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Toxicol Appl Pharmacol. 2017 Dec 1;336:55-65. doi: 10.1016/j.taap.2017.10.012. Epub 2017 Oct 18.

The anthelminthic drug praziquantel is a selective agonist of the sensory transient receptor potential melastatin type 8 channel.

Author information

1
Department of Anatomy, Physiology and Biophysics, Faculty of Biology, University of Bucharest, Romania; Department of Biophysics, Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.
2
Department of Anatomy, Physiology and Biophysics, Faculty of Biology, University of Bucharest, Romania.
3
Department of Anatomy, Physiology and Biophysics, Faculty of Biology, University of Bucharest, Romania. Electronic address: alex@biologie.kappa.ro.

Abstract

Praziquantel is the most effective anthelminthic drug for the treatment of schistosomiasis, an infectious disease caused by the platyhelminth Schistosoma mansoni. While praziquantel is known to trigger calcium influx into schisostomes, followed by spastic paralysis of the worms and tegumental disruption, the mechanism of action of the drug is not completely understood. Although relatively well tolerated, praziquantel has been reported to cause mild adverse effects, including nausea, abdominal pain and headaches. As a number of putative Transient Receptor Potential (TRP) channel genes have recently been predicted in S. mansoni, we sought to investigate the effect of praziquantel on three mammalian TRP channels, TRP melastatin type 8 (TRPM8), TRP vanilloid type 1 (TRPV1) and TRP ankyrin type 1 (TRPA1). Using calcium microfluorimetry and the patch clamp technique, we recorded the effect of praziquantel on HEK293T cells expressing recombinant TRPM8, TRPV1 or TRPA1, as well as on cultured dorsal root ganglion (DRG) neurons from wild type and TRPM8 null mutant mice. We discovered that praziquantel is a relatively potent and selective partial agonist of the mammalian and avian cold and menthol receptor TRPM8. The activation of cultured DRG neurons by clinically relevant concentrations of praziquantel is predominantly mediated by TRPM8. Our results may provide clues to a better understanding of praziquantel's mechanism of action and its adverse effects.

KEYWORDS:

Calcium imaging; Dorsal root ganglion; Praziquantel; Schisostoma mansoni; Transient Receptor Potential

PMID:
29054683
DOI:
10.1016/j.taap.2017.10.012
[Indexed for MEDLINE]

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