Action of Carvacrol on <i>Parascaris</i> sp. and Antagonistic Effect on Nicotinic Acetylcholine Receptors

<i>Parascaris</i> sp. is the only ascarid parasitic nematode in equids and one of the most threatening infectious organisms in horses. Only a limited number of compounds are available for treatment of horse helminthiasis, and <i>Parascaris</i> sp. worms have developed resista...

Full description

Saved in:
Bibliographic Details
Main Authors: Sasa M. Trailovic (Author), Milan Rajkovic (Author), Djordje S. Marjanovic (Author), Cédric Neveu (Author), Claude L. Charvet (Author)
Format: Book
Published: MDPI AG, 2021-05-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:<i>Parascaris</i> sp. is the only ascarid parasitic nematode in equids and one of the most threatening infectious organisms in horses. Only a limited number of compounds are available for treatment of horse helminthiasis, and <i>Parascaris</i> sp. worms have developed resistance to the three major anthelmintic families. In order to overcome the appearance of resistance, there is an urgent need for new therapeutic strategies. The active ingredients of herbal essential oils are potentially effective antiparasitic drugs. Carvacrol is one of the principal chemicals of essential oil from <i>Origanum</i>, <i>Thymus</i>, <i>Coridothymus</i>, <i>Thymbra</i>, <i>Satureja</i> and <i>Lippia</i> herbs. However, the antiparasitic mode of action of carvacrol is poorly understood. Here, the objective of the work was to characterize the activity of carvacrol on <i>Parascaris</i> sp. nicotinic acetylcholine receptor (nAChR) function both in vivo with the use of worm neuromuscular flap preparations and in vitro with two-electrode voltage-clamp electrophysiology on nAChRs expressed in <i>Xenopus</i> oocytes. We developed a neuromuscular contraction assay for <i>Parascaris</i> body flaps and obtained acetylcholine concentration-dependent contraction responses. Strikingly, we observed that 300 µM carvacrol fully and irreversibly abolished <i>Parascaris</i> sp. muscle contractions elicited by acetylcholine. Similarly, carvacrol antagonized acetylcholine-induced currents from both the nicotine-sensitive AChR and the morantel-sensitive AChR subtypes. Thus, we show for the first time that body muscle flap preparation is a tractable approach to investigating the pharmacology of <i>Parascaris</i> sp. neuromuscular system. Our results suggest an intriguing mode of action for carvacrol, being a potent antagonist of muscle nAChRs of <i>Parascaris</i> sp. worms, which may account for its antiparasitic potency.
Item Description:10.3390/ph14060505
1424-8247