Lipton S A, Rasmussen H, Dowling J E
J Gen Physiol. 1977 Dec;70(6):771-91. doi: 10.1085/jgp.70.6.771.
Substances known to alter cyclic nucleotide levels in cells were applied to the isolated toad retina and effects on rod electrical and adaptive behavior were studied. The retina was continually superfused in control ringer's or ringer's containing one or a combination of drugs, and rod activity was recorded intracellularly. Superfusion with cGMP, Bu(2)GMP, isobutylmethylxanthine (IBMX; a phosphodiesterase inhibitor), or PGF(2alpha) (a prostaglandin) caused effects in rods that closely match those observed when extracellular Ca(2+) levels were lowered. For example, short exposures (up to 6 min) of the retina to these substances caused depolarization of the membrane potential, increase in response amplitudes, and some changes in waveform; but under dark-adapted or partially light-adapted conditions receptor sensitivity was virtually unaffected. That is, the position of the V-log I curve on the intensity axis was determined by the prevailing light level, not by drug level. These drugs, like lowered extracellular Ca(2+), also decreased the period of receptor saturation after a bright-adapting flash, resulting in an acceleration of the onset of membrane and sensitivity recovery during dark adaptation. Long-term (6-15 min) exposure of a dark-adapted retina to 5 mM IBMX or a combination of IBMX and cGMP caused a loss of response amplitude and a desensitization of the rods that was similar to that observed in rods after a long-term low Ca(2+) (10(-9)M) treatment. Application of high (3.2 mM) Ca(2+) to the retina blocked the effects of applied Bu(2)cGMP. PGE(1) superfusion mimicked the effects of increasing extracellular Ca(2+). The results show that increased cGMP and lowered Ca(2+) produce similar alterations in the electrical activity of rods. These findings suggest that Ca(2+) and cGMP are interrelated messengers. We speculate that low Ca(2+) may lead to increased intracellular cGMP, and/or that applied cGMP, and/or that applied cGMP may lower cytosol Ca(2+), perhaps by stimulating Ca(2+)- ATPase pumps in the outer segment.
将已知能改变细胞中环核苷酸水平的物质应用于分离的蟾蜍视网膜,并研究其对视杆细胞电活动和适应性行为的影响。视网膜在对照林格氏液或含有一种或多种药物组合的林格氏液中持续灌流,细胞内记录视杆细胞的活动。用环鸟苷酸(cGMP)、丁酰基环鸟苷酸(Bu(2)GMP)、异丁基甲基黄嘌呤(IBMX;一种磷酸二酯酶抑制剂)或前列腺素F2α(PGF(2α))灌流对视杆细胞产生的影响与细胞外钙离子(Ca(2+))水平降低时观察到的影响密切匹配。例如,视网膜短时间(长达6分钟)暴露于这些物质会导致膜电位去极化、反应幅度增加以及波形的一些变化;但在暗适应或部分光适应条件下,感受器敏感性实际上未受影响。也就是说,V-log I曲线在强度轴上的位置由当时的光照水平决定,而非药物水平。这些药物与降低细胞外Ca(2+)一样,还会缩短明适应闪光后感受器饱和的时间,导致暗适应期间膜电位和敏感性恢复的起始加速。将暗适应的视网膜长期(6 - 15分钟)暴露于5 mM IBMX或IBMX与cGMP的组合会导致反应幅度丧失和视杆细胞脱敏,这与长期低Ca(2+)(10(-9)M)处理后视杆细胞的情况相似。向视网膜施加高浓度(3.2 mM)的Ca(2+)可阻断所施加的丁酰基环鸟苷酸(Bu(2)cGMP)的作用。前列腺素E1(PGE(1))灌流模拟了增加细胞外Ca(2+)的作用。结果表明,cGMP增加和Ca(2+)降低对视杆细胞电活动产生相似的改变。这些发现提示Ca(2+)和cGMP是相互关联的信使。我们推测低Ca(2+)可能导致细胞内cGMP增加,和/或所施加的cGMP,和/或所施加的cGMP可能降低细胞质Ca(2+),也许是通过刺激外段中的Ca(2+)-ATP酶泵来实现的。