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Carbamazepine has also been shown to potentiate GABA receptors made up of alpha1, beta2, gamma2 subunits.<ref>Granger, P. et al. Modulati

...eceptors in the absence of the GABA molecule, whereas benzodiazepines need GABA to be present to have an effect: this may explain the more widespread effec ...0.1038/sj.bjp.0705942 | pmc = 1575970}}</ref> Such findings implicate (non-GABA-ergic) ligand-gated ion channels, e.g. the neuronal nAChR channel, in media

...trations, but not &alpha;₁&beta;₂&gamma;₂ receptors.<ref name="Korpi95"/><ref name="Wafford96"/> During development, the &alpha

...or|5-HT₃ receptor]]s, and slightly potentiates [[GABAA receptor|GABA_A]] and [[glycine receptor]]s.<ref name="pmid11020766">{{cite jou ...ytic effect in mice in the elevated plus maze: mediation by benzodiazepine receptors|author = Emmanouil, D.E., Johnson, C.H. & Quock, R.M.|journal = Psychopharm

...smitter GABA by binding to the benzodiazepine site on the [[GABAA receptor|GABA_A receptor]] leading to [[central nervous system]] depression.<re ...ing-2006">{{Cite journal | last1 = Whiting | first1 = PJ. | title = GABA-A receptors: a viable target for novel anxiolytics? | journal = Curr Opin Pharmacol | v

.... [http://www.nature.com/bjp/journal/v143/n4/full/0705974a.html "Selective GABA-receptor actions of amobarbital on thalamic neurons."] ''British Journal of

...ally diverse class of mostly synthetic substances that bind to cannabinoid receptors. The latter group encompasses a variety of distinct chemical classes: the ' == Cannabinoid receptors ==

...tin''') is a pharmaceutical drug, specifically a [[gamma-Aminobutyric acid|GABA]] [[Analogue (chemistry)|analogue]]. It was originally developed for the tr ...inobutyric acid ('''GABA'''), but is not believed to act on the same brain receptors.

...5 |pmc=430630}}</ref> what Eric Simon (who independently discovered opioid receptors in the brain) later termed "endorphin" by an [[abbreviation]] of "endogenou ...gastric and vascular function as well as possibly panic and satiation, and receptors are often found at postsynaptic locations as well as presynaptically.

...ocannabinoid noladin ether acts as a full agonist at human CB2 cannabinoid receptors }}</ref> It shows agonistic behaviour on both receptors and is a partial agonist for the [[TRPV1]] channel.<ref name="pmid15148262"

...st. In addition, oleamide potentiates several serotonin receptors and the GABA(A) receptor, and inhibits gap junction communication.

...beta, gamma or delta subunits (some consist of 5 alpha subunits). Cys-loop receptors possess a characteristic loop formed by a disulfide bond between two [[cyst ...l | author = Albuquerque et al | title = Mammalian Nicotinic Acetylcholine Receptors: from Structure to Function | journal = Physiol Rev| issue = 89| pages = 73

...r case the receptors are typically 7-membrane spanning [[G-protein coupled receptors]] while in the latter case they are [[ligand-gated ion channels]]. The form Most other neurotransmitters, on the other hand, e.g. [[glutamate]], [[GABA]] and [[glycine]], are used very generally throughout the central nervous s

...the activity of K_Ca2.3 channels on the [[cell membrane]]. In [[GABA]]ergic [[POA neurons]], estrogen enhanced the ability of [[alpha-1 adrenerg

...journal |author=Vicini S |title=New perspectives in the functional role of GABA(A) channel heterogeneity |journal=Mol. Neurobiol. |volume=19 |issue=2 |page ...ided into 6 subfamilies based on homology: classical ([[TRPC]]), vanilloid receptors ([[TRPV]]), melastatin ([[TRPM]]), polycystins ([[TRPP]]), mucolipins ([[TR

.../sup>]], [[calcium|Ca²⁺]], or [[chloride|Cl^-]]. Such receptors located at [[synapse]]s convert the chemical signal of [[presynaptic]]ally ...= Structure and function of the glycine receptor and related nicotinicoid receptors | journal = J. Biol. Chem. | volume = 279 | issue = 19 | pages = 19383–6

...etomidate and propofol at beta3-containing gamma-aminobutyric acid type A receptors. ''Neuropharmacology''. 2009 Sep;57(4):446-55. PMID 19555700</ref>

...ich is associated with Cl⁻ [[ionophore]]s at GABA_A receptors.<ref>Katzung, Bertram G., Basic and Clinical Pharmacology, 10th ed., p. 406

...propofol analogues: mapping binding sites for an anesthetic phenol on the GABA(A) receptor. ''Journal of Medicinal Chemistry''. 2002 Jul 18;45(15):3210–

...[[Henri Laborit]] to use in studying the neurotransmitter [[GABA receptor|GABA]].<ref>{{cite journal | author = H. Laborit, J.M. Jouany, J. Gerald, F. Fab .../pjp/pdf/2004/1_43.pdf|format=PDF}}</ref> GHB is probably synthesized from GABA in GABAergic [[neurons]], and released when the neurons fire.<ref name="mec