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藤壶光感受器在红光照射后准稳定去极化的离子机制。

Ionic mechanism of a quasi-stable depolarization in barnacle photoreceptor following red light.

作者信息

Brown H M, Cornwall M C

出版信息

J Physiol. 1975 Jul;248(3):579-93. doi: 10.1113/jphysiol.1975.sp010989.

Abstract
  1. The membrane mechanism of a quasi-stable membrane depolarization (latch-up) that persists in darkness following red light was examined in barnacle photoreceptor with micro-electrode techniques including voltage-clamp and Na+-sensitive micro-electrodes. 2. Current-voltage (I-V) relations of the membrane in darkness following red light (latch-up) and in darkness following termination of latch-up with green light, indicate that latch-up is associated with an increase of membrane conductance. 3. The latch-current (membrane current in darkness following red light minus membrane current in darkness following a gree flash that terminates latch-up) was inward at the resting potential, reversed sign at about +26mV (mean of six cells), and became outward at more positive membrance potentials. 4. Current-voltage relations of the membrane during green light (no latch-up) closely resembled those during latch-up. The light-induced current (LIC) elicited by green ligh (membrane current during the light flash minus membrane current in darkness following the light flash) was inward from the resting potential to +26mV (mean of six cells), then reversed sign and became outward. 5. The latch-current and LIC were both augmented in reduced Ca2+ solutions and decreased as Na-+ was reduced at a fixed Ca2+ concentration. 6. Both LIC and latch-current reversed sign at a more negative membrane potential (increment V equals 14mV) in solutions containing one quarter the normal amount of Na+. 7. The internal Na-+ activity (a-iNa) of a photoreceptor increased from about 10-18 mM upon illumination with long steps of intense red or white illumination. Five minutes in darkness after white light, a-iNa had recovered significantly, whereas a-iNa remained elecated following red illumination. 8. Latch-up seems to be a persistence in darkness of the same membrane mechanism that normally occurs during illumination; i.e. a conductance increase to Na+ ions. Ca2+ ions act primarily to suppress this current. There is evidence for a net Na+ influx during illumination that is sustained in darkness during latch-up.
摘要
  1. 利用电压钳和钠敏感微电极等微电极技术,在藤壶光感受器中研究了红光后在黑暗中持续存在的准稳定膜去极化(闭锁)的膜机制。2. 红光后(闭锁)以及用绿光终止闭锁后在黑暗中膜的电流-电压(I-V)关系表明,闭锁与膜电导增加有关。3. 闭锁电流(红光后黑暗中的膜电流减去终止闭锁的绿色闪光后黑暗中的膜电流)在静息电位时为内向电流,在约+26mV(六个细胞的平均值)时反转符号,并在更正的膜电位时变为外向电流。4. 绿光期间(无闭锁)膜的电流-电压关系与闭锁期间的关系非常相似。绿光诱发的光电流(LIC)(闪光期间的膜电流减去闪光后黑暗中的膜电流)从静息电位到+26mV(六个细胞的平均值)为内向电流,然后反转符号并变为外向电流。5. 在低钙溶液中,闭锁电流和LIC均增加,而在固定钙浓度下随着钠的减少而降低。6. 在含有正常钠量四分之一的溶液中,LIC和闭锁电流均在更负的膜电位(增量V等于14mV)时反转符号。7. 光感受器的内部钠活性(a-iNa)在长时间强烈红光或白光照射后从约10-18 mM增加。白光照射后五分钟处于黑暗中,a-iNa已显著恢复,而红光照射后a-iNa仍升高。8. 闭锁似乎是通常在光照期间发生的相同膜机制在黑暗中的持续存在;即对钠离子的电导增加。钙离子主要起抑制这种电流的作用。有证据表明在光照期间有净钠内流,在闭锁期间的黑暗中持续存在。

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