RÉSUMÉ
The cardioprotective effect of ischemic preconditioning (IPC) and ischemic postconditioning (IPoC) in adult hearts is mediated by nitric oxide (NO). During the early developmental period, rat hearts exhibit higher resistance to ischemia-reperfusion (I/R) injury, contain higher levels of serum nitrates, and their resistance cannot be further increased by IPC or IPoC. NOS blocker (L-NAME) lowers their high resistance. Wistar rat hearts (postnatal Days 1 and 10) were perfused according to Langendorff and exposed to 40 min of global ischemia followed by reperfusion with or without IPoC. NO and reactive oxygen species donors (DEA-NONO, SIN-1) and L-NAME were administered. Tolerance to ischemia decreased between Days 1 and 10. DEA-NONO (low concentrations) significantly increased tolerance to I/R injury on both Days 1 and 10. SIN-1 increased tolerance to I/R injury on Day 10, but not on Day 1. L-NAME significantly reduced resistance to I/R injury on Day 1, but actually increased resistance to I/R injury on Day 10. Cardioprotection by IPoC on Day 10 was not affected by either NO donors or L-NAME. It can be concluded that resistance of the neonatal heart to I/R injury is NO dependent, but unlike in adult hearts, cardioprotective interventions, such as IPoC, are most likely NO independent.
Sujet(s)
Animaux nouveau-nés , Postconditionnement ischémique , Lésion de reperfusion myocardique , L-NAME , Monoxyde d'azote , Rat Wistar , Animaux , Monoxyde d'azote/métabolisme , Postconditionnement ischémique/méthodes , Lésion de reperfusion myocardique/prévention et contrôle , Lésion de reperfusion myocardique/métabolisme , Rats , L-NAME/pharmacologie , Préconditionnement ischémique myocardique/méthodes , Donneur d'oxyde nitrique/pharmacologie , Mâle , Coeur/effets des médicaments et des substances chimiques , Myocarde/métabolisme , Molsidomine/pharmacologie , Molsidomine/analogues et dérivésRÉSUMÉ
Aim. This study aimed to investigate the correlation between seismocardiographic and echocardiographic systolic variables and whether a decrease in preload could be detected by the seismocardiography (SCG).Methods. This study included a total of 34 subjects. SCG and electrocardiography were recorded simultaneously followed by echocardiography (echo) in both supine and 30â¦head-up tilted position. The SCG signals was segmented into individual heartbeats and systolic fiducial points were defined using a detection algorithm. Statistical analysis included correlation coefficient calculations and paired sample tests.Results. SCG was able to measure a decrease in preload by almost all of the examined systolic SCG variables. It was possible to correlate certain echo variables to SCG time intervals, amplitudes, and peak to peak intervals. Also, changes between supineand tilted position of some SCG variables were possible to correlate to changes in echo variables. LVET, IVCT, S', strain, SR, SV, and LVEF were significantly correlated to relevant SCG variables.Conclusion. This study showed a moderate correlation, between systolic echo and systolic SCG variables. Additionally, systolic SCG variables were able to detect a decrease in preload.
Sujet(s)
Algorithmes , Échocardiographie , Électrocardiographie , Systole , Humains , Échocardiographie/méthodes , Systole/physiologie , Mâle , Femelle , Adulte , Électrocardiographie/méthodes , Rythme cardiaque/physiologie , Adulte d'âge moyen , Jeune adulte , Coeur/imagerie diagnostique , Coeur/physiologieRÉSUMÉ
BACKGROUND: A compromised cardiac autonomic function has been found in subjects with insulin resistance related disorders such as obesity, impaired glucose tolerance (IGT) and type 2 diabetes and confers an increased risk of adverse cardiovascular outcomes. Growing evidence indicate that 1 h plasma glucose levels (1hPG) during an oral glucose tolerance test (OGTT) ≥ 155 mg/dl identify amongst subjects with normal glucose tolerance (NGT) a new category of prediabetes (NGT 1 h-high), harboring an increased risk of cardiovascular organ damage. In this study we explored the relationship between 1 h post-load hyperglycemia and cardiac autonomic dysfunction. METHODS: Presence of cardiac autonomic neuropathy (CAN) defined by cardiovascular autonomic reflex tests (CARTs) and heart rate variability (HRV), assessed by 24-h electrocardiography were evaluated in 88 non-diabetic subjects subdivided on the basis of OGTT data in: NGT with 1 h PG < 155 mg/dl (NGT 1 h-low), NGT 1 h-high and IGT. RESULTS: As compared to subjects with NGT 1 h-low, those with NGT 1 h-high and IGT were more likely to have CARTs defined CAN and reduced values of the 24 h time domain HVR parameters including standard deviation of all normal heart cycles (SDNN), standard deviation of the average RR interval for each 5 min segment (SDANN), square root of the differences between adjacent RR intervals (RMSSD), percentage of beats with a consecutive RR interval difference > 50 ms (PNN50) and Triangular index. Univariate analyses showed that 1hPG, but not fasting and 2hPG, was inversely associated with all the explored HVR parameters and positively with CARTs determined presence of CAN. In multivariate regression analysis models including several confounders we found that 1hPG was an independent contributor of HRV and presence of CAN. CONCLUSION: Subjects with 1hPG ≥ 155 mg/dl have an impaired cardiac autonomic function.
Sujet(s)
Système nerveux autonome , Glycémie , Hyperglycémie provoquée , Rythme cardiaque , Hyperglycémie , Humains , Études transversales , Mâle , Femelle , Adulte d'âge moyen , Système nerveux autonome/physiopathologie , Glycémie/métabolisme , Hyperglycémie/physiopathologie , Hyperglycémie/sang , Hyperglycémie/diagnostic , Adulte , Facteurs temps , Marqueurs biologiques/sang , Maladies du système nerveux autonome/physiopathologie , Maladies du système nerveux autonome/diagnostic , Maladies du système nerveux autonome/sang , Coeur/innervation , Coeur/physiopathologie , Électrocardiographie ambulatoire , État prédiabétique/physiopathologie , État prédiabétique/diagnostic , État prédiabétique/sang , Intolérance au glucose/diagnostic , Intolérance au glucose/physiopathologie , Intolérance au glucose/sang , Facteurs de risqueRÉSUMÉ
Accurate motion estimation at high acceleration factors enables rapid motion-compensated reconstruction in Magnetic Resonance Imaging (MRI) without compromising the diagnostic image quality. In this work, we introduce an attention-aware deep learning-based framework that can perform non-rigid pairwise registration for fully sampled and accelerated MRI. We extract local visual representations to build similarity maps between the registered image pairs at multiple resolution levels and additionally leverage long-range contextual information using a transformer-based module to alleviate ambiguities in the presence of artifacts caused by undersampling. We combine local and global dependencies to perform simultaneous coarse and fine motion estimation. The proposed method was evaluated on in-house acquired fully sampled and accelerated data of 101 patients and 62 healthy subjects undergoing cardiac and thoracic MRI. The impact of motion estimation accuracy on the downstream task of motion-compensated reconstruction was analyzed. We demonstrate that our model derives reliable and consistent motion fields across different sampling trajectories (Cartesian and radial) and acceleration factors of up to 16x for cardiac motion and 30x for respiratory motion and achieves superior image quality in motion-compensated reconstruction qualitatively and quantitatively compared to conventional and recent deep learning-based approaches. The code is publicly available at https://github.com/lab-midas/GMARAFT.
Sujet(s)
Apprentissage profond , Coeur , Traitement d'image par ordinateur , Imagerie par résonance magnétique , Humains , Imagerie par résonance magnétique/méthodes , Traitement d'image par ordinateur/méthodes , Coeur/imagerie diagnostique , Algorithmes , Artéfacts , Mouvement/physiologie , Thorax/imagerie diagnostique , AdulteRÉSUMÉ
Without intervention, cardiac arrhythmias pose a risk of fatality. However, timely intervention can be challenging in environments where transporting a large, heavy defibrillator is impractical, or emergency surgery to implant cardiac stimulation devices is not feasible. Here, we introduce an injectable cardiac stimulator, a syringe loaded with a nanoparticle solution comprising a conductive polymer and a monomer that, upon injection, forms a conductive structure around the heart for cardiac stimulation. Following treatment, the electrode is cleared from the body, eliminating the need for surgical extraction. The mixture adheres to the beating heart in vivo without disrupting its normal rhythm. The electrofunctionalized injectable cardiac stimulator demonstrates a tissue-compatible Young's modulus of 21 kPa and a high conductivity of 55 S/cm. The injected electrode facilitates electrocardiogram measurements, regulates heartbeat in vivo, and rectifies arrhythmia. Conductive functionality is maintained for five consecutive days, and no toxicity is observed at the organism, organ, or cellular levels.
Sujet(s)
Troubles du rythme cardiaque , Animaux , Troubles du rythme cardiaque/thérapie , Troubles du rythme cardiaque/physiopathologie , Conductivité électrique , Coeur/physiologie , Nanoparticules/composition chimique , Électrocardiographie , Humains , Souris , Rythme cardiaque , Polymères/composition chimique , Mâle , Injections , Module d'élasticité , Électrothérapie/instrumentation , Électrothérapie/méthodes , Électrodes implantéesRÉSUMÉ
The analysis of cardiac wall mechanics is of importance for understanding coronary heart diseases (CHD). The inhalation of ultrafine particles could deteriorate CHD. The aim of the study is to investigate the effects of cardiac wall mechanics on rats of myocardial infarction (MI) after long-term inhalation of ultrafine Zn particles. Cardiac wall stresses and strains were computed, based on echocardiographic and hemodynamic measurements. It was found that MI resulted in the significantly elevated stresses and the reduced strains. The short-term inhalation of ultrafine Zn particles decreased stresses and increased strains in MI rats, but the long-term inhalation had the opposite effects. Hence, the short-term inhalation of ultrafine Zn particles could alleviate the MI-induced LV dysfunction while the long-term inhalation impaired it.
Sujet(s)
Infarctus du myocarde , Contrainte mécanique , Zinc , Infarctus du myocarde/physiopathologie , Animaux , Zinc/administration et posologie , Zinc/pharmacologie , Rats , Mâle , Facteurs temps , Administration par inhalation , Taille de particule , Rat Sprague-Dawley , Phénomènes biomécaniques , Coeur/effets des médicaments et des substances chimiques , Coeur/physiopathologie , Hémodynamique/effets des médicaments et des substances chimiquesRÉSUMÉ
Keaton Schuster completed his PhD in the lab of Rachel Smith-Bolton at the University of Illinois, USA, investigating Drosophila wing disc regeneration before joining Lionel Christiaen's lab at New York University, USA, for his postdoc studying heart regeneration in the chordate tunicate Ciona robusta (formerly Ciona intestinalis type A). Keaton is part of the second cohort of Development's Pathway to Independence Programme fellows and we spoke to him over Teams to learn more about his career to date and his future plans for starting his own group continuing to use emerging model systems to study cardiac regeneration.
Sujet(s)
Ciona intestinalis , Animaux , Histoire du 21ème siècle , Ciona intestinalis/physiologie , Régénération/physiologie , Histoire du 20ème siècle , Biologie du développement/histoire , Drosophila , Coeur/physiologieRÉSUMÉ
Macrophages regulate angiogenesis, repair, conduction, and homeostasis in heart tissue. Landau et al.1 demonstrate that incorporating primitive macrophages into engineered heart tissues significantly promotes long-term vascularization and cardiac maturation. This advance demonstrates the importance of resident immune-vascular microenvironments in cardiac tissue engineering, marking an important step forward for heart-on-chip technologies.
Sujet(s)
Macrophages , Néovascularisation physiologique , Ingénierie tissulaire , Ingénierie tissulaire/méthodes , Macrophages/métabolisme , Macrophages/cytologie , Humains , Animaux , Myocarde/cytologie , Coeur/physiologieRÉSUMÉ
To date, the role of NODAL in normal and abnormal L-R asymmetry has been well established. In a recent paper, mutations of this gene have been reported in heterotaxy but also in transposition with D- or L-ventricular loop. The effects of NODAL and other laterality genes can be recognized separately in all three cardiac segments: for topology and septation of the atria, for ventricular looping, and for spiralization and alignment of the great arteries.
Sujet(s)
Cardiopathies congénitales , Syndrome d'hétérotaxie , Humains , Syndrome d'hétérotaxie/génétique , Cardiopathies congénitales/génétique , Protéine Nodal/génétique , Protéine Nodal/métabolisme , Coeur , Mutation , AnimauxRÉSUMÉ
BACKGROUND: The ratio (E/Ea) of mitral Doppler inflow velocity to annular tissue Doppler wave velocity by transthoracic echocardiography and diaphragmatic excursion (DE) by diaphragm ultrasound have been confirmed to predict extubation outcomes. However, few studies focused on the predicting value of E/Ea and DE at different positions during a spontaneous breathing trial (SBT), as well as the effects of â³E/Ea and â³DE (changes in E/Ea and DE during a SBT). METHODS: This study was a reanalysis of the data of 60 difficult-to-wean patients in a previous study published in 2017. All eligible participants were organized into respiratory failure (RF) group and extubation success (ES) group within 48 h after extubation, or re-intubation (RI) group and non-intubation (NI) group within 1 week after extubation. The risk factors for respiratory failure and re-intubation including E/Ea and â³E/Ea, DE and â³DE at different positions were analyzed by multivariate logistic regression, respectively. The receiver operating characteristic (ROC) curves of E/Ea (septal, lateral, average) and DE (right, left, average) were compared with each other, respectively. RESULTS: Of the 60 patients, 29 cases developed respiratory failure within 48 h, and 14 of those cases required re-intubation within 1 week. Multivariate logistic regression showed that E/Ea were all associated with respiratory failure, while only DE (right) and DE (average) after SBT were related to re-intubation. There were no statistic differences among the ROC curves of E/Ea at different positions, nor between the ROC curves of DE. No statistical differences were shown in â³E/Ea between RF and ES groups, while â³DE (average) was remarkably higher in NI group than that in RI group. However, multivariate logistic regression analysis showed that â³DE (average) was not associated with re-intubation. CONCLUSIONS: E/Ea at different positions during a SBT could predict postextubation respiratory failure with no statistical differences among them. Likewise, only DE (right) and DE (average) after SBT might predict re-intubation with no statistical differences between each other.
Sujet(s)
Extubation , Muscle diaphragme , Insuffisance respiratoire , Sevrage de la ventilation mécanique , Humains , Mâle , Muscle diaphragme/imagerie diagnostique , Muscle diaphragme/physiopathologie , Femelle , Études rétrospectives , Insuffisance respiratoire/imagerie diagnostique , Insuffisance respiratoire/physiopathologie , Sujet âgé , Sevrage de la ventilation mécanique/méthodes , Adulte d'âge moyen , Courbe ROC , Échocardiographie/méthodes , Coeur/imagerie diagnostique , Facteurs de risqueRÉSUMÉ
BACKGROUND: The elevated blood pressure (BP) and lower cardiac autonomic modulation (CAM) are associated with higher morbidity mortality risk among older adults. Although exercise is an important intervention for cardiovascular promotion, it is unclear whether combat sports training could benefit cardiovascular outcomes as much as autonomic in this population. This study compared the effects of 12 weeks of Muay Thai (MT) training against functional training (FT) on CAM and hemodynamic parameters in older adults. METHODS: The sample consisted of 50 older adults (41 women; 66.0 ± 5.3 years old), who were equaly randomized into FT (n = 25) and MT (n = 25) intervention groups. CAM was measured by 30-min rest heart rate variability. Systolic blood pressure (SBP), diastolic blood pressure (DBP) and resting heart rate (RHR) were measured using an automatic oscillometric device. Pulse pressure (PP) and the double product (DP) were also calculated. The interventions were carried out three times a week, with 60-min length per session, during 12 consecutive weeks. The intensity of the interventions was measured using the subjective perception of exertion scale and by accelerometer. Two-factor repeated measures analysis of covariance was used for groups comparison, considering intervention group and body mass as factors. The 95% confidence interval of the difference (95%CIdif) was also calculated and the effect size was measured using partial eta squared (η2p). RESULTS: CAM indices did not show significant changes across moments and intervention groups. In hemodynamic parameters, only in DBP was there an effect of the moment (F1,39 = 8.206; P = 0.007; η2p = 0.174, large) and interaction effect between group*moment (F1,39 = 7.950; P = 0.008; η2p = 0.169, large). Specifically, the MT group at the post-training moment showed lower DBP (P = 0.010; 95%CIdif = -13.3; -1.89) in relation to the FT group. Furthermore, the MT group showed a decrease in DBP during training (P = 0.002; 95%CIdif = -10.3; -2.6). Also, an increase in training intensity was also found over the 12 weeks in FT, with no difference between the groups. CONCLUSION: After 12 weeks of MT practice there was a reduction in DBP compared to FT in older adults. TRIAL REGISTRATION: NCT03919968 Registration date: 01/02/2019.
Sujet(s)
Système nerveux autonome , Pression sanguine , Rythme cardiaque , Hémodynamique , Humains , Femelle , Mâle , Sujet âgé , Système nerveux autonome/physiopathologie , Facteurs temps , Adulte d'âge moyen , Résultat thérapeutique , Facteurs âges , Thaïlande , Traitement par les exercices physiques/méthodes , Coeur/innervation , Peuples d'Asie du Sud-EstRÉSUMÉ
To develop a deep learning-based model capable of segmenting the left ventricular (LV) myocardium on native T1 maps from cardiac MRI in both long-axis and short-axis orientations. Models were trained on native myocardial T1 maps from 50 healthy volunteers and 75 patients using manual segmentation as the reference standard. Based on a U-Net architecture, we systematically optimized the model design using two different training metrics (Sørensen-Dice coefficient = DSC and Intersection-over-Union = IOU), two different activation functions (ReLU and LeakyReLU) and various numbers of training epochs. Training with DSC metric and a ReLU activation function over 35 epochs achieved the highest overall performance (mean error in T1 10.6 ± 17.9 ms, mean DSC 0.88 ± 0.07). Limits of agreement between model results and ground truth were from -35.5 to + 36.1 ms. This was superior to the agreement between two human raters (-34.7 to + 59.1 ms). Segmentation was as accurate for long-axis views (mean error T1: 6.77 ± 8.3 ms, mean DSC: 0.89 ± 0.03) as for short-axis images (mean error ΔT1: 11.6 ± 19.7 ms, mean DSC: 0.88 ± 0.08). Fully automated segmentation and quantitative analysis of native myocardial T1 maps is possible in both long-axis and short-axis orientations with very high accuracy.
Sujet(s)
Apprentissage profond , Imagerie par résonance magnétique , Humains , Imagerie par résonance magnétique/méthodes , Mâle , Femelle , Adulte , Adulte d'âge moyen , Traitement d'image par ordinateur/méthodes , Myocarde , Ventricules cardiaques/imagerie diagnostique , Coeur/imagerie diagnostiqueRÉSUMÉ
Cardiovascular diseases represent a significant public health challenge and are responsible for more than 4 million deaths annually in Europe alone (45% of all deaths). Among these, coronary-related heart diseases are a leading cause of mortality, accounting for 20% of all deaths. Cardiac tissue engineering has emerged as a promising strategy to address the limitations encountered after myocardial infarction. This approach aims to improve regulation of the inflammatory and cell proliferation phases, thereby reducing scar tissue formation and restoring cardiac function. In cardiac tissue engineering, biomaterials serve as hosts for cells and therapeutics, supporting cardiac restoration by mimicking the native cardiac environment. Various bioengineered systems, such as 3D scaffolds, injectable hydrogels, and patches play crucial roles in cardiac tissue repair. In this context, self-healing hydrogels are particularly suitable substitutes, as they can restore structural integrity when damaged. This structural healing represents a paradigm shift in therapeutic interventions, offering a more native-like environment compared to static, non-healable hydrogels. Herein, we sharply review the most recent advances in self-healing hydrogels in cardiac tissue engineering and their potential to transform cardiovascular healthcare.
Sujet(s)
Hydrogels , Ingénierie tissulaire , Hydrogels/composition chimique , Hydrogels/pharmacologie , Humains , Animaux , Structures d'échafaudage tissulaires/composition chimique , Matériaux biocompatibles/composition chimique , Matériaux biocompatibles/pharmacologie , Coeur , Myocarde/cytologie , Myocarde/métabolisme , Myocarde/anatomopathologieRÉSUMÉ
The Dlk1-Dio3 domain is important for normal embryonic growth and development. The heart is the earliest developing and functioning organ of the embryo. In this study, we constructed a transcriptional termination model by inserting termination sequences and clarified that the lack of long non-coding RNA (lncRNA) expression in the Dlk1-Dio3 domain caused the death of maternal insertion mutant (MKI) and homozygous mutant (HOMO) mice starting from E13.5. Parental insertion mutants (PKI) can be born and grow normally. Macroscopically, dying MKI and HOMO embryos showed phenomena such as embryonic edema and reduced heart rate. Hematoxylin and eosin (H.E.) staining showed thinning of the myocardium in MKI and HOMO embryos. In situ hybridization (IHC) and quantitative reverse-transcription polymerase chain reaction (qRT-PCR) showed downregulation of lncGtl2, Rian, and Mirg expression in MKI and HOMO hearts. The results of single-cell RNA sequencing (scRNA-Seq) analysis indicated that the lack of lncRNA expression in the Dlk1-Dio3 domain led to reduced proliferation of epicardial cells and may be an important cause of cardiac dysplasia. In conclusion, this study demonstrates that Dlk1-Dio3 domain lncRNAs play an integral role in ventricular development.
Sujet(s)
Protéines de liaison au calcium , Régulation de l'expression des gènes au cours du développement , Coeur , Iodide peroxidase , ARN long non codant , Animaux , ARN long non codant/génétique , Souris , Protéines de liaison au calcium/génétique , Protéines de liaison au calcium/métabolisme , Coeur/embryologie , Coeur/croissance et développement , Iodide peroxidase/génétique , Iodide peroxidase/métabolisme , Femelle , Développement embryonnaire/génétique , Protéines et peptides de signalisation intercellulaire/génétique , Protéines et peptides de signalisation intercellulaire/métabolisme , Prolifération cellulaire/génétique , Embryon de mammifère/métabolisme , Protéines nucléairesRÉSUMÉ
Insulin signaling is vital for regulating cellular metabolism, growth, and survival pathways, particularly in tissues such as adipose, skeletal muscle, liver, and brain. Its role in the heart, however, is less well-explored. The heart, requiring significant ATP to fuel its contractile machinery, relies on insulin signaling to manage myocardial substrate supply and directly affect cardiac muscle metabolism. This review investigates the insulin-heart axis, focusing on insulin's multifaceted influence on cardiac function, from metabolic regulation to the development of physiological cardiac hypertrophy. A central theme of this review is the pathophysiology of insulin resistance and its profound implications for cardiac health. We discuss the intricate molecular mechanisms by which insulin signaling modulates glucose and fatty acid metabolism in cardiomyocytes, emphasizing its pivotal role in maintaining cardiac energy homeostasis. Insulin resistance disrupts these processes, leading to significant cardiac metabolic disturbances, autonomic dysfunction, subcellular signaling abnormalities, and activation of the renin-angiotensin-aldosterone system. These factors collectively contribute to the progression of diabetic cardiomyopathy and other cardiovascular diseases. Insulin resistance is linked to hypertrophy, fibrosis, diastolic dysfunction, and systolic heart failure, exacerbating the risk of coronary artery disease and heart failure. Understanding the insulin-heart axis is crucial for developing therapeutic strategies to mitigate the cardiovascular complications associated with insulin resistance and diabetes.
Sujet(s)
Insulinorésistance , Insuline , Transduction du signal , Humains , Animaux , Insuline/métabolisme , Myocarde/métabolisme , Myocytes cardiaques/métabolisme , Coeur/physiologie , Coeur/physiopathologie , Système rénine-angiotensine/physiologieRÉSUMÉ
There is limited information available on cardiovascular toxicity of 2-Aminobenzothiazole (NTH), a derivative of benzothiazole (BTH) commonly used in tire production, in aquatic organisms. In the present study, the zebrafish embryos were exposed to varying concentrations of NTH (0, 0.05, 0.5, and 5 mg/L) until adulthood and the potential cardiovascular toxicity was assessed. NTH exposure resulted in striking aberrations in cardiac development, including heart looping failure and interference with atrioventricular canal differentiation. RNA-sequencing analysis indicated that NTH causes oxidative damage to the heart via ferroptosis, leading to oxygen supply disruption, cardiac malformation, and ultimately, zebrafish death. Quantitative real-time polymerase chain reaction (qPCR) analysis demonstrated the dysregulation of genes associated with early heart development, contraction, and oxidative stress. Additionally, reactive oxygen species accumulation and glutathione/malondialdehyde levels changes suggested a potential link between cardiac developmental toxicity and oxidative stress. In adult zebrafish, NTH exposure led to ventricular enlargement, decreased heart rate, reduced blood flow, and prolonged RR, QRS, and QTc intervals. To the best of our knowledge, this study is the first to provide evidence of cardiac toxicity and the adverse effects of ontogenetic NTH exposure in zebrafish, revealing the underlying toxic mechanisms connected with oxidative stress damage. These findings may provide crucial insights into the environmental risks associated with NTH and other BTHs.
Sujet(s)
Benzothiazoles , Cardiotoxicité , Embryon non mammalien , Coeur , Stress oxydatif , Danio zébré , Animaux , Stress oxydatif/effets des médicaments et des substances chimiques , Cardiotoxicité/étiologie , Benzothiazoles/toxicité , Coeur/effets des médicaments et des substances chimiques , Embryon non mammalien/effets des médicaments et des substances chimiques , Espèces réactives de l'oxygène/métabolisme , Polluants chimiques de l'eau/toxicitéRÉSUMÉ
Automated identification of cardiac vortices is a formidable task due to the complex nature of blood flow within the heart chambers. This study proposes a novel approach that algorithmically characterizes the identification criteria of these cardiac vortices based on Lagrangian Averaged Vorticity Deviation (LAVD). For this purpose, the Recurrent All-Pairs Field Transforms (RAFT) is employed to assess the optical flow over the Phase Contrast Magnetic Resonance Imaging (PC-MRI), and to construct a continuous blood flow velocity field and reduce errors that arise from the integral process of LAVD. Additionally, Generalized Hough Transform (GHT) is applied for automated depiction of the structure of cardiac vortices. The effectiveness of this method is demonstrated and validated by the computation of the acquired cardiac flow data. The results of this comprehensive visual and analytical study show that the evolution of cardiac vortices can be effectively described and displayed, and the RAFT framework for optical flow can synthesize the in-between PC-MRIs with high accuracy. This allows cardiologists to acquire a deeper understanding of intracardiac hemodynamics and its impact on cardiac functional performance.