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BACKGROUND AND PURPOSE: Ionotropic GABA receptors are evolutionarily conserved proteins that mediate cellular and network inhibition in both vertebrates and invertebrates. A unique class of excitatory GABA receptors has been identified in several nematode species. Despite well-characterized functions in Caenorhabditis elegans, little is known about the pharmacology of the excitatory GABA receptors EXP-1 and LGC-35. Using a panel of compounds that differentially activate and modulate ionotropic GABA receptors, we investigated the agonist binding site and allosteric modulation of EXP-1 and LGC-35.
EXPERIMENTAL APPROACH: We used two-electrode voltage clamp recordings to characterize the pharmacological profile of EXP-1 and LGC-35 receptors expressed in Xenopus laevis oocytes.
KEY RESULTS: The pharmacology of EXP-1 and LGC-35 is different from that of GABAA and GABAA -ρ receptors. Both nematode receptors are resistant to the competitive orthosteric antagonist bicuculline and to classical ionotropic receptor pore blockers. The GABAA -ρ specific antagonist, TPMPA, was the only compound tested that potently inhibited EXP-1 and LGC-35. Neurosteroids have minimal effects on GABA-induced currents, but ethanol selectively potentiates LGC-35.
CONCLUSIONS AND IMPLICATIONS: The pharmacological properties of EXP-1 and LGC-35 more closely resemble the ionotropic GABAA -ρ family. However, EXP-1 and LGC-35 exhibit a unique profile that differs from vertebrate GABAA and GABAA -ρ receptors, insect GABA receptors and nematode GABA receptors. As a pair, EXP-1 and LGC-35 may be utilized to further understand the differential molecular mechanisms of agonist, antagonist and allosteric modulation at ionotropic GABA receptors and may aid in the design of new and more specific anthelmintics that target GABA neurotransmission.
Alexander,
The Concise Guide to PHARMACOLOGY 2015/16: Ligand-gated ion channels.
2015, Pubmed
Alexander,
The Concise Guide to PHARMACOLOGY 2015/16: Ligand-gated ion channels.
2015,
Pubmed
Bamber,
Pharmacological characterization of the homomeric and heteromeric UNC-49 GABA receptors in C. elegans.
2003,
Pubmed
,
Xenbase
Bamber,
The Caenorhabditis elegans unc-49 locus encodes multiple subunits of a heteromultimeric GABA receptor.
1999,
Pubmed
,
Xenbase
Beg,
EXP-1 is an excitatory GABA-gated cation channel.
2003,
Pubmed
,
Xenbase
Belelli,
Neurosteroids: endogenous regulators of the GABA(A) receptor.
2005,
Pubmed
Belelli,
The contraceptive agent Provera enhances GABA(A) receptor-mediated inhibitory neurotransmission in the rat hippocampus: evidence for endogenous neurosteroids?
2003,
Pubmed
Borghese,
Identification of an Inhibitory Alcohol Binding Site in GABAA ρ1 Receptors.
2016,
Pubmed
,
Xenbase
Bormann,
The 'ABC' of GABA receptors.
2000,
Pubmed
Chebib,
GABA-Activated ligand gated ion channels: medicinal chemistry and molecular biology.
2000,
Pubmed
Chen,
Cloning and functional expression of a Drosophila gamma-aminobutyric acid receptor.
1994,
Pubmed
,
Xenbase
Curtis,
Experimental design and analysis and their reporting: new guidance for publication in BJP.
2015,
Pubmed
Davies,
A central role of the BK potassium channel in behavioral responses to ethanol in C. elegans.
2003,
Pubmed
Hosie,
Agonist pharmacology of two Drosophila GABA receptor splice variants.
1996,
Pubmed
,
Xenbase
Hosie,
Endogenous neurosteroids regulate GABAA receptors through two discrete transmembrane sites.
2006,
Pubmed
Jobson,
Spillover transmission is mediated by the excitatory GABA receptor LGC-35 in C. elegans.
2015,
Pubmed
,
Xenbase
Johnston,
GABA(A) receptor channel pharmacology.
2005,
Pubmed
Johnston,
Muscimol as an ionotropic GABA receptor agonist.
2014,
Pubmed
Johnston,
Neurochemicals for the investigation of GABA(C) receptors.
2010,
Pubmed
Kaji,
A molecular characterization of the agonist binding site of a nematode cys-loop GABA receptor.
2015,
Pubmed
,
Xenbase
Kilkenny,
Animal research: reporting in vivo experiments: the ARRIVE guidelines.
2010,
Pubmed
Krogsgaard-Larsen,
Specific GABA(A) agonists and partial agonists.
2002,
Pubmed
Kusama,
Pharmacology of GABA rho 1 and GABA alpha/beta receptors expressed in Xenopus oocytes and COS cells.
1993,
Pubmed
,
Xenbase
Lambert,
Neurosteroid modulation of GABAA receptors.
2003,
Pubmed
Laskowski,
AQUA and PROCHECK-NMR: programs for checking the quality of protein structures solved by NMR.
1996,
Pubmed
Lobo,
GABA(A) receptors and alcohol.
2008,
Pubmed
Majewska,
Steroid hormone metabolites are barbiturate-like modulators of the GABA receptor.
1986,
Pubmed
Martí-Renom,
Comparative protein structure modeling of genes and genomes.
2000,
Pubmed
McGrath,
Implementing guidelines on reporting research using animals (ARRIVE etc.): new requirements for publication in BJP.
2015,
Pubmed
Michels,
GABAA receptors: properties and trafficking.
2007,
Pubmed
Mihic,
Sites of alcohol and volatile anaesthetic action on GABA(A) and glycine receptors.
1997,
Pubmed
,
Xenbase
Miller,
Crystal structure of a human GABAA receptor.
2014,
Pubmed
Morris,
Differential modulation of the gamma-aminobutyric acid type C receptor by neuroactive steroids.
1999,
Pubmed
,
Xenbase
Nicholl,
Pharmacological characterization of the excitatory 'Cys-loop' GABA receptor family in Caenorhabditis elegans.
2017,
Pubmed
,
Xenbase
Siddiqui,
An UNC-49 GABA receptor subunit from the parasitic nematode Haemonchus contortus is associated with enhanced GABA sensitivity in nematode heteromeric channels.
2010,
Pubmed
,
Xenbase
Sigel,
Structure, function, and modulation of GABA(A) receptors.
2012,
Pubmed
Southan,
The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands.
2016,
Pubmed
Stell,
Neuroactive steroids reduce neuronal excitability by selectively enhancing tonic inhibition mediated by delta subunit-containing GABAA receptors.
2003,
Pubmed
Thompson,
The structural basis of function in Cys-loop receptors.
2010,
Pubmed
Trott,
AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading.
2010,
Pubmed
Ueno,
Subunit mutations affect ethanol actions on GABA(A) receptors expressed in Xenopus oocytes.
1999,
Pubmed
,
Xenbase
Woodward,
Characterization of bicuculline/baclofen-insensitive (rho-like) gamma-aminobutyric acid receptors expressed in Xenopus oocytes. II. Pharmacology of gamma-aminobutyric acidA and gamma-aminobutyric acidB receptor agonists and antagonists.
1993,
Pubmed
,
Xenbase
Zhu,
Neurosteroid prolongs GABAA channel deactivation by altering kinetics of desensitized states.
1997,
Pubmed