Pharmacologic characterization of muscarinic receptors of insect brains
- 1 January 1991
- journal article
- research article
- Published by Wiley in Archives of Insect Biochemistry and Physiology
- Vol. 17 (2-3) , 107-118
- https://doi.org/10.1002/arch.940170205
Abstract
Muscarinic receptors in brain membranes from honey bees, houseflies, and the American cockroach were identified by their specific binding of the non‐selective muscarinic receptor antagonist [3H]quinuclidinyl benzilate ([3H]QNB) and the displacement of this binding by agonists as well as subtype‐selective antagonists, using filtration assays. The binding parameters, obtained from Scatchard analysis, indicated that insect muscarinic receptors, like those of mammalian brains, had high affinities for [3H]QNB (KD = 0.47 nM in honey bees, 0.17 nM in houseflies and 0.13 nM in the cockroach). However, the receptor concentration was low (108, 64.7, and 108 fmol/mg protein for the three species, respectively). The association and dissociation rates of [3H]QNB binding to honey bee brain membranes, sensitivity of [3H]QNB binding to muscarinic agonists, and high affinity for atropine were also features generally similar to muscarinic receptors of mammalian brains. In order to further characterize the three insect brain muscarinic receptors, the displacement of [3H]QNB binding by subtype‐selective antagonists was studied. The rank order of potency of pirenzepine (PZ), the M1 selective antagonist 11‐((2‐((dimethylamino)‐methyl)1‐ piperidinyl)acetyl)‐5, 11‐dihydro‐6H‐pyrido(2,3‐b)‐(1,4)‐benzodiazepin‐6 one (AF‐DX 116), the M2‐selective antagonist, and 4‐DAMP (4‐diphenylacetoxy‐N‐methylpiperidine methiodide) the M3‐selective antagonist, was also the same as that of mammalian brains, i.e., 4‐DAMP > PZ > AF‐DX 116. The three insect brain receptors had 27–50‐fold lower affinity for PZ (Ki 484–900 nM) than did the mammalian brain receptor (Ki 16 nM), but similar to that reported for the muscarinic receptor subtype cloned from Drosophila. Also, the affinity of insect receptors for 4‐DAMP (Ki 18.9–56.6 nM) was much lower than that of the M3 receptor, which predominates in rat submaxillary gland (Ki of 0.37 nM on [3H]QNB binding). These drug specificities of muscarinic receptors of brains from three insect species suggest that insect brains may be predominantly of a unique subtype that is close to, though significantly different from, the mammalian M3 subtype.Keywords
This publication has 25 references indexed in Scilit:
- Modulation of central muscarinic receptor binding in vitro by ultralow levels of the organophosphate paraoxonToxicology and Applied Pharmacology, 1989
- Cloning, sequence analysis and chromosome localization of a Drosophila muscarinic acetylcholine receptorFEBS Letters, 1989
- Direct actions of organophosphate anticholinesterases on nicotinic and muscarinic acetylcholine receptorsJournal of Biochemical Toxicology, 1988
- Binding profile of a novel cardioselective muscarine receptor antagonist, AF-DX 116, to membranes of peripheral tissues and brain in the ratLife Sciences, 1986
- Interactions of charatoxins and nereistoxin with the nicotinic acetylcholine receptors of insect cns and Torpedo electric organArchives of Insect Biochemistry and Physiology, 1986
- A practical computer-based approach to the analysis of radioligand binding experimentsComputer Programs in Biomedicine, 1983
- Properties of putative nicotinic and muscarinic cholinergic receptors in the central nervous system of Locusta migratoriaNeurochemistry International, 1981
- Quinuclidinyl Benzilate Binding in House Fly Heads and Rat BrainJournal of Neurochemistry, 1981
- Muscarinic cholinergic binding sites in an orthopteran central nervous systemJournal of Neurobiology, 1980
- Muscarinic receptor in Drosophila melanogaster demonstrated by binding of [3H]quinuclidinyl benzilateFEBS Letters, 1977