collimation-64 x 0,5 mm and 80 ml of iodinated contrast). Independent blinded observers with no knowledge of clinical data or other exams performed visual and quantitative analysis of CTP, CTA, SPECT and quantitative coronary angiography (QCA) analysis, that was performed on CCA. All 36 patients completed the CT protocol with no adverse events, mean radiation dose of 14.7 ± 3.0 mSv and with interpretable scans. CTP was positive in 27 of 36 patients (75%). From the 9 (25%) disagreements with normal CTP and positive SPECT, 6 patients had normal CCA or CTA and 2 had no coronary stenosis > 70 %. One had patent stents and the other had a diagonal branch with mild luminal reduction at CCA. The remaining patient had an occluded right posterior lateral branch with collateral flow detect by CTA and confirmed by CCA. Good agreement was demonstrated between CTP and SPECT on a per-patient analysis (kappa 0.53). In 26 patients using CCA as reference, sensitivity, specificity, positive predictive value, negative predictive values and accuracy for CTP were 88.0, 79.3, 66.7, 93.3%, 82,1% and for SPECT 68.8, 76.1, 66.7, 77.8% and 73,1% respectively. Rest and dipyridamole-stress computed tomography myocardial perfusion is feasible and results are similar to SPECT scintigraphy. The combined anatomical information provided by computed tomography coronary angiography may allow identification of false-positives on perfusion scans.

Introdução: recente estudo brasileiro detectou a presença concomitante do Mycoplasma pneumoniae e Chlamydia pneumoniae em lesões ateromatosas coronárias estáveis e instáveis. O objetivo do presente estudo foi testar a associação entre títulos sorológicos de anticorpos anti-Chlamydia pneumoniae e anti-Mycoplasma pneumoniae e as Síndromes Isquêmicas Miocárdicas Instáveis. Métodos: foram incluídos de forma prospectiva, 138 pacientes divididos em 4 grupos: 34 pacientes com Síndrome Isquêmica Miocárdica Instável com supradesnível do segmento ST, 40 pacientes com Síndrome Isquêmica Miocárdica Instável sem supradesnível ST, 30 pacientes com aterosclerose crônica assintomática e 34 doadores de sangue sem doença coronária conhecida. Nos dois primeiros grupos, as amostras sorológicas foram colhidas durante o evento agudo e com seis meses de seguimento, enquanto nos outros dois (aterosclerose crônica e controle) as mesmas foram colhidas uma única vez. Em todas as amostras foram dosados anticorpos da classe IgG anti-Chlamydia pneumoniae e anti-Mycoplasma pneumoniae utilizando a técnica de imunoflorescência indireta.. Resultados: seis meses após a internação, os pacientes com síndrome isquêmica miocárdica instável com supradesnível ST apresentaram significativa redução dos títulos sorológicos, em relação às sorologias colhidas durante o evento coronário agudo, o que ocorreu tanto com a chlamydia (307,5+47,5 versus 650+115,7 p=0,0001) quanto com o mycoplasma (21,5+3,5 versus 36,5+5 p=0,0004). O grupo sem supradesnível ST não teve variação significativa dos níveis sorológicos em seis meses de seguimento (522,6+102,7 versus 576+84,1 p=0,27) para chlamydia e 27,6+5,8 versus 27,6 + 5,8 p >0,99 para mycoplasma. Foi realizada também uma comparação entre os níveis sorológicos de todos os grupos analisados, e observou-se que os grupos com síndrome isquêmica miocárdica instável (com e sem supra ST), tiveram valores sorológicos mais elevados do que os grupos aterosclerose crônica e controle, mas as diferenças não foram significativas. Os valores para chlamydia foram: 650+115,7 (com supra), 576+84 (sem supra), 373,3+65 (aterosclerose crônica) e 343,5+57,2 (controle), p=0,083; e os valores para mycoplasma foram: 36,5+5 (com supra), 27,6+5,8 (sem supra), 23+4,3 (aterosclerose crônica) e 26,7+3,3 (controle), p=0,171. Conclusões: o presente estudo demonstra associação entre títulos de anticorpos anti-Chlamydia pneumoniae e anti-Mycoplasma pneumoniae e a instabilização da placa coronária. Demonstra ainda a normalização dos mesmos títulos em um período de até seis meses, a partir do quadro agudo. / Objective of the study: to test the association of serum titers of anti-Chlamydia pneumoniae and anti-Mycoplasma pneumoniae antibodies and Acute Coronary Syndrome (ACS). The patients were divided into 4 groups: ACS with ST-segment elevation, ACS without ST-segment elevation, chronic asymptomatic atherosclerosis and blood donors without known coronary disease. Serum samples were collected during the acute event and after six months of follow-up. Six months after the acute event, patients with ACS with St-segment elevation showed a significant decrease of serum titers, when compared to the other one. That\'s show the association between anti-Chlamydia pneumoniae and anti-Mycoplasma pneumoniae antibody titers and acute coronary syndrome.