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大鼠海马切片电活动诱发的钙和钡依赖性细胞外碱化转变

Calcium- and barium-dependent extracellular alkaline shifts evoked by electrical activity in rat hippocampal slices.

作者信息

Grichtchenko I I, Chesler M

机构信息

Department of Physiology and Neuroscience, New York University Medical Center, NY 10016, USA.

出版信息

Neuroscience. 1996 Dec;75(4):1117-26. doi: 10.1016/0306-4522(96)00293-x.

Abstract

Synaptic activation of central neurons has been associated with rapid extracellular alkalinization. In this report, we directly activated CA1 pyramidal cells by antidromic invasion, or by field stimulation. Antidromic activation produced no pH change, despite a robust population spike in five of 11 slices. In six slices, antidromic stimulation at 10 Hz evoked a small alkalinization in stratum pyramidale (0.04 +/- 0.01 unit pH) which grew to 0.10-0.20 unit pH at 50-100 Hz, and was blocked in 0 Ca2+ media. Simultaneous pH recordings revealed no alkalinizations in stratum radiatum, despite robust alkaline shifts in stratum pyramidale. When synaptic transmission was blocked by 6-cyano-7-nitroquinoxaline-2,3-dione, DL-2-amino-5-phosphonovalerate and picrotoxin, the Schaffer collateral-induced alkaline shift in stratum radiatum was abolished. With adequate stimulus strength and orientation, however, alkaline shifts in stratum radiatum could still be elicited, presumably by direct activation of the CA1 population. The non-synaptic alkaline shifts ranged from 0.10-0.20 unit pH, were amplified by benzolamide, and blocked by tetrodotoxin, 0 Ca2+ saline, and 300-400 microM Cd2+. Although directly activated alkaline shifts were never observed in 0 Ca2+ saline, large stimulus evoked responses could be elicited upon addition of 5-10 mM Ba2+. The Ba(2+)-dependent responses were also amplified by benzolamide and blocked by tetrodotoxin, Cd2+ or high Mg2+. These data demonstrate that stratum pyramidale can undergo an extracellular alkaline shift independent of stratum radiatum. The ionic dependence and pharmacologic sensitivity of the alkaline shifts suggest that voltage-gated Ca2+ channels are instrumental in triggering the alkalinizing mechanism. However, the ability of Ba2+ to support the alkaline shifts indicates that Ca2+ entry is not an absolute requirement. Implications for the mechanism of these pH changes are discussed.

摘要

中枢神经元的突触激活与细胞外快速碱化有关。在本报告中,我们通过逆向侵入或场刺激直接激活CA1锥体细胞。尽管在11个切片中有5个出现了强烈的群体峰电位,但逆向激活并未引起pH值变化。在6个切片中,10 Hz的逆向刺激在锥体层引起了小的碱化(0.04±0.01单位pH),在50 - 100 Hz时增至0.1-0.2单位pH,并在0 Ca2+培养基中被阻断。同时进行的pH记录显示,尽管锥体层出现了强烈的碱性变化,但放射层中没有碱化现象。当突触传递被6-氰基-7-硝基喹喔啉-2,3-二酮、DL-2-氨基-5-磷酸戊酸和印防己毒素阻断时,放射层中由Schaffer侧支诱导的碱性变化被消除。然而,在足够的刺激强度和方向下,放射层中的碱性变化仍然可以被诱发,推测是通过直接激活CA1群体。非突触性碱性变化范围为0.1-0.2单位pH,被苯甲酰胺放大,并被河豚毒素、0 Ca2+生理盐水和300 - 400 microM Cd2+阻断。尽管在0 Ca2+生理盐水中从未观察到直接激活的碱性变化,但加入5 - 10 mM Ba2+后可诱发大的刺激反应。Ba(2+)依赖性反应也被苯甲酰胺放大,并被河豚毒素、Cd2+或高镁阻断。这些数据表明,锥体层可以发生独立于放射层的细胞外碱性变化。碱性变化的离子依赖性和药理敏感性表明,电压门控Ca2+通道在触发碱化机制中起作用。然而,Ba2+支持碱性变化的能力表明Ca2+内流不是绝对必要的。文中讨论了这些pH变化机制的意义。

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