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快速、激动剂诱导的调节递质释放的α2自身受体脱敏。

Rapid, agonist-induced desensitization of alpha 2-autoreceptors modulating transmitter release.

作者信息

Boehm S, Huck S, Schwarz K, Agneter E, Drobny H, Singer E A

机构信息

Institutes of Neuropharmacology, University of Vienna, Austria.

出版信息

Br J Pharmacol. 1995 Mar;114(6):1143-8. doi: 10.1111/j.1476-5381.1995.tb13326.x.

Abstract
  1. The release of previously incorporated [3H]-noradrenaline was investigated in cultures of dissociated chick or rat sympathetic neurones and in cerebrocortical slices from neonatal or adult rats. Noradrenaline, in the presence of 10 mumol l-1 of the uptake inhibitor, cocaine, or the selective alpha 2-adrenoceptor agonist, 5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)-6-quinoxalinamine (UK 4,304), was applied for different periods of time in order to detect a possible time-dependence of the alpha 2-adrenoceptor-mediated inhibition of electrically evoked tritium outflow. 2. In chick sympathetic neurones, stimulation-evoked overflow was reduced to 30%, 42%, or 56% of control when noradrenaline (1 mumol l-1) was present for 2, 8, or 16 min, respectively. Likewise, UK 14,304 (1 mumol l-1) present for these periods of time reduced 3H overflow to 35%, 51%, and 53% of control, respectively. Addition of 1 nmol l-1 to 10 mumol l-1 UK 14,304 for either 2 or 16 min did not produce significantly different IC50 values, but the inhibitory effects were smaller with 16 min as compared to 2 min exposure at concentrations > or = 10 nmol l-1. 3. In rat sympathetic neurones, noradrenaline (100 nmol l-1) reduced stimulation-evoked overflow to 33%, 56%, or 57% of control, when present for 2, 8, or 16 min, respectively. Addition of UK 14,304 (1 mumol l-1) for these periods of time caused inhibition to 11%, 41%, and 46% of control. Applying UK14,304 for either 2 or 16 min did not result in significantly different IC5o values, but the inhibition induced by 16 min as compared to 2 min exposure was smaller at concentrations > 10 nmol 1-1.4. In cerebrocortical slices from either neonatal or adult rats, exposure to 0.1 to 1.0 micromol 1-1 UK14,304 for 16 min never caused a smaller inhibition than a corresponding 3 min exposure, although various experimental conditions were investigated.5 The results demonstrate that alpha 2-adrenoceptors which regulate noradrenaline release from sympathetic neurones undergo agonist-induced desensitization within minutes. Such rapid desensitization of alpha 2-autoreceptors was not detected in brain slice preparations.
摘要
  1. 在离体鸡或大鼠交感神经元培养物以及新生或成年大鼠的大脑皮质切片中,研究了先前摄取的[3H]-去甲肾上腺素的释放情况。在存在10 μmol l-1摄取抑制剂可卡因或选择性α2-肾上腺素能受体激动剂5-溴-N-(4,5-二氢-1H-咪唑-2-基)-6-喹喔啉胺(UK 4,304)的情况下,将去甲肾上腺素应用不同时间段,以检测α2-肾上腺素能受体介导的对电诱发氚流出的抑制作用是否可能存在时间依赖性。2. 在鸡交感神经元中,当去甲肾上腺素(1 μmol l-1)分别存在2、8或16分钟时,刺激诱发的溢出量分别降至对照的30%、42%或56%。同样,在这些时间段存在的UK 14,304(1 μmol l-1)分别将3H溢出量降至对照的35%、51%和53%。在2分钟或16分钟内添加1 nmol l-1至10 μmol l-1的UK 14,304,未产生显著不同的IC50值,但在浓度≥10 nmol l-1时,与2分钟暴露相比,16分钟暴露的抑制作用较小。3. 在大鼠交感神经元中,当去甲肾上腺素(100 nmol l-1)分别存在2、8或16分钟时,刺激诱发的溢出量分别降至对照的33%、56%或57%。在这些时间段添加UK 14,304(1 μmol l-1)导致抑制至对照的11%、41%和46%。应用UK14,304 2分钟或16分钟未产生显著不同的IC5o值,但在浓度>10 nmol 1-1时,与2分钟暴露相比,16分钟暴露诱导的抑制作用较小。4. 在新生或成年大鼠的大脑皮质切片中,尽管研究了各种实验条件,但暴露于0.1至1.0 μmol 1-1 UK14,304 16分钟从未导致比相应3分钟暴露更小的抑制作用。5. 结果表明,调节交感神经元去甲肾上腺素释放的α2-肾上腺素能受体在数分钟内会发生激动剂诱导的脱敏。在脑片制备中未检测到α2-自身受体的这种快速脱敏。

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