Nikonov S, Lamb T D, Pugh E N
Department of Ophthalmology and Institute of Neurological Sciences, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
J Gen Physiol. 2000 Dec;116(6):795-824. doi: 10.1085/jgp.116.6.795.
We investigated the kinetics and sensitivity of photocurrent responses of salamander rods, both in darkness and during adaptation to steady backgrounds producing 20-3,000 photoisomerizations per second, using suction pipet recordings. The most intense backgrounds suppressed 80% of the circulating dark current and decreased the flash sensitivity approximately 30-fold. To investigate the underlying transduction mechanism, we expressed the responses as a fraction of the steady level of cGMP-activated current recorded in the background. The fractional responses to flashes of any fixed intensity began rising along a common trajectory, regardless of background intensity. We interpret these invariant initial trajectories to indicate that, at these background intensities, light adaptation does not alter the gain of any of the amplifying steps of phototransduction. For subsaturating flashes of fixed intensity, the fractional responses obtained on backgrounds of different intensity were found to "peel off" from their common initial trajectory in a background-dependent manner: the more intense the background, the earlier the time of peeling off. This behavior is consistent with a background-induced reduction in the effective lifetime of at least one of the three major integrating steps in phototransduction; i.e., an acceleration of one or more of the following: (1) the inactivation of activated rhodopsin (R*); (2) the inactivation of activated phosphodiesterase (E*, representing the complex G(alpha)-PDE of phosphodiesterase with the transducin alpha-subunit); or (3) the hydrolysis of cGMP, with rate constant beta. Our measurements show that, over the range of background intensities we used, beta increased on average to approximately 20 times its dark-adapted value; and our theoretical analysis indicates that this increase in beta is the primary mechanism underlying the measured shortening of time-to-peak of the dim-flash response and the decrease in sensitivity of the fractional response.
我们使用吸管记录法,研究了蝾螈视杆细胞在黑暗中以及适应每秒产生20 - 3000次光异构化的稳定背景光时的光电流响应动力学和敏感性。最强的背景光抑制了约80%的循环暗电流,并使闪光敏感性降低了约30倍。为了研究潜在的转导机制,我们将响应表示为在背景光中记录的cGMP激活电流稳定水平的分数。对任何固定强度闪光的分数响应开始沿着一条共同的轨迹上升,而与背景强度无关。我们将这些不变的初始轨迹解释为表明,在这些背景强度下,光适应不会改变光转导任何放大步骤的增益。对于固定强度的亚饱和闪光,发现在不同强度背景上获得的分数响应以依赖背景的方式从它们共同的初始轨迹“剥离”:背景越强,剥离时间越早。这种行为与光转导中三个主要积分步骤中至少一个的有效寿命因背景而缩短一致;即以下一个或多个过程的加速:(1) 活化视紫红质(R*)的失活;(2) 活化磷酸二酯酶(E*,代表磷酸二酯酶与转导蛋白α亚基的复合物G(α)-PDE)的失活;或(3) cGMP的水解,速率常数为β。我们的测量表明,在我们使用的背景强度范围内,β平均增加到其暗适应值的约20倍;我们的理论分析表明,β的这种增加是测量到的暗闪光响应峰值时间缩短和分数响应敏感性降低的主要机制。