首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Spatiotemporal interaction of alpha(2) autoreceptors and noradrenaline transporters in the rat locus coeruleus: implications for volume transmission.
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Spatiotemporal interaction of alpha(2) autoreceptors and noradrenaline transporters in the rat locus coeruleus: implications for volume transmission.

机译:大鼠轨迹蓝斑中α(2)自身受体和去甲肾上腺素转运蛋白的时空相互作用:对体积传输的影响。

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摘要

We investigated the roles of alpha(2) autoreceptors and noradrenaline (NA) transporters on NA efflux and uptake in the rat locus coeruleus after electrical stimulation. NA efflux was evoked by various trains (50 pulses, 10-500 Hz) and measured by fast cyclic voltammetry. NA efflux and uptake half-time (t(1/2)) were stimulus-dependent, ranging from 43 +/- 3 nM and 2.45 +/- 0.21 s, respectively, with 500-Hz stimuli to 127 +/- 11 nM and 4.41 +/- 0.34 s, respectively, with 100-Hz trains. Based on these data, we calculate that each transporter removes 0.19 NA molecules from the extracellular space every second, a velocity compatible more with transporter-than channel-mode conduction. Dexmedetomidine (10 nM) decreased NA efflux by approximately 30% on stimulations of < or =1 s in duration. BRL 44408 (1 microM) increased NA efflux on stimuli of > or =2 s (by up to 92 +/- 16%). Desipramine (50 nM) increased NA efflux on stimuli of > or =1 s (by 113 +/- 24%) but slowed NA uptake on all stimuli. When given together, the effects of desipramine and BRL 44408 were additive at stimuli of >or =1 s but showed potentiation on shorter trains. There was a significant time delay for the elevation of NA efflux by blockade of uptake (0.79 s) or autoreceptors (1.14 s), suggesting that both are located extrasynaptically and that NA must diffuse through the extracellular space to these structures. We suggest that released NA may interact with alpha(2) autoreceptors and NA transporters as far as 10 microm from the release sites, an action compatible with a volume transmission role of NA in the locus coeruleus.
机译:我们调查了电刺激后大鼠外源蓝斑中α(2)自身受体和去甲肾上腺素(NA)转运蛋白对NA外排和摄取的作用。 NA流出被各种序列(50个脉冲,10-500Hz)诱发,并通过快速循环伏安法测量。 NA外排和吸收半衰期(t(1/2))取决于刺激,范围分别为43 +/- 3 nM和2.45 +/- 0.21 s,受500-Hz刺激至127 +/- 11 nM和100Hz火车分别为4.41 +/- 0.34 s和。根据这些数据,我们计算出每个转运蛋白每秒都会从细胞外空间清除0.19个NA分子,这种速度与转运蛋白的传导方式比与通道模式传导的相容性更高。持续时间<或= 1 s时,右美托咪定(10 nM)使NA外排减少约30%。 BRL 44408(1 microM)在>或= 2 s的刺激下增加了NA外排(最多92 +/- 16%)。 Desipramine(50 nM)在>或= 1 s的刺激下增加了NA的流出(增加113 +/- 24%),但在所有刺激下都降低了NA的吸收。当一起使用时,地昔帕明和BRL 44408的作用在>或= 1 s的刺激下是加和的,但在较短的列车上显示出增强作用。通过吸收(0.79 s)或自身受体(1.14 s)的阻滞,NA流出的升高存在明显的时间延迟,这表明两者均位于突触外,并且NA必须通过细胞外空间扩散至这些结构。我们建议释放的NA可能与α(2)自身受体和NA转运蛋白相互作用,距离释放部位最远为10微米,这一作用与基因在蓝斑中的体积传递作用兼容。

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