毒蕈碱乙酰胆碱受体
毒蕈碱乙酰胆碱受体M4
神经科学
毒蕈碱乙酰胆碱受体M3
受体
生物
乙酰胆碱
毒蕈碱乙酰胆碱受体M5
体内
毒蕈碱乙酰胆碱受体M1
变构调节
乙酰胆碱受体
中枢神经系统
毒蕈碱乙酰胆碱受体M2
药理学
生物化学
遗传学
标识
DOI:10.1007/978-3-642-23274-9_1
摘要
The physiological role of muscarinic receptors is highly complex and, although not completely understood, has become clearer over the last decade. Recent pharmacological evidence with novel compounds, together with data from transgenic mice, suggests that all five subtypes have defined functions in the nervous system as well as mediating the non neuronal, hormonal actions of acetylcholine. Numerous novel agonists, allosteric regulators, and antagonists have now been identified with authentic subtype specificity in vitro and in vivo. These compounds provide additional pharmacological opportunities for selective subtype modulation as well as a new generation of muscarinic receptor-based therapeutics.
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