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The anti-asthmatic drug pranlukast suppresses the delayed-phase vomiting and reverses intracellular indices of emesis evoked by cisplatin in the least shrew (Cryptotis parva).
- Source :
-
European journal of pharmacology [Eur J Pharmacol] 2017 Aug 15; Vol. 809, pp. 20-31. Date of Electronic Publication: 2017 May 10. - Publication Year :
- 2017
-
Abstract
- The introduction of second generation serotonin 5-HT <subscript>3</subscript> receptor (5-HT <subscript>3</subscript> ) antagonist palonosetron combined with long-acting substance P neurokinin NK <subscript>1</subscript> receptor (NK <subscript>1</subscript> ) antagonists (e.g. netupitant) has substantially improved antiemetic therapy against early- and delayed-phases of emesis caused by highly emetogenic chemotherapeutics such as cisplatin. However, the improved efficacy comes at a cost that many patients cannot afford. We introduce a new class of antiemetic, the antiasthmatic leukotriene CysLT1 receptor antagonist pranlukast for the suppression of cisplatin-evoked vomiting. Pranlukast (10mg/kg) by itself significantly reduced the mean frequency of vomits (70%) and fully protected least shrews from vomiting (46%) during the delayed-phase of cisplatin (10mg/kg)-evoked vomiting. Although, pranlukast tended to substantially reduce both the mean frequency of vomits and the number of shrews vomiting during the early-phase, these reductions failed to attain significance. When combined with a first (tropisetron)- or a second (palonosetron)-generation 5-HT <subscript>3</subscript> receptor antagonist, pranlukast potentiated their antiemetic efficacy during both phases of vomiting. In addition, pranlukast by itself prevented several intracellular signal markers of cisplatin-evoked delayed-vomiting such as phosphorylation of ERK1/2 and PKA. When pranlukast was combined with either palonosetron or tropisetron, these combinations suppressed the evoked phosphorylation of: i) ERK1/2 during both acute- and delayed-phase, ii) PKCα/β at the peak acute-phase, and iii) PKA at the peak delayed-phase. The current and our published findings suggest that overall behavioral and intracellular signaling effects of pranlukast via blockade of CysLT1 receptors generally appear to be similar to the NK <subscript>1</subscript> receptor antagonist netupitant with some differences.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Cyclic AMP-Dependent Protein Kinases metabolism
Drug Synergism
Female
Intracellular Space metabolism
Male
Mitogen-Activated Protein Kinase 1 metabolism
Mitogen-Activated Protein Kinase 3 metabolism
Phosphorylation drug effects
Protein Kinase C metabolism
Receptors, Serotonin metabolism
Serotonin Antagonists pharmacology
Shrews
Vomiting metabolism
Vomiting pathology
Anti-Asthmatic Agents pharmacology
Chromones pharmacology
Cisplatin adverse effects
Intracellular Space drug effects
Vomiting chemically induced
Vomiting prevention & control
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0712
- Volume :
- 809
- Database :
- MEDLINE
- Journal :
- European journal of pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 28501575
- Full Text :
- https://doi.org/10.1016/j.ejphar.2017.05.014