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改变沐浴液成分对甲壳类动物肌原纤维束中等长张力-pCa关系的影响。

Effect of changing the composition of the bathing solutions upon the isometric tension-pCa relationship in bundles of crustacean myofibrils.

作者信息

Ashley C C, Moisescu D G

出版信息

J Physiol. 1977 Sep;270(3):627-52. doi: 10.1113/jphysiol.1977.sp011972.

Abstract
  1. The relative isometric tension-pCa relationship has been determined for isolated bundles of barnacle myofibrils under a variety of ionic conditions using [Ca(2+)]-buffered solutions which also contained an ATP regenerating system (creatine phosphate and creatine kinase).2. The results are in better agreement with the ;consecutive' scheme of reaction rather than with the ;independent' alternative (Ashley & Moisescu, 1972) for the co-operative action of two Ca(2+) ions in the process of tension activation in crustacean skeletal muscle.3. Variations in the pH of the activating solutions did have a marked effect on the relative tension-Ca curve, although no effect was observed on the absolute maximum value for isometric tension. A shift in pH by 0.5 u. in the range 6.6-7.6 shifted the Ca(2+)-activation curve by 0.5 log u. towards lower free Ca(2+) concentrations.4. Changes in the free Mg(2+) concentration of the activating solutions in the millimolar range produced a pronounced shift of the relative tension-pCa curve along the pCa axis. Increasing [Mg(2+)] from 1 to 5 mM shifted the curve by about 0.7 log u. to higher free Ca(2+) concentrations, without significantly modifying its steepness.5. Changes in the MgATP concentration of the activating solutions in the range of 1-13 mM had no significant effect on the relative tension-pCa relationship.6. Varying the K(+) concentration in the activating solutions was also observed to have a marked effect upon the tension-pCa relationship in barnacle. An increase in the K(+) concentration from 90 to 170 mM shifted the curve by some 0.6 log u. towards higher free Ca(2+) concentrations.7. Cooling the standard activating solutions from room temperature to +4 degrees C made no apparent difference to the relative tension-pCa relationship, but decreased significantly the absolute tension responses.8. The results presented show that tonicity by itself has a marked effect upon the absolute steady-state tension levels in isolated bundles of myofibrils.9. Maximum isometric tension in this preparation was not simply related to ionic strength, or to the monovalent cation concentration, but it depended, as well, upon the anionic composition of the activating solution. In addition, a change in ionic strength of 25 mM over the range of 245-270 mM did not appear to modify the relative tension-pCa relationship.10. The effect of the physiologically occurring cations H(+), K(+), Mg(2+) upon the relative isometric tension-pCa relationship can be accounted for on the basis of a model of competitive inhibition between these cations and Ca(2+) for the functional unit for tension. This inhibitory effect appears to involve at least one H(+), one Mg(2+) and two K(+) per each Ca(2+) ion participating in the activation process of the functional unit for tension.
摘要
  1. 使用含有ATP再生系统(磷酸肌酸和肌酸激酶)的[Ca(2+)]缓冲溶液,在多种离子条件下测定了藤壶肌原纤维分离束的相对等长张力-pCa关系。

  2. 对于甲壳类动物骨骼肌张力激活过程中两个Ca(2+)离子的协同作用,结果与反应的“连续”模式比与“独立”模式(Ashley和Moisescu,1972)更相符。

  3. 激活溶液pH值的变化确实对相对张力-Ca曲线有显著影响,尽管对等长张力的绝对最大值未观察到影响。在6.6 - 7.6范围内pH值变化0.5个单位,使Ca(2+)激活曲线向较低的游离Ca(2+)浓度方向移动0.5个对数单位。

  4. 激活溶液中毫摩尔范围内游离Mg(2+)浓度的变化使相对张力-pCa曲线沿pCa轴发生明显移动。将[Mg(2+)]从1 mM增加到5 mM使曲线向较高的游离Ca(2+)浓度方向移动约0.7个对数单位,而不显著改变其斜率。

  5. 激活溶液中MgATP浓度在1 - 13 mM范围内的变化对相对张力-pCa关系没有显著影响。

  6. 还观察到激活溶液中K(+)浓度的变化对藤壶的张力-pCa关系有显著影响。K(+)浓度从90 mM增加到170 mM使曲线向较高的游离Ca(2+)浓度方向移动约0.6个对数单位。

  7. 将标准激活溶液从室温冷却到+4℃,对相对张力-pCa关系没有明显影响,但显著降低了绝对张力响应。

  8. 所呈现的结果表明,张力本身对肌原纤维分离束中的绝对稳态张力水平有显著影响。

  9. 该制剂中的最大等长张力不仅与离子强度或单价阳离子浓度有关,还取决于激活溶液的阴离子组成。此外,在245 - 270 mM范围内离子强度变化25 mM似乎并未改变相对张力-pCa关系。

  10. 生理上存在的阳离子H(+)、K(+)、Mg(2+)对相对等长张力-pCa关系的影响可以基于这些阳离子与Ca(2+)之间对张力功能单位的竞争性抑制模型来解释。这种抑制作用似乎涉及每个参与张力功能单位激活过程的Ca(2+)离子至少一个H(+)、一个Mg(2+)和两个K(+)。

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Requirement for calcium in the synaeresis of myofibrils.肌原纤维脱水收缩对钙的需求。
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Hydrogen ion buffers for biological research.用于生物学研究的氢离子缓冲剂。
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