首页> 美国卫生研究院文献>The Journal of Physiology >Mechanism of contracture on cooling of caffeine-treated frog skeletal muscle fibres.
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Mechanism of contracture on cooling of caffeine-treated frog skeletal muscle fibres.

机译:挛缩对咖啡因处理的青蛙骨骼肌纤维的冷却作用。

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1. In order to clarify the mechanism of contracture on cooling of caffeine-treated intact muscle fibres, the temperature dependence of a calcium (Ca2+) release mechanism, 'Ca2+-induced Ca2+ release', of the sarcoplasmic reticulum (SR) was examined in skinned frog muscle fibres. 2. Skinned fibres in a solution containing 1.2 mM-caffeine and 0.7 mM-EGTA (Mg2+, 1.5 mM, Mg-ATP, 3.5 mM, pH 7), contracted on cooling (from 22 to 2 degrees C) due to Ca2+ release from the SR. 3. The rate of Ca2+ release from skinned fibre SR in a medium which contained Ca2+ ions (with 10 mM-EGTA) and no ATP salts, was determined under various conditions using the 'caffeine method.' 4. In the absence of Mg2+ ions, adenine nucleotides and caffeine, the rates at room temperature (21-22 degrees C) were 3-4 times greater than those at a lower temperature (1.5-3 degrees C), at any concentrations of Ca2+ ions external to the SR. 5. In the presence of Mg2+ ions (1.5 mM) and beta,gamma-methylene ATP (1 mM), the effect of temperature on the rates disappeared in Ca2+-containing media, although the effect remained in Ca2+-free medium. 6. When caffeine (1.2 mM), which is a potentiator of the Ca2+-induced Ca2+ release, was added to the test medium with Mg2+ and beta,gamma-methylene ATP, the resulting potentiating effect was several times greater than that at lower temperature. 7. In order to examine the temperature dependence of the Ca2+ pump activity of the SR, the initial rate of Ca2+ uptake by the empty SR was determined under various conditions in the presence of Mg2+ ions (1.5 mM) and Mg-ATP (3.5 mM). The Q10 of the pump activity was around 2.0 at the Ca2+ ion concentrations examined (less than 10(-6) M). 8. A numerical model based on the results obtained, together with some reasonable assumptions, suggested that both suppression of the Ca2+ pump and enhancement of the Ca2+ release contribute to the cooling contracture of caffeinized fibres.
机译:1.为了阐明挛缩对咖啡因处理过的完整肌纤维的冷却作用,研究了肌浆网(SR)的钙(Ca2 +)释放机理,“ Ca2 +诱导的Ca2 +释放”的温度依赖性。蛙皮皮肤纤维。 2.在含有1.2 mM-咖啡因和0.7 mM-EGTA(Mg2 +,1.5 mM,Mg-ATP,3.5 mM,pH 7)的溶液中,由于冷却过程中Ca2 +释放,收缩后的纤维收缩(从22到2摄氏度)。 SR。 3.在各种条件下,使用“咖啡因法”确定了在含有Ca2 +离子(含10 mM-EGTA)且不含ATP盐的介质中,皮肤纤维SR中Ca2 +的释放速率。 4.在不存在Mg2 +离子,腺嘌呤核苷酸和咖啡因的情况下,在任何浓度下,室温(21-22摄氏度)的速率是较低温度(1.5-3摄氏度)的速率的3-4倍。 SR外部的Ca2 +离子。 5.在存在Mg2 +离子(1.5 mM)和β,γ-亚甲基ATP(1 mM)的情况下,温度对速率的影响在含Ca2 +的介质中消失了,尽管这种影响仍然存在于无Ca2 +的介质中。 6.当将咖啡因(1.2 mM)作为Ca2 +诱导的Ca2 +释放的增强剂添加到含有Mg2 +和β,γ-亚甲基ATP的测试培养基中时,所产生的增强作用是在较低温度下的增强作用的几倍。 。 7.为了检查SR的Ca2 +泵浦活动的温度依赖性,在存在Mg2 +离子(1.5 mM)和Mg-ATP(3.5 mM)的各种条件下,测定空SR吸收Ca2 +的初始速率。 )。在所检查的Ca2 +离子浓度下(小于10(-6)M),泵浦活动的Q10约为2.0。 8.基于获得的结果的数值模型,加上一些合理的假设,表明抑制Ca2 +泵和增强Ca2 +释放都有助于咖啡因纤维的冷却收缩。

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