Institute of Neurophysiology, University of Cologne, Koeln, Germany.
Acta Ophthalmol. 2011 Nov;89(7):e579-90. doi: 10.1111/j.1755-3768.2011.02167.x. Epub 2011 Aug 23.
Light-evoked responses from vertebrate retinas were recorded as an electroretinogram (ERG). The b-wave is the most prominent component of the ERG, and in the bovine retina its NiCl(2) -sensitive component was attributed to reciprocal signalling by pharmacoresistant R-type voltage-gated Ca(2+) channels, which similar to other voltage-dependent Ca(2+) channels trigger and control neurotransmitter release. The murine retina has the great advantage that the effect of gene inactivation for Ni(2+) -sensitive Ca(2+) channels can be analysed to prove or disprove that any of these Ca(2+) channels is involved in retinal signalling.
Superfused retinas from different murine genotypes lacking either one or both highly Ni(2+) -sensitive voltage-gated Ca(2+) channels were used to record their ex vivo ERGs.
The isolated retinas from mice lacking Ca(v)2.3 R-type or Ca(v)3.2 T-type or both voltage-gated Ca(2+) channels were superfused with a NiCl(2) (15 μm) containing nutrient solution. The change in the b-wave amplitude and implicit time, caused by NiCl(2), was calculated as a difference spectrum and compared to data from control animals. From the results, it can be deduced that Ca(v)2.3 contributes rather to a later component in the b-wave response, while in the absence of Ca(v)3.2 the gain of Ni(2+) -mediated increase in the b-wave amplitude is significantly increased, probably due to a loss of reciprocal inhibition to photoreceptors. Thus, each of the Ni(2+)-sensitive Ca(2+) channels contributes to specific features of the b-wave response.
Both high-affinity Ni(2+)-sensitive Ca(2+) channels contribute to transretinal signalling. Based on the results from the double knockout mice, additional targets for NiCl(2) must contribute to transretinal signalling, which will be most important for the structurally similar physiologically more important heavy metal cation Zn(2+).
通过记录视网膜电图(ERG)来记录脊椎动物视网膜的光诱反应。b 波是 ERG 中最显著的成分,在牛视网膜中,其 NiCl2 敏感成分归因于药理学抗性 R 型电压门控 Ca2+通道的相互信号传递,类似于其他电压依赖性 Ca2+通道,触发和控制神经递质释放。鼠视网膜具有很大的优势,可以分析 Ni2+敏感 Ca2+通道基因失活的效果,以证明或反驳任何这些 Ca2+通道都参与视网膜信号传递。
使用缺乏一种或两种高度 Ni2+敏感电压门控 Ca2+通道的不同鼠基因型的超孵育视网膜来记录其离体 ERG。
从缺乏 Ca(v)2.3 R 型或 Ca(v)3.2 T 型或两种电压门控 Ca2+通道的小鼠中分离出的视网膜用含有 NiCl2(15 μm)的营养溶液超孵育。用 NiCl2 引起的 b 波幅度和潜伏期变化作为差谱计算,并与对照动物的数据进行比较。结果表明,Ca(v)2.3 对 b 波反应的后期成分贡献较大,而在缺乏 Ca(v)3.2 的情况下,Ni2+介导的 b 波幅度增加的增益显著增加,可能是由于对光感受器的相互抑制丧失。因此,每种 Ni2+敏感 Ca2+通道都有助于 b 波反应的特定特征。
两种高亲和力 Ni2+敏感 Ca2+通道都有助于视网膜间信号传递。基于双敲除小鼠的结果,NiCl2 的其他靶标必须有助于视网膜间信号传递,这对于结构相似的生理上更重要的重金属阳离子 Zn2+来说将是最重要的。