首页> 美国卫生研究院文献>The Journal of Physiology >Modulation of Ca2+ transients and contractile properties by beta-adrenoceptor stimulation in ferret ventricular muscles.
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Modulation of Ca2+ transients and contractile properties by beta-adrenoceptor stimulation in ferret ventricular muscles.

机译:β-肾上腺素受体刺激雪貂心室肌对Ca2 +瞬变和收缩特性的调节。

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摘要

1. The mechanism of modulation of Ca2+ transients and contraction by beta-adrenoceptor stimulation was studied in ferret ventricular muscles using aequorin to measure intracellular Ca2+. 2. Peaks of tension and light transients were increased by isoprenaline (10(-9) - 5 x 10(-7) M) which also abbreviated their time courses. 3. Time-to-peak tension was significantly shortened by 5 x 10(-9) M-isoprenaline and time-to-peak light was abbreviated by 10(-9) M-isoprenaline. 4. The time for the light to decay was shortened at 10(-9) M-isoprenaline. However, a higher concentration of isoprenaline (10(-8) M) was required for significant shortening of the half-relaxation time (TR50). 5. When isoprenaline was removed and beta-blocker (bupranolol, 1 microM) was applied, the time course of the light transients recovered but the time course of relaxation did not recover. 6. The relationship between [Ca2+]i and tension in tetanic contraction produced in the presence of ryanodine (5 microM) was shifted to the right by isoprenaline (10(-8) M). This was recovered by the replacement of isoprenaline with bupranolol (1 microM). 7. Isoprenaline (10(-7) M) added to the solution containing 20 mM [Ca2+]O and Bay K 8644 (1 microM), which produced maximal tension, caused a large light signal and enhancement of the initial phasic tension in tetanic contraction. However, the replacement of isoprenaline with bupranolol after immersing the preparation in 20 mM [Ca2+]O solution with Bay K 8644 and isoprenaline, did not significantly change the tension level, although the light signal decreased. Similar results were obtained in the ventricular muscle of young rats. 8. These results suggest that the dose dependence of modulation of the contractile element and sarcoplasmic reticulum (SR) by beta-adrenoceptor stimulation differs, and that additional factors, other than the faster Ca2+ uptake by SR and the decrease in Ca2+ sensitivity of the contractile element, might be involved in the shortening of the half-relaxation time by beta-adrenoceptor stimulation. In addition, beta-adrenoceptor stimulation does not produce a marked change in the maximal tension level.
机译:1.利用水母发光蛋白测量细胞内Ca2 +,研究了β-肾上腺素能刺激Ca2 +瞬变和收缩的机制。 2.异丙肾上腺素(10(-9)-5 x 10(-7)M)增加了张力和光瞬变的峰值,这也缩短了它们的时间进程。 3.高峰时间明显缩短了5 x 10(-9)M-异丙肾上腺素,高峰时间缩短了10(-9)M-异丙肾上腺素。 4.将光衰减的时间缩短为10(-9)M-异丙肾上腺素。但是,需要显着缩短半松弛时间(TR50)的更高浓度的异丙肾上腺素(10(-8)M)。 5.当除去异丙肾上腺素并使用β-受体阻滞剂(丁丙诺醇,1 microM)时,光瞬态的时间进程得以恢复,但弛豫的时间进程并未恢复。 6. [Ca2 +] i与在ryanodine(5 microM)存在下产生的强直性收缩中的张力之间的关系被异丙肾上腺素(10(-8)M)向右移动。通过用丁苯那洛尔(1 microM)代替异丙肾上腺素来回收。 7.向含有20 mM [Ca2 +] O和Bay K 8644(1 microM)的溶液中添加异丙肾上腺素(10(-7)M),产生最大的张力,引起大的光信号并增强强直性中的初始相张力。收缩。但是,将制剂浸入带有Bay K 8644和异丙肾上腺素的20 mM [Ca2 +] O溶液中后,用丁丙诺尔代替异丙肾上腺素并没有显着改变张力水平,尽管光信号降低了。在年轻大鼠的心室肌中获得了相似的结果。 8.这些结果表明,β-肾上腺素受体刺激对收缩因子和肌浆网(SR)的调节的剂量依赖性有所不同,除了SR更快地吸收Ca2 +和降低对收缩剂的Ca2 +敏感性外,其他因素β-肾上腺素受体刺激可能参与了半松弛时间的缩短。另外,β-肾上腺素能受体刺激不会在最大张力水平上产生明显变化。

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