Positive and negative modulation of nicotinic receptors

Research output: Chapter in Book/Report/Conference proceedingChapter

52 Citations (Scopus)

Abstract

Nicotinic acetylcholine receptors (AChRs) are one of the best characterized ion channels from the Cys-loop receptor superfamily. The study of acetylcholine binding proteins and prokaryotic ion channels from different species has been paramount for the understanding of the structure - function relationship of the Cys-loop receptor superfamily. AChR function can be modulated by different ligand types. The neurotransmitter ACh and other agonists trigger conformational changes in the receptor, finally opening the intrinsic cation channel. The so-called gating process couples ligand binding, located at the extracellular portion, to the opening of the ion channel, located at the transmembrane region. After agonist activation, in the prolonged presence of agonists, the AChR becomes desensitized. Competitive antagonists overlap the agonist-binding sites inhibiting the pharmacological action of agonists. Positive allosteric modulators (PAMs) do not bind to the orthostetic binding sites but allosterically enhance the activity elicited by agonists by increasing the gating process (type I) and/or by decreasing desensitization (type II). Instead, negative allosteric modulators (NAMs) produce the opposite effects. Interestingly, this negative effect is similar to that found for another class of allosteric drugs, that is, noncompetitive antagonists (NCAs). However, the main difference between both categories of drugs is based on their distinct binding site locations. Although both NAMs and NCAs do not bind to the agonist sites, NACs bind to sites located in the ion channel, whereas NAMs bind to nonluminal sites. However, this classification is less clear for NAMs interacting at the extracellular - transmembrane interface where the ion channel mouth might be involved. Interestingly, PAMs and NAMs might be developed as potential medications for the treatment of several diseases involving AChRs, including dementia-, skin-, and immunological-related diseases, drug addiction, and cancer. More exciting is the potential combination of specific agonists with specific PAMs. However, we are still in the beginning of understanding how these compounds act and how these drugs can be used therapeutically.

Original languageEnglish
Title of host publicationAdvances in Protein Chemistry and Structural Biology
PublisherAcademic Press Inc.
Pages153-203
Number of pages51
EditionC
DOIs
StatePublished - 1 Jan 2010
Externally publishedYes

Publication series

NameAdvances in Protein Chemistry and Structural Biology
NumberC
Volume80
ISSN (Print)1876-1623

Fingerprint

Nicotinic Receptors
Ion Channels
Modulators
Modulation
Cysteine Loop Ligand-Gated Ion Channel Receptors
Cholinergic Receptors
Binding Sites
Pharmaceutical Preparations
Ligands
Immune System Diseases
Acetylcholine
Substance-Related Disorders
Neurotransmitter Agents
Dementia
Mouth
Cations
Carrier Proteins
Pharmacology
Skin
Chemical activation

Cite this

Arias, H. R. (2010). Positive and negative modulation of nicotinic receptors. In Advances in Protein Chemistry and Structural Biology (C ed., pp. 153-203). (Advances in Protein Chemistry and Structural Biology; Vol. 80, No. C). Academic Press Inc.. https://doi.org/10.1016/B978-0-12-381264-3.00005-9
Arias, Hugo R. / Positive and negative modulation of nicotinic receptors. Advances in Protein Chemistry and Structural Biology. C. ed. Academic Press Inc., 2010. pp. 153-203 (Advances in Protein Chemistry and Structural Biology; C).
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Arias, HR 2010, Positive and negative modulation of nicotinic receptors. in Advances in Protein Chemistry and Structural Biology. C edn, Advances in Protein Chemistry and Structural Biology, no. C, vol. 80, Academic Press Inc., pp. 153-203. https://doi.org/10.1016/B978-0-12-381264-3.00005-9

Positive and negative modulation of nicotinic receptors. / Arias, Hugo R.

Advances in Protein Chemistry and Structural Biology. C. ed. Academic Press Inc., 2010. p. 153-203 (Advances in Protein Chemistry and Structural Biology; Vol. 80, No. C).

Research output: Chapter in Book/Report/Conference proceedingChapter

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AB - Nicotinic acetylcholine receptors (AChRs) are one of the best characterized ion channels from the Cys-loop receptor superfamily. The study of acetylcholine binding proteins and prokaryotic ion channels from different species has been paramount for the understanding of the structure - function relationship of the Cys-loop receptor superfamily. AChR function can be modulated by different ligand types. The neurotransmitter ACh and other agonists trigger conformational changes in the receptor, finally opening the intrinsic cation channel. The so-called gating process couples ligand binding, located at the extracellular portion, to the opening of the ion channel, located at the transmembrane region. After agonist activation, in the prolonged presence of agonists, the AChR becomes desensitized. Competitive antagonists overlap the agonist-binding sites inhibiting the pharmacological action of agonists. Positive allosteric modulators (PAMs) do not bind to the orthostetic binding sites but allosterically enhance the activity elicited by agonists by increasing the gating process (type I) and/or by decreasing desensitization (type II). Instead, negative allosteric modulators (NAMs) produce the opposite effects. Interestingly, this negative effect is similar to that found for another class of allosteric drugs, that is, noncompetitive antagonists (NCAs). However, the main difference between both categories of drugs is based on their distinct binding site locations. Although both NAMs and NCAs do not bind to the agonist sites, NACs bind to sites located in the ion channel, whereas NAMs bind to nonluminal sites. However, this classification is less clear for NAMs interacting at the extracellular - transmembrane interface where the ion channel mouth might be involved. Interestingly, PAMs and NAMs might be developed as potential medications for the treatment of several diseases involving AChRs, including dementia-, skin-, and immunological-related diseases, drug addiction, and cancer. More exciting is the potential combination of specific agonists with specific PAMs. However, we are still in the beginning of understanding how these compounds act and how these drugs can be used therapeutically.

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Arias HR. Positive and negative modulation of nicotinic receptors. In Advances in Protein Chemistry and Structural Biology. C ed. Academic Press Inc. 2010. p. 153-203. (Advances in Protein Chemistry and Structural Biology; C). https://doi.org/10.1016/B978-0-12-381264-3.00005-9