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豚鼠海马切片中齿状回门区神经元的抑制作用

Inhibitory role of dentate hilus neurons in guinea pig hippocampal slice.

作者信息

Müller W, Misgeld U

机构信息

Abteilung Neurophysiologie, Max-Planck-Institut für Psychatrie, Martinsried, Federal Republic of Germany.

出版信息

J Neurophysiol. 1990 Jul;64(1):46-56. doi: 10.1152/jn.1990.64.1.46.

Abstract
  1. Current and voltage-clamp recording of CA3/CA4 pyramidal neurons, hilar neurons, and granule cells or pairs of these neurons were used to study the generation of Cl-dependent and K-dependent inhibitory postsynaptic potentials (IPSPs) in the guinea pig hippocampal slice preparation. 2. A sequence of an early Cl-dependent and a late K-dependent IPSP was evoked in CA3 neurons by electrical stimulation from the stratum moleculare of the dentate gyrus, the hilus, and the stratum oriens/alveus. Blockade of glutamatergic excitation by 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX, 10 microM) and D(-)-2-amino-5-phosphonovaleric acid (APV, 30 microM) abolished IPSPs evoked from the stratum moleculare of the dentate gyrus, but IPSPs could still be evoked from the hilus and the stratum oriens/alveus. 3. Repetitive giant IPSPs, which consisted of Cl-dependent and K-dependent components, were evoked by bath application of 4-aminopyridine (4-AP, 10-50 microM) in CA3 neurons and in granule cells. Giant IPSPs were blocked by bath-applied tetrodotoxin (TTX). In addition, 4-AP hyperpolarized CA3 neurons in a Cl-dependent and picrotoxin-sensitive way. 4. Focal application of TTX to the dentate gyrus or the hilus considerably reduced the amplitude of giant IPSPs evoked by 4-AP in CA3 neurons. In hilar neurons, 4-AP evoked repetitive bursts, eventually, but not necessarily intermingled with giant IPSPs. Bursts were observed in hilar neurons in presence as well as absence of CNQX and APV. 5. In paired recordings, bursts in hilar neurons induced by 4-AP occurred simultaneously to giant IPSPs in granule cells and CA3 neurons, and giant IPSPs in granule cells occurred simultaneously to giant IPSPs in CA3 neurons. Blockade of glutamatergic excitation by CNQX and APV did not abolish this synchrony. 6. 4-AP-evoked Cl- and K-dependent IPSPs were, unlike electrically evoked IPSPs, not strictly coupled: some 20% of large IPSPs and up to 90% of small IPSPs were either Cl or K dependent. In granule cells K-dependent components either preceded or followed Cl-dependent components. 7. K-dependent IPSPs only could be evoked in CA3 neurons by focal application of 4-AP (1 mM) to the hilus, the stratum lacunosum moleculare or the stratum pyramidale. Wash out of Ca for 15-20 min blocked the Cl-dependent but not the K-dependent component of giant IPSPs evoked by bath-applied 4-AP.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 使用豚鼠海马脑片标本,对CA3/CA4锥体神经元、海马门神经元、颗粒细胞或这些神经元对进行电流钳和电压钳记录,以研究氯离子依赖性和钾离子依赖性抑制性突触后电位(IPSPs)的产生。2. 通过对齿状回分子层、海马门、海马原层/齿状回下托进行电刺激,在CA3神经元中诱发了一系列早期氯离子依赖性和晚期钾离子依赖性IPSPs。用6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX,10微摩尔)和D-(-)-2-氨基-5-磷酸戊酸(APV,30微摩尔)阻断谷氨酸能兴奋,消除了从齿状回分子层诱发的IPSPs,但仍可从海马门和海马原层/齿状回下托诱发IPSPs。3. 通过在浴槽中应用4-氨基吡啶(4-AP,10 - 50微摩尔),在CA3神经元和颗粒细胞中诱发了由氯离子依赖性和钾离子依赖性成分组成的重复性巨大IPSPs。巨大IPSPs被浴槽中应用的河豚毒素(TTX)阻断。此外,4-AP以氯离子依赖性和苦味毒敏感的方式使CA3神经元超极化。4. 向齿状回或海马门局部应用TTX,可显著降低4-AP在CA3神经元中诱发的巨大IPSPs的幅度。在海马门神经元中,4-AP最终诱发了重复性爆发,但不一定与巨大IPSPs混合。在存在和不存在CNQX和APV的情况下,在海马门神经元中均观察到爆发。5. 在配对记录中,4-AP在海马门神经元中诱发的爆发与颗粒细胞和CA3神经元中的巨大IPSPs同时发生,颗粒细胞中的巨大IPSPs与CA神经元中的巨大IPSPs同时发生。CNQX和APV阻断谷氨酸能兴奋并没有消除这种同步性。及6. 与电诱发的IPSPs不同,4-AP诱发的氯离子和钾离子依赖性IPSPs并不严格耦合:约20%的大IPSPs和高达90%的小IPSPs要么是氯离子依赖性的,要么是钾离子依赖性的。在颗粒细胞中,钾离子依赖性成分要么先于要么后于氯离子依赖性成分。7. 通过向海马门、分子层隙状层或锥体层局部应用4-AP(1毫摩尔),仅在CA3神经元中诱发了钾离子依赖性IPSPs。冲洗15 - 20分钟的钙离子可阻断浴槽中应用4-AP诱发的巨大IPSPs的氯离子依赖性成分,但不阻断钾离子依赖性成分。(摘要截断于400字)

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