Kuhar M J, Taylor N, Wamsley J K, Hulme E C, Birdsall N J
Brain Res. 1981 Jul 6;216(1):1-9. doi: 10.1016/0006-8993(81)91274-9.
Muscarinic cholinergic receptors were labeled by the potent, specific, irreversible muscarinic cholinergic antagonist propylbenzilylcholine mustard. Slices of rat hippocampus and cerebral cortex were labeled in vitro under conditions such that workable specific to non-specific ratios of receptor binding were obtained. Light microscopic autoradiography of 1 micrometer sections revealed a limited penetration of drug into the tissue and, by grain counts, confirmed the specific to non-specific ratios observed in preliminary biochemical studies. Examination of thin sections with the electron microscope revealed a significant fraction of (but not all) autoradiographic grains associated with synapses. This fraction was reduced in tissues coincubated with quinuclidinylbenzilate to produce blanks. These results indicate an enrichment of cholinergic muscarinic receptors at synapses.
毒蕈碱型胆碱能受体用强效、特异性、不可逆的毒蕈碱型胆碱能拮抗剂丙基苄基胆碱芥子碱进行标记。大鼠海马体和大脑皮层切片在体外进行标记,条件是获得可行的受体结合特异性与非特异性比率。对1微米切片进行光镜放射自显影显示药物在组织中的渗透有限,通过颗粒计数,证实了在初步生化研究中观察到的特异性与非特异性比率。用电子显微镜检查薄切片发现相当一部分(但不是全部)放射自显影颗粒与突触相关。在用奎宁环基苯甲酸酯共同孵育以产生空白的组织中,这一比例降低。这些结果表明突触处胆碱能毒蕈碱型受体富集。