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从成年大鼠分离出的视上核大细胞神经元的特性

Properties of supraoptic magnocellular neurones isolated from the adult rat.

作者信息

Oliet S H, Bourque C W

机构信息

Centre for Research in Neuroscience, Montreal General Hospital, P.Q., Canada.

出版信息

J Physiol. 1992 Sep;455:291-306. doi: 10.1113/jphysiol.1992.sp019302.

Abstract
  1. Magnocellular neurosecretory cells (MNCs) were isolated from the supraoptic nucleus of adult Long-Evans rats using an enzymatic procedure. Immunocytochemical staining with antibodies against vasopressin and oxytocin revealed that MNCs can be identified by size. The membrane properties of these cells were examined at 32-34 degrees C using intracellular recording methods. 2. Isolated MNCs displayed a mean (+/- S.E.M.; n = 109) resting membrane potential of -64.1 +/- 1.0 mV, an input resistance of 571 +/- 34 M omega, and a time constant of 8.7 +/- 0.4 ms. Measurements of specific resistivity and input capacitance revealed that the soma of these cells accounts for a mere 20% of their total somato-dendritic membrane in situ. 3. Voltage-current relations measured near -60 mV were linear negative to spike threshold. From more hyperpolarized membrane potentials, voltage responses to depolarizing current steps displayed transient outward rectification and delayed impulse discharge. 4. Action potentials (76.6 +/- 0.9 mV) triggered from an apparent threshold of -59.3 +/- 0.1 mV broadened progressively at the onset of spontaneous or current-evoked spike trains. Steady-state spike duration increased as a logarithmic function of firing frequency with a maximum near 25 Hz. These effects were abolished in Ca(2+)-free solutions. 5. In all cells, evoked spike trains were followed by a prolonged Ca(2+)-sensitive after-hyperpolarization. In contrast, only a small proportion (16%) of MNCs displayed spontaneous bursting activity or depolarizing after-potentials following brief current-evoked bursts. 6. Isolated MNCs responded to amino acids (glutamate and GABA) and to the neuropeptide cholecystokinin, indicating that receptors for these neurotransmitters are expressed postsynaptically by MNCs and are retained following dissociation. 7. Increasing the osmolality of the superfusing solution by 5-30 mosmol kg-1 caused a membrane depolarization associated with a decrease of input resistance and accelerated spontaneous spike discharge in each of thirty-six MNCs tested. Current-clamp analysis suggested that these responses resulted from the activation of a cationic conductance. Excitatory effects of hyperosmolality were not observed in non-magnocellular neurones (n = 6).
摘要
  1. 采用酶解法从成年Long-Evans大鼠的视上核分离出大细胞神经分泌细胞(MNCs)。用抗加压素和抗催产素抗体进行免疫细胞化学染色显示,MNCs可通过大小来识别。使用细胞内记录方法在32 - 34摄氏度下检测这些细胞的膜特性。2. 分离出的MNCs的平均(±标准误;n = 109)静息膜电位为 - 64.1 ± 1.0 mV,输入电阻为571 ± 34 MΩ,时间常数为8.7 ± 0.4 ms。比电阻率和输入电容的测量结果显示,这些细胞的胞体在原位仅占其总胞体 - 树突膜的20%。3. 在接近 - 60 mV处测量的电压 - 电流关系在达到动作电位阈值之前呈线性负相关。从更超极化的膜电位开始,对去极化电流阶跃的电压响应表现出瞬时外向整流和延迟冲动发放。4. 动作电位(76.6 ± 0.9 mV)从明显的阈值 - 59.3 ± 0.1 mV触发,在自发或电流诱发的冲动发放开始时逐渐变宽。稳态动作电位持续时间随发放频率呈对数函数增加,在接近25 Hz时达到最大值。这些效应在无钙溶液中消失。5. 在所有细胞中,诱发的冲动发放后紧接着是一个延长的钙敏感超极化后电位。相比之下,只有一小部分(16%)的MNCs在短暂电流诱发的爆发后表现出自发爆发活动或去极化后电位。6. 分离出的MNCs对氨基酸(谷氨酸和γ-氨基丁酸)以及神经肽胆囊收缩素产生反应,表明这些神经递质的受体在MNCs的突触后表达,并且在解离后仍保留活性。7. 将灌流溶液的渗透压增加5 - 30 mosmol kg-1会导致膜去极化,同时伴有输入电阻降低,并加速了所测试的36个MNCs中每个细胞的自发冲动发放。电流钳分析表明,这些反应是由阳离子电导的激活引起的。在非大细胞神经元(n = 6)中未观察到高渗的兴奋作用。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bdc6/1175645/3499a14f4fae/jphysiol00427-0294-a.jpg

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