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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 364 (1976), S. 135-141 
    ISSN: 1432-2013
    Keywords: Vascular smooth muscle ; Force velocity relation ; pH ; Calcium ; Noradrenaline
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The kinetics of vascular smooth muscle activity was studied by means of afterloaded isotonic contractions of the tetanized rat portal vein at varied pH (8.0–5.9), pCa (3.4–2.1), and during noradrenaline incubation (0.4 μg/ml). Under control conditions (pH 7.3, pCa 2.6) the following parameters of the force velocity relation were calculated:a of Hill's equation (relating to the isometric peak tension)=0.36;b (relating to the actual muscle length)=0.19 ML/s;V M (relating to the actual muscle length)=0.56 ML/s. Within the range of pCa between 2.0 and 3.2 the amount of force generation (=ΔP) depended on the extracellular calcium level whereas the extrapolated velocity of shortening of the unloaded preparation (=V M) did not. Also pH changes between 8.0 and 6.8 as well as noradrenaline incubation at a pH of 5.9 affectedΔP quite considerably, butV M only scarcely. At a pH of 6.3, however,V M was distinctly diminished, and a reduced calcium sensitivity of the ATPase was inferred from the shift of ED50 of extracellular calcium from 0.66 mM Ca at a pH of 7.3 to 1.56 mM Ca at a pH of 6.3 (P〈0.0005). It is concluded from these results that the experimental conditions—pCa between 2.0 and 3.2, pH between 8.0 and 6.8, and noradrenaline added at a pH of 5.9—obviously change the intracellular calcium concentration which influences the number of activated interaction sites rather than the velocity of crossbridge movement.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Force-velocity relation ; Vascular smooth muscle ; Portal vein ; Calcium ; Temperature ; Contractility ; Staircase phenomenon
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The velocity of the contractile elementV CE of the rat portal vein during a single isometric twitch was calculated from the ratio of the rate of tension increase (dT/dt) to the stiffness (dT/dL) of the series elastic element. This stiffness was considered as a linear function of tension (dT/dL=k · T), and thus the respective term wasV CE=(dT/dt)/(kT). A polynome of the 10th order was fitted to the time course of tension change within the first seconds of stimulation. From this function, the instantaneous values of forceT, rate of tension increasedT/dt, as well as the ratio(dT/dt)/T were computed. The series elasticity was treated as the respective stiffness factor ‘k’.V max isV CE extrapolated to zero load, and this value gives an index of the turnover rate of the myosin cross-bridges. The experiments were carried out at different temperatures (37° C, 30° C, and 25° C) as well as at different intracellular calcium levels occurring as a staircase phenomenon in the first contractions after a period of non-stimulation of 20 min. With increasing temperature,T remained constant but there was an increase inV max (Q 10=1.9), peakV CE (Q 10=1.8) and in (dT/dt)max (Q 10=1.8). Furthermore, this so-called ‘tachytropic’ effect of temperature showed a reduction of the time to the maximumdT/dt (Q 10=1.4), and to the peakV CE (Q 10=1.2). During a staircase cycle the parameters describing the contractile state, i.e. theV max, the time to maximumdT/dt, and the time to peakV CE remained constant.T, maximumdT/dt and peakV CE were, however, considerably increased. These results are typical of the socalled ‘polytropic’ effect of calcium. The experimental results obtained from the isometric force-velocity relation were compared with those calculated by means of isotonic contractions in previous experiments. There were similar changes in the dynamics of contraction, irrespective of the method used for calculation ofV max; this was the case in experiments with varied temperatures and calcium levels. Therefore the determination ofV max from a single isometric contraction seems to be a suitable method of describing the elementary process of contraction in vascular smooth muscle. This method showed a higher time resolution as compared with other methods using isotonic contractions.
    Type of Medium: Electronic Resource
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