Nicotinic acetylcholine receptor

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Acetylcholine Acetylcholine.svg
Acetylcholine
Nicotine Nicotine.svg
Nicotine

Nicotinic acetylcholine receptors, or nAChRs, are receptor polypeptides that respond to the neurotransmitter acetylcholine. Nicotinic receptors also respond to drugs such as the agonist nicotine. They are found in the central and peripheral nervous system, muscle, and many other tissues of many organisms. At the neuromuscular junction they are the primary receptor in muscle for motor nerve-muscle communication that controls muscle contraction. In the peripheral nervous system: (1) they transmit outgoing signals from the presynaptic to the postsynaptic cells within the sympathetic and parasympathetic nervous system, and (2) they are the receptors found on skeletal muscle that receive acetylcholine released to signal for muscular contraction. In the immune system, nAChRs regulate inflammatory processes and signal through distinct intracellular pathways. [1] In insects, the cholinergic system is limited to the central nervous system. [2]

Contents

The nicotinic receptors are considered cholinergic receptors, since they respond to acetylcholine. Nicotinic receptors get their name from nicotine which does not stimulate the muscarinic acetylcholine receptors but selectively binds to the nicotinic receptors instead. [3] [4] [5] The muscarinic acetylcholine receptor likewise gets its name from a chemical that selectively attaches to that receptor—muscarine. [6] Acetylcholine itself binds to both muscarinic and nicotinic acetylcholine receptors. [7]

As ionotropic receptors, nAChRs are directly linked to ion channels. Some evidence suggests that these receptors can also use second messengers (as metabotropic receptors do) in some cases. [8] Nicotinic acetylcholine receptors are the best-studied of the ionotropic receptors. [3]

Since nicotinic receptors help transmit outgoing signals for the sympathetic and parasympathetic systems, nicotinic receptor antagonists such as hexamethonium interfere with the transmission of these signals. Thus, for example, nicotinic receptor antagonists interfere with the baroreflex [9] that normally corrects changes in blood pressure by sympathetic and parasympathetic stimulation of the heart.

Structure

Nicotinic receptor structure NAChR.png
Nicotinic receptor structure

Nicotinic receptors, with a molecular mass of 290 kDa, [10] are made up of five subunits, arranged symmetrically around a central pore. [3] Each subunit comprises four transmembrane domains with both the N- and C-terminus located extracellularly. They possess similarities with GABAA receptors, glycine receptors, and the type 3 serotonin receptors (which are all ionotropic receptors), or the signature Cys-loop proteins. [11]

In vertebrates, nicotinic receptors are broadly classified into two subtypes based on their primary sites of expression: muscle-type nicotinic receptors and neuronal-type nicotinic receptors. In the muscle-type receptors, found at the neuromuscular junction, receptors are either the embryonic form, composed of α1, β1, γ, and δ subunits in a 2:1:1:1 ratio ((α1)2β1γδ), or the adult form composed of α1, β1, δ, and ε subunits in a 2:1:1:1 ratio ((α1)2β1δε). [3] [4] [5] [12] The neuronal subtypes are various homomeric (all one type of subunit) or heteromeric (at least one α and one β) combinations of twelve different nicotinic receptor subunits: α2−α10 and β2−β4. Examples of the neuronal subtypes include: (α4)3(β2)2, (α4)2(β2)3, (α3)2(β4)3, α4α6β3(β2)2, (α7)5, and many others. In both muscle-type and neuronal-type receptors, the subunits are very similar to one another, especially in the hydrophobic regions. [13]

A number of electron microscopy and x-ray crystallography studies have provided very high resolution structural information for muscle and neuronal nAChRs and their binding domains. [10] [14] [15] [16]

Binding

As with all ligand-gated ion channels, opening of the nAChR channel pore requires the binding of a chemical messenger. Several different terms are used to refer to the molecules that bind receptors, such as ligand, agonist, or transmitter. As well as the endogenous agonist acetylcholine, agonists of the nAChR include nicotine, epibatidine, and choline. Nicotinic antagonists that block the receptor include mecamylamine, dihydro-β-erythroidine, and hexamethonium. [13]

In muscle-type nAChRs, the acetylcholine binding sites are located at the α and either ε or δ subunits interface. In neuronal nAChRs, the binding site is located at the interface of an α and a β subunit or between two α subunits in the case of α7 receptors. The binding site is located in the extracellular domain near the N terminus. [4] [17] When an agonist binds to the site, all present subunits undergo a conformational change and the channel is opened [18] and a pore with a diameter of about 0.65 nm opens. [4]

Channel opening

Nicotinic AChRs may exist in different interconvertible conformational states. Binding of an agonist stabilizes the open and desensitized states. In normal physiological conditions, the receptor needs exactly two molecules of ACh to open. [19] Opening of the channel allows positively charged ions to move across it; in particular, sodium enters the cell and potassium exits. The net flow of positively charged ions is inward.

The nAChR is a non-selective cation channel, meaning that several different positively charged ions can cross through. [3] It is permeable to Na+ and K+, with some subunit combinations that are also permeable to Ca2+. [4] [20] [21] The amount of sodium and potassium the channels allow through their pores (their conductance) varies from 50 to 110  pS, with the conductance depending on the specific subunit composition as well as the permeant ion. [22]

Many neuronal nAChRs can affect the release of other neurotransmitters. [5] The channel usually opens rapidly and tends to remain open until the agonist diffuses away, which usually takes about 1 millisecond. [4] AChRs can spontaneously open with no ligands bound or can spontaneously close with ligands bound, and mutations in the channel can shift the likelihood of either event. [23] [18] Therefore, ACh binding changes the probability of pore opening, which increases as more ACh binds.

The nAChR is unable to bind ACh when bound to any of the snake venom α-neurotoxins. These α-neurotoxins antagonistically bind tightly and noncovalently to nAChRs of skeletal muscles and in neurons, thereby blocking the action of ACh at the postsynaptic membrane, inhibiting ion flow and leading to paralysis and death. The nAChR contains two binding sites for snake venom neurotoxins. Progress in discovering the dynamics of binding action of these sites has proved difficult, although recent studies using normal mode dynamics [24] have aided in predicting the nature of both the binding mechanisms of snake toxins and of ACh to nAChRs. These studies have shown that a twist-like motion caused by ACh binding is likely responsible for pore opening, and that one or two molecules of α-bungarotoxin (or other long-chain α-neurotoxin) suffice to halt this motion. The toxins seem to lock together neighboring receptor subunits, inhibiting the twist and therefore, the opening motion. [25]

Effects

The activation of receptors by nicotine modifies the state of neurons through two main mechanisms. On one hand, the movement of cations causes a depolarization of the plasma membrane (which results in an excitatory postsynaptic potential in neurons) leading to the activation of voltage-gated ion channels. On the other hand, the entry of calcium acts, either directly or indirectly, on different intracellular cascades. This leads, for example, to the regulation of activity of some genes or the release of neurotransmitters.[ citation needed ]

Regulation

Desensitization

Ligand-bound desensitization of receptors was first characterized by Katz and Thesleff in the nicotinic acetylcholine receptor. [26]

Prolonged or repeated exposure to a stimulus often results in decreased responsiveness of that receptor toward a stimulus, termed desensitization. nAChR function can be modulated by phosphorylation [27] by the activation of second messenger-dependent protein kinases. PKA [26] and PKC, [28] as well as tyrosine kinases, [29] have been shown to phosphorylate the nAChR resulting in its desensitization. It has been reported that, after prolonged receptor exposure to the agonist, the agonist itself causes an agonist-induced conformational change in the receptor, resulting in receptor desensitization. [30]

Desensitized receptors can revert to a prolonged open state when an agonist is bound in the presence of a positive allosteric modulator, for example PNU-120,596. [31] Also, there is evidence that indicates specific chaperone molecules have regulatory effects on these receptors. [32]

Roles

The subunits of the nicotinic receptors belong to a multigene family (16 members in humans) and the assembly of combinations of subunits results in a large number of different receptors (for more information see the Ligand-Gated Ion Channel database). These receptors, with highly variable kinetic, electrophysiological and pharmacological properties, respond to nicotine differently, at very different effective concentrations. This functional diversity allows them to take part in two major types of neurotransmission. Classical synaptic transmission (wiring transmission) involves the release of high concentrations of neurotransmitter, acting on immediately neighboring receptors. In contrast, paracrine transmission (volume transmission) involves neurotransmitters released by axon terminals, which then diffuse through the extra-cellular medium until they reach their receptors, which may be distant. [33] Nicotinic receptors can also be found in different synaptic locations; for example the muscle nicotinic receptor always functions post-synaptically. The neuronal forms of the receptor can be found both post-synaptically (involved in classical neurotransmission) and pre-synaptically [34] where they can influence the release of multiple neurotransmitters.

Subunits

17 vertebrate nAChR subunits have been identified, which are divided into muscle-type and neuronal-type subunits. Although an α8 subunit/gene is present in avian species such as the chicken, it is not present in human or mammalian species. [35]

The nAChR subunits have been divided into four subfamilies (I–IV) based on similarities in protein sequence. [36] In addition, subfamily III has been further divided into three types.

Neuronal-typeMuscle-type
IIIIIIIV
α9, α10 α7, α8 123 α1, β1, δ, γ, ε
α2, α3, α4, α6 β2, β4 β3, α5

Neuronal nAChRs are transmembrane proteins that form pentameric structures assembled from a family of subunits composed of α2–α10 and β2–β4. [37] These subunits were discovered from the mid-1980s through the early 1990s, when cDNAs for multiple nAChR subunits were cloned from rat and chicken brains, leading to the identification of eleven different genes (twelve in chickens) that code for neuronal nAChR subunits; The subunit genes identified were named α2–α10 (α8 only found in chickens) and β2–β4. [38] It has also been discovered that various subunit combinations could form functional nAChRs that could be activated by acetylcholine and nicotine, and the different combinations of subunits generate subtypes of nAChRs with diverse functional and pharmacological properties. [39] When expressed alone, α7, α8, α9, and α10 are able to form functional receptors, but other α subunits require the presence of β subunits to form functional receptors. [37] In mammals, nAchR subunits have been found to be encoded by 17 genes, and of these, nine genes encoding α-subunits and three encoding β-subunits are expressed in the brain. β2 subunit-containing nAChRs (β2nAChRs) and α7nAChRs are widely expressed in the brain, whereas other nAChR subunits have more restricted expression. [40] The pentameric assembly of nAChRs is subjected to the subunits that are produced in various cell types such as in the human lung where epithelial and muscular pentamers largely differ. [41]

CHRNA5/A3/B4

An important nAchR gene cluster (CHRNA5/A3/B4) contains the genes encoding for the α5, α3 and β4 subunits. Genetic studies have identified single nucleotide polymorphisms (SNPs) in the chromosomal locus encoding these three nAChR genes as risk factors for nicotine dependence, lung cancer, chronic obstructive pulmonary disease, alcoholism, and peripheral arterial disease. [37] [42] The CHRNA5/A3/B4 nAChR subunit genes are found in a tight cluster in chromosomal region 15q24–25. The nAChR subunits encoded by this locus form the predominant nicotinic receptor subtypes expressed in the peripheral nervous system (PNS) and other key central nervous system (CNS) sites, such as the medial habenula, a structure between the limbic forebrain and midbrain involved in major cholinergic circuitry pathways. [37] Further research of the CHRNA5/A3/B4 genes have revealed that "neuronal" nAChR genes are also expressed in non-neuronal cells where they are involved in various fundamental processes, such as inflammation. [43] The CHRNA5/A3/B4 genes are co-expressed in many cell types and the transcriptional activities of the promoter regions of the three genes are regulated by many of the same transcription factors, demonstrating that their clustering may reflect control of gene expression. [37]

CHRNA6/CHRNB3

CHRNB3 and CHRNA6 are also grouped in a gene cluster, located on 8p11. [42] Multiple studies have shown that SNPS in the CHRNB3–CHRNA6 have been linked to nicotine dependence and smoking behavior, such as two SNPs in CHRNB3, rs6474413 and rs10958726. [42] Genetic variation in this region also displays influence susceptibility to use drugs of abuse, including cocaine and alcohol consumption. [44] Nicotinic receptors containing α6 or β3 subunits expressed in brain regions, especially in the ventral tegmental area and substantia nigra, are important for drug behaviors due to their role in dopamine release. [45] Genetic variation in these genes can alter sensitivity to drugs of abuse in numerous ways, including changing the amino acid structure of the protein or cause alterations in transcriptional and translational regulation. [44]

CHRNA4/CHRNB2

Other well studied nAChR genes include the CHRNA4 and CHRNB2, which have been associated as Autosomal Dominant Nocturnal Frontal Lobe Epilepsy (ADNFLE) genes. [42] [46] Both of these nAChR subunits are present in the brain and the occurrence of mutations in these two subunits cause a generalized type of epilepsy. Examples include the CHRNA4 insertion mutation 776ins3 that is associated with nocturnal seizures and psychiatric disorders, and the CHRNB2 mutation I312M that seems to cause not only epilepsy but also very specific cognitive deficits, such as deficits in learning and memory. [46] [47] There is naturally occurring genetic variation between these two genes and analysis of single nucleotide polymorphisms (SNPs) and other gene modifications show a higher variation in the CHRNA4 gene than in the CHRNB2 gene, implying that nAChR β2, the protein encoded by CHRNB2, associates with more subunits than α4. CHRNA2 has also been reported as a third candidate for nocturnal frontal lobe seizures. [42] [46]

CHRNA7

Several studies have reported an association between CHRNA7 and endophenotypes of psychiatric disorders and nicotine dependence, contributing to the significant clinical relevance of α7 and research being done on it. [46] CHRNA7 was one of the first genes that had been considered to be involved with schizophrenia. Studies identified several CHRNA7 promoter polymorphisms that reduce the genes transcriptional activity to be associated with schizophrenia, which is consistent with the finding of reduced levels of a7 nAChRs in the brain of schizophrenic patients. [46] Both nAChRs subtypes, α4β2 and α7, have been found to be significantly reduced in post-mortem studies of individuals with schizophrenia. [48] Additionally, smoking rates are significantly higher in those with schizophrenia, implying that smoking nicotine may be a form of self-medicating. [49]

Notable variations

Nicotinic receptors are pentamers of these subunits; i.e., each receptor contains five subunits. Thus, there is immense potential of variation of these subunits, some of which are more commonly found than others. The most broadly expressed subtypes include (α1)2β1δε (adult muscle-type), (α3)2(β4)3 (ganglion-type), (α4)2(β2)3 (CNS-type) and (α7)5 (another CNS-type). [50] A comparison follows:

Receptor-typeLocationEffect; functions Nicotinic agonists Nicotinic antagonists
Muscle-type:
(α1)2β1δε [50]
or
(α1)2β1δγ		 Neuromuscular junction EPSP, mainly by increased Na+ and K+ permeability
Ganglion-type:
(α3)2(β4)3		 autonomic ganglia EPSP, mainly by increased Na+ and K+ permeability
Heteromeric CNS-type:
(α4)2(β2)3 		Brain Post- and presynaptic excitation, [50] mainly by increased Na+ and K+ permeability. Major subtype involved in the attention-enhancing and rewarding effects of nicotine as well as the pathophysiology of nicotine addiction. [52] [53] [54]
Further CNS-type:
(α3)2(β4)3
Brain Post- and presynaptic excitation
Homomeric CNS-type:
(α7)5
Brain Post- and presynaptic excitation, [50] mainly by increased Na+, K+ and Ca2+ permeability. Major subtype involved in some of the cognitive effects of nicotine. [55] Moreover, activation of (α7)5 could improve neurovascular coupling response in neurodegenerative disease [56] and neurogenesis in ischemic stroke. [57] Also involved in the pro-angiogenic effects of nicotine and accelerate the progression of chronic kidney disease in smokers. [58] [59] [60]

See also

Related Research Articles

<span class="mw-page-title-main">Acetylcholine</span> Organic chemical and neurotransmitter

Acetylcholine (ACh) is an organic compound that functions in the brain and body of many types of animals as a neurotransmitter. Its name is derived from its chemical structure: it is an ester of acetic acid and choline. Parts in the body that use or are affected by acetylcholine are referred to as cholinergic.

<span class="mw-page-title-main">Acetylcholine receptor</span> Integral membrane protein

An acetylcholine receptor or a cholinergic receptor is an integral membrane protein that responds to the binding of acetylcholine, a neurotransmitter.

<span class="mw-page-title-main">Muscarinic acetylcholine receptor</span> Acetylcholine receptors named for their selective binding of muscarine

Muscarinic acetylcholine receptors, or mAChRs, are acetylcholine receptors that form G protein-coupled receptor complexes in the cell membranes of certain neurons and other cells. They play several roles, including acting as the main end-receptor stimulated by acetylcholine released from postganglionic fibers. They are mainly found in the parasympathetic nervous system, but also have a role in the sympathetic nervous system in the control of sweat glands.

<span class="mw-page-title-main">Epibatidine</span> Toxic chemical from some poison dart frogs

Epibatidine is a chlorinated alkaloid that is secreted by the Ecuadoran frog Epipedobates anthonyi and poison dart frogs from the Ameerega genus. It was discovered by John W. Daly in 1974, but its structure was not fully elucidated until 1992. Whether epibatidine occurs naturally remains controversial due to challenges in conclusively identifying the compound from the limited samples collected by Daly. By the time that high-resolution spectrometry was used in 1991, there remained less than one milligram of extract from Daly's samples, raising concerns about possible contamination. Samples from other batches of the same species of frog failed to yield epibatidine.

α-Bungarotoxin Chemical compound

α-Bungarotoxin is one of the bungarotoxins, components of the venom of the elapid Taiwanese banded krait snake. It is a type of α-neurotoxin, a neurotoxic protein that is known to bind competitively and in a relatively irreversible manner to the nicotinic acetylcholine receptor found at the neuromuscular junction, causing paralysis, respiratory failure, and death in the victim. It has also been shown to play an antagonistic role in the binding of the α7 nicotinic acetylcholine receptor in the brain, and as such has numerous applications in neuroscience research.

<span class="mw-page-title-main">Methyllycaconitine</span> Chemical compound

Methyllycaconitine (MLA) is a diterpenoid alkaloid found in many species of Delphinium (larkspurs). In common with many other diterpenoid alkaloids, it is toxic to animals, although the acute toxicity varies with species. Methyllycaconitine was identified one of the principal toxins in larkspurs responsible for livestock poisoning in the mountain rangelands of North America. Methyllycaconitine has been explored as a possible therapeutic agent for the treatment of spastic paralysis, and it has been shown to have insecticidal properties. It has become an important molecular probe for studying the pharmacology of the nicotinic acetylcholine receptor.

A nicotinic agonist is a drug that mimics the action of acetylcholine (ACh) at nicotinic acetylcholine receptors (nAChRs). The nAChR is named for its affinity for nicotine.

Muscarinic acetylcholine receptor M<sub>2</sub> Protein-coding gene in the species Homo sapiens

The muscarinic acetylcholine receptor M2, also known as the cholinergic receptor, muscarinic 2, is a muscarinic acetylcholine receptor that in humans is encoded by the CHRM2 gene. Multiple alternatively spliced transcript variants have been described for this gene. It is Gi-coupled, reducing intracellular levels of cAMP.

<span class="mw-page-title-main">CHRNB2</span> Protein-coding gene in the species Homo sapiens

Neuronal acetylcholine receptor subunit beta-2 is a protein that in humans is encoded by the CHRNB2 gene.

<span class="mw-page-title-main">CHRNA3</span> Protein-coding gene in the species Homo sapiens

Neuronal acetylcholine receptor subunit alpha-3, also known as nAChRα3, is a protein that in humans is encoded by the CHRNA3 gene. The protein encoded by this gene is a subunit of certain nicotinic acetylcholine receptors (nAchR). Research with mecamylamine in animals has implicated alpha-3-containing nAChRs in the abusive and addictive properties of ethanol.

<span class="mw-page-title-main">CHRNA1</span> Protein-coding gene in the species Homo sapiens

Neuronal acetylcholine receptor subunit alpha-1, also known as nAChRα1, is a protein that in humans is encoded by the CHRNA1 gene. The protein encoded by this gene is a subunit of certain nicotinic acetylcholine receptors (nAchR).

<span class="mw-page-title-main">CHRNB4</span> Protein-coding gene in the species Homo sapiens

Neuronal acetylcholine receptor subunit beta-4 is a protein that in humans is encoded by the CHRNB4 gene.

The alpha-4 beta-2 nicotinic receptor, also known as the α4β2 receptor, is a type of nicotinic acetylcholine receptor implicated in learning, consisting of α4 and β2 subunits. It is located in the brain, where activation yields post- and presynaptic excitation, mainly by increased Na+ and K+ permeability.

<span class="mw-page-title-main">Alpha-7 nicotinic receptor</span> Type of cell receptor found in humans

The alpha-7 nicotinic receptor, also known as the α7 receptor, is a type of nicotinic acetylcholine receptor implicated in long-term memory, consisting entirely of α7 subunits. As with other nicotinic acetylcholine receptors, functional α7 receptors are pentameric [i.e., (α7)5 stoichiometry].

<span class="mw-page-title-main">CHRNB3</span> Protein-coding gene in the species Homo sapiens

Neuronal acetylcholine receptor subunit beta-3 is a protein that in humans is encoded by the CHRNB3 gene. This gene has been identified as a candidate for predisposition to tobacco dependence.

<span class="mw-page-title-main">CHRNA2</span> Protein-coding gene in the species Homo sapiens

Neuronal acetylcholine receptor subunit alpha-2, also known as nAChRα2, is a protein that in humans is encoded by the CHRNA2 gene. The protein encoded by this gene is a subunit of certain nicotinic acetylcholine receptors (nAchR).

<span class="mw-page-title-main">CHRNA6</span> Protein-coding gene in the species Homo sapiens

Cholinergic receptor, nicotinic, alpha 6, also known as nAChRα6, is a protein that in humans is encoded by the CHRNA6 gene. The CHRNA6 gene codes for the α6 nicotinic receptor subunit that is found in certain types of nicotinic acetylcholine receptors found primarily in the brain. Neural nicotinic acetylcholine receptors containing α6 subunits are expressed on dopamine-releasing neurons in the midbrain, and dopamine release following activation of these neurons is thought to be involved in the addictive properties of nicotine. Due to their selective localisation on dopaminergic neurons, α6-containing nACh receptors have also been suggested as a possible therapeutic target for the treatment of Parkinson's disease. In addition to nicotine, research in animals has implicated alpha-6-containing nAChRs in the abusive and addictive properties of ethanol, with mecamylamine demonstrating a potent ability to block these properties.

The alpha-3 beta-4 nicotinic receptor, also known as the α3β4 receptor and the ganglion-type nicotinic receptor, is a type of nicotinic acetylcholine receptor, consisting of α3 and β4 subunits. It is located in the autonomic ganglia and adrenal medulla, where activation yields post- and/or presynaptic excitation, mainly by increased Na+ and K+ permeability.

The alpha-3 beta-2 nicotinic receptor, also known as the α3β2 receptor, is a type of nicotinic acetylcholine receptor, consisting of α3 and β2 subunits.

The neuronal acetylcholine receptor subunit alpha-5, or alpha-5 nicotinic acetylcholine receptor(α5 nAChR) also known as the α5 receptor is a type of ligand gated neuronal type subunit of the nicotinic acetylcholine receptor involved in pain regulation encoded in the human by the CHRNA5 gene. This receptor is commonly associated with nicotine addiction, immunotherapy, cancer, pain and attention.

References

  1. ↑ Lu B, Kwan K, Levine YA, Olofsson PS, Yang H, Li J, et al. (August 2014). "α7 nicotinic acetylcholine receptor signaling inhibits inflammasome activation by preventing mitochondrial DNA release". Molecular Medicine. 20 (1): 350–8. doi:10.2119/molmed.2013.00117. PMC   4153835 . PMID   24849809.
  2. ↑ Yamamoto I (1999). "Nicotine to Nicotinoids: 1962 to 1997". Nicotinoid Insecticides and the Nicotinic Acetylcholine Receptor. pp. 3–27. doi:10.1007/978-4-431-67933-2_1. ISBN   978-4-431-68011-6.
  3. 1 2 3 4 5 6 7 8 9 10 11 Purves D, Augustine GJ, Fitzpatrick D, Hall WC, LaMantia AS, McNamara JO, White LE (2008). Neuroscience (4th ed.). Sinauer Associates. pp.  122–6. ISBN   978-0-87893-697-7.
  4. 1 2 3 4 5 6 Siegel GJ, Agranoff BW, Fisher SK, Albers RW, Uhler MD (1999). "GABA Receptor Physiology and Pharmacology". Basic Neurochemistry: Molecular, Cellular and Medical Aspects (6th ed.). American Society for Neurochemistry. Retrieved 2008-10-01.{{cite book}}: |website= ignored (help)
  5. 1 2 3 Itier V, Bertrand D (August 2001). "Neuronal nicotinic receptors: from protein structure to function". FEBS Letters. 504 (3): 118–25. Bibcode:2001FEBSL.504..118I. doi: 10.1016/s0014-5793(01)02702-8 . PMID   11532443.
  6. ↑ Ishii M, Kurachi Y (1 October 2006). "Muscarinic acetylcholine receptors". Current Pharmaceutical Design. 12 (28): 3573–81. doi:10.2174/138161206778522056. PMID   17073660.
  7. ↑ Lott EL, Jones EB (2020). "Cholinergic Toxicity". StatPearls. StatPearls Publishing. PMID   30969605.
  8. ↑ Kabbani N, Nordman JC, Corgiat BA, Veltri DP, Shehu A, Seymour VA, Adams DJ (December 2013). "Are nicotinic acetylcholine receptors coupled to G proteins?". BioEssays. 35 (12): 1025–34. doi:10.1002/bies.201300082. PMID   24185813. S2CID   9441100.
  9. ↑ Henderson CG, Ungar A (April 1978). "Effect of cholinergic antagonists on sympathetic ganglionic transmission of vasomotor reflexes from the carotid baroreceptors and chemoreceptors of the dog". The Journal of Physiology. 277 (1): 379–385. doi: 10.1113/jphysiol.1978.sp012278 . PMC   1282395 . PMID   206690.
  10. 1 2 Unwin N (March 2005). "Refined structure of the nicotinic acetylcholine receptor at 4A resolution". Journal of Molecular Biology. 346 (4): 967–89. doi:10.1016/j.jmb.2004.12.031. PMID   15701510.
  11. ↑ Cascio M (May 2004). "Structure and function of the glycine receptor and related nicotinicoid receptors". The Journal of Biological Chemistry. 279 (19): 19383–6. doi: 10.1074/jbc.R300035200 . PMID   15023997.
  12. ↑ Giniatullin R, Nistri A, Yakel JL (July 2005). "Desensitization of nicotinic ACh receptors: shaping cholinergic signaling". Trends in Neurosciences. 28 (7): 371–8. doi:10.1016/j.tins.2005.04.009. PMID   15979501. S2CID   19114228.
  13. 1 2 Matera, Carlo; Papotto, Claudio; Dallanoce, Clelia; De Amici, Marco (August 2023). "Advances in small molecule selective ligands for heteromeric nicotinic acetylcholine receptors". Pharmacological Research. 194: 106813. doi:10.1016/j.phrs.2023.106813. hdl: 2434/978688 . PMID   37302724.
  14. ↑ Brejc K, van Dijk WJ, Klaassen RV, Schuurmans M, van Der Oost J, Smit AB, Sixma TK (May 2001). "Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors". Nature. 411 (6835): 269–76. Bibcode:2001Natur.411..269B. doi:10.1038/35077011. PMID   11357122. S2CID   4415937.
  15. ↑ Zouridakis M, Giastas P, Zarkadas E, Chroni-Tzartou D, Bregestovski P, Tzartos SJ (November 2014). "Crystal structures of free and antagonist-bound states of human α9 nicotinic receptor extracellular domain". Nature Structural & Molecular Biology. 21 (11): 976–80. doi:10.1038/nsmb.2900. PMID   25282151. S2CID   30096256.
  16. ↑ Morales-Perez CL, Noviello CM, Hibbs RE (October 2016). "X-ray structure of the human α4β2 nicotinic receptor". Nature. 538 (7625): 411–415. Bibcode:2016Natur.538..411M. doi:10.1038/nature19785. PMC   5161573 . PMID   27698419.
  17. ↑ Squire L (2003). Fundamental neuroscience (2nd ed.). Amsterdam: Acad. Press. p. 1426. ISBN   978-0-12-660303-3.
  18. 1 2 Colquhoun D, Sivilotti LG (June 2004). "Function and structure in glycine receptors and some of their relatives". Trends in Neurosciences. 27 (6): 337–44. CiteSeerX   10.1.1.385.3809 . doi:10.1016/j.tins.2004.04.010. PMID   15165738. S2CID   19008547.
  19. ↑ Aidley DJ (1998). The physiology of excitable cells (4th ed.). Cambridge, UK: Cambridge University Press. ISBN   978-0521574150. OCLC   38067558.[ page needed ]
  20. ↑ Beker F, Weber M, Fink RH, Adams DJ (September 2003). "Muscarinic and nicotinic ACh receptor activation differentially mobilize Ca2+ in rat intracardiac ganglion neurons". Journal of Neurophysiology. 90 (3): 1956–64. doi:10.1152/jn.01079.2002. PMID   12761283. S2CID   8684707.
  21. ↑ Weber M, Motin L, Gaul S, Beker F, Fink RH, Adams DJ (January 2005). "Intravenous anesthetics inhibit nicotinic acetylcholine receptor-mediated currents and Ca2+ transients in rat intracardiac ganglion neurons". British Journal of Pharmacology. 144 (1): 98–107. doi:10.1038/sj.bjp.0705942. PMC   1575970 . PMID   15644873.
  22. ↑ Mishina M, Takai T, Imoto K, Noda M, Takahashi T, Numa S, et al. (May 1986). "Molecular distinction between fetal and adult forms of muscle acetylcholine receptor". Nature. 321 (6068): 406–11. Bibcode:1986Natur.321..406M. doi:10.1038/321406a0. PMID   2423878. S2CID   4356336.
  23. ↑ Einav T, Phillips R (April 2017). "Monod-Wyman-Changeux Analysis of Ligand-Gated Ion Channel Mutants". The Journal of Physical Chemistry B. 121 (15): 3813–3824. arXiv: 1701.06122 . Bibcode:2017arXiv170106122E. doi:10.1021/acs.jpcb.6b12672. PMC   5551692 . PMID   28134524.
  24. ↑ Levitt M, Sander C, Stern PS (February 1985). "Protein normal-mode dynamics: trypsin inhibitor, crambin, ribonuclease and lysozyme". Journal of Molecular Biology. 181 (3): 423–47. doi:10.1016/0022-2836(85)90230-x. PMID   2580101.
  25. ↑ Samson AO, Levitt M (April 2008). "Inhibition mechanism of the acetylcholine receptor by alpha-neurotoxins as revealed by normal-mode dynamics". Biochemistry. 47 (13): 4065–70. doi:10.1021/bi702272j. PMC   2750825 . PMID   18327915.
  26. 1 2 Pitchford S, Day JW, Gordon A, Mochly-Rosen D (November 1992). "Nicotinic acetylcholine receptor desensitization is regulated by activation-induced extracellular adenosine accumulation". The Journal of Neuroscience. 12 (11): 4540–4. doi:10.1523/JNEUROSCI.12-11-04540.1992. PMC   6576003 . PMID   1331363.
  27. ↑ Huganir RL, Greengard P (February 1983). "cAMP-dependent protein kinase phosphorylates the nicotinic acetylcholine receptor". Proceedings of the National Academy of Sciences of the United States of America. 80 (4): 1130–4. Bibcode:1983PNAS...80.1130H. doi: 10.1073/pnas.80.4.1130 . PMC   393542 . PMID   6302672.
  28. ↑ Safran A, Sagi-Eisenberg R, Neumann D, Fuchs S (August 1987). "Phosphorylation of the acetylcholine receptor by protein kinase C and identification of the phosphorylation site within the receptor delta subunit". The Journal of Biological Chemistry. 262 (22): 10506–10. doi: 10.1016/S0021-9258(18)60990-1 . PMID   3038884.
  29. ↑ Hopfield JF, Tank DW, Greengard P, Huganir RL (December 1988). "Functional modulation of the nicotinic acetylcholine receptor by tyrosine phosphorylation". Nature. 336 (6200): 677–80. Bibcode:1988Natur.336..677H. doi:10.1038/336677a0. PMID   3200319. S2CID   4239105.
  30. ↑ Barrantes FJ (September 1978). "Agonist-mediated changes of the acetylcholine receptor in its membrane environment". Journal of Molecular Biology. 124 (1): 1–26. doi:10.1016/0022-2836(78)90144-4. PMID   712829.
  31. ↑ Hurst RS, Hajós M, Raggenbass M, Wall TM, Higdon NR, Lawson JA, et al. (April 2005). "A novel positive allosteric modulator of the alpha7 neuronal nicotinic acetylcholine receptor: in vitro and in vivo characterization". The Journal of Neuroscience. 25 (17): 4396–405. doi:10.1523/JNEUROSCI.5269-04.2005. PMC   6725110 . PMID   15858066.
  32. ↑ Sadigh-Eteghad S, Majdi A, Talebi M, Mahmoudi J, Babri S (May 2015). "Regulation of nicotinic acetylcholine receptors in Alzheimer׳s disease: a possible role of chaperones". European Journal of Pharmacology. 755: 34–41. doi:10.1016/j.ejphar.2015.02.047. PMID   25771456. S2CID   31929001.
  33. ↑ Picciotto MR, Higley MJ, Mineur YS (October 2012). "Acetylcholine as a neuromodulator: cholinergic signaling shapes nervous system function and behavior". Neuron. 76 (1): 116–29. doi:10.1016/j.neuron.2012.08.036. PMC   3466476 . PMID   23040810.
  34. ↑ Wonnacott S (February 1997). "Presynaptic nicotinic ACh receptors". Trends in Neurosciences. 20 (2): 92–8. doi:10.1016/S0166-2236(96)10073-4. PMID   9023878. S2CID   42215860.
  35. ↑ Graham A, Court JA, Martin-Ruiz CM, Jaros E, Perry R, Volsen SG, et al. (2002). "Immunohistochemical localization of nicotinic acetylcholine receptor subunits in human cerebellum". Neuroscience. 113 (3): 493–507. doi:10.1016/S0306-4522(02)00223-3. PMID   12150770. S2CID   39839166.
  36. ↑ Le Novère N, Changeux JP (February 1995). "Molecular evolution of the nicotinic acetylcholine receptor: an example of multigene family in excitable cells". Journal of Molecular Evolution. 40 (2): 155–72. Bibcode:1995JMolE..40..155L. doi:10.1007/BF00167110. PMID   7699721. S2CID   2040912.
  37. 1 2 3 4 5 Improgo MR, Scofield MD, Tapper AR, Gardner PD (October 2010). "The nicotinic acetylcholine receptor CHRNA5/A3/B4 gene cluster: dual role in nicotine addiction and lung cancer". Progress in Neurobiology. 92 (2): 212–26. doi:10.1016/j.pneurobio.2010.05.003. PMC   2939268 . PMID   20685379.
  38. ↑ Tammimäki A, Horton WJ, Stitzel JA (October 2011). "Recent advances in gene manipulation and nicotinic acetylcholine receptor biology". Biochemical Pharmacology. 82 (8): 808–19. doi:10.1016/j.bcp.2011.06.014. PMC   3162071 . PMID   21704022.
  39. ↑ Graham A, Court JA, Martin-Ruiz CM, Jaros E, Perry R, Volsen SG, et al. (September 2002). "Immunohistochemical localization of nicotinic acetylcholine receptor subunits in human cerebellum". Neuroscience. 113 (3): 493–507. doi:10.1016/S0306-4522(02)00223-3. PMID   12150770. S2CID   39839166.
  40. ↑ Changeux JP (June 2010). "Nicotine addiction and nicotinic receptors: lessons from genetically modified mice". Nature Reviews. Neuroscience. 11 (6): 389–401. doi:10.1038/nrn2849. PMID   20485364. S2CID   661315.
  41. ↑ Diabasana, Z; Perotin, JM; Belgacemi, R; Ancel, J; Mulette, P; Delepine, G; Gosset, P; Maskos, U; Polette, M; Deslée, G; Dormoy, V (2020). "Nicotinic Receptor Subunits Atlas in the Adult Human Lung". Int. J. Mol. Sci. 21 (20): 7446. doi: 10.3390/ijms21207446 . PMC   7588933 . PMID   33050277.
  42. 1 2 3 4 5 Greenbaum L, Lerer B (October 2009). "Differential contribution of genetic variation in multiple brain nicotinic cholinergic receptors to nicotine dependence: recent progress and emerging open questions". Molecular Psychiatry. 14 (10): 912–45. doi: 10.1038/mp.2009.59 . PMID   19564872.
  43. ↑ Gahring LC, Rogers SW (January 2006). "Neuronal nicotinic acetylcholine receptor expression and function on nonneuronal cells". The AAPS Journal. 7 (4): E885-94. doi:10.1208/aapsj070486. PMC   2750958 . PMID   16594641.
  44. 1 2 Kamens HM, Corley RP, Richmond PA, Darlington TM, Dowell R, Hopfer CJ, et al. (September 2016). "Evidence for Association Between Low Frequency Variants in CHRNA6/CHRNB3 and Antisocial Drug Dependence". Behavior Genetics. 46 (5): 693–704. doi:10.1007/s10519-016-9792-4. PMC   4975622 . PMID   27085880.
  45. ↑ Grady SR, Salminen O, Laverty DC, Whiteaker P, McIntosh JM, Collins AC, Marks MJ (October 2007). "The subtypes of nicotinic acetylcholine receptors on dopaminergic terminals of mouse striatum". Biochemical Pharmacology. 74 (8): 1235–46. doi:10.1016/j.bcp.2007.07.032. PMC   2735219 . PMID   17825262.
  46. 1 2 3 4 5 Steinlein OK, Bertrand D (November 2008). "Neuronal nicotinic acetylcholine receptors: from the genetic analysis to neurological diseases". Biochemical Pharmacology. 76 (10): 1175–83. doi:10.1016/j.bcp.2008.07.012. PMID   18691557.
  47. ↑ Bertrand D, Elmslie F, Hughes E, Trounce J, Sander T, Bertrand S, Steinlein OK (December 2005). "The CHRNB2 mutation I312M is associated with epilepsy and distinct memory deficits". Neurobiology of Disease. 20 (3): 799–804. doi:10.1016/j.nbd.2005.05.013. PMID   15964197. S2CID   29811931.
  48. ↑ Breese CR, Lee MJ, Adams CE, Sullivan B, Logel J, Gillen KM, et al. (October 2000). "Abnormal regulation of high affinity nicotinic receptors in subjects with schizophrenia". Neuropsychopharmacology. 23 (4): 351–64. doi: 10.1016/S0893-133X(00)00121-4 . PMID   10989262.
  49. ↑ McLean SL, Grayson B, Idris NF, Lesage AS, Pemberton DJ, Mackie C, Neill JC (April 2011). "Activation of α7 nicotinic receptors improves phencyclidine-induced deficits in cognitive tasks in rats: implications for therapy of cognitive dysfunction in schizophrenia". European Neuropsychopharmacology. 21 (4): 333–43. doi:10.1016/j.euroneuro.2010.06.003. hdl: 10454/8464 . PMID   20630711. S2CID   41306366.
  50. 1 2 3 4 Rang HP (2003). Pharmacology (5th ed.). Edinburgh: Churchill Livingstone. ISBN   978-0-443-07145-4.[ page needed ]
  51. 1 2 Neurosci.pharm - MBC 3320 Acetylcholine Archived 2007-12-27 at the Wayback Machine
  52. ↑ Sarter M (August 2015). "Behavioral-Cognitive Targets for Cholinergic Enhancement". Current Opinion in Behavioral Sciences. 4: 22–26. doi:10.1016/j.cobeha.2015.01.004. PMC   5466806 . PMID   28607947.
  53. ↑ Wu J, Gao M, Shen JX, Shi WX, Oster AM, Gutkin BS (October 2013). "Cortical control of VTA function and influence on nicotine reward". Biochemical Pharmacology. 86 (8): 1173–80. doi:10.1016/j.bcp.2013.07.013. PMID   23933294.
  54. ↑ "Nicotine: Biological activity". IUPHAR/BPS Guide to Pharmacology. International Union of Basic and Clinical Pharmacology. Retrieved 7 February 2016. Kis as follows; α2β4=9900nM [5], α3β2=14nM [1], α3β4=187nM [1], α4β2=1nM [4,6]. Due to the heterogeneity of nACh channels we have not tagged a primary drug target for nicotine, although the α4β2 is reported to be the predominant high affinity subtype in the brain which mediates nicotine addiction [2-3].
  55. ↑ Levin ED (May 2012). "α7-Nicotinic receptors and cognition". Current Drug Targets. 13 (5): 602–6. doi:10.2174/138945012800398937. PMID   22300026.
  56. ↑ Sadigh-Eteghad S, Mahmoudi J, Babri S, Talebi M (November 2015). "Effect of alpha-7 nicotinic acetylcholine receptor activation on beta-amyloid induced recognition memory impairment. Possible role of neurovascular function". Acta Cirurgica Brasileira. 30 (11): 736–42. doi: 10.1590/S0102-865020150110000003 . PMID   26647792.
  57. ↑ Wang J, Lu Z, Fu X, Zhang D, Yu L, Li N, et al. (May 2017). "Alpha-7 Nicotinic Receptor Signaling Pathway Participates in the Neurogenesis Induced by ChAT-Positive Neurons in the Subventricular Zone". Translational Stroke Research. 8 (5): 484–493. doi:10.1007/s12975-017-0541-7. PMC   5704989 . PMID   28551702.
  58. ↑ Lee J, Cooke JP (November 2012). "Nicotine and pathological angiogenesis". Life Sciences. 91 (21–22): 1058–64. doi:10.1016/j.lfs.2012.06.032. PMC   3695741 . PMID   22796717.
  59. ↑ Jain G, Jaimes EA (October 2013). "Nicotine signaling and progression of chronic kidney disease in smokers". Biochemical Pharmacology. 86 (8): 1215–23. doi:10.1016/j.bcp.2013.07.014. PMC   3838879 . PMID   23892062.
  60. ↑ Mihalak KB, Carroll FI, Luetje CW (September 2006). "Varenicline is a partial agonist at alpha4beta2 and a full agonist at alpha7 neuronal nicotinic receptors". Molecular Pharmacology. 70 (3): 801–5. doi:10.1124/mol.106.025130. PMID   16766716. S2CID   14562170.
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