Steep decrease in the specific membrane resistance in the apical dendrites of hippocampal CA1 pyramidal neurons

被引:10
|
作者
Omori, Toshiaki [1 ,2 ]
Aonishi, Toru [2 ,3 ]
Miyakawa, Hiroyoshi [4 ]
Inoue, Masashi [4 ]
Okada, Masato [1 ,2 ]
机构
[1] Univ Tokyo, Grad Sch Frontier Sci, Dept Complex Sci & Engn, Chiba 2778561, Japan
[2] RIKEN, Brain Sci Inst, Wako, Saitama 3510198, Japan
[3] Tokyo Inst Technol, Interdisciplinary Grad Sch Sci & Engn, Dept Computat Intelligence & Syst Sci, Modori Ku, Kanagawa 2268502, Japan
[4] Tokyo Univ Pharm & Life Sci, Sch Life Sci, Lab Cellular Neurobiol, Tokyo 1920392, Japan
关键词
Dendrite; Detailed compartment model; Simulation; Passive membrane property; Extracellular electric field; EPSP spread; Hippocampus; SYNAPTIC POTENTIALS; VOLTAGE ATTENUATION; ELECTRIC-FIELDS; CURRENTS; STIMULATION; LOCATION; SLICES; MOTONEURONS; SIMULATION; CHANNELS;
D O I
10.1016/j.neures.2009.01.012
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Specific membrane resistance (R(m)), distributed non-uniformly over the dendrite, has a substantial effect on neuronal information processing, since it is a major determinant in subthreshold-synaptic integration. From experimental data of dendritic excitatory postsynaptic potential (EPSP) spread, we previously reported that non-uniform R(m) distribution in hippocampal CA1 pyramidal neurons could be expressed as a step function. However, it remains unclear how steeply R(m) decreases. Here, we estimated the R(m) distribution using sigmoid function to evaluate the steepness of decrease in R(m). Simulations were performed to find the distribution which reproduced experimental voltage responses to extracellular electric field applied to CA1 slices, in contrast to the EPSP spread. Distribution estimated from the responses to electric field was a steep-sigmoid function, similar to that from the EPSP spread. R(m) in distal dendrite was estimated to be less than or similar to 10(3.5) Omega cm(2) whereas that in proximal dendrite/soma was greater than or similar to 10(4.5) Omega cm(2). Our results not only supported previous studies, but, surprisingly, implied that R(m) decreases at a location more distal, and that distal dendrite was leakier, than previous estimates by other groups. Simulations satisfactorily reproduced the responses to two distinct perturbations, suggesting that steep decrease in R. is reliable. Our study suggests that the non-uniform Rm distribution plays an important role in information processing for spatially segregated synaptic inputs. (C) 2009 Elsevier Ireland Ltd and the Japan Neuroscience Society. All rights reserved.
引用
收藏
页码:83 / 95
页数:13
相关论文
共 50 条
  • [31] Membrane Potential Dynamics of CA1 Pyramidal Neurons during Hippocampal Ripples in Awake Mice
    Hulse, Brad K.
    Moreaux, Laurent C.
    Lubenov, Evgueniy V.
    Siapas, Athanassios G.
    NEURON, 2016, 89 (04) : 800 - 813
  • [32] Intrinsic Mechanisms of Frequency Selectivity in the Proximal Dendrites of CA1 Pyramidal Neurons
    Combe, Crescent L.
    Canavier, Carmen C.
    Gasparini, Sonia
    JOURNAL OF NEUROSCIENCE, 2018, 38 (38): : 8110 - 8127
  • [33] SIRT1 activation by resveratrol reverses atrophy of apical dendrites of hippocampal CA1 pyramidal neurons and neurobehavioral impairments in moderate grade hepatic encephalopathy rats
    Khanna, Archita
    Anamika
    Chakraborty, Suwarna
    Tripathi, Sunil Jamuna
    Acharjee, Arup
    Rao, Shankaranarayana B. S.
    Trigun, Surendra K.
    JOURNAL OF CHEMICAL NEUROANATOMY, 2020, 106
  • [34] Phosphorylation of CRMP2 is involved in proper bifurcation of the apical dendrite of hippocampal CA1 pyramidal neurons
    Niisato, Emi
    Nagai, Jun
    Yamashita, Naoya
    Nakamura, Fumio
    Goshima, Yoshio
    Ohshima, Toshio
    DEVELOPMENTAL NEUROBIOLOGY, 2013, 73 (02) : 142 - 151
  • [35] NMDA receptor-independent LTP in basal versus apical dendrites of CA1 pyramidal cells in rat hippocampal slice
    Çavus, I
    Teyler, TJ
    HIPPOCAMPUS, 1998, 8 (04) : 373 - 379
  • [36] GABAergic control of synaptic summation in hippocampal CA1 pyramidal neurons
    Enoki, R
    Inoue, M
    Hashimoto, Y
    Kudo, Y
    Miyakawa, H
    HIPPOCAMPUS, 2001, 11 (06) : 683 - 689
  • [37] Distance-dependent Ni2+-sensitivity of synaptic plasticity in apical dendrites of hippocampal CA1 pyramidal cells
    Isomura, Y
    Fujiwara-Tsukamoto, Y
    Imanishi, M
    Nambu, A
    Takada, M
    JOURNAL OF NEUROPHYSIOLOGY, 2002, 87 (02) : 1169 - 1174
  • [38] Differential Structure of Hippocampal CA1 Pyramidal Neurons in the Human and Mouse
    Benavides-Piccione, Ruth
    Regalado-Reyes, Mamen
    Fernaud-Espinosa, Isabel
    Kastanauskaite, Asta
    Tapia-Gonzalez, Silvia
    Leon-Espinosa, Gonzalo
    Rojo, Concepcion
    Insausti, Ricardo
    Segev, Idan
    DeFelipe, Javier
    CEREBRAL CORTEX, 2020, 30 (02) : 730 - 752
  • [39] ERG Channels Contribute to the Excitability of Pyramidal Neurons in Hippocampal CA1
    Yildirim, Caner
    Cakir, Ziya
    Bal, Ramazan
    EUROPEAN JOURNAL OF THERAPEUTICS, 2021, 27 (02): : 168 - 176
  • [40] Frequency-dependent response property of the dendrites in the hippocampal CA1 pyramidal cells
    Watanabe, Hidenori
    Tsubokawa, Hiroshi
    Aihara, Takeshi
    Tsukada, Minoru
    NEUROSCIENCE RESEARCH, 2007, 58 : S186 - S186