Precoccinelline Explained
Precoccinelline is an alkaloid produced by the Coccinella septempunctata, also known as the seven-spot ladybird.[1] The alkaloid is released from the joints in C. septempunctata legs when it is provoked to deter predators such as ants or birds.[2] [3] It binds to both insect and mammalian nicotinic acetylcholine receptors, giving it use as an insecticide or as a therapy to treat drug dependence.[4] [5]
Biosynthesis
It was determined that precoccinelline is produced de novo in the C. septempunctata as their diet, which is composed of aphids, does not contain this alkaloid. While the exact biosynthesis has not been fleshed out, precoccinelline is thought to be of polyketide origin. The hypothesized biosynthesis involves condensation of six acetates and methyl addition.[6]
Chemical synthesis
2,6-lutidine (1) is used as starting material, and its treatment with β-bromo-propionaldehyde dimethyl acetal in ether produces a monolithium derivative. In the presence of 2,6-lutidine in excess, the monolithium derivative becomes an acetal (2). Treatment of the acetal with phenyl-lithium and then adding an ethereal solution of acetonitrile produces the crude ketone (3), followed by immediate transformation into the diacetal (4). Using sodium-isoamyl alcohol, the diacetal can be reduced to give the cis piperidine (5). The trans-isomer of the cis piperidine can be isolated and hydrolyzed using aqueous hydrochloric acid to yield the ketol (6). The ketol can then be cyclized with the use of acetic acid and pyrrolidine in refluxing tetrahydrofuran which gives a mixture of ketones. Separation of structure 7 from the mixture and then treatment with methyllithium in ether to produce a carbinol (8). Dehydrating the carbinol with thionyl chloride in methylene chloride gives olefin which can be hydrogenated to produce precoccinelline.[7]
Mechanism of action
Precoccinelline is an alkaloid which acts as an inhibitor of nicotinic acetylcholine receptors (nAChRs). It binds to an allosteric site on nAChRs― a site separate from the ACh recognition site. Of the secreted ladybird alkaloids, precoccinelline was the most potent inhibitor, acting via a non-competitive mechanism.[8]
Targeting nAChRs has several implications including developing insecticides and modulating drug dependence relating to the reward pathway in the brain.[9]
Notes and References
- Daloze . Désiré . Braekman . Jean-Claude . Pasteels . Jacques M. . Ladybird defence alkaloids: Structural, chemotaxonomic and biosynthetic aspects (Col.: Coccinellidae) . Chemoecology . September 1994 . 5-6 . 3-4 . 173–183 . 10.1007/BF01240602.
- Blount . Jonathan D. . Rowland . Hannah M. . Drijfhout . Falko P. . Endler . John A. . Inger . Richard . Sloggett . John J. . Hurst . Gregory D. D. . Hodgson . David J. . Speed . Michael P. . How the ladybird got its spots: effects of resource limitation on the honesty of aposematic signals: Warning signal honesty in a ladybird . Functional Ecology . April 2012 . 26 . 2 . 334–342 . 10.1111/j.1365-2435.2012.01961.x. 10536/DRO/DU:30047055 . free .
- Lee . Benjamin W . Ugine . Todd A . Losey . John E . An Assessment of the Physiological Costs of Autogenous Defenses in Native and Introduced Lady Beetles . Environmental Entomology . 11 August 2018 . 47 . 4 . 1030–1038 . 10.1093/ee/nvy068.
- Gepner . J. I. . Hall . L. M. . Sattelle . D. B. . Insect acetylcholine receptors as a site of insecticide action . Nature . November 1978 . 276 . 5684 . 188–190 . 10.1038/276188a0.
- Wu . Jie . Gao . Ming . Taylor . Devin H . Neuronal nicotinic acetylcholine receptors are important targets for alcohol reward and dependence . Acta Pharmacologica Sinica . March 2014 . 35 . 3 . 311–315 . 10.1038/aps.2013.181. 4647894 .
- Daloze . Désiré . Braekman . Jean-Claude . Pasteels . Jacques M. . Ladybird defence alkaloids: Structural, chemotaxonomic and biosynthetic aspects (Col.: Coccinellidae) . Chemoecology . September 1994 . 5-6 . 3-4 . 173–183 . 10.1007/BF01240602.
- Ayer . William A. . Furuichi . Kimiaki . The total synthesis of coccinelline and precoccinelline . Canadian Journal of Chemistry . 1 May 1976 . 54 . 9 . 1494–1495 . 10.1139/v76-216. free .
- Leong . Ron L. . Xing . Hong . Braekman . Jean-Claude . Kem . William R. . Non-competitive Inhibition of Nicotinic Acetylcholine Receptors by Ladybird Beetle Alkaloids . Neurochemical Research . October 2015 . 40 . 10 . 2078–2086 . 10.1007/s11064-014-1466-0.
- Gepner . J. I. . Hall . L. M. . Sattelle . D. B. . Insect acetylcholine receptors as a site of insecticide action . Nature . November 1978 . 276 . 5684 . 188–190 . 10.1038/276188a0.