This study examined whether reduced [ATP], raised [Mg2+] and the presence of the metabolites AMP and inosine monophosphate (IMP) affected depolarization-induced Ca2+ release from the sarcoplasmic reticulum (SR) in mechanically skinned skeletal muscle fibres of the rat. The amount of Ca2+ released was determined from the extent of SR Ca2+ depletion following a depolarization in the specified conditions with 2 mM free EGTA present to chelate released Ca2+. 2. In the presence of 8 mM total ATP and 1 mM free Mg2+, most of the SR Ca2+ could be released by a single (2-3 s) depolarization. Paired comparisons in the same fibres showed that raising the [Mg2+] from 1 to 3 mM reduced the total amount of Ca2+ released by a single depolarization by approximately 40 %. At 1 mM Mg2+, lowering the [ATP] to 0.5 mM did not cause a detectable change in the total amount of Ca2+ released, but when the release rate was reduced by the presence of 3 mM Mg2+, lowering the [ATP] to 0.5 mM resulted in a further ( approximately 20 %) reduction in the total amount of Ca2+ released. 3. At 1 mM Mg2+ and 0.5 mM ATP, neither the presence of 3 mM AMP alone nor 3 mM AMP plus 3 mM IMP caused a significant change in total Ca2+ release. Furthermore, at 1 mM Mg2+, the combined effect of lowering the [ATP] from 8 to 0.5 mM and simultaneously adding 3 mM AMP and 3 mM IMP did not significantly alter total Ca2+ release. However, when Ca2+ release was already reduced by the presence of 3 mM Mg2+ and 0.5 mM ATP (to approximately 50 %), addition of 3 mM AMP and 3 mM IMP significantly reduced the amount of Ca2+ released a further 2-fold. 4. These results show that depolarization-induced Ca2+ release in mammalian muscle fibres is modulated by the concentration of ATP and its metabolic products, as well as by the free [Mg2+]. Consequently, the (reversible) reduction in Ca2+ release occurring in a muscle fibre after prolonged exercise could result not only from raised [Mg2+] but also from a severe reduction in [ATP] locally near the Ca2+ release channels, with the accompanying build-up of AMP and IMP further exacerbating this effect.
摘要
本研究检测了降低的[ATP]、升高的[Mg2+]以及代谢产物AMP和肌苷一磷酸(IMP)的存在是否会影响大鼠机械分离的骨骼肌纤维中去极化诱导的肌浆网(SR)钙释放。在存在2 mM游离EGTA以螯合释放的钙的特定条件下,通过去极化后SR钙耗竭的程度来确定释放的钙量。2. 在总ATP为8 mM且游离Mg2+为1 mM的情况下,大多数SR钙可通过单次(2-3秒)去极化释放。在同一纤维中的配对比较显示,将[Mg2+]从1 mM提高到3 mM可使单次去极化释放的总钙量减少约40%。在1 mM Mg2+时,将[ATP]降至0.5 mM不会导致释放的总钙量有可检测到的变化,但当由于存在3 mM Mg2+而使释放速率降低时,将[ATP]降至0.5 mM会导致释放的总钙量进一步(约20%)减少。3. 在1 mM Mg2+和0.5 mM ATP时,单独存在3 mM AMP或3 mM AMP加3 mM IMP均不会引起总钙释放的显著变化。此外,在1 mM Mg2+时,将[ATP]从8 mM降至0.5 mM并同时添加3 mM AMP和3 mM IMP的联合作用也不会显著改变总钙释放。然而,当由于存在3 mM Mg2+和0.5 mM ATP而使钙释放已经减少(至约50%)时,添加3 mM AMP和3 mM IMP会使释放的钙量进一步显著减少2倍。4. 这些结果表明,哺乳动物肌肉纤维中去极化诱导的钙释放受ATP及其代谢产物的浓度以及游离[Mg2+]的调节。因此,长时间运动后肌肉纤维中发生的(可逆的)钙释放减少不仅可能是由于[Mg2+]升高,还可能是由于钙释放通道附近局部[ATP]的严重降低,同时AMP和IMP的积累会进一步加剧这种效应。