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J Physiol. 1978 Feb;275:547-57. doi: 10.1113/jphysiol.1978.sp012207.
2
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本文引用的文献

1
EFFECTS PRODUCED ON INHIBITORY POSTSYNAPTIC POTENTIALS BY THE COUPLED INJECTIONS OF CATIONS AND ANIONS INTO MOTONEURONS.通过向运动神经元联合注入阳离子和阴离子对抑制性突触后电位产生的影响。
Proc R Soc Lond B Biol Sci. 1964 May 19;160:197-210. doi: 10.1098/rspb.1964.0036.
2
Anion permeability of the synaptic and non-synaptic motoneurone membrane.突触和非突触运动神经元膜的阴离子通透性。
J Physiol. 1961 Dec;159(3):410-35. doi: 10.1113/jphysiol.1961.sp006818.
3
Electrical activities in thin sections from the mammalian brain maintained in chemically-defined media in vitro.在体外化学限定培养基中维持的哺乳动物脑薄片中的电活动。
J Neurochem. 1966 Dec;13(12):1333-43. doi: 10.1111/j.1471-4159.1966.tb04296.x.
4
Anionic permeability of cortical neurones.皮质神经元的阴离子通透性。
Exp Brain Res. 1969;7(1):11-31. doi: 10.1007/BF00236105.
5
Structure of cat frontal olfactory cortex.
J Neurophysiol. 1969 Mar;32(2):184-92. doi: 10.1152/jn.1969.32.2.184.
6
Electrical activity observed in guinea-pig olfactory cortex maintained in vitro.在体外培养的豚鼠嗅觉皮层中观察到的电活动。
J Physiol. 1968 Aug;197(3):667-83. doi: 10.1113/jphysiol.1968.sp008581.
7
Anion permeability of the inhibitory subsynaptic membrane of the spinal motoneuron of the toad.蟾蜍脊髓运动神经元抑制性突触后膜的阴离子通透性
Jpn J Physiol. 1971 Jun;21(3):265-76. doi: 10.2170/jjphysiol.21.265.
8
Evoked surface-positive potentials in isolated mammalian olfactory cortex.在离体哺乳动物嗅觉皮层中诱发出的表面正电位。
Brain Res. 1974 Aug 16;76(2):235-45. doi: 10.1016/0006-8993(74)90457-0.
9
Current-density analysis of summed evoked potentials in opossum prepyriform cortex.
J Neurophysiol. 1973 Jul;36(4):789-802. doi: 10.1152/jn.1973.36.4.789.
10
Primary afferent neurones: the ionic mechanism of GABA-mediated depolarization.初级传入神经元:γ-氨基丁酸介导的去极化的离子机制
Neuropharmacology. 1974 Mar;13(3):215-9. doi: 10.1016/0028-3908(74)90110-5.

体外嗅皮质神经元中的去极化抑制电位

A depolarizing inhibitory potential in neurones of the olfactory cortex in vitro.

作者信息

Scholfield C N

出版信息

J Physiol. 1978 Feb;275:547-57. doi: 10.1113/jphysiol.1978.sp012207.

DOI:10.1113/jphysiol.1978.sp012207
PMID:633155
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1282562/
Abstract
  1. Stable intracellular recordings were obtained from neurones in slices of the guinea-pig olfactory cortex maintained in vitro. 2. Single stimuli applied to the lateral olfactory tract (l.o.t.) produced an excitatory post-synaptic potential (e.p.s.p.) usually generating a single spike. 3. The e.p.s.p. was followed by a long (200-500 msec) after-depolarization (l.a.d.) of peak amplitude 5-16 mV. This was accompanied by a very large conductance increase and was associated with an inhibition of the intracellularly recorded e.p.s.p. and of spike generation. 4. The l.a.d. was more susceptible than the e.p.s.p. to depression by (i) repetitive l.o.t. stimulation and (ii) raising external [Mg2+]. The l.a.d. could be generated without a preceding spike. 5. At an average resting membrane potential of -74 mV the average reversal potential for the l.a.d. (El.a.d.) was -63 mV.El.a.d. became more positive on reducing [Cl-]out or on using KCl-filled electrodes. 6. It is concluded that the l.a.d. represents a Cl- -mediated inhibitory post-synaptic potential, generated through deep-lying recurrent inhibitory loops.
摘要
  1. 从体外培养的豚鼠嗅觉皮层切片中的神经元获得了稳定的细胞内记录。2. 对外侧嗅束(l.o.t.)施加单个刺激产生兴奋性突触后电位(e.p.s.p.),通常引发单个峰电位。3. e.p.s.p. 之后是一个持续时间较长(200 - 500毫秒)的去极化后电位(l.a.d.),峰值幅度为5 - 16毫伏。这伴随着非常大的电导增加,并与细胞内记录的e.p.s.p. 和峰电位产生的抑制相关。4. l.a.d. 比e.p.s.p. 更容易受到以下因素的抑制:(i)外侧嗅束的重复刺激和(ii)提高细胞外[Mg2+]浓度。l.a.d. 可以在没有先前峰电位的情况下产生。5. 在平均静息膜电位为 -74毫伏时,l.a.d. 的平均反转电位(El.a.d.)为 -63毫伏。在降低细胞外[Cl-]浓度或使用充满KCl的电极时,El.a.d. 变得更正。6. 得出的结论是,l.a.d. 代表一种由Cl-介导的抑制性突触后电位,通过深层的反馈抑制环路产生。