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BN52021是一种血小板活化因子拮抗剂,是甘氨酸门控氯离子通道的选择性阻滞剂。

BN52021, a platelet activating factor antagonist, is a selective blocker of glycine-gated chloride channel.

作者信息

Kondratskaya Elena L, Lishko Polina V, Chatterjee Shyam S, Krishtal Oleg A

机构信息

Department of Cellular Membranology, A.A. Bogomoletz Institute of Physiology, National Academy of Sciences of Ukraine, Bogomoletz St. 4, Kiev 01024, Ukraine.

出版信息

Neurochem Int. 2002 Jun;40(7):647-53. doi: 10.1016/s0197-0186(01)00109-7.

Abstract

We have found that the platelet activating factor antagonist (BN52021) is an effective blocker of the glycine (Gly) receptor-mediated responses in the hippocampal pyramidal neurons of rat. Using the whole-cell voltage clamp and concentration clamp recording techniques, we investigated the mechanism underlying the inhibitory action of this terpenoid on the glycine-induced chloride current. BN52021 selectively and reversibly inhibits glycine current in a non-competitive and voltage-dependent fashion. The antagonistic effect of this substance is more pronounced at positive membrane potentials. At holding potential -70mV and in the presence of 200 microM glycine IC50 value for the blocking action of BN52021 was 270+/-10nM. Repetitive applications of BN52021 reveal the use-dependence of its blocking action. When co-applied with strychnine (STR), a competitive glycine receptor antagonist, BN52021 does not alter the IC50 value for strychnine. The inhibitory effect of BN52021 on gamma-aminobutyric acid (GABA) current is at least 25 times less potent than the effect on glycine current. This substance fails to affect AMPA and NMDA responses. It may be concluded that BN52021 inhibits glycine-gated Cl- channels by interacting with the pore region and does not compete for the strychnine-binding centre.

摘要

我们发现血小板激活因子拮抗剂(BN52021)是大鼠海马锥体细胞中甘氨酸(Gly)受体介导反应的有效阻断剂。运用全细胞电压钳和浓度钳记录技术,我们研究了这种萜类化合物对甘氨酸诱导的氯离子电流产生抑制作用的机制。BN52021以非竞争性和电压依赖性方式选择性且可逆地抑制甘氨酸电流。该物质的拮抗作用在膜电位为正时更为显著。在钳制电位为-70mV且存在200微摩尔甘氨酸的情况下,BN52021阻断作用的IC50值为270±10纳摩尔。重复应用BN52021揭示了其阻断作用的使用依赖性。当与竞争性甘氨酸受体拮抗剂士的宁(STR)共同应用时,BN52021不会改变士的宁的IC50值。BN52021对γ-氨基丁酸(GABA)电流的抑制作用比对甘氨酸电流的抑制作用至少弱25倍。该物质不会影响α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)和N-甲基-D-天冬氨酸(NMDA)反应。可以得出结论,BN52021通过与孔区域相互作用抑制甘氨酸门控氯离子通道,且不与士的宁结合中心竞争。

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