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蟹肌纤维的去极化后电位。由细胞内钙介导的钠依赖性过程。

The depolarizing afterpotential of crab muscle fibres. A sodium-dependent process mediated by intracellular calcium.

作者信息

Suarez-Kurtz G

出版信息

J Physiol. 1979 Jan;286:317-29. doi: 10.1113/jphysiol.1979.sp012621.

Abstract
  1. A study was made of the depolarizing afterpotential (d.a.p.) which follows the initial graded electrogenesis of crab muscle fibres. 2. Increasing the strength, duration or amplitude of the stimulating current pulses enhanced both the d.a.p. and the local contractions. 3. Arsenazo III was injected intracellularly and changes in light absorbance by the dye were used to monitor the increase in free sarcoplasmic Ca concentration during excitation-contraction (E-C) coupling. The onset of the absorbance changes occurred during the depolarizing phase of the initial electrogenesis and the maximum value coincided with the peak of the d.a.p. An exponential decay of the absorbance signal occurred during the repolarizing phase of the d.a.p. 4. Ionophoretic injection of EGTA into the sarcoplasm did not affect the initial electrogenesis but did reduce changes in dye absorbance, blocked tension development and abolished the d.a.p. 5. Caffeine (0.1--0.4 mM) markedly enhanced both the d.a.p. and the local contractions, but had no effect on the initial electrogenesis. 6. Replacement of extracellular Na ions with Li, Tris or choline abolished the d.a.p. The initial electrogenesis was enhanced in the choline-containing medium, but was not affected by Li or Tris. The rate of relaxation of the local contractions and the rate of decay of the light absorbance changes were slowed in Na-free saline. 7. Tetrodotoxin (10(-5) g/ml.) had no effect on either the membrane responses or tension development. 8. For initial graded responses of comparable peak amplitude a threefold reduction of [Ca-a1o shortened the d.a.p., but had little effect onits peak amplitude. A fivefold increase in [Ca]o reduced both the amplitude and duration of the d.a.p. 9. Changes in [Mg]o had little effect on the d.a.p., but both Mn (4--10 mM) and La (0.1 mM) blocked the initial electrogenesis and the d.a.p. 10. It is concluded that distinct ionic mechanisms give rise to the initial electrogenesis and the d.a.p. While the former is due to activation of Ca conductance, the d.a.p. is a Na-dependent phenomenon that is tetrodotoxin-insensitive, and mediated by the rise of intracellular Ca concentration during E--C coupling.
摘要
  1. 对蟹肌纤维初始分级电活动之后的去极化后电位(d.a.p.)进行了研究。2. 增加刺激电流脉冲的强度、持续时间或幅度,会增强去极化后电位和局部收缩。3. 将偶氮胂III注入细胞内,利用染料吸光度的变化来监测兴奋 - 收缩(E - C)偶联过程中游离肌浆钙浓度的增加。吸光度变化的起始发生在初始电活动的去极化阶段,最大值与去极化后电位的峰值一致。在去极化后电位的复极化阶段,吸光度信号呈指数衰减。4. 向肌浆中离子电泳注入乙二醇双四乙酸(EGTA)不影响初始电活动,但会减少染料吸光度的变化,阻断张力发展并消除去极化后电位。5. 咖啡因(0.1 - 0.4 mM)显著增强去极化后电位和局部收缩,但对初始电活动无影响。6. 用锂、三羟甲基氨基甲烷(Tris)或胆碱替代细胞外钠离子会消除去极化后电位。在含胆碱的培养基中初始电活动增强,但不受锂或Tris的影响。在无钠盐溶液中,局部收缩的松弛速率和吸光度变化的衰减速率减慢。7. 河豚毒素(10⁻⁵ g/ml)对膜反应或张力发展均无影响。8. 对于峰值幅度相当的初始分级反应,细胞外钙浓度([Ca]o)降低三倍会缩短去极化后电位,但对其峰值幅度影响不大。细胞外钙浓度增加五倍会降低去极化后电位的幅度和持续时间。9. 细胞外镁浓度([Mg]o)的变化对去极化后电位影响不大,但锰(4 - 10 mM)和镧(0.1 mM)均阻断初始电活动和去极化后电位。10. 得出的结论是,不同的离子机制导致了初始电活动和去极化后电位。前者是由于钙电导的激活,而去极化后电位是一种对河豚毒素不敏感的钠依赖性现象,由兴奋 - 收缩偶联过程中细胞内钙浓度的升高介导。

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