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未成熟大鼠海马CA3区神经元中的巨大突触电位

Giant synaptic potentials in immature rat CA3 hippocampal neurones.

作者信息

Ben-Ari Y, Cherubini E, Corradetti R, Gaiarsa J L

机构信息

Unité 29, INSERM, Hôpital de Port-Royal, Paris, France.

出版信息

J Physiol. 1989 Sep;416:303-25. doi: 10.1113/jphysiol.1989.sp017762.

Abstract
  1. Intracellular recordings were made from rat CA3 hippocampal neurones in vitro during the first eighteen days of postnatal life. The cells had resting membrane potentials more negative than -51 mV, action potentials greater than 55 mV and membrane input resistances of 117 +/- 12 M omega. An unusual characteristic of these cells was the presence of spontaneous giant depolarizing potentials (GDPs) which were observed during the first eight postnatal (P) days in over 85% of neurones. They were less frequent between P9 and P12 (48%) and disappeared after P12. 2. The GDPs were synchronously generated by a population of neurones; they reversed polarity at -27 mV when recorded with KCl-containing electrodes and at -51 mV with potassium acetate- or potassium methylsulphate-filled electrodes. 3. The GDPs were blocked by bath application of bicuculline (10 microM) or picrotoxin (100-200 microM). Exogenously applied gamma-aminobutyric acid (GABA; 0.2-1 mM) induced at resting membrane potential a bicuculline-sensitive membrane depolarization which reversed polarity at -25 and -51 mV when recorded with KCl- or potassium methylsulphate-filled electrodes respectively. 4. The GDPs were reduced in frequency or blocked by the N-methyl-D-aspartate (NMDA) receptor antagonists DL-2-amino-7-phosphonoheptanoate (AP-7; 50 microM), D(-)2-amino-5-phosphonovalerate (AP-5, 10-50 microM) and (+-)3-(2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP, 10-50 microM) or NMDA channel blockers phencyclidine (2 microM) and ketamine (20 microM). 5. Stimulation of the hilus during the first week of life evoked a GDP followed by a hyperpolarization. The GDPs were generated by a population of synchronized neurones and reversed polarity at -27 mV with KCl-filled electrodes and at -52 mV with potassium acetate- or potassium methylsulphate-containing electrodes. 6. Bath application of bicuculline (1-10 microM) or picrotoxin (100-200 microM) reversibly blocked the evoked GDPs in the majority of cells. The NMDA receptor antagonists AP-5 (50 microM), AP-7 (50 microM) and CPP (30 microM) usually reduced the amplitude and the duration of the evoked GDPs. In neurones in which evoked GDPs were blocked by bicuculline, a NMDA-mediated component was revealed by increasing the strength or the frequency of stimulation. 7. During the second week of postnatal life, when spontaneous GDPs were extremely rare or absent, superfusion with bicuculline (10 microM) induced, as in adult slices, interictal discharges. These reversed polarity near 0 mV with KCl- or potassium acetate-containing electrodes and were reduced in amplitude and duration by AP-5 (50 microM).(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 在出生后的头18天内,对体外培养的大鼠CA3海马神经元进行细胞内记录。这些细胞的静息膜电位比-51 mV更负,动作电位大于55 mV,膜输入电阻为117±12 MΩ。这些细胞的一个不寻常特征是存在自发的巨大去极化电位(GDPs),在出生后的前8天,超过85%的神经元中可观察到这种电位。在出生后第9天至第12天期间,它们出现的频率较低(48%),在出生后第12天之后消失。2. GDPs由一群神经元同步产生;当用含KCl的电极记录时,它们在-27 mV时极性反转,而用充满醋酸钾或甲基硫酸钾的电极记录时,在-51 mV时极性反转。3. 通过浴加荷包牡丹碱(10 μM)或印防己毒素(100 - 200 μM)可阻断GDPs。外源性施加γ-氨基丁酸(GABA;0.2 - 1 mM)在静息膜电位时诱导出一种对荷包牡丹碱敏感的膜去极化,当分别用含KCl或甲基硫酸钾的电极记录时,该去极化在-25 mV和-51 mV时极性反转。4. GDPs的频率降低或被N-甲基-D-天冬氨酸(NMDA)受体拮抗剂DL-2-氨基-7-膦酰庚酸(AP-7;50 μM)、D-(-)-2-氨基-5-膦酰戊酸(AP-5,10 - 50 μM)和(±)-3-(2-羧基哌嗪-4-基)-丙基-1-膦酸(CPP,10 - 50 μM)或NMDA通道阻滞剂苯环己哌啶(2 μM)和氯胺酮(20 μM)阻断。5. 在出生后的第一周刺激海马齿状回可诱发一个GDP,随后是超极化。GDPs由一群同步的神经元产生,当用含KCl的电极记录时,它们在-27 mV时极性反转,而用含醋酸钾或甲基硫酸钾的电极记录时,在-52 mV时极性反转。6. 浴加荷包牡丹碱(1 - 10 μM)或印防己毒素(100 - 200 μM)可在大多数细胞中可逆地阻断诱发的GDPs。NMDA受体拮抗剂AP-5(50 μM)、AP-7(50 μM)和CPP(30 μM)通常会降低诱发的GDPs的幅度和持续时间。在荷包牡丹碱阻断诱发的GDPs的神经元中,通过增加刺激强度或频率可揭示出一个NMDA介导的成分。7. 在出生后的第二周,当自发的GDPs极其罕见或不存在时,用荷包牡丹碱(10 μM)灌注,如同在成年切片中一样,可诱发发作间期放电。这些放电在用含KCl或醋酸钾的电极记录时,在接近0 mV时极性反转,并被AP-5(50 μM)降低幅度和持续时间。(摘要截选至400字)
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4e6/1189216/0cfbb8891beb/jphysiol00481-0323-a.jpg

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