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Functional characterization of three G protein-coupled acetylcholine receptors in parasitic nematode Trichinella spiralis. | LitMetric

Functional characterization of three G protein-coupled acetylcholine receptors in parasitic nematode Trichinella spiralis.

Int J Parasitol Drugs Drug Resist

Laboratoire de Santé Animale, UMR BIPAR, Ecole Nationale Vétérinaire d'Alfort, INRAE, ANSES, F-94700 Maisons-Alfort, France. Electronic address:

Published: December 2023

AI Article Synopsis

  • - The study identified three metabotropic acetylcholine receptors (TsGAR-1, -2, and -3) in the parasitic nematode Trichinella spiralis and explored their physiological roles and genetic relationships.
  • - TsGAR-1 and -2 are distinct from mammalian receptors, while TsGAR-3 is similar to mammalian-type receptors, and all three were found to trigger a G protein pathway when activated by acetylcholine.
  • - The unique pharmacological profiles of TsGAR-1 and -2, along with their evolutionary distance from mammalian counterparts, suggest they could be important targets for creating new drugs to combat nematode infections.

Article Abstract

The physiological significance of metabotropic acetylcholine receptors in parasitic nematodes remains largely unexplored. Here, three different Trichinella spiralis G protein-coupled acetylcholine receptors (TsGAR-1, -2, and -3) were identified in the genome of T. spiralis. The phylogenetic analyses showed that TsGAR-1 and -2 receptors belong to a distinct clade specific to invertebrates, while TsGAR-3 is closest to the cluster of mammalian-type muscarinic acetylcholine receptors (mAChR). The mRNA of TsGAR-1, -2, and -3 was detected in muscle larvae, newborn larvae, and adults. The functional aequorin-based assay in Chinese hamster ovary cells revealed that all three types of T. spiralis GARs trigger the G pathway upon activation of the receptor with the acetylcholine ligand. TsGAR-1 and TsGAR-2 showed atypical affinity with classical muscarinic agonists, while TsGAR-3 was sensitive to all muscarinic agonists tested. High concentrations of propiverine antagonist blocked the activities of all three TsGARs, while atropine and scopolamine antagonists effectively inhibited only TsGAR-3. Our data indicate that the distinct pharmacological profile of TsGAR-1 and -2 receptors, as well as the phylogenetic distance between them and their mammalian orthologs, place them as attractive targets for the development of selective anthelmintic drugs interfering with nematodes' cholinergic system.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10731000PMC
http://dx.doi.org/10.1016/j.ijpddr.2023.11.005DOI Listing

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