Dendritic properties of hippocampal CA1 pyramidal neurons in the rat: Intracellular staining in vivo and in vitro

被引:0
|
作者
Pyapali, GK
Sik, A
Penttonen, M
Buzsaki, G
Turner, DA
机构
[1] Duke Univ, Med Ctr, Dept Neurosurg, Durham, NC 27710 USA
[2] Vet Affairs Med Ctr, Durham, NC 27710 USA
[3] Rutgers State Univ, Ctr Mol & Behav Neurosci, Newark, NJ 07102 USA
[4] Duke Univ, Dept Neurobiol, Durham, NC 27710 USA
关键词
CA1 pyramidal cells; neuronal reconstructions; electrotonic modeling; synaptic integration; dendritic function;
D O I
10.1002/(SICI)1096-9861(19980216)391:3<335::AID-CNE4>3.0.CO;2-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Dendritic morphology and passive cable properties determine many aspects of synaptic integration in complex neurons, together with voltage-dependent membrane conductances. We investigated dendritic properties of CA1 pyramidal neurons intracellularly labeled during in vivo and in vitro physiologic recordings, by using similar intracellular staining and three-dimensional reconstruction techniques. Total dendritic length of the in vive neurons was similar to that of the in vitro cells. After correction for shrinkage, cell extent in three-dimensional representation was not different between the two groups. Both in vive and in vitro neurons demonstrated a variable degree of symmetry, with some neurons showing more cylindrical symmetry around the main apical axis, whereas other neurons were more elliptical, with the variation likely due to preparation and preservation conditions. Branch order analysis revealed no difference in the number of branch orders or dendritic complexity. Passive conduction of dendritic signals to the soma in these neurons shows considerable attenuation, particularly with higher frequency signals (such as synaptic potentials compared with steady-state signals), despite a relatively short electrotonic length. Essential aspects of morphometric appearance and complex dendritic integration critical to CA1 pyramidal cell functioning are preserved across neurons defined from the two different hippocampal preparations used in this study. (C) 1998 Wiley-Liss, Inc.
引用
收藏
页码:335 / 352
页数:18
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