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软体动物爆发性和搏动性起搏神经元电流的定量差异。

Quantitative differences in the currents of bursting and beating molluscan pace-maker neurones.

作者信息

Gorman A L, Hermann A

出版信息

J Physiol. 1982 Dec;333:681-99. doi: 10.1113/jphysiol.1982.sp014475.

Abstract
  1. The spontaneous activity and the membrane conductances to Na(+), Ca(2+) and K(+) ions of the bursting pace-maker neurone R-15 and the repetitively discharging (beating) pace-maker neurone L-11 in the abdominal ganglion of the marine mollusc, Aplysia californica, were compared.2. The bursting pace-maker R-15 can be converted to a beating pace-maker neurone by the removal of external Ca(2+) or by the injection of EGTA intracellularly. Bursting pace-maker activity is not restored by changes in the resting potential.3. Spontaneous action potentials of cell R-15 are reduced, but not abolished, by the addition of tetrodotoxin (TTX) to block Na(+) currents or by the removal of external Ca(2+) to abolish Ca(2+) currents, whereas the spontaneous action potentials of cell L-11 are abolished by external TTX, but are unaffected by external Ca(2+) removal.4. The membranes of both cells contain Na(+) and Ca(2+) inward currents. The specific Na(+) conductance of both cells is of similar magnitude, whereas the specific Ca(2+) conductance is about half the Na(+) conductance in R-15 cells and an order of magnitude smaller in L-11 cells.5. The delayed K(+) conductance of cell L-11 is about 1.2 times greater than this conductance in cell R-15. The transient K(+) currents of the two cells are about the same magnitude.6. The Ca(2+)-activated K(+) conductance of cell R-15 and cell L-11 was estimated using two methods. The Ca(2+)-activated K(+) conductance of cell R-15 estimated from the difference in the total outward current in normal external solution and the delayed K(+) current in Ca(2+)-free solution (to preclude Ca(2+) influx) or after internal EGTA injection (to prevent Ca(2+) accumulation) is about 23 times greater than this conductance in cell L-11. The Ca(2+)-activated K(+) conductance of cell R-15, estimated from local internal Ca(2+) injections in Ca(2+)-free solution, is about 3 times greater than this conductance in cell L-11.7. The leakage conductance of cell L-11 is about 1.3 times greater than this conductance in cell R-15. This conductance increases by a factor of about 2 in both cells in Ca(2+)-free external solutions containing 1 mM-EGTA, but is unchanged or is decreased slightly by injection of EGTA internally.8. It is concluded that the Ca(2+) conductance and the Ca(2+)-activated K(+) conductance are appreciably greater in the bursting pace-maker neurone R-15 than in the beating pace-maker neurone L-11, whereas other voltage-dependent conductances to Na(+) and K(+) ions as well as the leakage conductance are quite similar. These quantitative differences provide a basis for understanding the different spontaneous activities of the two cells.
摘要
  1. 对海生软体动物加州海兔腹神经节中爆发性起搏神经元R - 15和重复性放电(搏动)起搏神经元L - 11的自发活动以及对Na⁺、Ca²⁺和K⁺离子的膜电导进行了比较。

  2. 通过去除细胞外Ca²⁺或细胞内注射乙二醇双(2 - 氨基乙基醚)四乙酸(EGTA),爆发性起搏神经元R - 15可转变为搏动性起搏神经元。静息电位的改变不能恢复爆发性起搏活动。

  3. 加入河豚毒素(TTX)阻断Na⁺电流或去除细胞外Ca²⁺以消除Ca²⁺电流时,细胞R - 15的自发动作电位降低但未消除,而细胞L - 11的自发动作电位被细胞外TTX消除,但不受去除细胞外Ca²⁺的影响。

  4. 两种细胞的膜均含有Na⁺和Ca²⁺内向电流。两种细胞的比Na⁺电导大小相似,而比Ca²⁺电导在R - 15细胞中约为Na⁺电导的一半,在L - 11细胞中则小一个数量级。

  5. 细胞L - 11的延迟K⁺电导比细胞R - 15中的该电导大约大1.2倍。两种细胞的瞬时K⁺电流大小大致相同。

  6. 用两种方法估计了细胞R - 15和细胞L - 11的Ca²⁺激活K⁺电导。根据正常细胞外溶液中的总外向电流与无Ca²⁺溶液(以排除Ca²⁺内流)或细胞内注射EGTA后(以防止Ca²⁺积累)的延迟K⁺电流之差估计,细胞R - 15的Ca²⁺激活K⁺电导比细胞L - 11中的该电导大约大23倍。在无Ca²⁺溶液中通过局部细胞内注射Ca²⁺估计,细胞R - 15的Ca²⁺激活K⁺电导比细胞L - 11中的该电导大约大3倍。

  7. 细胞L - 11的漏电导比细胞R - 15中的该电导大约大1.3倍。在含有1 mM EGTA的无Ca²⁺细胞外溶液中,两种细胞的该电导均增加约2倍,但细胞内注射EGTA时该电导不变或略有降低。

  8. 得出结论:爆发性起搏神经元R - 15中的Ca²⁺电导和Ca²⁺激活K⁺电导明显大于搏动性起搏神经元L - 11,而其他对Na⁺和K⁺离子的电压依赖性电导以及漏电导则非常相似。这些数量差异为理解两种细胞不同的自发活动提供了基础。

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Ionic currents in molluscan soma.软体动物体细胞中的离子电流。
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