Benishin C G
Department of Physiology, Faculty of Medicine, University of Alberta, Edmonton, Canada.
J Neurochem. 1990 Dec;55(6):2086-90. doi: 10.1111/j.1471-4159.1990.tb05799.x.
Modulation of acetylcholine (ACh) release from superfused hippocampal slices was examined when the release of ACh was stimulated by exposure of slices to elevated K+ concentration. Evoked release was not sensitive to inhibition by 0.1 microM tetrodotoxin, but it could be inhibited in a dose-dependent manner by a muscarinic agonist (10-100 nM oxotremorine) and a purinergic agonist (10-100 nM 2-chloroadenosine). The alpha-dendrotoxin (100 nM), which selectively blocks voltage-gated inactivating K+ channels in nerve endings, did not affect the release of ACh under resting or depolarized conditions. However, alpha-dendrotoxin reduced the 2-chloroadenosine-induced inhibition of release, but did not alter the oxotremorine-induced inhibition. These results suggest that an alpha-dendrotoxin-sensitive K+ channel may be activated as an obligatory step in the modulation of ACh release by presynaptic purinergic receptor activation, but not in the modulation by presynaptic muscarinic receptors.
当通过将海马切片暴露于高钾浓度来刺激乙酰胆碱(ACh)释放时,研究了从灌流海马切片中释放的ACh的调节情况。诱发释放对0.1微摩尔河豚毒素的抑制不敏感,但可被毒蕈碱激动剂(10 - 100纳摩尔氧化震颤素)和嘌呤能激动剂(10 - 100纳摩尔2 - 氯腺苷)以剂量依赖方式抑制。α - 树眼镜蛇毒素(100纳摩尔)选择性阻断神经末梢中的电压门控失活钾通道,在静息或去极化条件下不影响ACh的释放。然而,α - 树眼镜蛇毒素降低了2 - 氯腺苷诱导的释放抑制,但不改变氧化震颤素诱导的抑制。这些结果表明,α - 树眼镜蛇毒素敏感的钾通道可能作为突触前嘌呤能受体激活调节ACh释放的必要步骤被激活,但在突触前毒蕈碱受体调节中不被激活。