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Nicotinic Ganglion-Stimulating Agents

  • Chapter
Pharmacology of Ganglionic Transmission

Part of the book series: Handbook of Experimental Pharmacology ((HEP,volume 53))

Abstract

The classic subgrouping of cholinoceptive sites proposed by Dale is based on the different pharmacological properties of muscarine and nicotine. Stated in the simplest terms, a drug is said to be a nicotinic agonist when it causes the general bi-phasic pattern of excitation and depression of excitable tissues that is produced by nicotine. More rigorous definitions of nicotinic agonists include susceptibility to blockade by specific antagonists, of which hexamethonium and d-tubocurarine can be regarded as prototypical drugs. It is generally understood that the responses to nicotinic agents are resistant to blockade by atropine or adrenergic blocking drugs. It is in this context that the term nicotinic agent is used in this chapter.

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Volle, R.L. (1980). Nicotinic Ganglion-Stimulating Agents. In: Kharkevich, D.A. (eds) Pharmacology of Ganglionic Transmission. Handbook of Experimental Pharmacology, vol 53. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-67397-9_11

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  • DOI: https://doi.org/10.1007/978-3-642-67397-9_11

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