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蛙类视杆光感受器中钠离子和环鸟苷酸诱导的钙离子通量。

Na+- and cGMP-induced Ca2+ fluxes in frog rod photoreceptors.

作者信息

Schnetkamp P P, Bownds M D

出版信息

J Gen Physiol. 1987 Mar;89(3):481-500. doi: 10.1085/jgp.89.3.481.

Abstract

We have examined the Ca2+ content and pathways of Ca2+ transport in frog rod outer segments using the Ca2+-indicating dye arsenazo III. The experiments employed suspensions of outer segments of truncated, but physiologically functional, frog rods (OS-IS), intact isolated outer segments (intact OS), and leaky outer segments (leaky OS with a plasma membrane leaky to small solutes, but with sealed disk membranes). We observed the following. Intact OS or OS-IS isolated and purified in Percoll-Ringer's solution contained an average of 2.2 mM total Ca2+, while leaky OS contained 2.0 mM total Ca2+. This suggests that most of the Ca2+ in OS-IS is contained inside OS disks. Phosphodiesterase inhibitors increased the Ca2+ content to approximately 4.2 mM in intact OS or OS-IS, whereas the Ca2+ content of leaky OS was not altered. Na-Ca exchange was the dominant pathway for Ca2+ efflux in both intact and leaky OS/OS-IS. The rate of Na-Ca exchange in intact OS/OS-IS was half-maximal between 30 and 50 mM Na+; at 50 mM Na+, this amounted to 5.8 X 10(7) Ca2+/OS X s or 0.05 mM total Ca2+/s. This is much larger than the Ca2+ component of the dark current. Other alkali cations could not replace Na+ in Na-Ca exchange in either OS-IS or leaky OS. They inhibited the rate of Na-Ca exchange (K greater than or equal to Rb greater than Cs greater than or equal to Li greater than TMA) and, as the inhibition became greater, a delay developed in the onset of Na-Ca exchange. The inhibition of Na-Ca exchange by alkali cations correlates with the prolonged duration of the photoresponse induced by these cations (Hodgkin, A. L., P. A. McNaughton, and B. J. Nunn. 1985. Journal of Physiology. 358:447-468). In addition to Na-Ca exchange, disk membranes in leaky OS showed a second pathway of Ca2+ transport activated by cyclic GMP (cGMP). The cGMP-activated pathway required the presence of alkali cations and had a maximal rate of 9.7 X 10(6) Ca2+/OS X s. cGMP caused the release of only 30% of the total Ca2+ from leaky OS. The rate of Na-Ca exchange in leaky OS amounted to 1.9 X 10(7) Ca2+/OS X s.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

我们使用钙指示染料偶氮胂III检测了蛙视杆细胞外段中的钙离子含量及钙离子转运途径。实验采用了截断但生理功能正常的蛙视杆细胞外段(OS-IS)、完整分离的外段(完整OS)以及渗漏外段(质膜对小分子溶质渗漏但盘膜密封的渗漏OS)的悬浮液。我们观察到以下情况。在Percoll-林格氏溶液中分离纯化的完整OS或OS-IS平均总钙离子含量为2.2 mM,而渗漏OS的总钙离子含量为2.0 mM。这表明OS-IS中的大部分钙离子包含在视杆细胞外段盘膜内。磷酸二酯酶抑制剂使完整OS或OS-IS中的钙离子含量增加到约4.2 mM,而渗漏OS的钙离子含量未改变。钠钙交换是完整和渗漏OS/OS-IS中钙离子外流的主要途径。完整OS/OS-IS中钠钙交换速率在30至50 mM钠离子浓度之间达到半数最大速率;在50 mM钠离子浓度时,这相当于5.8×10⁷个钙离子/视杆细胞外段×秒或0.05 mM总钙离子/秒。这比暗电流中的钙离子成分大得多。在OS-IS或渗漏OS中,其他碱金属阳离子在钠钙交换中不能替代钠离子。它们抑制钠钙交换速率(钾离子≥铷离子>铯离子≥锂离子>四甲基铵离子),并且随着抑制作用增强,钠钙交换开始出现延迟。碱金属阳离子对钠钙交换的抑制作用与这些阳离子诱导的光反应持续时间延长相关(霍奇金,A.L.,P.A.麦克诺顿和B.J.纳恩。1985年。《生理学杂志》。358:447 - 468)。除了钠钙交换外,渗漏OS中的盘膜还显示出由环磷酸鸟苷(cGMP)激活的第二条钙离子转运途径。cGMP激活的途径需要碱金属阳离子的存在,最大速率为9.7×10⁶个钙离子/视杆细胞外段×秒。cGMP仅导致渗漏OS中30%的总钙离子释放。渗漏OS中钠钙交换速率为1.9×10⁷个钙离子/视杆细胞外段×秒。(摘要截断于400字)

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