Dual effect of muscarinic receptor agonists on Ca2+ mobilization in SH-SY5Y neuroblastoma cells

Jaak Järv , Rasmus Hautala , Karl E.O. Åkerman
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引用次数: 10

Abstract

The muscarinic receptor-stimulated mobilisation of calcium ions in SH-SY5Y neuroblastoma cells was measured as function of the concentration of seven muscarinic receptor agonists and partial agonists: carbamoylcholine, acetylcholine, propionylcholine, butyrylcholine, acetylthiocholine, methylfurmethide and tetrametylammonium. The dose-response curves reached a clear maximum followed by a downturn of the curve. The concentration interval where the activatory and inhibitory effects occured depended on the structure of the ligand. The bell-shaped dose-response curves were analysed assuming that the drugs interact with two sites, which are responsible for agonistic and antagonistic effects, on the muscarinic receptors. The results indicate that full vs. partial agonism is at least in part determined by relative affinities of these two sites.

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毒蕈碱受体激动剂对SH-SY5Y神经母细胞瘤细胞Ca2+动员的双重影响
通过7种毒蕈碱受体激动剂和部分激动剂(氨甲酰胆碱、乙酰胆碱、丙酰胆碱、丁基胆碱、乙酰硫胆碱、甲氧基甲氧胺和四甲基铵)浓度的变化,测量了SH-SY5Y神经母细胞瘤细胞中受毒蕈碱受体刺激的钙离子动员。剂量-反应曲线达到一个明显的最大值,然后曲线下降。激活和抑制作用发生的浓度间隔取决于配体的结构。假设药物与毒蕈碱受体上负责激动和拮抗作用的两个位点相互作用,分析钟形剂量-反应曲线。结果表明,完全或部分激动作用至少部分取决于这两个位点的相对亲和力。
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