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腺苷A1受体对大鼠视网膜神经节细胞中谷氨酸诱导的钙内流的调节作用。

Adenosine A1-receptor modulation of glutamate-induced calcium influx in rat retinal ganglion cells.

作者信息

Hartwick Andrew T E, Lalonde Mélanie R, Barnes Steven, Baldridge William H

机构信息

Retina and Optic Nerve Research Laboratory, Department of Anatomy and Neurobiology, Dalhousie University, Halifax, Nova Scotia, Canada.

出版信息

Invest Ophthalmol Vis Sci. 2004 Oct;45(10):3740-8. doi: 10.1167/iovs.04-0214.

Abstract

PURPOSE

Although adenosine receptors (A(1)-Rs and A(2)-Rs) have been identified in the mammalian retina, the role of adenosine in this tissue is not fully understood. The purpose of this work was to investigate the action of adenosine on glutamate-induced calcium influx in rat retinal ganglion cells (RGCs) and to determine whether adenosine modulates RGC voltage-gated calcium channels.

METHODS

Purified RGC cultures were generated from neonatal rats with a two-step panning procedure. Isolated RGCs were loaded with the ratiometric calcium-indicator dye fura-2, and the effect of adenosine (and related agonists and antagonists) on intracellular calcium levels (Ca(2+)) during exposure to glutamate (10 microM with 10 microM glycine) was assessed. The effect of adenosine on calcium channel currents was also studied in isolated RGCs with whole-cell patch-clamp techniques. In addition, the effect of adenosine on Ca(2+) was investigated in fura dextran-loaded RGCs in an intact adult rat retina preparation.

RESULTS

In isolated RGCs, adenosine (10 and 100 microM) significantly reduced the glutamate-induced increase in Ca(2+) ( approximately 30%). The effect of adenosine was blocked by the A(1)-R antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX), but not by the A(2)-R antagonist 3,7-dimethyl-1-propargylxanthine (DMPX). Adenosine (10 microM) inhibited calcium channel currents by 43%, and again this effect was blocked by DPCPX, but not DMPX. Adenosine (100 microM) also significantly reduced the elevation of Ca(2+) in RGCs in the intact retina during exposure to N-methyl-d-aspartate (NMDA; 100 microM).

CONCLUSIONS

Adenosine can inhibit glutamate-induced calcium influx and voltage-gated calcium currents in rat RGCs through A(1)-R activation. This work supports a role for adenosine as a neuromodulator of mammalian RGCs.

摘要

目的

尽管在哺乳动物视网膜中已鉴定出腺苷受体(A(1)受体和A(2)受体),但腺苷在该组织中的作用尚未完全明确。本研究旨在探讨腺苷对大鼠视网膜神经节细胞(RGCs)中谷氨酸诱导的钙内流的作用,并确定腺苷是否调节RGC的电压门控钙通道。

方法

采用两步淘选法从新生大鼠中培养纯化的RGCs。将分离的RGCs用比率钙指示剂染料fura-2加载,并评估腺苷(及相关激动剂和拮抗剂)对暴露于谷氨酸(10微摩尔与10微摩尔甘氨酸)期间细胞内钙水平([Ca(2+)]i)的影响。还利用全细胞膜片钳技术在分离的RGCs中研究腺苷对钙通道电流的影响。此外,在完整成年大鼠视网膜标本中,对加载fura葡聚糖的RGCs研究腺苷对[Ca(2+)]i的影响。

结果

在分离的RGCs中,腺苷(10和100微摩尔)显著降低谷氨酸诱导的[Ca(2+)]i增加(约30%)。腺苷的作用被A(1)受体拮抗剂8-环戊基-1,3-二丙基黄嘌呤(DPCPX)阻断,但未被A(2)受体拮抗剂3,7-二甲基-1-丙炔基黄嘌呤(DMPX)阻断。腺苷(10微摩尔)使钙通道电流抑制43%,同样,该作用被DPCPX阻断,但未被DMPX阻断。腺苷(100微摩尔)在暴露于N-甲基-D-天冬氨酸(NMDA;100微摩尔)期间也显著降低完整视网膜中RGCs的[Ca(2+)]i升高。

结论

腺苷可通过激活A(1)受体抑制大鼠RGCs中谷氨酸诱导的钙内流和电压门控钙电流。本研究支持腺苷作为哺乳动物RGCs神经调节剂的作用。

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