Abstract
The advent of selective antimuscarinic drugs such as pirenzepine has led to increased acceptance of the concept of distinct subclasses of muscarinic recegtors. This chapter focuses upon our studies of [3H]pirenzepine ([3H]PZ), which we suggested is an effective ligand for the investigation of putative M1 receptor- effector mechanisms (26–31). Data indicating that [3H]PZ labels putative M1 muscarinic receptors with high affinity is discussed in relation to the growing body of evidence which supports the M1/M2 hypothesis. Emphasis is placed upon our studies of human stellate ganglia. Several relevant reviews have recently appeared in the literature (3, 22, 23, 29).
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Watson, M. et al. (1986). Identification of Putative M1 Muscarinic Receptors Using [3H]Pirenzepine: Characterization of Binding and Autoradiographic Localization in Human Stellate Ganglia. In: Hanin, I. (eds) Dynamics of Cholinergic Function. Advances in Behavioral Biology, vol 30. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-5194-8_4
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DOI: https://doi.org/10.1007/978-1-4684-5194-8_4
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