4.6 Article

The Caenorhabditis elegans DEG-3/DES-2 Channel Is a Betaine-Gated Receptor Insensitive to Monepantel

Journal

MOLECULES
Volume 27, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/molecules27010312

Keywords

nAChR; betaine; Caenorhabditis elegans; Xenopus laevis; DEG-3; DES-2; monepantel

Funding

  1. NIH Office of Research Infrastructure Programs [P40 OD010440]

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This study investigates the pharmacological characteristics of the DEG-3/DES-2 channel in C. elegans. The results show that the channel is more sensitive to betaine than ACh and choline, but less sensitive to monepantel and monepantel sulfone. These findings provide important insights into the function of the DEG-3/DES-2 channel in C. elegans.
Natural plant compounds, such as betaine, are described to have nematocidal properties. Betaine also acts as a neurotransmitter in the free-living model nematode Caenorhabditis elegans, where it is required for normal motility. Worm motility is mediated by nicotinic acetylcholine receptors (nAChRs), including subunits from the nematode-specific DEG-3 group. Not all types of nAChRs in this group are associated with motility, and one of these is the DEG-3/DES-2 channel from C. elegans, which is involved in nociception and possibly chemotaxis. Interestingly, the activity of DEG-3/DES-2 channel from the parasitic nematode of ruminants, Haemonchus contortus, is modulated by monepantel and its sulfone metabolite, which belong to the amino-acetonitrile derivative anthelmintic drug class. Here, our aim was to advance the pharmacological knowledge of the DEG-3/DES-2 channel from C. elegans by functionally expressing the DEG-3/DES-2 channel in Xenopus laevis oocytes and using two-electrode voltage-clamp electrophysiology. We found that the DEG-3/DES-2 channel was more sensitive to betaine than ACh and choline, but insensitive to monepantel and monepantel sulfone when used as direct agonists and as allosteric modulators in co-application with betaine. These findings provide important insight into the pharmacology of DEG-3/DES-2 from C. elegans and highlight the pharmacological differences between non-parasitic and parasitic nematode species.

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