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  • Articles  (2)
  • Active stress  (2)
  • 1985-1989
  • 1980-1984  (2)
  • 1945-1949
  • 1925-1929
  • 1984  (2)
  • Technology  (2)
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  • Articles  (2)
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  • 1985-1989
  • 1980-1984  (2)
  • 1945-1949
  • 1925-1929
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  • 1984  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Annals of biomedical engineering 12 (1984), S. 481-496 
    ISSN: 1573-9686
    Keywords: Dose-response curve ; Length-tension relationship ; Autoregulation ; Preload ; Regional differences ; Active stress ; Dog ; Anterior tibial artery ; Mechanics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract This study examines the effect of length on the dose-response (D-R) relationship and the effect of agonist concentration on the length-tension (L-T) relationship in vascular smooth muscle. The experiments used 2-mm rings from isolated segments of the dog anterior tibial artery. In D-R experiments the length (internal ring circumference) for maximum active force (Lmax) was determined first. D-R relationships were obtained from cumulative responses to increasing concentrations of norepinephrine (NE) or potassium (K+). L-T relationships were obtained from individual responses to a specific concentration of agonist as the ring was stretched in increments of L0 (the initial length for resting force). Dimensions of the arterial rings were measured with a video caliper. For NE and K+ stimulations at lengths equal to and less than Lmax: (a) The concentration for half maximal response (ED50) was lowest (most sensitive) at Lmax and increased significantly as length decreased from Lmax; (b) When the direction of length change was reversed, the direction of change in ED50 was reversed; and (c) The ED50 of repeated dose-response experiments at Lmax was not significantly different. For NE: (a) the ED50 decreased significantly when length was increased from Lmax; and (b) the ED50 increased significantly when length was decreased to Lmax. The results of L-T experiments show Lmax is significantly longer for a low concentration of NE (10−6 M) than for a high concentration (10−5 M). With force normalized to the maximum force, the L-T curve is significantly lower, and the initial length for an active response was 80% longer for 10−6 M than for 10−5 M NE. It may be concluded that vascular smooth muscle has a length-dependent dose-response relationship and a concentration-dependent length-tension relationship.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Annals of biomedical engineering 12 (1984), S. 497-510 
    ISSN: 1573-9686
    Keywords: Passive mechanics ; Active stress ; Active constriction ; Elastic modulus ; Series elastic element ; Anisotropy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine , Technology
    Notes: Abstract Vascular smooth muscle mechanics have been studied in vitro in cylindrical segments of dog carotid artery, human internal mammary artery, and human saphenous vein. Such cylindrical preparations maintain normal vessel geometry and also permit correlation of mechanical phenomena with transmural pressure. These studies show that the vascular muscle in cylindrical arteries develops a maximum active stress of 1.1×105 N/m2 for the whole wall, or 2.2–3.7×105 N/m2 for the volume of the wall occupied by vascular muscle. These values are similar to those reported for strip studies of vascular muscle and various preparations of skeletal muscle, but are two to five times that reported for cardiac papillary muscle preparations. In cylindrical preparations of arteries, maximum isometric active stress occurs at 150 mm Hg, whereas that in veins occurs at less than 15 mm Hg. Quick release experiments of cylindrical segments of vessels avoid the compliance of inactive tissue trapped beneath ligatures in strip studies. Quick release experiments in cylindrical segments of dog carotid artery reveal that at maximum isometric stress, the series elastic component (SEC) is extended 8–11%. Experiments employing temperature variations and degradative enzymes show that the SEC is located largely in elastin, with a lesser portion located in the contractile apparatus. At short-and long-muscle lengths, the active muscle develops decreased active stress and that developed at long lengths persists at all muscle lengths, even after shortening. This has been termed “attenuation” and appears to contribute to the static length-stress and pressure-diameter hysteresis exhibited by vessels. Excitation of vascular muscle in vessel segments held at constant pressure discloses that isobaric contraction decreases artery diameter a maximum of approximately 25%. This occurs at a dimension corresponding to approximately 100 mm Hg in the relaxed vessel. Isometrically and isobarically contracted vessels tend to fall along the same pressure-diameter coordinates, indicating equivalence of both modes of contraction. Distention of contracted vessels indicates that active vascular muscle markedly resists distention up to 150–250 mm Hg; at higher pressures the contracted vessel exhibits decreased stiffness as the contracted muscle yields. The vascular muscle, therefore, has a biphasic effect on circumferential elastic modulus relative to that of the relaxed vessel. Although controversial, evaluation of the effects of the active muscle on wall elastic modulus probably is most meaningful when the modulus is examined as a function of stress, or as a function of strain, where strain is computed with respect to a single initial dimension for both the relaxed and contracted vessel.
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