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Activation of host transient receptor potential (TRP) channels by praziquantel stereoisomers
by
Dosa, Peter I.
, Gunaratne, Gihan S.
, Yahya, Nawal A.
, Marchant, Jonathan S.
in
Activation
/ Animals
/ Anthelmintic agents
/ Anthelmintics - pharmacology
/ Antiparasitic agents
/ Arteries
/ Biology and Life Sciences
/ Blood vessels
/ Channels
/ Complications and side effects
/ Depolarization
/ Dosage and administration
/ Drug therapy
/ Eggs
/ Female
/ G protein-coupled receptors
/ HEK293 Cells
/ Humans
/ Medicine and Health Sciences
/ Mesenteric Arteries - drug effects
/ Mice
/ Molecular chains
/ Neurosciences
/ Paralysis
/ Parasites
/ Persistence
/ Pharmacology
/ Physical Sciences
/ Potassium
/ Praziquantel
/ Praziquantel - pharmacology
/ Proteins
/ Receptors
/ Research and Analysis Methods
/ Schistosoma mansoni
/ Schistosomiasis
/ Serotonin
/ Stereoisomerism
/ Stereoisomers
/ Tegument
/ Therapy
/ Tissue
/ Tissues
/ Transient receptor potential proteins
/ Tropical diseases
/ TRPM Cation Channels - drug effects
/ TRPM Cation Channels - metabolism
/ Vasoactive agents
/ Vasodilator Agents - pharmacology
/ Worms
2018
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Activation of host transient receptor potential (TRP) channels by praziquantel stereoisomers
by
Dosa, Peter I.
, Gunaratne, Gihan S.
, Yahya, Nawal A.
, Marchant, Jonathan S.
in
Activation
/ Animals
/ Anthelmintic agents
/ Anthelmintics - pharmacology
/ Antiparasitic agents
/ Arteries
/ Biology and Life Sciences
/ Blood vessels
/ Channels
/ Complications and side effects
/ Depolarization
/ Dosage and administration
/ Drug therapy
/ Eggs
/ Female
/ G protein-coupled receptors
/ HEK293 Cells
/ Humans
/ Medicine and Health Sciences
/ Mesenteric Arteries - drug effects
/ Mice
/ Molecular chains
/ Neurosciences
/ Paralysis
/ Parasites
/ Persistence
/ Pharmacology
/ Physical Sciences
/ Potassium
/ Praziquantel
/ Praziquantel - pharmacology
/ Proteins
/ Receptors
/ Research and Analysis Methods
/ Schistosoma mansoni
/ Schistosomiasis
/ Serotonin
/ Stereoisomerism
/ Stereoisomers
/ Tegument
/ Therapy
/ Tissue
/ Tissues
/ Transient receptor potential proteins
/ Tropical diseases
/ TRPM Cation Channels - drug effects
/ TRPM Cation Channels - metabolism
/ Vasoactive agents
/ Vasodilator Agents - pharmacology
/ Worms
2018
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Activation of host transient receptor potential (TRP) channels by praziquantel stereoisomers
by
Dosa, Peter I.
, Gunaratne, Gihan S.
, Yahya, Nawal A.
, Marchant, Jonathan S.
in
Activation
/ Animals
/ Anthelmintic agents
/ Anthelmintics - pharmacology
/ Antiparasitic agents
/ Arteries
/ Biology and Life Sciences
/ Blood vessels
/ Channels
/ Complications and side effects
/ Depolarization
/ Dosage and administration
/ Drug therapy
/ Eggs
/ Female
/ G protein-coupled receptors
/ HEK293 Cells
/ Humans
/ Medicine and Health Sciences
/ Mesenteric Arteries - drug effects
/ Mice
/ Molecular chains
/ Neurosciences
/ Paralysis
/ Parasites
/ Persistence
/ Pharmacology
/ Physical Sciences
/ Potassium
/ Praziquantel
/ Praziquantel - pharmacology
/ Proteins
/ Receptors
/ Research and Analysis Methods
/ Schistosoma mansoni
/ Schistosomiasis
/ Serotonin
/ Stereoisomerism
/ Stereoisomers
/ Tegument
/ Therapy
/ Tissue
/ Tissues
/ Transient receptor potential proteins
/ Tropical diseases
/ TRPM Cation Channels - drug effects
/ TRPM Cation Channels - metabolism
/ Vasoactive agents
/ Vasodilator Agents - pharmacology
/ Worms
2018
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Activation of host transient receptor potential (TRP) channels by praziquantel stereoisomers
Journal Article
Activation of host transient receptor potential (TRP) channels by praziquantel stereoisomers
2018
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Overview
The anthelmintic praziquantel (±PZQ) serves as a highly effective antischistosomal therapy. ±PZQ causes a rapid paralysis of adult schistosome worms and deleterious effects on the worm tegument. In addition to these activities against the parasite, ±PZQ also modulates host vascular tone in blood vessels where the adult worms reside. In resting mesenteric arteries ±PZQ causes a constriction of basal tone, an effect mediated by (R)-PZQ activation of endogenous serotoninergic G protein coupled receptors (GPCRs). Here, we demonstrate a novel vasodilatory action of ±PZQ in mesenteric vessels that are precontracted by high potassium-evoked depolarization, an effect previously reported to be associated with agonists of the transient receptor potential melastatin 8 channel (TRPM8). Pharmacological profiling a panel of 17 human TRPs demonstrated ±PZQ activity against a subset of human TRP channels. Several host TRP channels (hTRPA1, hTRPC3, hTRPC7) were activated by both (R)-PZQ and (S)-PZQ over a micromolar range whereas hTRPM8 showed stereoselective activation by (S)-PZQ. The relaxant effect of ±PZQ in mesenteric arteries was caused by (S)-PZQ, and mimicked by TRPM8 agonists. However, persistence of both (S)-PZQ and TRPM8 agonist evoked vessel relaxation in TRPM8 knockout tissue suggested that canonical TRPM8 does not mediate this (S)-PZQ effect. We conclude that (S)-PZQ is vasoactive over the micromolar range in mesenteric arteries although the molecular mediators of this effect remain to be identified. These data expand our knowledge of the polypharmacology and host vascular efficacy of this clinically important anthelmintic.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Animals
/ Anthelmintics - pharmacology
/ Arteries
/ Channels
/ Complications and side effects
/ Eggs
/ Female
/ Humans
/ Medicine and Health Sciences
/ Mesenteric Arteries - drug effects
/ Mice
/ Proteins
/ Research and Analysis Methods
/ Tegument
/ Therapy
/ Tissue
/ Tissues
/ Transient receptor potential proteins
/ TRPM Cation Channels - drug effects
/ TRPM Cation Channels - metabolism
/ Vasodilator Agents - pharmacology
/ Worms
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