Ashmore J F, Copenhagen D R
J Physiol. 1983 Jul;340:569-97. doi: 10.1113/jphysiol.1983.sp014781.
Voltage noise was recorded from centre-hyperpolarizing bipolar cells in the retina of the snapping turtle. The identity of the cells was confirmed by intracellular staining. The variance of the voltage fluctuations of the membrane potential present in the dark was suppressed by up to 30-fold by 100 microns diameter light spot stimuli centred on the cell's receptive field. Such noise reduction is expected when light hyperpolarizes the photoreceptors and reduces the rate of release of transmitter from the terminals. The spectra of the fluctuations were analysed as the sum of two components: (a), a component with power band width limited to below approximately 10 Hz, and (b), a component Sh(f) of the form Sh(f) = Sh(0)/(1 + (f/f0)2)2, with f0 = 27 Hz. The two components were attributed (a) to the noise generated in the cones and transmitted through the synapse to the bipolar cells and (b) to the action of transmitter on the bipolar cell membrane. The component Sh(f) attributed to the action of transmitter on the bipolar cells corresponded to an event approximately 14 ms in duration. The event had a peak amplitude in the range 17.6-223 microV with a mean of 69.5 microV. It is estimated that, in the dark, the number of such events contributing to the noise is about 9200 s-1. It is estimated that each elementary noise event in the cones controls approximately thirty of the transmitter-related events at the synapse. Responses to flashes of darkness applied on steady illumination were analysed by a method of matched filtering. The responses fluctuated in amplitude, and the analysis of this fluctuation suggested an elementary event of approximately the same amplitude as found from the noise analysis. Enlarging the diameter of the stimulus spot to 1500 microns repolarized the bipolar cells with an associated increase in voltage noise. Implications for the synaptic mechanisms of the centre-surround organization are discussed.
从啮龟视网膜的中心超极化双极细胞记录了电压噪声。通过细胞内染色确认了细胞的身份。以细胞感受野为中心的直径100微米的光斑刺激可将黑暗中存在的膜电位电压波动的方差抑制高达30倍。当光使光感受器超极化并降低来自终末的递质释放速率时,预计会出现这种噪声降低。波动的光谱被分析为两个成分的总和:(a),一个功率带宽限制在约10Hz以下的成分,以及(b),形式为Sh(f)=Sh(0)/(1+(f/f0)2)2的成分Sh(f),其中f0 = 27Hz。这两个成分被归因于(a)在视锥细胞中产生并通过突触传递到双极细胞的噪声,以及(b)递质对双极细胞膜的作用。归因于递质对双极细胞作用的成分Sh(f)对应于持续时间约14毫秒的一个事件。该事件的峰值幅度在17.6 - 223微伏范围内,平均值为69.5微伏。据估计,在黑暗中,导致噪声的此类事件的数量约为9200次/秒。据估计,视锥细胞中的每个基本噪声事件在突触处控制大约三十个与递质相关的事件。通过匹配滤波方法分析了在稳定光照下施加的暗闪光的响应。响应的幅度波动,对这种波动的分析表明存在一个幅度与噪声分析中发现的大致相同的基本事件。将刺激光斑的直径扩大到1500微米会使双极细胞复极化,同时电压噪声增加。讨论了对中心 - 周边组织突触机制的影响。