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锰离子对青蛙心脏收缩的影响。

The effects of manganese ions on the contraction of the frog's heart.

作者信息

Chapman R A, Ellis D

出版信息

J Physiol. 1977 Nov;272(2):331-54. doi: 10.1113/jphysiol.1977.sp012047.

Abstract
  1. The effects of Mn(2+) in particular but also of Ni(2+), Co(2+), Cd(2+), verapamil and D600 on the contraction of isolated frog atrial trabeculae have been investigated. Contraction was initiated either by electrical stimulation, or by raising the K or by lowering the Na.2. Mn ions like Ca ions cause a hyperpolarization of the cell membrane and a rise in the threshold for the action potential and twitch. Mn ions, particularly at low concentrations, reduce the overshoot of the ventricular action potential.3. Mn ions reduce the strength of the regularly evoked heart beats. Prolonged exposure, in beating hearts, results in a rise in resting tension and often a small recovery of the heart beat.4. In normal Ringer solution and in Ringer free of Na ions, the addition of Mn causes the tension-depolarization curve to be displaced by an amount equivalent to an 18 mV hyperpolarization of the membrane potential for a tenfold increase in the divalent cation concentration.5. Mn, Co, Ni and Cd ions all cause a marked reduction in the tension generated by exclusion of Na ions from the bathing fluid. In the presence of these divalent cations the contracture divides into an initial phasic and a later tonic contraction. This inhibition is reversed by raising the Ca, while the tension developed during the initial phasic contraction varies with the Ca/Mn quotient.6. A similar tonic contracture is initiated after exposure to Na-free fluid containing a high Mn by the addition of a small concentration of Na, Li, hydrazinium or hydroxylammonium ions.7. The organic ;Ca antagonists' verapamil and D600 have little effect on the contracture induced by lowering Na even after prolonged exposure at relatively high concentrations but they do inhibit the twitch contraction and the K contractures.8. The effects of Mn on the Na-withdrawal contracture of frog heart can be interpreted in terms of an exclusively extracellular effect where Mn ions resemble Na ions in their action, and both antagonize the movement of Ca across the cell membrane.9. The experimental evidence suggests that the K contracture in frog heart is initiated by a mechanism which is, in some ways different to that underlying the Na-withdrawal contracture, and may involve two different sources of activator Ca.10. The several different effects of Mn on the frog heart probably reflects the ability of this cation to interfere with many processes involving Ca, and that there are a number of such processes involved in the results described in this work. The effects of Mn are more complex than might be generally supposed.
摘要
  1. 研究了锰离子(特别是Mn²⁺)以及镍离子(Ni²⁺)、钴离子(Co²⁺)、镉离子(Cd²⁺)、维拉帕米和D600对离体蛙心耳小梁收缩的影响。收缩可通过电刺激、提高细胞外钾离子浓度([K]ₒ)或降低细胞外钠离子浓度([Na]ₒ)引发。

  2. 锰离子与钙离子一样,可引起细胞膜超极化,并使动作电位和抽搐阈值升高。锰离子,尤其是低浓度时,可降低心室动作电位的超射值。

  3. 锰离子可降低正常诱发心跳的强度。在跳动的心脏中长时间暴露,会导致静息张力升高,且心跳常略有恢复。

  4. 在正常任氏液和无钠离子的任氏液中,添加锰会使张力 - 去极化曲线发生位移,相当于膜电位超极化18 mV,二价阳离子浓度增加10倍。

  5. 锰、钴、镍和镉离子都会使因从浴液中排除钠离子而产生的张力显著降低。在这些二价阳离子存在时,挛缩分为初始的相性收缩和随后的强直性收缩。通过提高细胞外钙离子浓度([Ca]ₒ)可逆转这种抑制作用,而初始相性收缩期间产生的张力随[Ca]ₒ/[Mn]ₒ商值而变化。

  6. 在暴露于含有高浓度[Mn]ₒ的无钠溶液后,添加低浓度的钠离子、锂离子、肼离子或羟铵离子会引发类似的强直性挛缩。

  7. 有机“钙拮抗剂”维拉帕米和D600对因降低[Na]ₒ引起的挛缩几乎没有影响,即使在相对高浓度下长时间暴露也是如此,但它们确实能抑制抽搐收缩和钾离子挛缩。

  8. 锰对蛙心钠缺失挛缩的影响可以用一种仅为细胞外效应来解释,其中锰离子在作用上类似于钠离子,两者都拮抗钙离子跨细胞膜的移动。

  9. 实验证据表明,蛙心的钾离子挛缩是由一种机制引发的,该机制在某些方面与钠缺失挛缩的机制不同,可能涉及两种不同的激活钙离子来源。

  10. 锰对蛙心的几种不同影响可能反映了这种阳离子干扰许多涉及钙离子过程的能力,并且在本工作中描述的结果涉及许多这样的过程。锰的影响比一般认为的更为复杂。

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Effects of calcium on the contraction of the hypodynamic frog heart.钙对低动力蛙心收缩的影响。
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