首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Pharmacological characterization of ionotropic glutamate receptors in the zebrafish olfactory bulb.
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Pharmacological characterization of ionotropic glutamate receptors in the zebrafish olfactory bulb.

机译:斑马鱼嗅球中离子型谷氨酸受体的药理特性。

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摘要

The distribution of N-methyl-D-aspartate- (NMDA) and kainic acid- (KA) sensitive ionotropic glutamate receptors (iGluR) in the zebrafish olfactory bulb was assessed using an activity-dependent labeling method. Olfactory bulbs were incubated with an ion channel permeant probe, agmatine (AGB), and iGluR agonists in vitro, and the labeled neurons containing AGB were visualized immunocytochemically. Preparations exposed to 250 microM KA in the presence of a NMDA receptor antagonist (D-2-amino-5-phosphono-valeric acid) and an alpha-amino-3-hydroxyl-5-methylisoxazole-4-propionic acid (AMPA) receptor antagonist (sym 2206), revealed KA receptor-mediated labeling of approximately 60-70% of mitral cells, juxtaglomerular cells, tyrosine hydroxylase-positive cells and granule cells. A higher proportion of ventral olfactory bulb neurons were KA-sensitive. Application of 333 microM NMDA in the presence of an AMPA/KA receptor antagonist (6-cyano-7-nitroquinoxaline-2,3-dione) resulted in NMDA receptor-mediated labeling of almost all neurons. The concentrations eliciting 50% of the maximal response (effective concentration: EC(50)s) for NMDA-stimulated labeling of different cell types were not significantly different and ranged from 148 microM to 162 microM. These results suggest that while NMDA receptors with similar binding affinities are widely distributed in the neurons of the zebrafish olfactory bulb, KA receptors are heterogeneously expressed among these cells and may serve unique roles in different regions of the olfactory bulb.
机译:使用活性依赖性标记方法评估了斑马鱼嗅球中N-甲基-D-天冬氨酸-(NMDA)和海藻酸-(KA)离子型谷氨酸受体(iGluR)的分布。嗅球与离子通道渗透探针,胍丁胺(AGB)和iGluR激动剂在体外孵育,并通过免疫细胞化学可视化包含AGB的标记神经元。在NMDA受体拮抗剂(D-2-氨基-5-膦酰基戊酸)和α-氨基-3-羟基-5-甲基异恶唑-4-丙酸(AMPA)受体存在下暴露于250 microM KA的制剂拮抗剂(符号2206),揭示了KA受体介导的二尖瓣细胞,近肾小球细胞,酪氨酸羟化酶阳性细胞和颗粒细胞的标记。较高比例的腹嗅球神经元对KA敏感。在AMPA / KA受体拮抗剂(6-氰基-7-硝基喹喔啉-2,3-二酮)存在下应用333 microM NMDA导致几乎所有神经元的NMDA受体介导的标记。 NMDA刺激标记不同细胞类型引起最大反应的50%浓度(有效浓度:EC(50)s)没有显着差异,范围为148 microM至162 microM。这些结果表明,虽然具有相似结合亲和力的NMDA受体广泛分布在斑马鱼嗅球的神经元中,但KA受体在这些细胞之间异质表达,并可能在嗅球的不同区域发挥独特作用。

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