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在蟾蜍截短的视杆外段中研究的3',5'-环磷酸鸟苷激活的电导。

Guanosine 3',5'-cyclic monophosphate-activated conductance studied in a truncated rod outer segment of the toad.

作者信息

Nakatani K, Yau K W

机构信息

Howard Hughes Medical Institute, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

J Physiol. 1988 Jan;395:731-53. doi: 10.1113/jphysiol.1988.sp016943.

DOI:10.1113/jphysiol.1988.sp016943
PMID:2457686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1192018/
Abstract
  1. In darkness, a single rod outer segment isolated from the toad retina was sucked partially, tip first, into a tight-fitting, Ringer solution-filled glass pipette for recording membrane current. The basal end of the outer segment outside the pipette was sheared off with a probe to allow internal dialysis. The potential between the inside and the outside of the pipette was held at 0 mV. 2. With cyclic GMP and IBMX (isobutylmethylxanthine) in the dialysis solution, a large inward current appeared across the plasma membrane of the outer segment; this current saturated at around 1 mM-cyclic GMP. IBMX by itself was ineffective. 3. The saturated cyclic GMP-induced current recorded varied in size with the length of outer segment (L) within the suction pipette. For L less than 25 micron, the relation was linear, with a current density of 4-20 pA micron-1. 4. At short L (less than 25 micron), the dose-response relation between current magnitude and cyclic GMP concentration was sigmoidal, with a Hill coefficient (n) of 1.8-3.1 and a half-saturating cyclic GMP concentration (K1/2) of 30-85 microM. 5. In the presence of IBMX and the absence of GTP, the dose-response relation was the same in continuous bleaching light as in darkness. This indicates that both the characteristics of cyclic GMP binding and the intrinsic conduction properties of the open conductance are not affected by light. 6. Removing IBMX from the dialysing solution had little effect on the saturated current, but substantially reduced the current induced at low concentrations of cyclic GMP. When the analogue 8-bromo cyclic GMP was used instead, however, the presence of IBMX was relatively unimportant even at low agonist concentrations. These observations indicated that significant phosphodiesterase activity was present within the truncated outer segment. 7. In the absence of IBMX and the presence of GTP, the cyclic GMP-induced current could be suppressed by light. When ATP was also present in the dialysing solution, the effect of light was significantly reduced and the suppression also became more transient. 8. We conclude from the above results that the cyclic GMP-gated conductance is indeed present in the plasma membrane of the rod outer segment, and that this conductance and the light-sensitive conductance are one and the same entity. 9. From the results, we estimate that only about 1% of the conductance is normally open in darkness. This fraction of open conductance corresponds to a free cyclic GMP concentration of a few micromolar.
摘要
  1. 在黑暗中,将从蟾蜍视网膜分离出的单个视杆细胞外段,先将其尖端部分吸入充满林格氏液的紧密贴合的玻璃微管中,用于记录膜电流。用探针将微管外视杆细胞外段的基部剪断,以便进行内部透析。微管内外的电位保持在0 mV。2. 在透析液中加入环鸟苷酸(cGMP)和异丁基甲基黄嘌呤(IBMX)后,视杆细胞外段质膜上出现了一个大的内向电流;该电流在约1 mM的cGMP浓度时达到饱和。单独使用IBMX无效。3. 记录到的饱和cGMP诱导电流的大小随微管内视杆细胞外段的长度(L)而变化。当L小于25微米时,这种关系是线性的,电流密度为4 - 20 pA/微米。4. 在短L(小于25微米)时,电流大小与cGMP浓度之间的剂量 - 反应关系呈S形,希尔系数(n)为1.8 - 3.1,半饱和cGMP浓度(K1/2)为30 - 85 microM。5. 在存在IBMX且不存在鸟苷三磷酸(GTP)的情况下,连续漂白光下的剂量 - 反应关系与黑暗中相同。这表明cGMP结合的特性和开放电导的内在传导特性均不受光的影响。6. 从透析液中去除IBMX对饱和电流影响不大,但显著降低了低浓度cGMP诱导的电流。然而,当使用类似物8 - 溴环鸟苷酸代替时,即使在低激动剂浓度下,IBMX的存在相对来说也不那么重要。这些观察结果表明,截断的视杆细胞外段内存在显著的磷酸二酯酶活性。7. 在不存在IBMX且存在GTP的情况下,cGMP诱导的电流可被光抑制。当透析液中也存在三磷酸腺苷(ATP)时,光的影响显著降低,抑制作用也变得更加短暂。8. 从上述结果我们得出结论,环鸟苷酸门控电导确实存在于视杆细胞外段的质膜中,并且这种电导和光敏感电导是同一实体。9. 根据结果,我们估计在黑暗中通常只有约1%的电导是开放的。这种开放电导的比例对应于几微摩尔的游离cGMP浓度。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/9c515a0c997a/jphysiol00517-0744-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/0538bac491c5/jphysiol00517-0740-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/3b6a0b4c255a/jphysiol00517-0742-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/a92108c6ac48/jphysiol00517-0743-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/9c515a0c997a/jphysiol00517-0744-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/0538bac491c5/jphysiol00517-0740-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/3b6a0b4c255a/jphysiol00517-0742-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/a92108c6ac48/jphysiol00517-0743-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5bd/1192018/9c515a0c997a/jphysiol00517-0744-a.jpg

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