Cross A J, Johnson J A, Frith C, Taylor G R
Biochem Biophys Res Commun. 1984 Feb 29;119(1):163-7. doi: 10.1016/0006-291x(84)91633-4.
The high affinity binding of the muscarinic ligand 3H-N-methylscopolamine (3H-NMS) to intact cells of the rat pheochromocytoma cell line PC12 was studied. A single class of saturable binding sites was observed with a density of about 5000 sites per cell, and a pharmacological profile consistent with muscarinic receptors. The inhibition of 3H-NMS binding by the antagonist pirenzepine was of low affinity suggesting PC12 muscarinic receptors may be similar to those found on rat sympathetic nerve terminals.
研究了毒蕈碱配体3H-N-甲基东莨菪碱(3H-NMS)与大鼠嗜铬细胞瘤细胞系PC12完整细胞的高亲和力结合。观察到一类单一的可饱和结合位点,密度约为每细胞5000个位点,其药理学特征与毒蕈碱受体一致。拮抗剂哌仑西平对3H-NMS结合的抑制作用亲和力较低,提示PC12毒蕈碱受体可能与大鼠交感神经末梢上发现的受体相似。