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

机译:Na +和cGMP诱导的蛙杆感光细胞中的Ca2 +通量

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摘要

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)
机译:我们已经使用指示Ca2 +的染料砷偶氮III检验了青蛙杆外部段中的Ca2 +含量和Ca2 +的运输途径。实验采用截短但具有生理功能的青蛙棒(OS-IS)外部段,完整的隔离外部段(int OS)和泄漏外部段(有质膜泄漏到小的溶质但密封的泄漏OS)的悬浮液。圆盘膜)。我们观察到以下情况。在Percoll-Ringer溶液中分离和纯化的完整OS或OS-IS平均含有2.2 mM的总Ca2 +,而泄漏OS含有2.0 mM的总Ca2 +。这表明OS-IS中的大多数Ca2 +都包含在OS磁盘中。在完整的OS或OS-IS中,磷酸二酯酶抑制剂可使Ca2 +含量增至约4.2 mM,而泄漏OS的Ca2 +含量未发生变化。在完整和泄漏的OS / OS-IS中,Na-Ca交换都是Ca2 +外排的主要途径。在完整的OS / OS-IS中,Na-Ca交换的速率在30至50 mM Na +之间达到最大值的一半。在50 mM Na +下,这相当于5.8 X 10(7)Ca2 + / OS X s或0.05 mM总Ca2 + / s。这比暗电流的Ca2 +分量大得多。在OS-IS或泄漏OS中,其他碱阳离子无法在Na-Ca交换中取代Na +。他们抑制了Na-Ca交换的速率(K大于或等于Rb大于Cs大于或等于Li大于TMA),并且随着抑制作用的增大,Na-Ca交换的开始出现延迟。碱性阳离子对Na-Ca交换的抑制与这些阳离子诱导的光响应的持续时间有关(Hodgkin,A.L.,P.A.McNaughton,和B.J.Nunn.1985。生理学杂志358:447-468)。除了Na-Ca交换外,泄漏OS中的盘状膜还显示了由循环GMP(cGMP)激活的Ca2 +转运的第二条途径。 cGMP激活的途径需要存在碱性阳离子,并且最大速率为9.7 X 10(6)Ca2 + / OS X s。 cGMP导致泄漏的OS仅释放了全部Ca2 +的30%。泄漏OS中Na-Ca交换的速率为1.9 X 10(7)Ca2 + / OS X s(抽象截断为400字)

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