Abstract:This overview addresses the remarkable efficiency of the mammalian heart as a pump of unique capacity to quickly vary output and ejection velocity and its relation to ventricular geometry, fiber architecture, integrity of collagen scaffold and microvasculature and appropriate electrical activation. The unique functional capacity of the ventricle depends critically on the organization of cardiac muscle fibers in layers of counter-wound helices encircling the ventricular cavity in a pattern that allows a special… Show more
“…It is known that cardiac fiber arrangement as counter-wound helices encircling the ventricles is crucial for achieving sufficient ejection fractions [36]. Fiber direction is oriented predominantly in the base-apex direction on the epicardial and endocardial surfaces and is rotated to a circumferential direction in the midwall only [20].…”
Background/Aims: Cardiac function is increasingly studied using murine models. However, current multicellular preparations to investigate contractile properties have substantial technical and biological limitations and are especially difficult to apply to the developing murine heart. Methods: Newborn murine hearts were cut with a vibratome into viable tissue slices. The structural and functional integrity of the tissue was shown by histology, ATP content and sharp electrode recordings. Results: Within the first 48 hours after slicing structure remained intact without induction of apoptosis. ATP concentrations and action potential parameters were comparable to those of physiological tissue. Isometric force measurements demonstrated a physiological force-frequency relationship with a ‘primary-phase’ negative force-frequency relationship up to 1-2 Hz and a ‘secondary-phase’ positive force-frequency relationship up to 8 Hz. (-)-Isoproterenol (10-6 mol/l) increased active force to 251±35% (n=15) of baseline values and shortened relaxation times indicating a preserved beta-adrenergic regulation of contraction. Changes of the force-frequency relationship after application of ryanodine and nifedipine indicated functionality of calcium release from the sarcoplasmic reticulum and of L-type calcium channels. Conclusion: Generation of viable, physiological intact ventricular slices from neonatal hearts is feasible and provides a robust model to study loaded contractions.
“…It is known that cardiac fiber arrangement as counter-wound helices encircling the ventricles is crucial for achieving sufficient ejection fractions [36]. Fiber direction is oriented predominantly in the base-apex direction on the epicardial and endocardial surfaces and is rotated to a circumferential direction in the midwall only [20].…”
Background/Aims: Cardiac function is increasingly studied using murine models. However, current multicellular preparations to investigate contractile properties have substantial technical and biological limitations and are especially difficult to apply to the developing murine heart. Methods: Newborn murine hearts were cut with a vibratome into viable tissue slices. The structural and functional integrity of the tissue was shown by histology, ATP content and sharp electrode recordings. Results: Within the first 48 hours after slicing structure remained intact without induction of apoptosis. ATP concentrations and action potential parameters were comparable to those of physiological tissue. Isometric force measurements demonstrated a physiological force-frequency relationship with a ‘primary-phase’ negative force-frequency relationship up to 1-2 Hz and a ‘secondary-phase’ positive force-frequency relationship up to 8 Hz. (-)-Isoproterenol (10-6 mol/l) increased active force to 251±35% (n=15) of baseline values and shortened relaxation times indicating a preserved beta-adrenergic regulation of contraction. Changes of the force-frequency relationship after application of ryanodine and nifedipine indicated functionality of calcium release from the sarcoplasmic reticulum and of L-type calcium channels. Conclusion: Generation of viable, physiological intact ventricular slices from neonatal hearts is feasible and provides a robust model to study loaded contractions.
“…These are predominantly longitudinal in the subendocardial region (right-handed helix), become circumferential in the mid-wall, and resume a longitudinal orientation at the subepicardial surface (left-handed helix). [28][29][30] During ejection, the ventricular volume is reduced as a result of contraction of both the subendocardial and subepicardial layers. 1-3 Whenever one of these is damaged (subendocardium in myocardial infarction, subepicardium in focal acute myocarditis), longitudinal function is impaired.…”
Background:The aim of our study was to assess longitudinal (L), circumferential (C) and radial (R) strain (S) of the left ventricle (LV) in patients with acute myocarditis and preserved LV wall motion.
Methods and Results:Of the 26 male patients that were enrolled, 13 patients (26±8 years) suffered from acute myocarditis and 13 (25±2 years) were healthy participants (controls). Both patients and controls underwent cardiac magnetic resonance (CMR) and 2-dimensional S imaging (2D-S) echocardiography on the same day. Myocardial strains (RS, LS and CS) were quantified by 2D-S. In patients with myocarditis, a delayed enhancement (DE) CMR study was performed to identify damaged myocardial segments. In the myocarditis group there was a significant LS reduction compared with controls (-25±7 vs -20±7, P<0.0001), whereas no difference was found between the 2 groups concerning CS and RS. Subepicardial DE areas were found in 12 of 13 patients. Segments with DE showed a significantly lower LS in comparison with segments without DE (-19±4 vs -23±6, P<0.0001). In contrast, no difference in CS and RS was found when comparing segments with DE vs segments without DE.
Conclusions:In patients with acute myocarditis, evidence of subepicardial damage and no wall motion abnormalities, longitudinal deformation is diffusely impaired, whereas circumferential impairment is regionally sited in the areas of subepicardial damage. (Circ J 2010; 74: 1205 - 1213
“…Although the adult giraffe heart has the same relative mass as that of mammals in general (22,76), it has a different shape than that of the human heart, being much more elliptical (29). This shape allows the left ventricle of the giraffe heart to generate the pressures required to maintain adequate cerebral perfusion (29).…”
Section: Cardiovascular Physiology Of the Giraffementioning
confidence: 98%
“…This shape allows the left ventricle of the giraffe heart to generate the pressures required to maintain adequate cerebral perfusion (29). Although the giraffe heart is not unusually large, the left ventricular and interventricular walls are massively thickened (44,76) with wall thickness being linearly related to neck length (76).…”
Section: Cardiovascular Physiology Of the Giraffementioning
Evolution represents a natural experimental process for testing animal design features. Driven by environmental pressures, animals have evolved adaptations which can give valuable insights into human biomedical conditions. The giraffe by virtue of its extremely long neck has a mean arterial pressure much higher than other mammals. However, the giraffe does not develop vascular damage or heart failure despite its high mean arterial pressure. The giraffe's cardiovascular physiology challenges a number of current concepts concerning the genesis of hypertensive vascular damage in the human. All animals senesce, and, in general, the manifestations of this senescence are similar to the aging features observed in humans. The characteristics of aging in natural animals strongly suggest that the so-called chronic degenerative diseases of humans are not really diseases but actually manifestations of the aging phenotype. Glucose regulation in birds and the naked mole rat has features which mimic the characteristics of the diabetic state, yet these animals do not develop the complications occurring in humans with diabetes. Disruptions in the functioning of the circadian molecular clock are thought to underlie certain neuropsychiatric disorders. The honeybee and the zebrafish have emerged as natural animal models for studying the regulation of molecular clocks and the mechanisms underlying plasticity of circadian rhythms. These examples underscore the valuable insights that natural animals can furnish with respect to biomedical disorders. Yet, this information data base remains a largely untapped resource.
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