Suard I, Pery-Man N, Coirault C, Pourny J C, Lecarpentier Y, Chemla D
Institut National de la Santé et de la Recherche Médicale Unité 275, Laboratoire d'Optique Appliquee, Ecole Nationale Supérieure de Techniques Avancées, Palaiseau, France.
Am J Physiol. 1994 Nov;267(5 Pt 2):H1814-23. doi: 10.1152/ajpheart.1994.267.5.H1814.
The purpose of this study was to test the hypothesis that loading patterns (i.e., loading sequence, total load, and preload) modulate the relaxant effects of isoproterenol. The effects of isoproterenol (10(-6) M) on peak rate of force decline (-dF/dt) were studied in rat left ventricular papillary muscle (n = 24) with respect to two sequences of relaxation: the classical, isotonic-isometric sequence, in which tension fall occurs at initial muscle length, and the physiological, isometric-isotonic sequence, in which tension fall occurs at end-systolic muscle length. The influences of muscle load and initial length were accounted for in the evaluation of relaxation rate by plotting -dF/dt against the entire range of loads both at preload = maximum length (Lmax) and 90% Lmax. The main results are the following: 1) in the classical, isotonic-isometric sequence of relaxation, and whatever the preload, the magnitude of the relaxant effect of isoproterenol increased with load; 2) after reversal into the physiological, isometric-isotonic sequence of relaxation, the relaxant effect of isoproterenol behaved independently of load level in muscle preloaded at Lmax; 3) conversely, in muscle preloaded at 90% Lmax and relaxing according to the physiological sequence, the relaxant effect of isoproterenol increased with load; and 4) the peak relaxant effect of isoproterenol was proportionally higher in the physiological sequence of relaxation than in the classical one and occurred at a similar level of load, whatever the loading sequence and whatever the preload level. Our results indicate that loading patterns finely modulated the relaxant effects of isoproterenol and that muscle length, both before the contraction phase and at the onset of relaxation phase, influenced the effects of isoproterenol on myocardial relaxation rate.
本研究的目的是检验负荷模式(即负荷顺序、总负荷和预负荷)调节异丙肾上腺素舒张作用这一假设。在大鼠左心室乳头肌(n = 24)中,针对两种舒张顺序研究了异丙肾上腺素(10⁻⁶ M)对最大力下降速率(-dF/dt)的影响:经典的等张-等长顺序,即张力下降发生在初始肌肉长度时;生理性的等长-等张顺序,即张力下降发生在收缩末期肌肉长度时。通过绘制在预负荷 = 最大长度(Lmax)和90% Lmax时 -dF/dt 相对于整个负荷范围的曲线,在评估舒张速率时考虑了肌肉负荷和初始长度的影响。主要结果如下:1)在经典的等张-等长舒张顺序中,无论预负荷如何,异丙肾上腺素的舒张效应大小随负荷增加;2)在转变为生理性的等长-等张舒张顺序后,在Lmax预负荷的肌肉中,异丙肾上腺素的舒张效应与负荷水平无关;3)相反,在90% Lmax预负荷并按生理性顺序舒张的肌肉中,异丙肾上腺素的舒张效应随负荷增加;4)无论负荷顺序和预负荷水平如何,异丙肾上腺素的最大舒张效应在生理性舒张顺序中比在经典顺序中更高且成比例,并且在相似的负荷水平出现。我们的结果表明,负荷模式精细地调节了异丙肾上腺素的舒张效应,并且收缩期前和舒张期开始时的肌肉长度影响了异丙肾上腺素对心肌舒张速率的作用。