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鉴定介导虎蝾螈视网膜中双极细胞和神经节细胞输入的谷氨酸受体亚型。

Identification of glutamate receptor subtypes mediating inputs to bipolar cells and ganglion cells in the tiger salamander retina.

作者信息

Hensley S H, Yang X L, Wu S M

机构信息

Cullen Eye Institute, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Neurophysiol. 1993 Jun;69(6):2099-107. doi: 10.1152/jn.1993.69.6.2099.

Abstract
  1. The effects of glutamate receptor agonists and antagonists on bipolar cells and ganglion cells were studied with the use of intracellular and extracellular recording in the superfused, isolated, flat-mounted tiger salamander retina. The goal of the experiments was to correlate glutamate receptor subtypes with their localization at specific synaptic sites in the tiger salamander retina. The drugs tested were the kainate/alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), the N-methyl-D-aspartate (NMDA) receptor antagonist 3-(C+/-)-2-carboxy-piperazin-4-yl)-propyl-1-phosphonic acid (CPP) and L-2-amino-4-phosphonobutyrate (L-AP4). 2. The light responses of hyperpolarizing bipolar cells were suppressed by 20 microM CNQX, whereas L-AP4 had no effect on their light responses. In contrast, 20 microM CNQX had no effect on depolarizing bipolar cells, whereas L-AP4 abolished the light responses of these cells. 3. The light offset responses of OFF and ON-OFF ganglion cells were completely blocked by concentrations of CNQX as low as 5 microM. The light onset responses of ON-OFF ganglion cells were blocked when the concentration of CNQX was raised to 20 microM. In addition, 30 microM CPP partially blocked the light onset responses of ON-OFF ganglion cells but had a lesser effect on the light offset responses. 4. Twenty micromolars of CNQX blocked a transient component, and 20 microM CPP blocked a sustained component of the light response of sustained-ON ganglion cells.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 利用细胞内和细胞外记录技术,在灌注、分离、平铺的虎蝾螈视网膜上研究了谷氨酸受体激动剂和拮抗剂对双极细胞和神经节细胞的影响。实验目的是将谷氨酸受体亚型与其在虎蝾螈视网膜特定突触位点的定位相关联。所测试的药物有海人藻酸/α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)、N-甲基-D-天冬氨酸(NMDA)受体拮抗剂3-(C+/-)-2-羧基-哌嗪-4-基)-丙基-1-膦酸(CPP)和L-2-氨基-4-膦酰丁酸(L-AP4)。2. 在20微摩尔CNQX作用下,超极化双极细胞的光反应受到抑制,而L-AP4对其光反应无影响。相反,20微摩尔CNQX对去极化双极细胞无影响,而L-AP4消除了这些细胞的光反应。3. 低至5微摩尔的CNQX浓度就能完全阻断OFF和ON-OFF神经节细胞的光消退反应。当CNQX浓度升至20微摩尔时,ON-OFF神经节细胞的光起始反应被阻断。此外,30微摩尔CPP部分阻断ON-OFF神经节细胞的光起始反应,但对光消退反应的影响较小。4. 20微摩尔CNQX阻断了持续ON神经节细胞光反应的一个瞬态成分,20微摩尔CPP阻断了其一个持续成分。(摘要截短至250字)

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