Larkman A U, Major G, Stratford K J, Jack J J
University Laboratory of Physiology, Oxford University, United Kingdom.
J Comp Neurol. 1992 Sep 8;323(2):137-52. doi: 10.1002/cne.903230202.
Features of the dendritic morphology of pyramidal neurones of the visual cortex of the rat that are relevant to the development of models of their passive electrical geometry were investigated. The sample of 39 neurones that was used came from layers 2/3 and 5. They had been recorded from and injected intracellularly with horseradish peroxidase (HRP) in vitro as part of a previous study (Larkman and Mason, J. Neurosci 10:1407, 1990). These cells had been reconstructed and measured previously by light microscopy. The relationship between the diameters of parent and daughter dendrites during branching was examined. It was found that most dendrites did not closely obey the "3/2 branch power relationship" required for representation of the dendrites as single equivalent cylinders. Estimates of total neuronal membrane area ranged from 27,100 +/- 7,900 microns2 for layer 2/3 cells to 52,200 +/- 11,800 microns2 for thick layer 5 cells. Dendritic spines contributed approximately half the total membrane area. Both neuronal input resistance and the ratio of membrane time constant to input resistance were correlated with neuronal membrane area as measured anatomically. The relative electrical lengths of the different dendrites of individual neurones were investigated, by using simple transformations to take account of the differences in diameter and spine density between dendritic segments. A novel "morphotonic" transformation is described that represents the purely morphological component of electrotonic length. Morphotonic lengths can be converted into electrotonic lengths by division by a "morphoelectric factor" ([Rm/Ri]1/2). This procedure has the advantage of separating the steps involving anatomical and electrical parameters. These transformations indicated that the dendrites of the apical terminal arbor were much longer electrically than the basal or apical oblique dendrites. In relative electrical terms, most apical oblique trees arose extremely close to the soma, and terminated at similar distances to the basals. These results indicate that the dendrites of these pyramidal cells cannot be represented as single equivalent cylinders. The electrotonic lengths of the dendrites were calculated by using the electrical parameters specific membrane capacitance (Cm), intracellular resistivity (Ri), and specific membrane resistivity (Rm). Conventional values were assumed for Cm (1.0 muFcm-2) and Ri (100 omega cm), but three different Rm values were used for each cell. Two of these were within the conventionally accepted range (10,000-20,000 omega cm2), while the third value was an order of magnitude higher, in line with some recent evidence from modeling and whole-cell recording studies.(ABSTRACT TRUNCATED AT 400 WORDS)
研究了大鼠视觉皮层锥体细胞树突形态的特征,这些特征与它们被动电几何模型的建立相关。所使用的39个神经元样本来自第2/3层和第5层。作为先前一项研究(Larkman和Mason,《神经科学杂志》10:1407,1990)的一部分,它们在体外被记录并进行了辣根过氧化物酶(HRP)的细胞内注射。这些细胞先前已通过光学显微镜进行了重建和测量。研究了分支过程中母树突和子树突直径之间的关系。发现大多数树突并不严格遵循将树突表示为单个等效圆柱体所需的“3/2分支幂关系”。神经元总膜面积的估计值范围为,第2/3层细胞为27,100±7,900平方微米,厚第5层细胞为52,200±11,800平方微米。树突棘约占总膜面积的一半。神经元输入电阻以及膜时间常数与输入电阻的比值,与通过解剖学测量的神经元膜面积相关。通过使用简单变换来考虑树突段之间直径和棘密度的差异,研究了单个神经元不同树突的相对电长度。描述了一种新颖的“形态电导率”变换,它代表了电紧张长度的纯形态学成分。形态电导率长度可以通过除以“形态电因子”([Rm/Ri]1/2)转换为电紧张长度。该过程具有分离涉及解剖学和电学参数步骤的优点。这些变换表明,顶端终末树突的电长度比基部或顶端斜向树突长得多。从相对电学角度来看,大多数顶端斜向树突极靠近胞体起始,并在与基部相似的距离处终止。这些结果表明,这些锥体细胞的树突不能表示为单个等效圆柱体。通过使用特定膜电容(Cm)、细胞内电阻率(Ri)和特定膜电阻率(Rm)等电学参数来计算树突的电紧张长度。假设Cm(1.0微法/平方厘米)和Ri(100欧姆厘米)为常规值,但每个细胞使用三个不同的Rm值。其中两个在常规接受的范围内(10,000 - 20,000欧姆平方厘米),而第三个值高一个数量级,这与建模和全细胞记录研究最近的一些证据一致。(摘要截断于400字)