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细胞质钙作为蝾螈视杆细胞中光适应的信使。

Cytoplasmic calcium as the messenger for light adaptation in salamander rods.

作者信息

Fain G L, Lamb T D, Matthews H R, Murphy R L

机构信息

Physiological Laboratory, University of Cambridge.

出版信息

J Physiol. 1989 Sep;416:215-43. doi: 10.1113/jphysiol.1989.sp017757.

Abstract
  1. In order to study the role of cytoplasmic calcium concentration (Ca2+i) in rod photoreceptor light adaptation, we have attempted to prevent light-induced changes in Ca2+i by minimizing calcium fluxes across the outer segment plasma membrane. This was achieved by exposing the outer segment to a low-Ca2+, 0-Na+ solution, in which sodium was replaced with either guanidinium or lithium and the external calcium concentration (Ca2+o) was reduced to micromolar levels. 2. With guanidinium and 1-3 microM-Ca2+o, the circulating current in darkness was maintained for a period of at least 15 s, consistent with approximate stability of Ca2+i. With Li+ rather than guanidinium most of the initial current was suppressed, but the residual current was again relatively stable. 3. During prolonged exposures (greater than 30 s) to low-Ca2+, 0-Na+ solution followed by dim illumination, the circulating current did not remain constant but slowly increased. Incorporation of calcium buffer into the cytoplasm greatly reduced the rate of change of current, consistent with the idea that the increase arose from a gradual decrease in Ca2+i. 4. Light responses of rods exposed to low-Ca2+, 0-Na+ solution in darkness were altered in a characteristic manner. Although the initial rising phase of the light response was little changed, the peak amplitude of the response was larger and occurred later, and the response decayed more slowly than in control. The response-intensity relation was steepened and was shifted towards lower intensities both for flashes and for steps of light. The normal sag in the response to steps disappeared, and the waveform of the step response could be predicted to a close approximation from the integral of the dim flash response. 5. Presentation of background illumination in Ringer solution produced a marked acceleration of the response to a subsequent bright flash. No such acceleration was observed if the background was given in low-Ca2+, 0-Na+ solution. 6. The results described in paragraphs 4 and 5 indicate that, under conditions expected to minimize changes in Ca2+i, all manifestations of light adaptation disappear, and the rod simply sums the effects of incident photons with an invariant integration time. 7. Exposure of a light-adapted rod to low-Ca2+, 0-Na+ solution altered the responses to superimposed test flashes in much the same way as for rods in darkness. The initial rising phases in low-Ca2+, 0-Na+ solution were unchanged, but the responses were larger, reached peak later and decayed more slowly.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 为了研究细胞质钙浓度(Ca2+i)在视杆光感受器光适应中的作用,我们试图通过最小化跨外段质膜的钙通量来防止光诱导的Ca2+i变化。这是通过将外段暴露于低钙、零钠溶液中来实现的,其中钠被胍或锂取代,外部钙浓度(Ca2+o)降低至微摩尔水平。2. 使用胍和1 - 3微摩尔的Ca2+o时,黑暗中的循环电流至少维持15秒,这与Ca2+i的大致稳定性一致。使用Li+而非胍时,大部分初始电流被抑制,但残余电流再次相对稳定。3. 在长时间暴露于低钙、零钠溶液(超过30秒)后再进行弱光照射期间,循环电流并非保持恒定,而是缓慢增加。将钙缓冲剂掺入细胞质可大大降低电流变化率,这与电流增加源于Ca2+i逐渐降低的观点一致。4. 在黑暗中暴露于低钙、零钠溶液的视杆的光反应以一种特征性方式改变。尽管光反应的初始上升阶段变化不大,但反应的峰值幅度更大且出现得更晚,并且反应衰减比对照组更慢。对于闪光和光阶跃,反应 - 强度关系变陡并向更低强度偏移。对阶跃反应中的正常凹陷消失,并且阶跃反应的波形可以根据弱闪光反应的积分进行近似预测。5. 在林格氏溶液中施加背景光照会显著加速对随后强光闪光的反应。如果在低钙、零钠溶液中施加背景光照,则未观察到这种加速现象。6. 第4段和第5段中描述的结果表明,在预期可最小化Ca2+i变化的条件下,光适应的所有表现都消失,并且视杆仅以不变的积分时间对入射光子的效应进行求和。7. 将光适应的视杆暴露于低钙、零钠溶液中,对视杆对叠加测试闪光的反应的改变方式与黑暗中的视杆大致相同。在低钙、零钠溶液中的初始上升阶段不变,但反应更大,达到峰值更晚且衰减更慢。(摘要截断于400字)

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